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Submission ID | Confirmed | Registered | Date | Stream | International Chair | Turkish Chair | presentingauthor | presentingauthoremail | Title | eposterdate | posterstream | contactauthor | contactauthoremail | |||||
675 | No | No | Esra Özpınar | dr.esraozpinar@gmail.com | An overview of drug-resistant epilepsies based on advances in genetics: a cohort study | Betül Kılıç | betulklc82@gmail.com | |||||||||||
607 | Yes | No | Achmad Rafli | achmad.rafli@gmail.com | "Subacute Sclerosing Panencephalitis in Children: A Case Series in Dr. Cipto Mangunkusumo Tertiary General Hospital | Jakarta | Indonesia" | Achmad Rafli | achmad.rafli@gmail.com | |||||||||
635 | Yes | No | 4th Oct 2022 | Epilepsy: Treatment 3 – ASM/ Dietary Treatments | J Sahu | Achmad Rafli | achmad.rafli@gmail.com | Modified Atkins Diet for the Treatment of Refractory Epilepsy in Children: A Pilot Study from Indonesia | Achmad Rafli | achmad.rafli@gmail.com | ||||||||
681 | Yes | No | 4th Oct 2022 | Epilepsy: Genetics 3 | L Lagae | Asli Kübra Atasever | akubrat@gmail.com | Novel ANKRD11 gene mutation in an individual with a phenotype of KBG syndrome presenting like West syndrome | Asli Kübra Atasever | akubrat@gmail.com | ||||||||
375 | Yes | No | 6th Oct 2022 | Education | "Jorge Vidaurre | US" | Alexandra Santana Almansa | alexandra.santanaalmansa@childrens.harvard.edu | Construction of an introductory curriculum for new child neurology and neurodevelopmental disabilities trainees | Alexandra Santana Almansa | alexandra.santanaalmansa@childrens.harvard.edu | |||||||
324 | Yes | No | 6th Oct 2022 | "Metabolic 5 Neurodegenerative diseases (NBIAs | metabolic causes of stroke | CDG | NCLs | NKH" | Suvasini Sharma India | Ami Shah | ami.en1neuro@gmail.com | Fatty Acid Hydroxylase associated Neurodegeneration (FAHN) – A case report from India highlighting its heterogenous nature. | Ami Shah | ami.en1neuro@gmail.com | ||||
463 | Yes | No | 6th Oct 2022 | Metabolic 3 Mitochondrial disorders II: Etiologies and mechanisms | Saskia Wortmann Netherlands | Ami Shah | ami.en1neuro@gmail.com | Thiamine Pyrophosphokinase Deficiency in Indian origin Siblings - Expanding the phenotype | Ami Shah | ami.en1neuro@gmail.com | ||||||||
290 | Yes | No | 5th Oct 2022 | Spasticity and ataxia | C Catsman | Amita Moirangthem | amis.72000@gmail.com | Neurodegeneration with brain iron accumulation in 18 Indian families: a case series highlighting phenotypic and genotypic diversity | Amita Moirangthem | amis.72000@gmail.com | ||||||||
666 | Yes | No | 4th Oct 2022 | Epilepsy: Status epilepticus and Miscellaneous | T Loddenkemper | Amna Al Futaisi | amnaf@squ.edu.om | Childhood status epilepticus in children of 1-12 years of age SQUH: demographics and outcome of treatment | Amna Al Futaisi | amnaf@squ.edu.om | ||||||||
372 | Yes | No | Andrew Hey | andrew.hey@louisville.edu | Reactivation of HSV-1 Encephalitis in an Infant Within One-Month of Completing Acyclovir Treatment: A Case Study | Andrew Hey | andrew.hey@louisville.edu | |||||||||||
231 | Yes | No | 4th Oct 2022 | Epilepsy: Genetics 2 | N Specchio | Ana Carolina Coan | anghelescu.cristina@gmail.com | Clinical predictors of positive genetic investigation of the developmental and epileptic encephalopathies | Maria Benevides | benevidesmarialuiza@gmail.com | ||||||||
447 | Yes | No | 6th Oct 2022 | Neuroradiology 2 | "Kshitij Mankand | UK" | Anish Ainapure | anish.ainapure1@gmail.com | Basal ganglia germinoma in an adolescent: A case report | Anish Ainapure | anish.ainapure1@gmail.com | |||||||
451 | Yes | No | 6th Oct 2022 | Metabolic 2 Mitochondrial disorders I : clinical phenotypes and tx | "Rita Horvath | UK" | Anish Ainapure | anish.ainapure1@gmail.com | Progressive Mitochondrial Leukoencephalopathy in a one and half year-old boy: A Case Report | Anish Ainapure | anish.ainapure1@gmail.com | |||||||
454 | Yes | No | 6th Oct 2022 | "Movement 3 Ataxias | opsoclonus myoclonus and covid 19 impact" | "Russell Dale | Australia" | Anish Ainapure | anish.ainapure1@gmail.com | Autosomal recessive spastic ataxia of Charlevoix–Saguenay : Two case reports | Anish Ainapure | anish.ainapure1@gmail.com | ||||||
441 | Yes | No | 6th Oct 2022 | "Movement 2 Dystonia | Parkinsons | tremor and epidemiology" | "Jon Mink | US" | Ayşe Nur Coşkun | anurcoskun@gmail.com | A Case of Childhood Onset Dystonia Due to KMT2B Gene Mutation | Ayşe Nur Coşkun | anurcoskun@gmail.com | |||||
461 | Yes | No | Areeba Wasim | areeba.wasim2@gmail.com | "VARIATIONS IN CLINICAL PRESENTATION | NEUROIMAGING AND ELECTROENCEPHALOGRAPHIC PATTERNS OF SUBACUTE SCLEROSING PANENCEPHALITIS" | Areeba Wasim | areeba.wasim2@gmail.com | ||||||||||
298 | Yes | No | 6th Oct 2022 | "Metabolic 5 Neurodegenerative diseases (NBIAs | metabolic causes of stroke | CDG | NCLs | NKH" | Suvasini Sharma India | Ayşe Aksoy | aysechild@gmail.com | A Mutation in Neurodegeneration with Brain Iron Accumulation – Two Brothers | Seren Aydin | serenaydin5228@gmail.com | ||||
550 | Yes | No | 4th Oct 2022 | Epilepsy: Investigations | P Madaan | Aysen Gok | aysenngok@gmail.com | Cases with Seizures During Routine Video Electroencephalography: Clinical and Electroencephalographic Characteristics | Aysen Gok | aysenngok@gmail.com | ||||||||
711 | Yes | No | 6th Oct 2022 | Metabolic 6 Defects of bioenergetic and intermediary metab | Ingrid Tein Canada | Sachendra Badal | badalsachendra@yahoo.com | Chylous blood in an infant with febrile encephalopathy: Clues to metabolic etiology (Very Long Chain Acyl CoA Dehydrogenase Deficiency) | Sachendra Badal | badalsachendra@yahoo.com | ||||||||
717 | Yes | No | 6th Oct 2022 | Neuroradiology 2 | "Kshitij Mankand | UK" | Sachendra Badal | badalsachendra@yahoo.com | Intracranial haemorrhage in two infant siblings: hereditary or acquired? | Sachendra Badal | badalsachendra@yahoo.com | |||||||
721 | Yes | No | 6th Oct 2022 | Neuroradiology 3 | "Ajay Taranath | Australia" | Sachendra Badal | badalsachendra@yahoo.com | Paroxysmal sympathetic hyperactivity in a child with High Grade Glioma post resection surgery. | Sachendra Badal | badalsachendra@yahoo.com | |||||||
401 | Yes | No | 5th Oct 2022 | General II | M Sönmez | Bushra Alattas | balattas@seha.ae | Diagnostic yield of Whole Exome and Whole Genome Sequencing in pediatric neurological disorders. A UAE Tertiary hospital experience | Bushra Alattas | balattas@seha.ae | ||||||||
308 | Yes | No | 4th Oct 2022 | "Epilepsy: Neuroimaging | Surgery and Basic Science" | C Akman | Bilal Berke Ayvaz | bilalberke.ayvaz@ogr.iuc.edu.tr | Comparison of 3D Printing Techniques with Patient-Specific Models for Epilepsy Surgery | Bilal Berke Ayvaz | bilalberke.ayvaz@ogr.iuc.edu.tr | |||||||
388 | Yes | No | 6th Oct 2022 | Metabolic 2 Mitochondrial disorders I : clinical phenotypes and tx | "Rita Horvath | UK" | Dan Sun | bloveriver@163.com | Efficacy and Safety of the Ketogenic Diet for Mitochondrial Disease with Epilepsy: A Prospective Controlled Study | Dan Sun | bloveriver@163.com | |||||||
210 | Yes | No | 5th Oct 2022 | General I | J Vajsar | Bita Poorshiri | bpskam@yahoo.com | The Co-existence of Phenylketonuria and Myasthenia Gravis: A CaseReport | Bita Poorshiri | bpskam@yahoo.com | ||||||||
724 | Yes | No | 6th Oct 2022 | Neuroradiology 2 | "Kshitij Mankand | UK" | Burçin Şanlıdağ | burcinsanlidag@yahoo.com | Intracranial cysts in pediatric age group: Incidental or developmental? | Burçin Şanlıdağ | burcinsanlidag@yahoo.com | |||||||
292 | Yes | No | 6th Oct 2022 | Metabolic 1 Clinical phenotypes | "Brahim Tabarki | KSA" | Cemile Busra Olculu | busra.olculu@ege.edu.tr | A Rare Cause of Developmental Epileptic Encephalopathy: D-Bifunctional Protein Deficiency with a Novel Pathogenic Variant | Cemile Busra Olculu | busra.olculu@ege.edu.tr | |||||||
625 | Yes | No | 6th Oct 2022 | Headache 1 | "Ken Mack | US" | Cemile Busra Olculu | busra.olculu@ege.edu.tr | Pseudotumor cerebri in childhood: a new vision to clinical spectrum and predictors for visual outcome | Cemile Busra Olculu | busra.olculu@ege.edu.tr | |||||||
181 | Yes | No | 6th Oct 2022 | Headache 1 | "Ken Mack | US" | Çağatay Günay | cagataygunaymd@gmail.com | Recurrent Painful Ophthalmoplegic Neuropathy: Report of the Two New Pediatric Cases | Çağatay Günay | cagataygunaymd@gmail.com | |||||||
182 | Yes | No | 4th Oct 2022 | "Epilepsy: Syndromes 1 – Self-limited | EE/DEE-SWAS" | C Joshi | Çağatay Günay | cagataygunaymd@gmail.com | The fate of spikes in self-limited epilepsy with centrotemporal spikes: Are clinical and baseline EEG features effective? | Çağatay Günay | cagataygunaymd@gmail.com | |||||||
548 | Yes | No | 6th Oct 2022 | CNS Infections 1 Covid-related | "Charles Newton | Kenya" | Çiğdem Genç Sel | cigdemsel@yahoo.com | A Rare Neurological Manifestation of Coronavirus Disease 2019 (COVID-19) in a Single Reference Center: Ramsay Hunt Syndrome | Çiğdem Genç Sel | cigdemsel@yahoo.com | |||||||
673 | Yes | No | 6th Oct 2022 | "Movement 3 Ataxias | opsoclonus myoclonus and covid 19 impact" | "Russell Dale | Australia" | Çi̇si̇l Çerçi̇ Kubur | cisilcerci@gmail.com | A study in a Turkish family with ataxia and points to MTCL1 as a candidate gene for autosomal dominant cerebellar ataxia | Çi̇si̇l Çerçi̇ Kubur | cisilcerci@gmail.com | ||||||
376 | Yes | No | 5th Oct 2022 | "CNS Malformations | NGS" | A Narayan | Chew Thye Choong | ctfan88@gmail.com | Filamin A associated periventricular nodular heterotopia presenting with mutism | Chew Thye Choong | ctfan88@gmail.com | |||||||
527 | Yes | No | 5th Oct 2022 | General I | J Vajsar | Duygu Aykol | d_aykol@hotmail.com | "Electromyography in Pediatric Population | A Single Center Experience" | Duygu Aykol | d_aykol@hotmail.com | |||||||
248 | Yes | No | 4th Oct 2022 | Epilepsy: Semiology and Clinical | H Cross | Deniz Menderes | denizkrgn@gmail.com | Hand Postures and Localization Value in Patients at Video EEG Monitorization | Deniz Menderes | denizkrgn@gmail.com | ||||||||
304 | Yes | No | 6th Oct 2022 | Headache/Stroke 2 | "Mahendra Moharir | Canada" | Dhanalakshmi Angappan | Dhanalakshmivj@gmail.com | "Stroke secondary to thoracic outlet syndrome | treated successfully with thrombolytics and thrombectomy in a teenager: a case report" | Dhanalakshmi Angappan | Dhanalakshmivj@gmail.com | ||||||
663 | Yes | No | 6th Oct 2022 | Headache/Stroke 3 | "Mubeen Rafay | Canada" | Sarolta Dobner | dobnersara@gmail.com | A retrospective study of central nervous system vasculitis patients | Zoltán Liptai | zliptai@gmail.com | |||||||
466 | Yes | No | 4th Oct 2022 | Epilepsy: Outcomes and Epidemiology | E Kija | Nicholas Odero | docodero@gmail.com | Risk Factors for Seizure Recurrence After Initial Withdrawal of Anti-Seizure Medication in Childhood Epilepsy | Nicholas Odero | docodero@gmail.com | ||||||||
339 | Yes | No | 4th Oct 2022 | Epilepsy: Treatment 2 – ASMs | Ramachandran Nair | Mahmut Aslan | dr_mahmut_21@hotmail.com | Effectiveness of zonisamide in childhood refractory epilepsy | Mahmut Aslan | dr_mahmut_21@hotmail.com | ||||||||
475 | Yes | No | 4th Oct 2022 | "Epilepsy: Syndromes 1 – Self-limited | EE/DEE-SWAS" | C Joshi | Sibel Oz Yildiz | dr_sibeloz@hotmail.com | Electrical status epilepticus during sleep: A study of 67 patients | Sibel Oz Yildiz | dr_sibeloz@hotmail.com | |||||||
720 | Yes | No | 5th Oct 2022 | Molecular genetics | T Sultan | Ayten Güleç | dr.aytengulec@gmail.com | "National Based | Retrospective Study on the Evaluation of Clinical | Laboratory | and Imaging Research of Angelman Syndrome- Turkey's Multicenter Study" | Ayten Güleç | dr.aytengulec@gmail.com | |||||
296 | Yes | No | 4th Oct 2022 | Epilepsy: Treatment 1 – ASMs | B Sanchez-Gan | Ebru Arhan | dr.elif.ksglyldrm@gmail.com | Reversible Leigh’s-like brain abnormalities with Vigabatrin: A Case Series | Ramesh Konanki | rameshkonanki@gmail.com | ||||||||
632 | Yes | No | 4th Oct 2022 | Epilepsy: Treatment 3 – ASM/ Dietary Treatments | J Sahu | Esra Özpınar | dr.esraozpinar@gmail.com | Ketogenic diet treatment success in our two patients with epilepsy of infancy with migrating focal seizures | Betül Kılıç | betulklc82@gmail.com | ||||||||
672 | Yes | No | 4th Oct 2022 | Epilepsy: Genetics 3 | L Lagae | Esra Özpınar | dr.esraozpinar@gmail.com | "Epileptic encephalopathy | visual impairment and developmental retardation: CDKL5 deficiency disorder" | Betül Kılıç | betulklc82@gmail.com | |||||||
278 | Yes | No | 6th Oct 2022 | Headache/Stroke 2 | "Mahendra Moharir | Canada" | Gülnur Esenülkü | dr.gesenulku@gmail.com | Unilateral internal carotid artery and middle cerebral artery thrombosis in a pediatric patient with mildly symptomatic COVID-19: Case report and literature review | Gülnur Esenülkü | dr.gesenulku@gmail.com | |||||||
718 | Yes | No | 6th Oct 2022 | Headache/Stroke 3 | "Mubeen Rafay | Canada" | Gülnur Esenülkü | dr.gesenulku@gmail.com | Does the presence of Friedman criteria always spesific for pseudotumor cerebri? | Gülnur Esenülkü | dr.gesenulku@gmail.com | |||||||
316 | Yes | No | 4th Oct 2022 | "Epilepsy: Neuroimaging | Surgery and Basic Science" | C Akman | Hilal Altas | dr.hilalaltas@gmail.com | Is There a Relation Between Hippocampal Measurements and Childhood Idiopathic Generalized Epilepsy? | Hilal Altas | dr.hilalaltas@gmail.com | |||||||
457 | Yes | No | 4th Oct 2022 | Epilepsy: Genetics 3 | L Lagae | Merve Hilal Dolu | dr.mervehilal@hotmail.com | A Rare Cause of Developmental Epileptic Encephalopathy; UBA5 Gene Mutation | Merve Hilal Dolu | dr.mervehilal@hotmail.com | ||||||||
269 | Yes | No | 6th Oct 2022 | Headache 1 | "Ken Mack | US" | Müge Baykan | dr.mugebaykan@gmail.com | ASSESSMENT OF CHILDHOOD HEADACHES: A SINGLE CENTER EXPERIENCE | Müge Baykan | dr.mugebaykan@gmail.com | |||||||
453 | Yes | No | 5th Oct 2022 | Molecular genetics | T Sultan | Müge Baykan | dr.mugebaykan@gmail.com | Duplication 9 p Syndrome; Case Report | Müge Baykan | dr.mugebaykan@gmail.com | ||||||||
567 | Yes | No | 6th Oct 2022 | Headache/Stroke 2 | "Mahendra Moharir | Canada" | Payal Shah | dr.payalshah@gmail.com | POSTERIOR CIRCULATION ARTERIAL ISCHEMIC STROKE IN CHILDREN | Payal Shah | dr.payalshah@gmail.com | |||||||
593 | Yes | No | 6th Oct 2022 | Metabolic 6 Defects of bioenergetic and intermediary metab | Ingrid Tein Canada | Ami Shah | drami.rajesh.shah@gmail.com | Fuel for Thought – Case series of Beta-Ketothiolase patients presenting with metabolic encephalopathy | Ami Shah | drami.rajesh.shah@gmail.com | ||||||||
332 | Yes | No | 4th Oct 2022 | Epilepsy: Genetics 3 | L Lagae | Canan Üstün | drcananustun@hotmail.com | Two Cases of ACTL6B Mutation-Associated Epileptic Encephalopathy | Canan Üstün | drcananustun@hotmail.com | ||||||||
338 | Yes | No | 4th Oct 2022 | Epilepsy: Genetics 2 | N Specchio | Canan Üstün | drcananustun@hotmail.com | CDKL5 Mutation-Associated Epileptic Encephalopathy Case | Canan Üstün | drcananustun@hotmail.com | ||||||||
342 | Yes | No | 4th Oct 2022 | Epilepsy: Genetics 2 | N Specchio | Canan Üstün | drcananustun@hotmail.com | A Case of Dup15q Syndrome Presenting with WEST Syndrome | Canan Üstün | drcananustun@hotmail.com | ||||||||
216 | Yes | No | 4th Oct 2022 | Epilepsy: Genetics 2 | N Specchio | Emine Tekin | dreminetekin@yahoo.com | "A case with developmental delay | resistant epilepsy and invuluntary movements diagnosed as SCN8A mutation" | Emine Tekin | dreminetekin@yahoo.com | |||||||
230 | Yes | No | 5th Oct 2022 | Genetics and epilepsy I | W Hakami | Gül Yücel | drgulyucel@hotmail.com | Novel Mutations in AP3B2 Gene Cause an Early Onset Developmental and Epileptic Encephalopathy: A Rare Clinical Entity | Gül Yücel | drgulyucel@hotmail.com | ||||||||
355 | Yes | No | 4th Oct 2022 | Epilepsy: Treatment 2 – ASMs | Ramachandran Nair | Hilal Aydin | drhilalaydin@gmail.com | The Effect Of Levetiracetam Therapy On Electrocardiography Parameters | Hilal Aydin | drhilalaydin@gmail.com | ||||||||
303 | Yes | No | 4th Oct 2022 | "Epilepsy: Syndromes 2 – IESS | Dravet | HHE | EMAS" | E Wirrell | Mahesh Kamate | drmaheshkamate@gmail.com | Idiopathic Hemiconvulsion Hemiplegia Epilepsy (IHHE) in an 8 yr old boy | Mahesh Kamate | drmaheshkamate@gmail.com | |||||
505 | Yes | No | 6th Oct 2022 | "Metabolic 5 Neurodegenerative diseases (NBIAs | metabolic causes of stroke | CDG | NCLs | NKH" | Suvasini Sharma India | Mahesh Kamate | drmaheshkamate@gmail.com | Atypical presentation of PLAN-associated NBIA | Mahesh Kamate | drmaheshkamate@gmail.com | ||||
207 | Yes | No | 5th Oct 2022 | Genetics and epilepsy I | W Hakami | Özlem Özsoy | drozlemozsoypediatri@gmail.com | "CASE REPORT: DOCK7 MUTATION AS A RARE CAUSE OF EPILEPTIC ENCEPHALOPATHY WITH CORTICAL BLINDNESS | DYSMORPHIC FINDINGS" | Özlem Özsoy | drozlemozsoypediatri@gmail.com | |||||||
735 | Yes | No | 4th Oct 2022 | Epilepsy: Treatment 1 – ASMs | B Sanchez-Gan | Pinar Ozkan Kart | drpinar_ozkan@yahoo.com | Evaluation of Efficacy and Tolerability of Lacosamide in Children with Drug-Resistant Epilepsy: A Multicenter Cohort Study | Pinar Ozkan Kart | drpinar_ozkan@yahoo.com | ||||||||
744 | Yes | No | 4th Oct 2022 | "Epilepsy: Syndromes 2 – IESS | Dravet | HHE | EMAS" | E Wirrell | Pi̇nar Ozkan Kart | drpinar_ozkan@yahoo.com | The Role of Genetic Factors in Electroclinic and Therapeutic Effectiveness in Children with Dravet Syndrome: A Multi-Center Cohort Study | Pi̇nar Ozkan Kart | drpinar_ozkan@yahoo.com | |||||
743 | Yes | No | 4th Oct 2022 | Epilepsy: Status epilepticus and Miscellaneous | T Loddenkemper | Ramya Bandi | drramyabandi@gmail.com | "Clinical spectrum | treatment response and outcomes in children with Febrile Infection Related Epilepsy Syndrome (FIRES) : A case series from India" | Ramesh Konanki | rameshkonanki@gmail.com | |||||||
487 | Yes | No | 6th Oct 2022 | CNS Infections 1 Covid-related | "Charles Newton | Kenya" | Rekha Mittal | drrekhamittal2008@gmail.com | Profile of Neurological manifestations of Covid 19 in a Pediatric hospital in Delhi | Rekha Mittal | drrekhamittal2008@gmail.com | |||||||
682 | Yes | No | 5th Oct 2022 | General I | J Vajsar | Yavuz Sayar | drsayar3@hotmail.com | A case of TUBGCP2-associated tubulinopathy with a novel missense variant | Miraç Yıldırım | miracyildirim81@hotmail.com | ||||||||
685 | Yes | No | Yavuz Sayar | drsayar3@hotmail.com | A case of posttransplant acute limbic encephalitis associated with human herpesvirus-6 | Miraç Yıldırım | miracyildirim81@hotmail.com | |||||||||||
740 | Yes | No | 6th Oct 2022 | CNS Infections 1 Covid-related | "Charles Newton | Kenya" | Yavuz Sayar | drsayar3@hotmail.com | A case of acute ophthalmoplegia presenting after multisystem inflammatory syndrome in children (MIS-C) | Miraç Yıldırım | miracyildirim81@hotmail.com | |||||||
739 | Yes | No | 4th Oct 2022 | "Epilepsy: DEEs | TSC | RETT and Comorbidities" | Y Jiang | Seda Kanmaz | drsedakanmaz@gmail.com | Developmental Epileptic Encephalopathies in A National Cohort Study (Turkish EPISTEP -1): A Step-based Approachment for Etiologic Diagnosis | Seda Kanmaz | drsedakanmaz@gmail.com | ||||||
384 | Yes | No | 6th Oct 2022 | "Movement 2 Dystonia | Parkinsons | tremor and epidemiology" | "Jon Mink | US" | Serdar Saritas | drserdarsaritas@gmail.com | A case of dopa responsive dystonia due to compound heterozygous TH gene mutation in a Turkish Girl. | Serdar Saritas | drserdarsaritas@gmail.com | |||||
726 | Yes | No | 5th Oct 2022 | Spasticity and ataxia | C Catsman | Süleyman Şahin | drsulimen2003@hotmail.com | Rare dual diagnoses in an infant: Aicardi-Goutieres and Moyamoya Syndromes | Süleyman Şahin | drsulimen2003@hotmail.com | ||||||||
665 | Yes | No | 4th Oct 2022 | "Epilepsy: Syndromes 1 – Self-limited | EE/DEE-SWAS" | C Joshi | Emine Tekin | emine.tekin@giresun.edu.tr | Research of autoimmunity clues in electrical status epilepticus (ESES) during sleep | Turgay Cokyaman | drturgay@comu.edu.tr | |||||||
591 | Yes | No | 6th Oct 2022 | "Metabolic 5 Neurodegenerative diseases (NBIAs | metabolic causes of stroke | CDG | NCLs | NKH" | Suvasini Sharma India | Fatema Al Amrani | fatemaamrani@gmail.com | Autosomal recessive NOTCH3-related leukodystrophy in two siblings and review of the literature | Fatema Al Amrani | fatemaamrani@gmail.com | ||||
277 | Yes | No | 6th Oct 2022 | Headache 1 | "Ken Mack | US" | Fatih Mehmet Akif Özdemi̇r | fatihmehmetakif@hotmail.com | "EVALUATION OF THE RISK FACTORS | FUNCTIONALITIES | LIFE QUALITIES OF THE PATIENTS WITH THE DIAGNOSIS OF PEDIATRIC ACUTE ARTERIAL ISCHEMIC STROKE" | Fatih Mehmet Akif Özdemi̇r | fatihmehmetakif@hotmail.com | |||||
630 | Yes | No | 5th Oct 2022 | Genetics and epilepsy II | Ramachandran Nair | Fatma Hanci | fatmah.arslan@gmail.com | A Photosensitivite Trichothiodystrophy Patient With A Mutation in ERCC2 Gene | Fatma Hanci | fatmah.arslan@gmail.com | ||||||||
706 | Yes | No | 4th Oct 2022 | Epilepsy: Genetics 3 | L Lagae | Florinela Gisela Rotaru | florirotaru9@gmail.com | Clinical features of KCNQ2 mutation in a Romanian family | Florinela Gisela Rotaru | florirotaru9@gmail.com | ||||||||
223 | Yes | No | 4th Oct 2022 | "Epilepsy: Syndromes 1 – Self-limited | EE/DEE-SWAS" | C Joshi | Zhijie Zhang | flyzoe423@sjtu.edu.cn | Immune mechanism in Benign Epilepsy with Centrotempral Spikes | Ling Li | liling@xinhuamed.com.cn | |||||||
659 | Yes | No | Franzina Coutinho | franzina.research@gmail.com | The Enabling Inclusion (EI) App: A story from Rural South India about COVID-19 and digital techno | Franzina Coutinho | franzina.research@gmail.com | |||||||||||
669 | Yes | No | Franzina Coutinho | franzina.research@gmail.com | Health coaching and COVID-19: Parent reports from India | Franzina Coutinho | franzina.research@gmail.com | |||||||||||
688 | Yes | No | 6th Oct 2022 | Education | "Jorge Vidaurre | US" | Franzina Coutinho | franzina.research@gmail.com | Early Intervention app and Digital technology: Bridging the rehabilitation service gap in India | Franzina Coutinho | franzina.research@gmail.com | |||||||
209 | Yes | No | 4th Oct 2022 | Epilepsy: Treatment 1 – ASMs | B Sanchez-Gan | Gamze Sarıkaya Uzan | gamzeuzan36@gmail.com | Levetiracetam Monotherapy For The Treatment Of Febrile and Febrile Induced Seizures | Gamze Sarıkaya Uzan | gamzeuzan36@gmail.com | ||||||||
350 | Yes | No | 5th Oct 2022 | Neurogenetics practice | T Lerman-Sagie | Gamze Sarıkaya Uzan | gamzeuzan36@gmail.com | Pontocerebellar Hypoplasia Associated With TTC 1 Mutation: Case Series | Gamze Sarıkaya Uzan | gamzeuzan36@gmail.com | ||||||||
649 | Yes | No | 4th Oct 2022 | "Epilepsy: Neuroimaging | Surgery and Basic Science" | C Akman | Gautam Kamila | gautamkamila7@gmail.com | Non-dominant hemisphere is more excitable compared to dominant hemisphere | Prashant Jauhari | pjauhari0@gmail.com | |||||||
340 | Yes | No | 6th Oct 2022 | Metabolic 3 Mitochondrial disorders II: Etiologies and mechanisms | Saskia Wortmann Netherlands | Gülbahar Kurt Bayir | gulbaharkurtbayir@gmail.com | Mutations of The E3 Beta Subunit of The Pyruvate Dehydrogenase (PDH) Complex Gene: A Case Report | Gülbahar Kurt Bayir | gulbaharkurtbayir@gmail.com | ||||||||
341 | Yes | No | 6th Oct 2022 | Metabolic 3 Mitochondrial disorders II: Etiologies and mechanisms | Saskia Wortmann Netherlands | Gülbahar Kurt Bayir | gulbaharkurtbayir@gmail.com | Two Different Phenotypes Caused by Mutation in the EARS2 Gene in Two Siblings | Gülbahar Kurt Bayir | gulbaharkurtbayir@gmail.com | ||||||||
343 | Yes | No | 5th Oct 2022 | General neurogenetics II | A R Tavasoli | Gülbahar Kurt Bayir | gulbaharkurtbayir@gmail.com | A Case of OTUD6B-Related Disorder | Gülbahar Kurt Bayir | gulbaharkurtbayir@gmail.com | ||||||||
610 | Yes | No | 6th Oct 2022 | CNS Infections 1 Covid-related | "Charles Newton | Kenya" | Gülcan Akyüz | gulcan.akyuz@hotmail.com | MOG ANTIBODY- ASSOCIATED ENCEPHALITIS SECONDER TO COVID 19 | Gülcan Akyüz | gulcan.akyuz@hotmail.com | |||||||
496 | Yes | No | 6th Oct 2022 | Headache/Stroke 2 | "Mahendra Moharir | Canada" | Gunce Basarir | guncebasarir@gmail.com | Ambulatory blood pressure monitoring in children diagnosed with primary headache | Pinar Gencpinar | pinargencpinar@gmail.com | |||||||
570 | Yes | No | 6th Oct 2022 | Metabolic 6 Defects of bioenergetic and intermediary metab | Ingrid Tein Canada | Gunjan Didwal | gunjan276@gmail.com | "Clinical | Biochemical and Genetic analysis of 6 North Indian families: Biotinidase deficiency in 86% of the children" | Gunjan Didwal | gunjan276@gmail.com | |||||||
543 | Yes | No | 6th Oct 2022 | Metabolic 4 Therapeutic approaches | Samantha Marin Canada | Gurdeep Sekhon | gurdeep.sekhon@gosh.nhs.uk | Uridine-responsive epileptic encephalopathy: precision treatment across the age spectrum | Gurdeep Sekhon | gurdeep.sekhon@gosh.nhs.uk | ||||||||
694 | Yes | No | Wen-xiong Chen | gzchcwx@126.com | Clinical analysis of 26 children with recurrent bacterial meningitis | Wen-xiong Chen | gzchcwx@126.com | |||||||||||
612 | Yes | No | 4th Oct 2022 | "Epilepsy: DEEs | TSC | RETT and Comorbidities" | Y Jiang | Hakan Ercelebi | hakanerc@hotmail.com | Application of a Recently Proposed Semiological Classification to Psychogenic Nonepileptic Seizures in Children | Hakan Ercelebi | hakanerc@hotmail.com | ||||||
778 | Yes | No | 6th Oct 2022 | Metabolic 3 Mitochondrial disorders II: Etiologies and mechanisms | Saskia Wortmann Netherlands | İsmail Hakkı Akbeyaz | hakkiakbeyaz@gmail.com | A CHALLENGING CASE: WERNICKE ENCEPAHALOPATHY AFTER GASTRIC SLEEVE SURGERY | İsmail Hakkı Akbeyaz | hakkiakbeyaz@gmail.com | ||||||||
263 | Yes | No | 4th Oct 2022 | "Epilepsy: Neuroimaging | Surgery and Basic Science" | C Akman | Hale Atalay Celik | hale.atalay@gmail.com | Acute encephalopathy with biphasic seizures and late reduced diffusion (AESD); 2 different clinical outcome | Hale Atalay Celik | hale.atalay@gmail.com | |||||||
365 | Yes | No | 6th Oct 2022 | Metabolic 3 Mitochondrial disorders II: Etiologies and mechanisms | Saskia Wortmann Netherlands | Hale Atalay Celik | hale.atalay@gmail.com | A Rare Mitochondrial disease; Naxe Gene Mutation | Hale Atalay Celik | hale.atalay@gmail.com | ||||||||
446 | Yes | No | 6th Oct 2022 | "Metabolic 5 Neurodegenerative diseases (NBIAs | metabolic causes of stroke | CDG | NCLs | NKH" | Suvasini Sharma India | Hale Atalay Celi̇k | hale.atalay@gmail.com | Metabolic Stroke; A Rare Clinical Condition of Glycerol Kinase Deficiency | Hale Atalay Celi̇k | hale.atalay@gmail.com | ||||
334 | Yes | No | 6th Oct 2022 | Metabolic 1 Clinical phenotypes | "Brahim Tabarki | KSA" | Harshuti Shah | harshuti@yahoo.co.in | Genotypic phenotypic charecteristics of galactosemia in postneonatal age in western India | Harshuti Shah | harshuti@yahoo.co.in | |||||||
337 | Yes | No | 6th Oct 2022 | Metabolic 4 Therapeutic approaches | Samantha Marin Canada | Harshuti Shah | harshuti@yahoo.co.in | Study of 15 patients with early infantile neurometabolic epileptic encephalopathy-treatable etiologies | Harshuti Shah | harshuti@yahoo.co.in | ||||||||
660 | Yes | No | 5th Oct 2022 | General neurogenetics I | AR Zamani | Hossein Farshadmoghadam | Hossein772000@yahoo.com | Study of clinical and genetic characteristics of limb-girdle muscular dystrophy in Iranian patients | Hossein Farshadmoghadam | Hossein772000@yahoo.com | ||||||||
767 | Yes | No | 6th Oct 2022 | Neuroradiology 1 | "Manohar Schroff | Canada" | Hülya Maraş Genç | hulyamaras@gmail.com | Two cases with Pontine Tegmental Cap Dysplasia: a rare hindbrain anomaly which may be misdiagnosed as Moebius Sequence | Hülya Maraş Genç | hulyamaras@gmail.com | |||||||
398 | Yes | No | 4th Oct 2022 | Epilepsy: Treatment 2 – ASMs | Ramachandran Nair | Huriye Cetin | huriyeecetin@gmail.com | "Relationship Between Valproic Acid | Hepatosteatosis and Serum Betatrophin Levels" | Turgay Cokyaman | drturgay@comu.edu.tr | |||||||
287 | Yes | No | 6th Oct 2022 | "Movement 1 Chorea | dyskinesias | tremor | spasms & tx" | "Biju Hameed | UK" | Hüseyin Pür | huseyinpur@gmail.com | "CLINICAL EVALUATION OF CHILDREN DIAGNOSED WITH SYDENHAM CHOREA | SINGLE CENTER EXPERIENCE" | Hüseyin Pür | huseyinpur@gmail.com | |||
676 | Yes | No | 6th Oct 2022 | "Movement 2 Dystonia | Parkinsons | tremor and epidemiology" | "Jon Mink | US" | Çiğdem İlter Uçar | iltercigdem@gmail.com | Holmes tremor associated with two different etiologies | Miraç Yıldırım | miracyildirim81@hotmail.com | |||||
677 | Yes | No | 6th Oct 2022 | "Movement 3 Ataxias | opsoclonus myoclonus and covid 19 impact" | "Russell Dale | Australia" | Çiğdem İlter Uçar | iltercigdem@gmail.com | Acute cerebellitis associated with juvenile idiopathic arthritis | Miraç Yıldırım | miracyildirim81@hotmail.com | ||||||
692 | Yes | No | 6th Oct 2022 | Education | "Jorge Vidaurre | US" | Ipek Tekcicek | ipekt08@gmail.com | A pilot study on the opinions of future doctors about child neurology | Esra Serdaroglu | esra.serdaroglu@gmail.com | |||||||
686 | Yes | No | 4th Oct 2022 | Epilepsy: Outcomes and Epidemiology | E Kija | Irmak Simsek | irmaksimsek@gmail.com | Epilepsy prevalence and trends in antiepileptic medication use among children in Turkey between 2015-2020 | Irmak Simsek | irmaksimsek@gmail.com | ||||||||
361 | Yes | No | 5th Oct 2022 | General neurogenetics II | A R Tavasoli | Irmak Erdoğan | irmkerdgn@gmail.com | A report of a rare syndrom: Alazami Syndrom | Irmak Erdoğan | irmkerdgn@gmail.com | ||||||||
172 | Yes | No | 6th Oct 2022 | "Movement 2 Dystonia | Parkinsons | tremor and epidemiology" | "Jon Mink | US" | Jo-anna Allen | jallen@ptcbio.com | A Mobile Domiciliary Phlebotomy Service to Support Patients With Rare Disease and Screening Study Recruitment in the UK | Jo-anna Allen | jallen@ptcbio.com | |||||
258 | Yes | No | 4th Oct 2022 | Epilepsy: Genetics 2 | N Specchio | Johanna De Luca-ramirez | jdeluca20@stu.psm.edu | Epileptic Encephalopathy Secondary to Homozygous TBC1 Domain-Containing Kinase (TBCK) Mutation in Four Patients of Puerto Rican Descent | Orlando Torres | orlandotorres@psm.edu | ||||||||
320 | Yes | No | 6th Oct 2022 | Metabolic 2 Mitochondrial disorders I : clinical phenotypes and tx | "Rita Horvath | UK" | Jorge Vidaurre | jorge.vidaurre@nationwidechildrens.org | Ketamine: An effective and safe treatment for patients with MELAS and refractory status epilepticus | Ezgi Saylam | ezgi.saylam@nationwidechildrens.org | |||||||
321 | Yes | No | 4th Oct 2022 | Epilepsy: Status epilepticus and Miscellaneous | T Loddenkemper | Javeria Raza | jra_28@hotmail.com | OUTCOME OF REFRACTORY STATUS EPILEPTICUS IN CHILDREN | Javeria Raza | jra_28@hotmail.com | ||||||||
423 | Yes | No | 6th Oct 2022 | CNS Infections 1 Covid-related | "Charles Newton | Kenya" | Javeria Alvi | jra_28@hotmail.com | Post COVID anti-NMDAR Encephalitis in an adolescent girl | Javeria Alvi | jra_28@hotmail.com | |||||||
430 | Yes | No | 5th Oct 2022 | "CNS Malformations | NGS" | A Narayan | Javeria Alvi | jra_28@hotmail.com | "PSEUDO-TORCH- A rare mutation causing global development delay | microcephaly and extensive band like brain calcification" | Javeria Alvi | jra_28@hotmail.com | ||||||
63 | Yes | No | 6th Oct 2022 | Metabolic 1 Clinical phenotypes | "Brahim Tabarki | KSA" | Judy Pipo-deveza | judepipo@yahoo.com | "S-adenosylhomocysteine hydrolase deficiency with associated masseter hypertrophy | bradykinesia | and cerebellar atrophy and alterations of creatine and choline homeostasis. Expansion of cerebrohepatomuscular phenotype" | Ingrid Tein | ingtein@sympatico.ca | |||||
770 | Yes | No | 4th Oct 2022 | Epilepsy: Outcomes and Epidemiology | E Kija | Kavita Srivastava | kavisri1970@gmail.com | Clinical profile and short term seizure outcome in children with Genetic Generalized Epilepsies | Kavita Srivastava | kavisri1970@gmail.com | ||||||||
774 | Yes | No | 4th Oct 2022 | Epilepsy: Treatment 1 – ASMs | B Sanchez-Gan | Kavita Srivastava | kavisri1970@gmail.com | "Effect of antiseizure medications on calcium profile | thyroid profile and bone mineral density in children" | Kavita Srivastava | kavisri1970@gmail.com | |||||||
252 | Yes | No | 5th Oct 2022 | General neurogenetics I | AR Zamani | Kursat Bora Carman | kbcarman@gmail.com | Evaluation of MicroRNAs in Pediatric Epilepsy | Kursat Bora Carman | kbcarman@gmail.com | ||||||||
253 | Yes | No | 6th Oct 2022 | Headache 1 | "Ken Mack | US" | Kursat Bora Carman | kbcarman@gmail.com | Neurological face of familial mediterranean fever | Kursat Bora Carman | kbcarman@gmail.com | |||||||
359 | Yes | No | 6th Oct 2022 | Cerebral palsy 2- Management; current and future | "Antigone Papavasiliou | Greece" | Kursat Bora Carman | kbcarman@gmail.com | Hippotherapy in children with cerebral palsy | Kursat Bora Carman | kbcarman@gmail.com | |||||||
379 | Yes | No | 4th Oct 2022 | Epilepsy: Semiology and Clinical | H Cross | Fatma Kusgoz | kusgozfatma@gmail.com | Ictal Nose Wiping in Frontal-Onset Absence Epilepsy; A case report | Fatma Kusgoz | kusgozfatma@gmail.com | ||||||||
380 | Yes | No | 5th Oct 2022 | Molecular genetics | T Sultan | Fatma Kusgoz | kusgozfatma@gmail.com | "Xp22.33-p11.4 Duplication and 46 | X+mar gonadal dysgenesis in a Patient with Epilepsy | Dysmorphisms | Hypotonia and Intellectual Disability | A case report" | Fatma Kusgoz | kusgozfatma@gmail.com | ||||
535 | Yes | No | 4th Oct 2022 | Epilepsy: Treatment 2 – ASMs | Ramachandran Nair | Mehmet Fatih Butun | M_FBUTUN@YAHOO.COM | "Rufinamide Experience in Childhood Epilepsy from a Tertiary Center | Turkey" | Mehmet Fatih Butun | M_FBUTUN@YAHOO.COM | |||||||
267 | Yes | No | 5th Oct 2022 | Genetics and epilepsy I | W Hakami | Magdalena Bliznakova | maggie.bliznakova@gmail.com | Hypocalcemic Seizure in a Girl with FOXG1-Gene–Related Encephalopathy | Zhivka Chuperkova | Zhivka.Chuperkova@mu-varna.bg | ||||||||
695 | Yes | No | 4th Oct 2022 | "Epilepsy: DEEs | TSC | RETT and Comorbidities" | Y Jiang | Manasa Thangella | manasa6548@gmail.com | EVALUATION OF HEALTH RELATED QUALITY OF LIFE IN CHILDREN WITH EPILEPSY USING QUALITY OF LIFE IN CHILDHOOD EPILEPSY QUESTIONNAIRE (QOLCE - 55) | Venkatesan Srinath Melpakkam | shribkcorp@gmail.com | ||||||
206 | Yes | No | 6th Oct 2022 | Headache 1 | "Ken Mack | US" | Mehmet Can Yeşilmen | mcanyesilmen@gmail.com | A case of first pediatric pseudotumor cerebri syndrome secondary to superior sagittal sinus thrombosis associated with SARS-CoV-2 | Mehmet Can Yeşilmen | mcanyesilmen@gmail.com | |||||||
589 | Yes | No | 4th Oct 2022 | Epilepsy: Status epilepticus and Miscellaneous | T Loddenkemper | Ayse Yasemin Celik | mdayasminc@gmail.com | "The effect of antiepileptic drugs on ischemia modified albumin | myeloperoxidase and catalase levels in children with idiopathic epilepsy" | Ayse Yasemin Celik | mdayasminc@gmail.com | |||||||
594 | Yes | No | 6th Oct 2022 | Metabolic 6 Defects of bioenergetic and intermediary metab | Ingrid Tein Canada | Ayse Yasemin Celik | mdayasminc@gmail.com | A rare cause of episodic vomiting: Late-onset multiple acyl-CoA dehydrogenase deficiency as a treatable metabolic myopathy | Ayse Yasemin Celik | mdayasminc@gmail.com | ||||||||
648 | Yes | No | 4th Oct 2022 | "Epilepsy: Syndromes 2 – IESS | Dravet | HHE | EMAS" | E Wirrell | Balamurugan Nagarajan | meetkabi@gmail.com | GENOTYPIC AND PHENOTYPIC SPECTRUM OF CHILDREN WITH GENETIC WEST SYNDROME FROM NORTHERN INDIA | Jitendra Kumar Sahu | jsh2003@gmail.com | |||||
427 | Yes | No | 5th Oct 2022 | "CNS Malformations | NGS" | A Narayan | Mohammed Alqahtani | mohammed.alqahtani@sickkids.ca | The Yield of Genetic and Metabolic Testing in Epileptic Spasms | Mohammed Alqahtani | mohammed.alqahtani@sickkids.ca | |||||||
585 | Yes | No | 4th Oct 2022 | Epilepsy: Investigations | P Madaan | Mehpare Sari Yanartas | mparesari2@gmail.com | Answer to seizures: The pediatric Covid-19 infection | Mehpare Sari Yanartas | mparesari2@gmail.com | ||||||||
587 | Yes | No | 4th Oct 2022 | Epilepsy: Treatment 2 – ASMs | Ramachandran Nair | Mehpare Sari Yanartas | mparesari2@gmail.com | "Lacosamide Experience in Childhood Epilepsy from a Tertiary Center | Turkey" | Mehpare Sari Yanartas | mparesari2@gmail.com | |||||||
336 | Yes | No | 6th Oct 2022 | Headache/Stroke 2 | "Mahendra Moharir | Canada" | Nesrin Şenbil | n.senbil.1965@gmail.com | Clinical Evaluation Of The Vestibular Functions In Pediatric Patients With Migraine And Probable Vestibular Migraine Of Childhood | Nesrin Şenbil | n.senbil.1965@gmail.com | |||||||
180 | Yes | No | 4th Oct 2022 | Epilepsy: Genetics 2 | N Specchio | Naznin Ruby | nazninruby73@gmail.com | Prevalence Proportion and Clinical Spectrum of Genetic Epilepsy in Children of Bangladesh: A Hospital Based Study | Naznin Ruby | nazninruby73@gmail.com | ||||||||
285 | Yes | No | 4th Oct 2022 | Epilepsy: Genetics 3 | L Lagae | Nefise Arıbaş Öz | nefisearibas@hotmail.com | Intractable epilepsy with Rahman Syndrome | Nefise Arıbaş Öz | nefisearibas@hotmail.com | ||||||||
387 | Yes | No | 5th Oct 2022 | Genetics and epilepsy I | W Hakami | Nefise Arıbaş Öz | nefisearibas@hotmail.com | TBC1D24 gene Mutations Presented with Familial Infantile Myoclonic Epilepsy | Nefise Arıbaş Öz | nefisearibas@hotmail.com | ||||||||
705 | Yes | No | 4th Oct 2022 | "Epilepsy: DEEs | TSC | RETT and Comorbidities" | Y Jiang | Nihal Yıldız | nihalyildiz661@gmail.com | "Evaluation of seizure semiology | genetic | magnetic resonance imaging and electroencephalogram findings in children with Rett syndrome: A multicenter retrospective study" | Nihal Yıldız | nihalyildiz661@gmail.com | ||||
227 | Yes | No | 5th Oct 2022 | Neurogenetics practice | T Lerman-Sagie | Nouha Bouayed Abdelmoula | nouha_abdelmoulabouayed@yahoo.fr | Sensorineural impairment in maternally inherited diabetes mellitus and deafness (MIDD) disorder | Nouha Bouayed Abdelmoula | nouha_abdelmoulabouayed@yahoo.fr | ||||||||
662 | Yes | No | 6th Oct 2022 | Metabolic 6 Defects of bioenergetic and intermediary metab | Ingrid Tein Canada | Nurşah Yeniay Süt | nursah_ny@hotmail.com | A rare metabolic disease causing infantile spasm: Argininosuccinate lyase deficiency | Nurşah Yeniay Süt | nursah_ny@hotmail.com | ||||||||
305 | Yes | No | 4th Oct 2022 | Epilepsy: Outcomes and Epidemiology | E Kija | Obrey Urio | obreyharold@rocketmail.com | "DRUG RESISTANT EPILEPSY AND ASSOCIATED FACTORS AMONG CHILDREN WITH EPILEPSIES IN TANZANIA | A CROSS SECTIONAL STUDY" | Obrey Urio | obreyharold@rocketmail.com | |||||||
522 | Yes | No | 4th Oct 2022 | Epilepsy: Outcomes and Epidemiology | E Kija | Mehmet Oguz Demiroglu | oguzdr66@gmail.com | The effect of anti-epileptic treatment selection on prognosis in traumatic brain injury | Mehmet Oguz Demiroglu | oguzdr66@gmail.com | ||||||||
698 | Yes | No | 5th Oct 2022 | Spasticity and ataxia | C Catsman | Olgay Bildik | olgaybildik@hotmail.com | Ring Chromosome 18 Case With 18p Deletion | Olgay Bildik | olgaybildik@hotmail.com | ||||||||
707 | Yes | No | 6th Oct 2022 | Metabolic 1 Clinical phenotypes | "Brahim Tabarki | KSA" | Olgay Bildik | olgaybildik@hotmail.com | A Case Of Vanishing White Matter Disease With Atypical Neuroimaging Presentation | Olgay Bildik | olgaybildik@hotmail.com | |||||||
389 | Yes | No | 5th Oct 2022 | Genetics and epilepsy I | W Hakami | Özgen Hür | ozgenozyazicioglu@yahoo.com | A case of ‘Joubert Syndrome 31’ due to CEP120 homozygous mutation | Özgen Hür | ozgenozyazicioglu@yahoo.com | ||||||||
414 | Yes | No | 5th Oct 2022 | Genetics and epilepsy II | Ramachandran Nair | Özgen Hür | ozgenozyazicioglu@yahoo.com | A Case of GRIN1 Mutation Presenting with Autistic Features | Özgen Hür | ozgenozyazicioglu@yahoo.com | ||||||||
422 | Yes | No | 6th Oct 2022 | "Movement 1 Chorea | dyskinesias | tremor | spasms & tx" | "Biju Hameed | UK" | Özgen Hür | ozgenozyazicioglu@yahoo.com | An autosomal dominant familial dyskinesia gene: ADCY5 mutation | Özgen Hür | ozgenozyazicioglu@yahoo.com | ||||
425 | Yes | No | 5th Oct 2022 | Genetics and epilepsy II | Ramachandran Nair | Özgen Hür | ozgenozyazicioglu@yahoo.com | A rare cause of progressive myoclonic epilepsy: KCTD7 mutation | Özgen Hür | ozgenozyazicioglu@yahoo.com | ||||||||
92 | Yes | No | 4th Oct 2022 | Epilepsy: Treatment 1 – ASMs | B Sanchez-Gan | Pawan Kashyape | pawankashyape@yahoo.co.uk | A Case of Carbamazepine Responsive Neonatal Epilepsy Secondary to PACS2 Gene mutation | Pawan Kashyape | pawankashyape@yahoo.co.uk | ||||||||
747 | Yes | No | 6th Oct 2022 | Metabolic 6 Defects of bioenergetic and intermediary metab | Ingrid Tein Canada | Pinar Edem | pinaredem@gmail.com | Phenotypic diversity of GLUT1 deficiency: A case report. | Pinar Edem | pinaredem@gmail.com | ||||||||
600 | Yes | No | 4th Oct 2022 | "Epilepsy: Neuroimaging | Surgery and Basic Science" | C Akman | Prashant Jauhari | pjauhari0@gmail.com | Real-time cortical excitability in children with DRE and ESES and its correlation with treatment response: A TMS based comparative study | Prashant Jauhari | pjauhari0@gmail.com | |||||||
773 | Yes | No | 5th Oct 2022 | General neurogenetics I | AR Zamani | Radu Perjoc | radu-stefan.perjoc@rez.umfcd.ro | Wolf-Hirschhorn syndrome and Dup15q – review of the literature and case report. | Radu Perjoc | radu-stefan.perjoc@rez.umfcd.ro | ||||||||
293 | Yes | No | 4th Oct 2022 | Epilepsy: Semiology and Clinical | H Cross | Ramesh Konanki | rameshkonanki@gmail.com | Electro-clinical spectrum of Absence epilepsy: A case series from India | Ramesh Konanki | rameshkonanki@gmail.com | ||||||||
439 | Yes | No | 6th Oct 2022 | Metabolic 3 Mitochondrial disorders II: Etiologies and mechanisms | Saskia Wortmann Netherlands | Ramesh Konanki | rameshkonanki@gmail.com | "High-dose Nicotinamide rescues from ‘Early-onset | progressive encephalopathy with brain edema and/or leukoencephalopathy-1 (PEBEL-1)’: All hope is not lost!" | Ramesh Konanki | rameshkonanki@gmail.com | |||||||
58 | Yes | No | 6th Oct 2022 | Cerebral palsy 2- Management; current and future | "Antigone Papavasiliou | Greece" | Razia Sultana | razia4m@yahoo.com | Association of Functional Ability with Nutritional status among Children with Cerebral Palsy | Razia Sultana | razia4m@yahoo.com | |||||||
683 | Yes | No | 4th Oct 2022 | Epilepsy: Semiology and Clinical | H Cross | Richard Idro | ridro1@gmail.com | Pathogenesis of nodding syndrome; Preliminary findings | Richard Idro | ridro1@gmail.com | ||||||||
746 | Yes | No | 6th Oct 2022 | Cerebral palsy 2- Management; current and future | "Antigone Papavasiliou | Greece" | Ruchika Jha | ruchicls@yahoo.com | To determine the prevalence of comorbidities among children with cerebral palsy (CP) and risk-factors predictive of different comorbidities. | Ruchika Jha | ruchicls@yahoo.com | |||||||
598 | Yes | No | 4th Oct 2022 | "Epilepsy: DEEs | TSC | RETT and Comorbidities" | Y Jiang | Zara Hamill | s1706726@sms.ed.ac.uk | Health Economic Analysis of Psychology Adding Value Epilepsy Screening (PAVES) - a Screening and Intervention Programme for the Epilepsy Clinic | Zara Hamill | s1706726@sms.ed.ac.uk | ||||||
225 | Yes | No | 6th Oct 2022 | Neuroradiology 2 | "Kshitij Mankand | UK" | Sandra Patricia Toelle | sandra.toelle@kispi.uzh.ch | Congenital tonic pupil - what's behind? | Sandra Patricia Toelle | sandra.toelle@kispi.uzh.ch | |||||||
57 | Yes | No | 6th Oct 2022 | "Cerebral palsy 1- Evaluation: clinic | neurophysiologic" | "Catherine Arnaud | France" | Sanjida Ahmed | sanjida.lipi@yahoo.com | Relationship Between the Level of Gross Motor Function and Magnetic Resonance Imaging Findings in Children with Cerebral Palsy in a Tertiary Care Hospital | Sanjida Ahmed | sanjida.lipi@yahoo.com | ||||||
426 | Yes | No | 6th Oct 2022 | "Movement 1 Chorea | dyskinesias | tremor | spasms & tx" | "Biju Hameed | UK" | Sara Sopena | sara.sopena@gstt.nhs.uk | A novel psychological therapy approach for children with PNKD | Sara Sopena | sara.sopena@gstt.nhs.uk | ||||
697 | Yes | No | 4th Oct 2022 | "Epilepsy: Syndromes 2 – IESS | Dravet | HHE | EMAS" | E Wirrell | Ingrid Scheffer | scheffer@unimelb.edu.au | Can vaccine-proximate seizures in Dravet syndrome be prevented? | Ingrid Scheffer | scheffer@unimelb.edu.au | |||||
586 | Yes | No | 6th Oct 2022 | Metabolic 1 Clinical phenotypes | "Brahim Tabarki | KSA" | Jan-christoph Schoene-bake | schoene-bake.christoph@mh-hannover.de | MPS-like disease presumably caused by VPS16-associated impairment of intracellular trafficking | Jan-christoph Schoene-bake | schoene-bake.christoph@mh-hannover.de | |||||||
449 | Yes | No | 6th Oct 2022 | Headache/Stroke 2 | "Mahendra Moharir | Canada" | Secil Doga Tunc | secildogatunc@gmail.com | THE COURSE OF PEDIATRIC HEADACHES DURING COVID-19 PANDEMIC | Hamit Ozyurek | hozyurekibu@hotmail.com | |||||||
601 | Yes | No | 6th Oct 2022 | Headache/Stroke 3 | "Mubeen Rafay | Canada" | Semra Saygi | semra_saygi@yahoo.com | The Prevalence of Adenoid Hypertrophy in Brain MRI Examination in Children with Headache in the Pediatric Neurology Outpatient Clinic | Semra Saygi | semra_saygi@yahoo.com | |||||||
318 | Yes | No | 6th Oct 2022 | Metabolic 2 Mitochondrial disorders I : clinical phenotypes and tx | "Rita Horvath | UK" | Seren Aydin | serenaydin5228@gmail.com | Three Different Phenotypic Presentations of Leigh Syndrome | Seren Aydin | serenaydin5228@gmail.com | |||||||
381 | Yes | No | 4th Oct 2022 | Epilepsy: Treatment 2 – ASMs | Ramachandran Nair | Sergiusz Jozwiak | sergiusz.jozwiak@gmail.com | "VIRAP - new randomized | double-blind | preventive study (vigabatrin vs sirolimus) on prevention of epilepsy in TSC" | Sergiusz Jozwiak | sergiusz.jozwiak@gmail.com | ||||||
52 | Yes | No | 4th Oct 2022 | Epilepsy: Treatment 1 – ASMs | B Sanchez-Gan | Esra Özpınar | seydabesen2000@gmail.com | Sirolimus in Tuberous Sclerosis Complex prior to epilepsy: evidence from a registry-based real-world study | Li-ping Zou | zouliping21@sina.com | ||||||||
450 | Yes | No | 4th Oct 2022 | "Epilepsy: DEEs | TSC | RETT and Comorbidities" | Y Jiang | Sharmila Manivannan | sharmila.manivannan@nhs.net | Quality Improvement Project to ameliorate the provision of mental health support to our children with epilepsy | Sharmila Manivannan | sharmila.manivannan@nhs.net | ||||||
508 | Yes | No | 6th Oct 2022 | Metabolic 4 Therapeutic approaches | Samantha Marin Canada | Yashu Sharma | shrma.yashu@gmail.com | Impact of COVID-19 on the care of children with neurometabolic disorders | Arushi Saini | doc.arushi@gmail.com | ||||||||
434 | Yes | No | Sonali Singh | sonali2017doc@gmail.com | Paroxysmal sympathetic hyperactivity in Pediatric Tuberculous meningitis: A New association | Prashant Jauhari | pjauhari0@gmail.com | |||||||||||
696 | Yes | No | 5th Oct 2022 | Molecular genetics | T Sultan | Didem Soydemir | soydemirdidem8@gmail.com | EXPANDING PHENOTYPIC DIVERSITY OF PRUNE1 RELATED DISORDERS: AN EXPERIENCE OF FOUR CASES IN A TERTIARY CENTER | Didem Soydemir | soydemirdidem8@gmail.com | ||||||||
347 | Yes | No | 6th Oct 2022 | "Movement 1 Chorea | dyskinesias | tremor | spasms & tx" | "Biju Hameed | UK" | Sukanya Vrushabhendra | sukanyavi2005@gmail.com | Caffeine significantly reduces frequency of Paroxysmal Dyskinesia in a child with an ADCY5 Mutation | Sukanya Vrushabhendra | sukanyavi2005@gmail.com | ||||
730 | Yes | No | 6th Oct 2022 | "Metabolic 5 Neurodegenerative diseases (NBIAs | metabolic causes of stroke | CDG | NCLs | NKH" | Suvasini Sharma India | Esra Ülgen Temel | ulgenesra@yahoo.com | An Infant With Movement Disorder And Infantile Spasm: Attenuated NKH | Esra Ülgen Temel | ulgenesra@yahoo.com | ||||
741 | Yes | No | 4th Oct 2022 | Epilepsy: Genetics 1 | S Perry | Esra Ülgen Temel | ulgenesra@yahoo.com | STXBP1 as a Novel Gene for Sleep-Related Hypermotor Epilepsy: A Video-EEG Documented Case Report | Esra Ülgen Temel | ulgenesra@yahoo.com | ||||||||
547 | Yes | No | 6th Oct 2022 | CNS Infections 1 Covid-related | "Charles Newton | Kenya" | Varghese Abraham | varghese.abraham@moscmc.edu.in | A Comparative Study On The Risk Of Seizure In Children During The Delta And The Omicron variants of SARS-COV-2 Infection | Varghese Abraham | varghese.abraham@moscmc.edu.in | |||||||
781 | Yes | No | 6th Oct 2022 | "Movement 2 Dystonia | Parkinsons | tremor and epidemiology" | "Jon Mink | US" | Wang-tso Lee | wangtsolee@ntu.edu.tw | "An open-label | single-dose study to evaluate the efficacy of probiotics PS128 in pediatric subjects with AADC deficiency" | Wang-tso Lee | wangtsolee@ntu.edu.tw | ||||
782 | Yes | No | 6th Oct 2022 | "Movement 3 Ataxias | opsoclonus myoclonus and covid 19 impact" | "Russell Dale | Australia" | Wang-tso Lee | wangtsolee@ntu.edu.tw | "Knockout of AGTPBP1 | a gene for cerebellar ataxia | lead to neuronal death and increased dopaminergic release" | Wang-tso Lee | wangtsolee@ntu.edu.tw | ||||
471 | Yes | No | 6th Oct 2022 | "Cerebral palsy 1- Evaluation: clinic | neurophysiologic" | "Catherine Arnaud | France" | Yilmaz Satirer | yilmaz.satirer@gmail.com | EVALUATION OF MOTOR AND SENSORY FUNCTIONS AND PSYCHOLOGICAL PROPERTIES IN CHILDREN WITH HEMIPARETIC CEREBRAL PALSY BETWEEN THE AGES OF 6 AND 16 YEARS | Yilmaz Satirer | yilmaz.satirer@gmail.com | ||||||
358 | Yes | No | 5th Oct 2022 | Neurogenetics practice | T Lerman-Sagie | Zahra Rezaei | zahra.rezaii84@gmail.com | Infantile Neuroaxonal Dystrophy; A Rare Or Underdiagnosed Disease? | Zahra Rezaei | zahra.rezaii84@gmail.com | ||||||||
485 | Yes | No | 6th Oct 2022 | Neuroradiology 2 | "Kshitij Mankand | UK" | Zahra Rezaei | zahra.rezaii84@gmail.com | A Common Neurologic Symptom Leads To A More Serious Oncologic Diagnosis! | Zahra Rezaei | zahra.rezaii84@gmail.com | |||||||
211 | Yes | No | 5th Oct 2022 | Neurogenetics practice | T Lerman-Sagie | Adelina Glangher | Not Available | Clinical and genetic profiles of grey matter heterotopia – report of 28 patients | Magdalena Budisteanu | magda_efrim@yahoo.com | ||||||||
356 | Yes | No | 4th Oct 2022 | "Epilepsy: Syndromes 1 – Self-limited | EE/DEE-SWAS" | C Joshi | TBC | Not Available | Clinical and electroencephalographic characteristics of childhood epilepsy with centrotemporal spikes for antiseizure medications: monotherapy versus dualtherapy in a multicenter cohort study | Beril Dilber | beriltem@gmail.com | |||||||
419 | Yes | No | 5th Oct 2022 | Genetics and epilepsy II | Ramachandran Nair | TBC | Not Available | A case of ‘Smith Magenis Syndrome’ with self-injurious behaviors and dysmorphic facial | Özgen Hür | ozgenozyazicioglu@yahoo.com | ||||||||
452 | Yes | No | 6th Oct 2022 | "Metabolic 5 Neurodegenerative diseases (NBIAs | metabolic causes of stroke | CDG | NCLs | NKH" | Suvasini Sharma India | TBC | Not Available | MRI pattern recognition of neuroceroid lipofuschinosis in children | Mahesh Kamate | drmaheshkamate@gmail.com | ||||
728 | Yes | No | 6th Oct 2022 | Neuroradiology 2 | "Kshitij Mankand | UK" | TBC | Not Available | Posterior reversible encephalopathy syndrome (PRES) without radiological correlate : Is it possible? | Sachendra Badal | badalsachendra@yahoo.com | |||||||
362 | No | No | 4th Oct 2022 | "Epilepsy: Syndromes 1 – Self-limited | EE/DEE-SWAS" | C Joshi | Aakanksha Anand | aakanksha.ucms@gmail.com | Continuous spikes and waves during sleep (CSWS): A Descriptive Clinical-epidemiological Profile from India | Aakanksha Anand | aakanksha.ucms@gmail.com | |||||||
364 | No | No | 5th Oct 2022 | General neurogenetics II | A R Tavasoli | Aakanksha Anand | aakanksha.ucms@gmail.com | STURGE WEBER SYNDROME WITH PHAKOMATOSIS PIGMENTOVASCULARIS: A CASE REPORT | Aakanksha Anand | aakanksha.ucms@gmail.com | ||||||||
59 | No | No | 4th Oct 2022 | Neonatal 2: Neonatal neurology – other | Lakshmi | Abdullahel Amaan | abdullahelamaan@gmail.com | Improvement of Hand Hygiene Practices among the Healthcare Workers in a Neonatal Intensive Care Unit | Abdullahel Amaan | abdullahelamaan@gmail.com | ||||||||
323 | No | No | 6th Oct 2022 | Metabolic 2 Mitochondrial disorders I : clinical phenotypes and tx | "Rita Horvath | UK" | Abir Zioudi | abir.zioudi@gmail.com | Mitochondrial disorders: a descriptive study of a Tunisian pediatric series | Abir Zioudi | abir.zioudi@gmail.com | |||||||
175 | No | No | 4th Oct 2022 | ASD/NDD/ADHD 1 ASD genetic / biomarkers / | Chahnez Triki | Adelina Glangher | adelina.glangher@gmail.com | "Epileptiform discharges and epilepsy in non-syndromic ASD patients. Pre | peri | post-natal risk factors for epilepsy." | Adelina Glangher | adelina.glangher@gmail.com | ||||||
411 | No | No | 6th Oct 2022 | "Movement 3 Ataxias | opsoclonus myoclonus and covid 19 impact" | "Russell Dale | Australia" | Adnan Deniz | adnandeniz85@hotmail.com | COVID-19 vaccine induced opsoclonus-myoclonus-ataxia syndrome | Adnan Deniz | adnandeniz85@hotmail.com | ||||||
413 | No | No | 5th Oct 2022 | Neuromuscular 1 | H Lochmüller | Adnan Deniz | adnandeniz85@hotmail.com | Paraneoplastic polyneuropathy associated with inflammatory myofibroblastic tumor in a pediatric patient | Adnan Deniz | adnandeniz85@hotmail.com | ||||||||
429 | No | No | 4th Oct 2022 | ASD/NDD/ADHD 2 ASD assessments / management / Rett syndrome / high risk infants | Antigone Papavasiliou | Annie Brandes-aitken | aitkenannie@gmail.com | "A Comprehensive | Personalized | Medically Based Care Model Improves Adaptive Behavior Outcomes in Autism vs Standard of Care" | Annie Brandes-aitken | aitkenannie@gmail.com | ||||||
671 | No | No | 6th Oct 2022 | Neuroradiology 3 | "Ajay Taranath | Australia" | Asli Kübra Atasever | akubrat@gmail.com | A case with an epidermoid cyst in the cerebellopontine angle presenting with hemifacial spasm | Asli Kübra Atasever | akubrat@gmail.com | |||||||
383 | No | No | 5th Oct 2022 | Genetics and epilepsy I | W Hakami | Ali Modaweb | ali.modaweb@ajch.ae | Early recurrent encephalopathy and subsequent hemiplegic migraine and intellectual disability caused by a de novo mutation in ATP2A2 gene | Ahmed Abd Alwahab Nugud | Ahmed.Nugud@ajch.ae | ||||||||
101 | No | No | 4th Oct 2022 | Epilepsy: Genetics 1 | S Perry | Alyssa Robison | alyssarobison1@gmail.com | Arthrogryposis multiplex congenita and SCN1A mutations: Another reported case and treatment guidance | Alyssa Robison | alyssarobison1@gmail.com | ||||||||
102 | No | No | 5th Oct 2022 | "Neuropathy | GBS | and CMS" | C Bönnemann | Alyssa Robison | alyssarobison1@gmail.com | Paraneoplastic Guillain-Barre Syndrome: A case report and call for modified diagnostic criteria | Alyssa Robison | alyssarobison1@gmail.com | ||||||
526 | No | No | 5th Oct 2022 | General II | M Sönmez | Amal Kentab | Amkentab@hotmail.com | Vici syndrome: Experience at tertiary care center | Amal Kentab | Amkentab@hotmail.com | ||||||||
532 | No | No | 5th Oct 2022 | "CNS Malformations | NGS" | A Narayan | Amal Kentab | Amkentab@hotmail.com | Clinical Characteristics and Aetiology of Corpus Callosum Abnormalities: A single Centre Experience in Saudi Arabia. | Amal Kentab | Amkentab@hotmail.com | |||||||
120 | No | No | 5th Oct 2022 | Neuroimmunology 2 Antibody mediated disorders / monophasic demyel disorder | Banu Anlar | Ángeles Schteinschnaider | angeles@fleni.org.ar | "FLAMES (FLAIR Hyperintense Lesions in Anti-Myelin Oligodendrocyte Glycoprotein-associated Encephalitis with Seizures) | a case report." | Ángeles Schteinschnaider | angeles@fleni.org.ar | |||||||
121 | No | No | 6th Oct 2022 | Neuroradiology 1 | "Manohar Schroff | Canada" | Ángeles Schteinschnaider | angeles@fleni.org.ar | POSTERIOR REVERSIBLE ENCEPHALOPATHY SYNDROME IN PEDIATRICS | Ángeles Schteinschnaider | angeles@fleni.org.ar | |||||||
125 | No | No | 6th Oct 2022 | "Tuberous sclerosis | Radiology" | K Aydın | Angeles Schteinschnaider | angeles@fleni.org.ar | NEUROCUTANEOUS MELANOSIS: CLINICAL AND IMAGING CHARACTERISTICS IN 7 PATIENTS | Angeles Schteinschnaider | angeles@fleni.org.ar | |||||||
126 | No | No | 5th Oct 2022 | Peripheral nerve | D Selcen | Angeles Schteinschnaider | angeles@fleni.org.ar | HIRAYAMA DISEASE: ABOUT TWO CASES | Angeles Schteinschnaider | angeles@fleni.org.ar | ||||||||
473 | No | No | 6th Oct 2022 | Headache/Stroke 3 | "Mubeen Rafay | Canada" | Ángeles Schteinschnaider | angeles@fleni.org.ar | "Pediatric Bow Hunter Syndrome | a case report." | Ángeles Schteinschnaider | angeles@fleni.org.ar | ||||||
653 | No | No | 5th Oct 2022 | Treatment | F Muntoni | Natalija Angelkova | angelkovan@gmail.com | Three years follow up of 6-minute walk test and North Star Ambulatory Assessment in 30 ambulant DMD boys since the beginning of steroid treatment | Natalija Angelkova | angelkovan@gmail.com | ||||||||
479 | No | No | 4th Oct 2022 | Epilepsy: Outcomes and Epidemiology | E Kija | Angela Schulz | anschulz@uke.de | Seizures in children with CLN2 disease receiving cerliponase alfa for >5 years | Sara Dosenovic | sara.dosenovic@bmrn.com | ||||||||
443 | No | No | 5th Oct 2022 | "Neuropathy | GBS | and CMS" | C Bönnemann | Ayşe Nur Coşkun | anurcoskun@gmail.com | "Charcot-Marie-Tooth Disease | So Which Type?" | Ayşe Nur Coşkun | anurcoskun@gmail.com | |||||
448 | No | No | 5th Oct 2022 | General II | M Sönmez | Arijit Chattopadhyay | arijitchatto@hotmail.com | Identification of a novel variant of the CDKl5 gene associated with atypical Rett Syndrome | Arijit Chattopadhyay | arijitchatto@hotmail.com | ||||||||
204 | No | No | 4th Oct 2022 | "Epilepsy: Syndromes 2 – IESS | Dravet | HHE | EMAS" | E Wirrell | Aristides Hadjinicolaou | aris.hadjinicolaou@gmail.com | Challenges of determination in date of onset of infantile spasms: A tertiary health center’s experience | Aristides Hadjinicolaou | aris.hadjinicolaou@gmail.com | |||||
412 | No | No | 6th Oct 2022 | Neuroradiology 3 | "Ajay Taranath | Australia" | Aristides Hadjinicolaou | aris.hadjinicolaou@gmail.com | Variation in neuroimaging and outcomes in patients with SWS type III | Aristides Hadjinicolaou | aris.hadjinicolaou@gmail.com | |||||||
396 | No | No | 5th Oct 2022 | Neuroimmunology 2 Antibody mediated disorders / monophasic demyel disorder | Banu Anlar | Arzu Yilmaz | arzuotken@yahoo.com | Human Herpes Virüs-7 Enfeksiyonu Sonrası Gelişen Subakut Sklerozan Panensefalit Olgusu | Arzu Yilmaz | arzuotken@yahoo.com | ||||||||
97 | No | No | 5th Oct 2022 | Neurogenetics practice | T Lerman-Sagie | Ashna Kumar | ashnakumar99@gmail.com | Dancing eyes and lazy gut in an infant with developmental delay | Ashna Kumar | ashnakumar99@gmail.com | ||||||||
155 | No | No | 4th Oct 2022 | "Epilepsy: Syndromes 1 – Self-limited | EE/DEE-SWAS" | C Joshi | Ashna Kumar | ashnakumar99@gmail.com | Self-Limited Epilepsy with Autonomic Seizures (SeLEAS): A Case series | Ashna Kumar | ashnakumar99@gmail.com | |||||||
167 | No | No | 5th Oct 2022 | Genetics and epilepsy I | W Hakami | Ahmet Yaramis | ayaramis@gmail.com | COL4A1-related autosomal recessive encephalopathy in 2 Turkish children | Ahmet Yaramis | ayaramis@gmail.com | ||||||||
280 | No | No | 5th Oct 2022 | "İon channel myopathy | and metabolic" | R Horvath | Ahmet Yaramış | ayaramis@gmail.com | Compliance with riboflavin treatment in a patient with late-diagnosed Brovn-Vialetto-Van Laere syndrome | Ahmet Yaramış | ayaramis@gmail.com | |||||||
281 | No | No | 5th Oct 2022 | "İon channel myopathy | and metabolic" | R Horvath | Ahmet Yaramış | ayaramis@gmail.com | Riboflavin treatment in 3 cases with ETFDH gene mutation | Ahmet Yaramış | ayaramis@gmail.com | |||||||
521 | No | No | 4th Oct 2022 | Epilepsy: Genetics 3 | L Lagae | Ayşe Yasemin Çelik | ayasminc@hotmail.com | A Rare Cause of Epilepsy In A Child: Mosaic Ring Chromosome 21 | Ayşe Yasemin Çelik | ayasminc@hotmail.com | ||||||||
737 | No | No | 6th Oct 2022 | Headache/Stroke 3 | "Mubeen Rafay | Canada" | Aysen Gok | aysenngok@gmail.com | A rare dual pathology: Idiopathic intracranial hypertension presenting with isolated unilateral facial nerve palsy | Aysen Gok | aysenngok@gmail.com | |||||||
732 | No | No | 6th Oct 2022 | Neuroradiology 3 | "Ajay Taranath | Australia" | Sachendra Badal | badalsachendra@yahoo.com | Mirror movements in children: Case series | Sachendra Badal | badalsachendra@yahoo.com | |||||||
753 | No | No | 6th Oct 2022 | Metabolic 1 Clinical phenotypes | "Brahim Tabarki | KSA" | Sachendra Badal | badalsachendra@yahoo.com | "Congenital Icthyosis and neurological manifestations | Sjogren Larsson and beyond: A study of seven children." | Sachendra Badal | badalsachendra@yahoo.com | ||||||
229 | No | No | 4th Oct 2022 | Neonatal 2: Neonatal neurology – other | Lakshmi | Bülent Kara | bkuskudar@gmail.com | Is Screening of Congenital CMV Infection in Saliva by RT-PCR Feasible? | Bülent Kara | bkuskudar@gmail.com | ||||||||
416 | No | No | 5th Oct 2022 | Peripheral nerve | D Selcen | Burcin Nazli Karacabey | bnazlikaracabey@hotmail.com | SHEAR WAVE ELASTOGRAPHY IN PATIENTS WITH SPINAL MUSCULAR ATROPHY TYPE 2-3 | Burcin Nazli Karacabey | bnazlikaracabey@hotmail.com | ||||||||
690 | No | No | 6th Oct 2022 | "Cerebral palsy 1- Evaluation: clinic | neurophysiologic" | "Catherine Arnaud | France" | Burce Emine Dortkardesler | burceyasar@gmail.com | "Assessment of Nutritional Status | Resuscitation Modalities of Malnutrition | and Enteral Feeding Products for Children with Neurological Disorders" | Burce Emine Dortkardesler | burceyasar@gmail.com | ||||
606 | No | No | 5th Oct 2022 | "CNS Malformations | NGS" | A Narayan | Cemile Busra Olculu | busra.olculu@ege.edu.tr | A Dynamic Genetic Testing Approachment for Neurological Disorders in The Pediatric Neurogenetic Case-Management Councils | Cemile Busra Olculu | busra.olculu@ege.edu.tr | |||||||
183 | No | No | 5th Oct 2022 | Neuroimmunology 1 Demyelinating / MS related | Russell Dale | Çağatay Günay | cagataygunaymd@gmail.com | Optic Neuritis in CD59 Deficiency: An Extremely Rare Presentation | Çağatay Günay | cagataygunaymd@gmail.com | ||||||||
369 | No | No | 5th Oct 2022 | Spasticity and ataxia | C Catsman | Chahnez Charfi Triki | chahnezct@gmail.com | ALPHA-FŒTOPROTEINE PROGNOSIS VALUE IN PATIENTS MONITORING WITH ATAXIA-TELANGIECTASIA | Salma Zouari Mallouli | mallouli.salma26@gmail.com | ||||||||
626 | No | No | 6th Oct 2022 | CNS Infections 1 Covid-related | "Charles Newton | Kenya" | Chahnez Charfi Triki | chahnezct@gmail.com | Post-COVID-19 related neurological features in a pediatric population | Salma Zouari Mallouli | mallouli.salma26@gmail.com | |||||||
123 | No | No | 4th Oct 2022 | ASD/NDD/ADHD 3 NDD / ID | Charuta Joshi | Nandita Chattopadhyay | chattnan@gmail.com | OVERCOMING ADVERSITIES TO PROMOTE EARLY BRAIN DEVELOPMENT IN CHILDREN - A STUDY FROM RURAL INDIA | Nandita Chattopadhyay | chattnan@gmail.com | ||||||||
146 | No | No | 5th Oct 2022 | General neurogenetics I | AR Zamani | Miaomiao Cheng | chengmiaomiao57@126.com | Genetics and clinical phenotypes of epilepsy associated with Dup15q syndrome | Yuehua Zhang | zhangyhdr@126.com | ||||||||
191 | No | No | 4th Oct 2022 | Epilepsy: Treatment 1 – ASMs | B Sanchez-Gan | Si-jia Chu | chu_sj@163.com | Efficacy and tolerability of adjunctive perampanel in pediatric patients (aged 4–12 years) with inadequately controlled focal-onset seizures | Si-jia Chu | chu_sj@163.com | ||||||||
128 | No | No | 5th Oct 2022 | Neuromuscular 1 | H Lochmüller | Çiğdem Genç Sel | cigdemsel@yahoo.com | Continuous Glucose Monitoring in Obese/Overweight Children and Adolescents with Neurological Manifestations: A Single Reference Center Experience | Çiğdem Genç Sel | cigdemsel@yahoo.com | ||||||||
162 | No | No | 5th Oct 2022 | Treatment | F Muntoni | Christian Werner | cwerner@ptcbio.com | Updated demographics and safety data from patients with nonsense mutation Duchenne muscular dystrophy receiving ataluren in the STRIDE Registry | Christian Werner | cwerner@ptcbio.com | ||||||||
165 | No | No | 5th Oct 2022 | Treatment | F Muntoni | Christian Werner | cwerner@ptcbio.com | Age at loss of ambulation in STRIDE Registry and CINRG Natural History Study patients with DMD: a matched cohort analysis | Christian Werner | cwerner@ptcbio.com | ||||||||
169 | No | No | 5th Oct 2022 | Treatment | F Muntoni | Christian Werner | cwerner@ptcbio.com | Pulmonary function in Duchenne muscular dystrophy patients from the STRIDE Registry and CINRG Natural History Study: a matched cohort analysis | Christian Werner | cwerner@ptcbio.com | ||||||||
525 | No | No | Xiaolu Chen | cxlnj@qq.com | The first case of Streptococcus intermedius brain abscess with hemophagocyic histiocytosis | Xiaolu Chen | cxlnj@qq.com | |||||||||||
545 | No | No | 6th Oct 2022 | Neuroradiology 2 | "Kshitij Mankand | UK" | Xiaolu Chen | cxlnj@qq.com | Clinical characteristics of 50 cases of cerebral cystic necrosis in children | Xiaolu Chen | cxlnj@qq.com | |||||||
260 | No | No | 5th Oct 2022 | "Neuropathy | GBS | and CMS" | C Bönnemann | Darshan Das | darshan.das@rajagirihospital.com | Isolated unilateral Palatal Palsy- a postinfectious inflammatory mononeuritis of the pharyngeal branch of the vagal nerve | Darshan Das | darshan.das@rajagirihospital.com | ||||||
202 | No | No | 5th Oct 2022 | General neurogenetics I | AR Zamani | Xianru Jiao | dc1981021@163.com | Phenotype of heterozygous variants of dehydrodolichol diphosphate synthase | Xianru Jiao | dc1981021@163.com | ||||||||
399 | No | No | 4th Oct 2022 | Epilepsy: Genetics 2 | N Specchio | Xianru Jiao | dc1981021@163.com | "A rare presentation characterized by epileptic spasms in ALDH7A1 | pyridox(am)ine-5’-phosphate oxidase (PNPO) | and PLPBP deficiency" | Xianru Jiao | dc1981021@163.com | ||||||
400 | No | No | 4th Oct 2022 | "Epilepsy: Syndromes 2 – IESS | Dravet | HHE | EMAS" | E Wirrell | Xianru Jiao | dc1981021@163.com | The clinical features and long-term follow-up of vitamin B6-responsive infantile spasms in a Chinese cohort | Xianru Jiao | dc1981021@163.com | |||||
212 | No | No | 6th Oct 2022 | Metabolic 4 Therapeutic approaches | Samantha Marin Canada | Defne Alikılıç | defnekocaoglu@hotmail.com | "Pyrimidine Metabolism Disorders as Rare Cause of Psycho-motor Retardation | Dysmorphism and Epilepsy" | Defne Alikılıç | defnekocaoglu@hotmail.com | |||||||
213 | No | No | 5th Oct 2022 | "İon channel myopathy | and metabolic" | R Horvath | Defne Alikılıç | defnekocaoglu@hotmail.com | Clinical Features Beyond Myopathy: Three Calpainopathy Patients with CAPN3 Mutation | Defne Alikılıç | defnekocaoglu@hotmail.com | |||||||
538 | No | No | 4th Oct 2022 | Neonatal 2: Neonatal neurology – other | Lakshmi | Demet Terek | demet.terek@yahoo.com | Investigation of Risk Factors in Neural Tube Defects in Newborns | Demet Terek | demet.terek@yahoo.com | ||||||||
588 | No | No | 4th Oct 2022 | ASD/NDD/ADHD 2 ASD assessments / management / Rett syndrome / high risk infants | Antigone Papavasiliou | Demet Terek | demet.terek@yahoo.com | Our cases with hypoxic ischemic encephalopathy in which we applied hypothermia | Demet Terek | demet.terek@yahoo.com | ||||||||
185 | No | No | 6th Oct 2022 | CNS Infections 1 Covid-related | "Charles Newton | Kenya" | Ari̇fe Derda Yücel Şen | derdayucel@hotmail.com | A pediatric case of reversible splenial lesion syndrome associated with SARS-CoV-2: Case report | Ari̇fe Derda Yücel Şen | derdayucel@hotmail.com | |||||||
193 | No | No | 5th Oct 2022 | SMA | N Chrestian | Ari̇fe Derda Yücel Şen | derdayucel@hotmail.com | CLİNİCAL CHARACTERİSTİCS OF CASES WİTH SPİNAL MUSCULAR ATROPHY | Ari̇fe Derda Yücel Şen | derdayucel@hotmail.com | ||||||||
584 | No | No | 6th Oct 2022 | Neuroradiology 1 | "Manohar Schroff | Canada" | Dhanalakshmi Angappan | Dhanalakshmivj@gmail.com | Ante-natal and post-natal factors affecting the rate of growth of corpus callosum in preterm infants: a retrospective study | Dhanalakshmi Angappan | Dhanalakshmivj@gmail.com | |||||||
224 | No | No | 4th Oct 2022 | ASD/NDD/ADHD 3 NDD / ID | Charuta Joshi | Dhanya Lakshmi Narayanan | dhanya.lakshmi@manipal.edu | Phenotypic and genotypic expansion of TRAPPC12-related disorder | Dhanya Lakshmi Narayanan | dhanya.lakshmi@manipal.edu | ||||||||
438 | No | No | 5th Oct 2022 | "İon channel myopathy | and metabolic" | R Horvath | Didem Ardicli | didem.aydogdu@gmail.com | "A rare cause of hypotonia | arthrogryposis | and early-onset scoliosis: Autosomal recessive PIEZO2-associated neuromuscular disease" | Didem Ardicli | didem.aydogdu@gmail.com | |||||
760 | No | No | 5th Oct 2022 | Peripheral nerve | D Selcen | Didem Ardicli | didem.aydogdu@gmail.com | Cardiac impairment in Duchenne Muscular Dystrophy: A single-center retrospective experience | Didem Ardicli | didem.aydogdu@gmail.com | ||||||||
701 | No | No | 5th Oct 2022 | Neuroimmunology 3 Autoimmune encephalitis plus | Silvia Tenenbaum | Dilara Ece Toprak | dilaraecetoprak@yahoo.com | Acute disseminated encephalomyelitis (ADEM) in children: a multicenter retrospective study | Seda Kanmaz | seda.kanmaz@ege.edu.tr | ||||||||
704 | No | No | 5th Oct 2022 | Neuroimmunology 3 Autoimmune encephalitis plus | Silvia Tenenbaum | Dilara Ece Toprak | dilaraecetoprak@yahoo.com | Anti-Hu associated encephalitis as the initial presentation of neuroblastoma | Dilara Ece Toprak | dilaraecetoprak@yahoo.com | ||||||||
51 | No | No | 5th Oct 2022 | Neuromuscular 1 | H Lochmüller | Dilek Cavusoglu | dilekcavusoglu83@gmail.com | Subcutaneous immunoglobulin in anti-HMGCR myopathy with children for long-term maintenance | Dilek Cavusoglu | dilekcavusoglu83@gmail.com | ||||||||
297 | No | No | 5th Oct 2022 | Neurogenetics practice | T Lerman-Sagie | Dilek Cavusoglu | dilekcavusoglu83@gmail.com | "Evaluation of clinical | laboratory | and imaging findings of patients with the diagnosis of Pontocerebellar Hypoplasia: A multicenter national study" | Dilek Cavusoglu | dilekcavusoglu83@gmail.com | ||||||
514 | No | No | 5th Oct 2022 | General neurogenetics I | AR Zamani | Dilek Cebeci | dilekcebeci@yahoo.com | "Lafora disease: Case report of a 13 years old patient with cognitive decline | ataxia and seizures" | Dilek Cebeci | dilekcebeci@yahoo.com | |||||||
476 | No | No | 4th Oct 2022 | Neonatal 2: Neonatal neurology – other | Lakshmi | Dipak Ram | dipak.ram@mft.nhs.uk | Neonatal Spinal Cord Injury: Not To be Missed | Dipak Ram | dipak.ram@mft.nhs.uk | ||||||||
501 | No | No | 5th Oct 2022 | "CNS Malformations | NGS" | A Narayan | Arushi Saini | doc.arushi@gmail.com | Exploring the genetic basis of Leukodystrophies through an in-house targeted panel approach in resource-poor settings | Arushi Saini | doc.arushi@gmail.com | |||||||
266 | No | No | 5th Oct 2022 | Neuroimmunology 2 Antibody mediated disorders / monophasic demyel disorder | Banu Anlar | Gülen Gül Mert | dr_gulen@hotmail.com | Evaluation of Prognostic Factors in Pediatric Transverse Myelitis: A Multicenter Cohort Study | Sevim Şahin | sevimsahin1@yahoo.com | ||||||||
114 | No | No | 5th Oct 2022 | "CNS Malformations | NGS" | A Narayan | Maha Zaki | dr_mahazaki@yahoo.com | The landscape of Lissencephaly among Egyptian Patients | Maha Zaki | dr_mahazaki@yahoo.com | |||||||
103 | No | No | 5th Oct 2022 | Neuroimmunology 3 Autoimmune encephalitis plus | Silvia Tenenbaum | Ayten Güleç | dr.aytengulec@gmail.com | "PREVALENCE AND OUTCOMES OF AUTOIMMUNE ENCEPHALITIS IN A TERTIARY HOSPITAL IN BAGUIO CITY | PHILIPPINES" | Jaidi Sagay | jdee2308@gmail.com | |||||||
762 | No | No | 4th Oct 2022 | Epilepsy: Genetics 3 | L Lagae | Ayten Güleç | dr.aytengulec@gmail.com | "National Based | Retrospective Study on the Evaluation of Clinical | Laboratory | and Imaging Research of Tuberous Sclerosis Cases" | Hüseyin Per | huseyinper@yahoo.com | |||||
325 | No | No | 4th Oct 2022 | ASD/NDD/ADHD 1 ASD genetic / biomarkers / | Chahnez Triki | Bilgihan Bikmazer | dr.bilgihan@hotmail.com | Association Between Sleep Problems and Perinatal Factors and Maternal Psychopathology in Toddlers at Risk for Autism | Bilgihan Bikmazer | dr.bilgihan@hotmail.com | ||||||||
725 | No | No | 4th Oct 2022 | ASD/NDD/ADHD 4 ADHD and Behav / syndromes / LD | Pratibha Singhi | Bilgihan Bikmazer | dr.bilgihan@hotmail.com | Neurocognitive Functions and Behavior Outcome of Preschool-Age Children with a History of Febrile Convulsions | Bilgihan Bikmazer | dr.bilgihan@hotmail.com | ||||||||
129 | No | No | 4th Oct 2022 | Epilepsy: Investigations | P Madaan | Elif Yildirim | dr.elif.ksglyldrm@gmail.com | Do Hyponatremia and Anemia in Simple Febrile Convulsions Affect Reccurence in The First 24 Hours? | Huseyin Tan | htan@atauni.edu.tr | ||||||||
133 | No | No | Elif Yildirim | dr.elif.ksglyldrm@gmail.com | Chronic meningitis mimicking idiopathic intracranial hypertension: a surprising diagnosis | Elif Yildirim | dr.elif.ksglyldrm@gmail.com | |||||||||||
135 | No | No | 4th Oct 2022 | Epilepsy: Genetics 1 | S Perry | Elif Yildirim | dr.elif.ksglyldrm@gmail.com | New two findings in idiopathic generalized epilepsy-15 (EIG-15); happy demeanor and gait disturbance: a case report | Elif Yildirim | dr.elif.ksglyldrm@gmail.com | ||||||||
709 | No | No | 6th Oct 2022 | "Movement 3 Ataxias | opsoclonus myoclonus and covid 19 impact" | "Russell Dale | Australia" | Esra Ozpinar | dr.esraozpinar@gmail.com | A rare neurodegenerative disorder mimicking autoimmune encephalitis induced by COVID-19: CONDSIAS | Esra Ozpinar | dr.esraozpinar@gmail.com | ||||||
713 | No | No | 6th Oct 2022 | Metabolic 2 Mitochondrial disorders I : clinical phenotypes and tx | "Rita Horvath | UK" | Esra Ozpi̇nar | dr.esraozpinar@gmail.com | A case with mutation of Vps13D: Leigh syndrome or spinocerebellar ataxia? | Esra Ozpi̇nar | dr.esraozpinar@gmail.com | |||||||
736 | No | No | 6th Oct 2022 | Neuroradiology 1 | "Manohar Schroff | Canada" | Esra Özpınar | dr.esraozpinar@gmail.com | Brain computed tomography still plays a critical role in the diagnosis of Aicardi-Goutières syndrome | Kürşad Aydın | kursadaydin@hotmail.com | |||||||
199 | No | No | 4th Oct 2022 | Neonatal 1: Neonatal seizures and EEG | Hannah Glass | Vrushabh Gavali | dr.vrushabhgavali@gmail.com | An Observational Study to Assess Inter-observer agreement for neonatal EEG Interpretation | Vrushabh Gavali | dr.vrushabhgavali@gmail.com | ||||||||
433 | No | No | 4th Oct 2022 | Neonatal 2: Neonatal neurology – other | Lakshmi | Vrushabh Gavali | dr.vrushabhgavali@gmail.com | A prospective observational study to determine difference in motor developmental outcomes & effect of early intervention in Full Term vs. Late Preterm neonates using INFANIB. | Vrushabh Gavali | dr.vrushabhgavali@gmail.com | ||||||||
76 | No | No | 6th Oct 2022 | "Movement 1 Chorea | dyskinesias | tremor | spasms & tx" | "Biju Hameed | UK" | Dramane Coulibaly | dramanecoul@yahoo.fr | "Diagnosis challenges of child abnormal movement in limited settings countries | the case of a little girl abandoned on the way to care" | Dramane Coulibaly | dramanecoul@yahoo.fr | |||
597 | No | No | 6th Oct 2022 | "Tuberous sclerosis | Radiology" | K Aydın | Ami Shah | drami.rajesh.shah@gmail.com | Unravelling the diagnostic dilemma – A case series of radiologically diagnosed pontocerebellar hypoplasia. | Ami Shah | drami.rajesh.shah@gmail.com | |||||||
136 | No | No | 6th Oct 2022 | Metabolic 1 Clinical phenotypes | "Brahim Tabarki | KSA" | Arzu Ekici | drarzuekici@gmail.com | Temporary Consciousness Disturbance in Van der Knaap disease after Minor Head Trauma | Arzu Ekici | drarzuekici@gmail.com | |||||||
710 | No | No | 4th Oct 2022 | ASD/NDD/ADHD 2 ASD assessments / management / Rett syndrome / high risk infants | Antigone Papavasiliou | Ayfer Arduc Akcay | drayfer@gmail.com | The Determinants of Quality of Life in Rett Syndrome: A Cross-sectional Study | Ayfer Arduc Akcay | drayfer@gmail.com | ||||||||
652 | No | No | 4th Oct 2022 | ASD/NDD/ADHD 2 ASD assessments / management / Rett syndrome / high risk infants | Antigone Papavasiliou | Ayşe Kaçar Bayram | draysebayram@gmail.com | Autonomic Nervous System Function Changes during Arousals in Children with Primary Nocturnal Enuresis | Ayşe Kaçar Bayram | draysebayram@gmail.com | ||||||||
478 | No | No | 5th Oct 2022 | Neuroimmunology 1 Demyelinating / MS related | Russell Dale | Seyfeddine Baouia | drbaouiaseyf@gmail.com | Devic's neuromyelitis optica (NMO) or a pediatric onset multiple sclerosis (MS)? A case report | Seyfeddine Baouia | drbaouiaseyf@gmail.com | ||||||||
480 | No | No | 6th Oct 2022 | Metabolic 2 Mitochondrial disorders I : clinical phenotypes and tx | "Rita Horvath | UK" | Seyfeddine Baouia | drbaouiaseyf@gmail.com | "A case of mitochondrial neuro-gastrointestinal encephalopathy or MNGIE syndrome | why not?" | Seyfeddine Baouia | drbaouiaseyf@gmail.com | ||||||
335 | No | No | 5th Oct 2022 | Neurogenetics practice | T Lerman-Sagie | Canan Üstün | drcananustun@hotmail.com | An Aicardi-Goutieres Syndrome 2 Case | Canan Üstün | drcananustun@hotmail.com | ||||||||
255 | No | No | 5th Oct 2022 | Neuroimmunology 1 Demyelinating / MS related | Russell Dale | Deniz Yuksel | drdeniz_yuksel@yahoo.com.tr | Clinical efficacy and safety of intrathecal methotrexate in the treatment of Balo’s concentric sclerosis: a case report | Deniz Yuksel | drdeniz_yuksel@yahoo.com.tr | ||||||||
360 | No | No | 5th Oct 2022 | Muscular dystrophy | Y Nevo | Derya Guder | drderyaguderkurt@gmail.com | LİMBE GİRDLE MUSCULAR DYSTROPHY WİTH A MUTATİON İN THE CAVEOLİN-3 (CAV-3) GENE | Derya Guder | drderyaguderkurt@gmail.com | ||||||||
363 | No | No | 5th Oct 2022 | General neurogenetics I | AR Zamani | Derya Guder | drderyaguderkurt@gmail.com | A RARE CAUSE OF AUTISM AND EPILEPSY COMBINATION: GRM7 GENE MUTATION | Derya Guder | drderyaguderkurt@gmail.com | ||||||||
71 | No | No | 5th Oct 2022 | Neuromuscular 1 | H Lochmüller | Gokce Eser | drgokceeser@gmail.com | CLINICAL SPECTRUM OF THE LIMB-GIRDLE MUSCULAR DYSTROPHY TYPE 2E (LGMD2E) | Gokce Eser | drgokceeser@gmail.com | ||||||||
72 | No | No | 6th Oct 2022 | Metabolic 2 Mitochondrial disorders I : clinical phenotypes and tx | "Rita Horvath | UK" | Gokce Eser | drgokceeser@gmail.com | THE MIRACLE OF NUCLEOSIDE TREATMENT IN THYMIDINE KINASE 2 DEFICIENCY | Gokce Eser | drgokceeser@gmail.com | |||||||
641 | No | No | 4th Oct 2022 | Epilepsy: Status epilepticus and Miscellaneous | T Loddenkemper | Harshkumar Patel | drharsh9@gmail.com | Novel treatment approach to NORSE (new onset refractory status epilepticus) in children: Skipping the pharmacological coma | Harshkumar Patel | drharsh9@gmail.com | ||||||||
624 | No | No | Ibrahim Oncel | dribrahimoncel@gmail.com | Global burden of measles: A registry of neurological complications | Ibrahim Oncel | dribrahimoncel@gmail.com | |||||||||||
315 | No | No | 4th Oct 2022 | "Epilepsy: DEEs | TSC | RETT and Comorbidities" | Y Jiang | İpek Dokurel Cetin | dripekdokurel@gmail.com | The Impact of Epilepsy on Sleep Characteristics in Epileptic Adolescents and their Caregivers | İpek Dokurel Cetin | dripekdokurel@gmail.com | ||||||
486 | No | No | 4th Oct 2022 | Neonatal 1: Neonatal seizures and EEG | Hannah Glass | İpek Dokurel Cetin | dripekdokurel@gmail.com | "Clinical | electrophysiological | and neuroimaging predictors for antiseizure medication in infants with neonatal clinical seizures" | İpek Dokurel Cetin | dripekdokurel@gmail.com | ||||||
564 | No | No | 4th Oct 2022 | Neonatal 2: Neonatal neurology – other | Lakshmi | Lokesh Saini | drlokeshsaini@gmail.com | General Movement Assessment for predicting the neurodevelopmental outcomes in cohort of infants exposed to severe hyperbilirubinemia and hypoxic ischaemic encephalopathy respectively in the neonatal period | Lokesh Saini | drlokeshsaini@gmail.com | ||||||||
733 | No | No | 6th Oct 2022 | Neuroradiology 3 | "Ajay Taranath | Australia" | Marya Hameed | drmash84@gmail.com | KEEP AN AYE ON LUMPY BUMPY HEAD: A CASE SERIES HIGHLIGHTING SPECTRUM OF PRESENTATION IN CRANIOSYNOSTOSIS | Marya Hameed | drmash84@gmail.com | |||||||
689 | No | No | 6th Oct 2022 | Metabolic 4 Therapeutic approaches | Samantha Marin Canada | Mert Altıntaş | drmertcanaltintas@gmail.com | A case of asparagine synthetase deficiency successfully treated with ketogenic diet | Miraç Yıldırım | miracyildirim81@hotmail.com | ||||||||
107 | No | No | 6th Oct 2022 | "Tuberous sclerosis | Radiology" | K Aydın | Maureen Njoroge | drmuthoninjoroge@gmail.com | NEUROIMAGING CHARACTERISTICS OF TUBEROUS SCLEROSIS COMPLEX IN PAEDIATRIC PATIENTS AT A TERTIARY HEALTH FACILITY IN KENYA: A CASE SERIES | Maureen Njoroge | drmuthoninjoroge@gmail.com | |||||||
302 | No | No | 4th Oct 2022 | ASD/NDD/ADHD 4 ADHD and Behav / syndromes / LD | Pratibha Singhi | Maureen Njoroge | drmuthoninjoroge@gmail.com | BROAD SPECTRUM MICRONUTRIENT SUPPLEMENTATION IN THE MANAGEMENT OF ADHD: A CLINICAL TRIAL AND SYSTEMATIC REVIEW | Maureen Njoroge | drmuthoninjoroge@gmail.com | ||||||||
242 | No | No | 4th Oct 2022 | ASD/NDD/ADHD 4 ADHD and Behav / syndromes / LD | Pratibha Singhi | Ömer Karaca | dromerkaraca@gmail.com | PURA Syndrome: A Specific Phenotype | Ömer Karaca | dromerkaraca@gmail.com | ||||||||
243 | No | No | 6th Oct 2022 | "Movement 1 Chorea | dyskinesias | tremor | spasms & tx" | "Biju Hameed | UK" | Ömer Karaca | dromerkaraca@gmail.com | Efficacy of zinc treatment in 2 cases with Arg209Cys mutation in GNAO1 gene | Ömer Karaca | dromerkaraca@gmail.com | ||||
751 | No | No | 5th Oct 2022 | Neuroimmunology 1 Demyelinating / MS related | Russell Dale | Özben Akıncı Göktaş | drozben@gmail.com | Two Pediatric Cases of Initial Manifestation of Multiple Sclerosis After Immunization with the Pfizer-BioNTech COVID 19 Vaccine | Özben Akıncı Göktaş | drozben@gmail.com | ||||||||
78 | No | No | 6th Oct 2022 | "Tuberous sclerosis | Radiology" | K Aydın | Özlem Yayıcı Köken | drozlemkoken@gmail.com | Thinning of the corpus callosum prominent in the splenium and colpocephaly: the AP-4 deficiency syndrome | Özlem Yayıcı Köken | drozlemkoken@gmail.com | |||||||
95 | No | No | 5th Oct 2022 | Neuromuscular 1 | H Lochmüller | Özlem Yayıcı Köken | drozlemkoken@gmail.com | Muscle cramps may be a clue for GFPT1 gene related congenital myasthenic syndrome | Özlem Yayıcı Köken | drozlemkoken@gmail.com | ||||||||
88 | No | No | 6th Oct 2022 | Education | "Jorge Vidaurre | US" | Pınar Özkan Kart | drpinar_ozkan@yahoo.com | Online Mother and Baby Yoga for Preterm-Born Infants and Their Mothers in the Time of COVID-19 Pandemic | Dilara Bozgan | dilarabozgan@gmail.com | |||||||
650 | No | No | 4th Oct 2022 | Epilepsy: Status epilepticus and Miscellaneous | T Loddenkemper | Pınar Özkan Kart | drpinar_ozkan@yahoo.com | Increased Post-Seizure ACTH Peak May Have a Role in the Benign Characteristics of Febrile Seizures | Sevim Şahin | sevimsahin1@yahoo.com | ||||||||
132 | No | No | 4th Oct 2022 | Epilepsy: Investigations | P Madaan | Rahul Sinha | drrahul_2000@yahoo.com | The Diagnostic Utility of the Video EEG at a Tertiary Care Center of North India: A Retrospective Study | Rahul Sinha | drrahul_2000@yahoo.com | ||||||||
691 | No | No | Renu Suthar | drrenusuthar@gmail.com | Serious neurological complication associated with COVID 19 and MISC: Do we need to be more vigilant? | Renu Suthar | drrenusuthar@gmail.com | |||||||||||
592 | No | No | 5th Oct 2022 | Genetics and epilepsy II | Ramachandran Nair | Sakir Genc | drsakirgenc@yahoo.com | A Cause of Severe Hypotonia in Infancy: Allan-Herndon-Dudley Syndrome | Sakir Genc | drsakirgenc@yahoo.com | ||||||||
613 | No | No | 4th Oct 2022 | Neonatal 1: Neonatal seizures and EEG | Hannah Glass | Seda Kanmaz | drsedakanmaz@gmail.com | A new scoring model for outcomes in neonates with seizures: ENEOSS (Ege Neonatal Seizure Scoring Model) | Seda Kanmaz | drsedakanmaz@gmail.com | ||||||||
620 | No | No | 4th Oct 2022 | Neonatal 2: Neonatal neurology – other | Lakshmi | Seda Kanmaz | drsedakanmaz@gmail.com | A multimodal prognostic evaluation of preterm and term infants with neonatal encephalopathy in a prospective follow-up study | Seda Kanmaz | drsedakanmaz@gmail.com | ||||||||
757 | No | No | 5th Oct 2022 | Peripheral nerve | D Selcen | Selcan Öztürk | drselcanozturk@gmail.com | Evaluation Of Pediatric Cases With Gullian Barre Syndrome: A National Multicenter Study | Mehmet Canpolat | drmehmetcanpolat@gmail.com | ||||||||
474 | No | No | 6th Oct 2022 | Headache/Stroke 3 | "Mubeen Rafay | Canada" | Sevcan İpek | drsevcanipek@gmail.com | The Case of a 15-year-old Adolescent with Cerebral and Pulmonary Fat Embolism Syndrome without Dermatologic Involvement | Sevcan İpek | drsevcanipek@gmail.com | |||||||
301 | No | No | 5th Oct 2022 | SMA | N Chrestian | Smilu Mohanlal | drsmilu@gmail.com | Setting up of a standard of care for children with spinal muscular atrophy at a tertiary care center in North Kerala: South India | Smilu Mohanlal | drsmilu@gmail.com | ||||||||
489 | No | No | Suhani Shah | drsuhaniashah@gmail.com | "Efficacy | safety and tolerability of Gabapentin as monotherapy for dystonic cerebral palsy" | Suhani Shah | drsuhaniashah@gmail.com | ||||||||||
493 | No | No | 6th Oct 2022 | Cerebral palsy 2- Management; current and future | "Antigone Papavasiliou | Greece" | Suhani Shah | drsuhaniashah@gmail.com | Gabapentin: Efficacy and tolerability as adjuvant therapy for dystonic cerebral palsy | Suhani Shah | drsuhaniashah@gmail.com | |||||||
565 | No | No | 6th Oct 2022 | "Movement 2 Dystonia | Parkinsons | tremor and epidemiology" | "Jon Mink | US" | Suhani Shah | drsuhaniashah@gmail.com | Spectrum of genetically determined movement disorder in Indian Cohort | Suhani Shah | drsuhaniashah@gmail.com | |||||
410 | No | No | 4th Oct 2022 | Epilepsy: Status epilepticus and Miscellaneous | T Loddenkemper | Sevim Türay | drsvm@yahoo.com | Can the gut microbiota be a guide in the diagnosis and treatment of childhood epilepsy? | Sevim Türay | drsvm@yahoo.com | ||||||||
627 | No | No | 4th Oct 2022 | Epilepsy: Treatment 3 – ASM/ Dietary Treatments | J Sahu | Edibe Pembegul Yildiz | edibepembegul@hotmail.com | Management of Valproat Monotherapy in Adolescent Girls with Epilepsy; Evaluation of Predictive Factors of Seizure Recurrens | Edibe Pembegul Yildiz | edibepembegul@hotmail.com | ||||||||
643 | No | No | 4th Oct 2022 | ASD/NDD/ADHD 1 ASD genetic / biomarkers / | Chahnez Triki | Elif Didinmez Taşkırdı | edidinmez@hotmail.com | Neurological Evaluation and Electroencephalographic Findings in Children with Autism Diagnosis | Elif Didinmez Taşkırdı | edidinmez@hotmail.com | ||||||||
546 | No | No | 5th Oct 2022 | SMA | N Chrestian | Eli̇f Acar Arslan | elifacararslan@gmail.com | Spinal Muscular Atrophy with Two SMN2 Copies and Preserved Deep Tendon Reflexes: An Extremely Rare Case | Eli̇f Acar Arslan | elifacararslan@gmail.com | ||||||||
561 | No | No | 5th Oct 2022 | SMA | N Chrestian | Eli̇f Acar Arslan | elifacararslan@gmail.com | The effect of Nusinersen and starting age on the improvement of motor performance in Spinal Muscular Atrophy (SMA): Preliminary results | Eli̇f Acar Arslan | elifacararslan@gmail.com | ||||||||
571 | No | No | 5th Oct 2022 | Treatment | F Muntoni | Eli̇f Acar Arslan | elifacararslan@gmail.com | Interobserver Reliability of the Turkish Translation of Timed Tests in Duchenne Muscular Dystrophy | Eli̇f Acar Arslan | elifacararslan@gmail.com | ||||||||
577 | No | No | 6th Oct 2022 | Headache/Stroke 3 | "Mubeen Rafay | Canada" | Eli̇f Acar Arslan | elifacararslan@gmail.com | A Child with Cerebral Venous Thrombosis Secondary to COVID 19 Infection Successfully Treated with Thrombectomy | Eli̇f Acar Arslan | elifacararslan@gmail.com | |||||||
651 | No | No | 4th Oct 2022 | Epilepsy: Semiology and Clinical | H Cross | Elif Karatoprak | elifyuksel2001@yahoo.com | Evaluation of Childhood Epilepsies with Frontal Paroxysm | Elif Karatoprak | elifyuksel2001@yahoo.com | ||||||||
160 | No | No | 4th Oct 2022 | "Epilepsy: Syndromes 1 – Self-limited | EE/DEE-SWAS" | C Joshi | Emily Innes | emily.innes@health.nsw.gov.au | Neurodevelopmental outcomes and clinical utility of genetic testing in a cohort of Australian families with self-limited (familial) epilepsy (neonatal/infantile onset) | Emily Innes | emily.innes@health.nsw.gov.au | |||||||
91 | No | No | 6th Oct 2022 | Education | "Jorge Vidaurre | US" | Emine Tekin | emine.tekin@giresun.edu.tr | Online paediatric EEG handbook: a survey on its usefulness | Veena Kander | veena.kander@uct.ac.za | |||||||
512 | No | No | 4th Oct 2022 | ASD/NDD/ADHD 3 NDD / ID | Charuta Joshi | Enise Avci Durmusalioglu | eniseavci.ea@gmail.com | A Novel Candidate Gene For Neurodevelopmental Disorders: JKAMP | Enise Avci Durmusalioglu | eniseavci.ea@gmail.com | ||||||||
141 | No | No | 6th Oct 2022 | "Movement 2 Dystonia | Parkinsons | tremor and epidemiology" | "Jon Mink | US" | Esra Serdaroglu | esra.serdaroglu@gmail.com | An Investigation of the relationship between dystonia severity and functional independence and quality of life in children with dystonia: A Preliminary Study | Kamile Uzun Akkaya | kuzun87@hotmail.com | |||||
134 | No | No | 6th Oct 2022 | "Cerebral palsy 1- Evaluation: clinic | neurophysiologic" | "Catherine Arnaud | France" | Esra Serdaroglu | esras@gazi.edu.tr | Clinical characteristic of oropharyngeal dysphagia and swallowing safety in children with dystonia: a preliminary report | Muserrefe Nur Keles | muserrefkeles19@gmail.com | ||||||
569 | No | No | 4th Oct 2022 | ASD/NDD/ADHD 3 NDD / ID | Charuta Joshi | Elena Sukarova-angelovska | esukarova@doctor.com | Application of advanced molecular technologies in revealing the etiology of intellectual disability – clarification or more questions | Elena Sukarova-angelovska | esukarova@doctor.com | ||||||||
556 | No | No | 6th Oct 2022 | "Movement 2 Dystonia | Parkinsons | tremor and epidemiology" | "Jon Mink | US" | Eugenia Roza | eugenia.roza@umfcd.ro | Novel mutation variant in GCH1 gene - a new cause for infantile-onset severe dystonic encephalopathy? | Eugenia Roza | eugenia.roza@umfcd.ro | |||||
590 | No | No | 5th Oct 2022 | "İon channel myopathy | and metabolic" | R Horvath | Fatema Al Amrani | fatemaamrani@gmail.com | MLIP-associated myopathy; report of a patient and review of the literature | Fatema Al Amrani | fatemaamrani@gmail.com | |||||||
780 | No | No | 4th Oct 2022 | ASD/NDD/ADHD 3 NDD / ID | Charuta Joshi | Francisco Carratalá-marco | fcarratalamarco@gmail.com | "PATHOLOGICAL | PROBABLY PATHOLOGICAL OR OF UNCERTAIN SIGNIFICANCE COPY NUMBER VARIANT IN A POPULATION OF PATIENTS WITH NEURODEVELOPMENTAL DISORDERS WITH EPIDEMIOLOGICAL REPRESENTATION." | Francisco Carratalá-marco | fcarratalamarco@gmail.com | |||||||
491 | No | No | 5th Oct 2022 | Spasticity and ataxia | C Catsman | Faruk Incecik | fincecik@yahoo.com | Hereditary spastic paraplegia type 26 with a novel mutation in B4GALNT1 gene and literature review of the clinical features | Faruk Incecik | fincecik@yahoo.com | ||||||||
492 | No | No | 5th Oct 2022 | Spasticity and ataxia | C Catsman | Faruk Incecik | fincecik@yahoo.com | Homozygous mutation in CWF19L1 with recessive ataxia syndrome in a Turkish child | Faruk Incecik | fincecik@yahoo.com | ||||||||
288 | No | No | 5th Oct 2022 | Neuromuscular 1 | H Lochmüller | Gamze Sarıkaya Uzan | gamzeuzan36@gmail.com | Pediatric Onset Chronic Inflammatory Demyelinating Polyneuropathy: A Multicenter Study from Türkiye | Gamze Sarıkaya Uzan | gamzeuzan36@gmail.com | ||||||||
574 | No | No | 6th Oct 2022 | "Movement 3 Ataxias | opsoclonus myoclonus and covid 19 impact" | "Russell Dale | Australia" | Gautam Kamila | gautamkamila7@gmail.com | CLINICO-EPIDEMIOLOGICAL PROFILE OF CHILDREN WITH OPSOCLONUS MYOCLONUS ATAXIA SYNDROME: A DECADE’S EXPERIENCE FROM A TERTIARY CARE CENTRE IN NORTH INDIA | Sheffali Gulati | sheffaligulati1@gmail.com | ||||||
633 | No | No | 5th Oct 2022 | Neuroimmunology 3 Autoimmune encephalitis plus | Silvia Tenenbaum | Gautam Kamila | gautamkamila7@gmail.com | Anti-NMDA receptor encephalitis in children – tale of ten years at a tertiary care center | Sheffali Gulati | sheffaligulati1@gmail.com | ||||||||
456 | No | No | 4th Oct 2022 | Epilepsy: Genetics 1 | S Perry | Hande Gazeteci Tekin | gazetecihande@yahoo.com.tr | "Very rare novel DHDDS mutation of infant with severe mental-motor retardation | resistant epilepsy | movement disorder" | Hande Gazeteci Tekin | gazetecihande@yahoo.com.tr | ||||||
279 | No | No | 5th Oct 2022 | Muscular dystrophy | Y Nevo | Gokcen Oz Tuncer | gokcenoz@hotmail.com | A Multicenter Retrospective Study in Turkish Children with Myotonic Dystrophy Type 1 | Gokcen Oz Tuncer | gokcenoz@hotmail.com | ||||||||
282 | No | No | 5th Oct 2022 | "İon channel myopathy | and metabolic" | R Horvath | Gokcen Oz Tuncer | gokcenoz@hotmail.com | Clinical And Genetic Spectrum of Myotonia Congenita in Turkish Children | Gokcen Oz Tuncer | gokcenoz@hotmail.com | |||||||
482 | No | No | 4th Oct 2022 | ASD/NDD/ADHD 3 NDD / ID | Charuta Joshi | Hideyo Goma | goma@kyokyo-u.ac.jp | Developmental trends and changes in children: Comparing assessment data of Japanese children from 1983 and 2020 | Hideyo Goma | goma@kyokyo-u.ac.jp | ||||||||
417 | No | No | 4th Oct 2022 | Epilepsy: Genetics 1 | S Perry | Hyo Jeong Kim | greatelena@naver.com | Missense variants in RHOBTB2 in a patient with developmental and epileptic encephalopathy and paroxysmal movement disorder | Hyo Jeong Kim | greatelena@naver.com | ||||||||
611 | No | No | 5th Oct 2022 | Neuroimmunology 2 Antibody mediated disorders / monophasic demyel disorder | Banu Anlar | Gülcan Akyüz | gulcan.akyuz@hotmail.com | A VERY YOUNG GİRL LİMBİC ENCEPHALİTİS WİTH LGI1 ANTİBODİES | Gülcan Akyüz | gulcan.akyuz@hotmail.com | ||||||||
306 | No | No | Pembe Gültutan | gultutanp@gmail.com | Acute Cerebellit: Is it always benign? | Pembe Gültutan | gultutanp@gmail.com | |||||||||||
572 | No | No | 4th Oct 2022 | Epilepsy: Status epilepticus and Miscellaneous | T Loddenkemper | Pembe Gültutan | gultutanp@gmail.com | Posterior Ocular Structure Parameters by Optical Coherence Tomography Angiography in Pediatric Epilepsy patients | Pembe Gültutan | gultutanp@gmail.com | ||||||||
435 | No | No | 5th Oct 2022 | General neurogenetics II | A R Tavasoli | Gunce Basarir | guncebasarir@gmail.com | Phenotypic diversity of 15q11.2 copy number variants: a case series and review of the literature | Nihal Olgac Dundar | nodundar@gmail.com | ||||||||
144 | No | No | 4th Oct 2022 | Epilepsy: Treatment 1 – ASMs | B Sanchez-Gan | Timothy B Saurer | gw2022encoresubmissions@heliosmedcomms.com | Efficacy and Safety of Cannabidiol Dose Adjustment in Patients with Lennox-Gastaut Syndrome in a Phase 3 Trial and Open-label Extension | Timothy B Saurer | gw2022encoresubmissions@heliosmedcomms.com | ||||||||
541 | No | No | 4th Oct 2022 | ASD/NDD/ADHD 1 ASD genetic / biomarkers / | Chahnez Triki | Wen-xiong Chen | gzchcwx@126.com | "Parental age | socioeconomic status and parity related with the clinical phenotypes in children with autism spectrum disorder" | Wen-xiong Chen | gzchcwx@126.com | |||||||
772 | No | No | 5th Oct 2022 | Neuroimmunology 3 Autoimmune encephalitis plus | Silvia Tenenbaum | Hale Atalay Celik | hale.atalay@gmail.com | Anti-NMDA receptor encephalitis after Human Bocavirus infection | Hale Atalay Celik | hale.atalay@gmail.com | ||||||||
776 | No | No | 5th Oct 2022 | "İon channel myopathy | and metabolic" | R Horvath | Hale Atalay Celi̇k | hale.atalay@gmail.com | Clinical Spectrum of Voltage-gated Sodium Channelopaties; One-center Experience | Hale Atalay Celi̇k | hale.atalay@gmail.com | |||||||
77 | No | No | 6th Oct 2022 | Cerebral palsy 2- Management; current and future | "Antigone Papavasiliou | Greece" | Naja'atu Hamza | hamzanajaatu@gmail.com | HEALTH-RELATED QUALITY OF LIFE OF CHILDREN \WITH CEREBRAL PALSY AT A TERTIARY HOSPITAL IN NIGERIA | Naja'atu Hamza | hamzanajaatu@gmail.com | |||||||
119 | No | No | 4th Oct 2022 | Epilepsy: Treatment 1 – ASMs | B Sanchez-Gan | Naja'atu Hamza | hamzanajaatu@gmail.com | Pyridoxine in Management of Super-Refractory Status Epilepticus: A Case Report | Naja'atu Hamza | hamzanajaatu@gmail.com | ||||||||
250 | No | No | 6th Oct 2022 | "Cerebral palsy 1- Evaluation: clinic | neurophysiologic" | "Catherine Arnaud | France" | Hanan Azouz | hananazouz@hotmail.com | Clinical and electophysiological evaluation of autonomic dysfunction in children with spastic cerebral palsy | Hanan Azouz | hananazouz@hotmail.com | ||||||
472 | No | No | 6th Oct 2022 | Headache/Stroke 2 | "Mahendra Moharir | Canada" | Hanan Azouz | hananazouz@hotmail.com | CLINICAL PROFILE OF HEADACHE AMONG CHILDREN ATTENDING EMERGENCY DEPARTMENT AT ALEXANDRIA UNIVERSITY CHILDREN'S HOSPITAL | Hanan Azouz | hananazouz@hotmail.com | |||||||
171 | No | No | 5th Oct 2022 | Molecular genetics | T Sultan | Handan Kava | handankava@gmail.com | Evaluation of the etiology of epilepsy and/or developmental delay in children with next generation sequencing: A single center experience | Handan Kava | handankava@gmail.com | ||||||||
458 | No | No | 5th Oct 2022 | General neurogenetics I | AR Zamani | Hande Dilber | handecozeli@hotmail.com | PROGRESSIVE MYOCLONIC EPILEPSY RELATED TO SEMA6B GENE MUTATION | Hande Dilber | handecozeli@hotmail.com | ||||||||
616 | No | No | 5th Oct 2022 | Molecular genetics | T Sultan | Jiyoon Han | hanji024@naver.com | "Bi-allelic POLR3A null variants cause autosomal recessive leukodystrophy | hypomyelinating | 7" | Jiyoon Han | hanji024@naver.com | ||||||
351 | No | No | 6th Oct 2022 | Neuroradiology 2 | "Kshitij Mankand | UK" | Hans Hartmann | hartmann.hans@mh-hannover.de | Cerebral microstructural changes in children suffering from hemolytic uremic syndrome | Hans Hartmann | hartmann.hans@mh-hannover.de | |||||||
386 | No | No | 6th Oct 2022 | Headache/Stroke 3 | "Mubeen Rafay | Canada" | Hans Hartmann | hartmann.hans@mh-hannover.de | Anterior spinal artery syndrome due to fibrocartilaginous embolism – case report and treatment options | Hans Hartmann | hartmann.hans@mh-hannover.de | |||||||
407 | No | No | 4th Oct 2022 | "Epilepsy: Syndromes 2 – IESS | Dravet | HHE | EMAS" | E Wirrell | Hasan Tekgul | hasan.tekgul@ege.edu.tr | Electro-clinic features and outcome in children with “pure” epilepsy with myoclonic atonic seizures (EMAS) | Hasan Tekgul | hasan.tekgul@ege.edu.tr | |||||
621 | No | No | 4th Oct 2022 | Neonatal 1: Neonatal seizures and EEG | Hannah Glass | Hasan Tekgul | hasan.tekgul@ege.edu.tr | The clinical value of amplitude-integrated EEG for neonatal seizures: comparison of short-term (6-12 hours) and long-term (24-48 hours) monitoring | Hasan Tekgul | hasan.tekgul@ege.edu.tr | ||||||||
734 | No | No | 4th Oct 2022 | Neonatal 1: Neonatal seizures and EEG | Hannah Glass | Hasan Tekgul | hasan.tekgul@ege.edu.tr | The adaptability of health care professionals to the new neonatal seizure classification : ILAE-2020 | Seda Kanmaz | seda.kanmaz@ege.edu.tr | ||||||||
65 | No | No | 5th Oct 2022 | Neuroimmunology 1 Demyelinating / MS related | Russell Dale | Hayder Kadhim Jabbar | hayderkadhim84@gmail.com | "Neuromyelitis Optica Spectrum Disorder in a sample of children: Experience of Children Welfare Teaching Hospital | Baghdad" | Nebal Waill Saadi | nebalpedneu2013@gmail.com | |||||||
562 | No | No | 4th Oct 2022 | Epilepsy: Genetics 1 | S Perry | Hazem Eltoukhy | hazemeltoukhy98@gmail.com | SPTAN1 related epileptic encephalopathy- a case study | Hazem Eltoukhy | hazemeltoukhy98@gmail.com | ||||||||
331 | No | No | 6th Oct 2022 | "Tuberous sclerosis | Radiology" | K Aydın | Hepsen Mine Serin | hepsenmine@yahoo.com | Clinical and molecular spectrum of tuberous sclerosis complex in a regional cohort: an efficacy and outcome study with antiseizure medication plus mTOR inhibitor therapy | Hepsen Mine Serin | hepsenmine@yahoo.com | |||||||
518 | No | No | 5th Oct 2022 | SMA | N Chrestian | Hoi Ning Hayley Ip | hnhayleyip@gmail.com | The impact of Nusinersen treatment on scoliosis progression in patients with Spinal Muscular Atrophy | Hoi Ning Hayley Ip | hnhayleyip@gmail.com | ||||||||
498 | No | No | 4th Oct 2022 | Epilepsy: Treatment 2 – ASMs | Ramachandran Nair | Hamit Özyürek | hozyurekibu@hotmail.com | Topiramate alters the erythrocyte osmotic fragility and whole blood viscosity | Ayşe Meltem Sevgili | msevgili@gazi.edu.tr | ||||||||
138 | No | No | 5th Oct 2022 | Neuroimmunology 2 Antibody mediated disorders / monophasic demyel disorder | Banu Anlar | Huseyin Tan | htan@atauni.edu.tr | Myelin oligodendrocyte glycoprotein antibody-associated disorder due to COVID 19 infection: a child case report | Huseyin Tan | htan@atauni.edu.tr | ||||||||
322 | No | No | 5th Oct 2022 | Neuromuscular 1 | H Lochmüller | Huseyin Tan | htan@atauni.edu.tr | Guillain–Barre Syndrome due to COVID 19 in a child with acute lymphoblastic leukemia: a case report | Huseyin Tan | htan@atauni.edu.tr | ||||||||
275 | No | No | 4th Oct 2022 | ASD/NDD/ADHD 3 NDD / ID | Charuta Joshi | Hülya Maraş Genç | hulyamaras@gmail.com | Clinical characteristics of children with neurodevelopmental delay and pathogenic copy number variations who underwent microarray analysis | Hülya Maraş Genç | hulyamaras@gmail.com | ||||||||
460 | No | No | 4th Oct 2022 | ASD/NDD/ADHD 4 ADHD and Behav / syndromes / LD | Pratibha Singhi | Hussein Abdeldayem | husseindayem@hotmail.com | Study of computerized cognitive training technique for treatment of children with attention deficit hyperactivity disorder. A new treatment modality experience. | Hussein Abdeldayem | husseindayem@hotmail.com | ||||||||
79 | No | No | 4th Oct 2022 | Epilepsy: Genetics 1 | S Perry | İlknur Erol | ilknur_erol@yahoo.com | CHEDDA syndrome associated with epileptic encephalopathy and hand stereotypies | İlknur Erol | ilknur_erol@yahoo.com | ||||||||
83 | No | No | 5th Oct 2022 | General neurogenetics II | A R Tavasoli | İlknıur Erol | ilknur_erol@yahoo.com | A novel mutation in the RUNX2 gene; a rare cause of enlarged fontanel | İlknıur Erol | ilknur_erol@yahoo.com | ||||||||
236 | No | No | 5th Oct 2022 | General neurogenetics II | A R Tavasoli | İlknur Erol | ilknur_erol@yahoo.com | First case of Bohring-Opitz syndrome inherited from the father | İlknur Erol | ilknur_erol@yahoo.com | ||||||||
237 | No | No | 4th Oct 2022 | Epilepsy: Genetics 1 | S Perry | İlknur Erol | ilknur_erol@yahoo.com | FOXG1 gene related epileptic diskinetic encephalopathy | Yasemin Özkale | dryaseminozkale@gmail.com | ||||||||
238 | No | No | 6th Oct 2022 | Metabolic 1 Clinical phenotypes | "Brahim Tabarki | KSA" | İlknur Erol | ilknur_erol@yahoo.com | Intermediate severe Salla Disease in differential diagnosis of hypomyelinating leukodystrophy: the second and third case from Turkey | İlknur Erol | ilknur_erol@yahoo.com | |||||||
405 | No | No | 5th Oct 2022 | "İon channel myopathy | and metabolic" | R Horvath | İlknur Erol | ilknur_erol@yahoo.com | Ketogenic diet for 134 cases of SCN1A related drug-resistant epilepsy | Jianxiang Liao | liaojianxiang@vip.sina.com | |||||||
326 | No | No | 4th Oct 2022 | Neonatal 1: Neonatal seizures and EEG | Hannah Glass | Ilknur Cankurt | ilknurcankurt@gmail.com | "Neonatal Amplitude Integrated EEG (aEEG): Contribution to Clinical | Etiologic | and Prognosis" | Ilknur Cankurt | ilknurcankurt@gmail.com | ||||||
327 | No | No | 4th Oct 2022 | "Epilepsy: Neuroimaging | Surgery and Basic Science" | C Akman | İlknur Cankurt | ilknurcankurt@gmail.com | PRE-SURGERY PHASE 1 EVALUATION RESULTS AND CONTRIBUTION TO SURGERY IN PEDIATRIC PATIENTS WITH DRUG-RESISTANT EPILEPSY | İlknur Cankurt | ilknurcankurt@gmail.com | |||||||
366 | No | No | 4th Oct 2022 | Epilepsy: Treatment 2 – ASMs | Ramachandran Nair | Ilknur Cankurt | ilknurcankurt@gmail.com | COMPARISON OF CORTİCOSTEROİDS VERSUS CLOBAZAM TREATMENT OF EPİLEPTİC ENCEPHALOPATHY WİTH ELECTRİCAL STATUS EPİLEPTİCUS FOR ELECTROCLINICAL REMISSION | Ilknur Cankurt | ilknurcankurt@gmail.com | ||||||||
75 | No | No | 6th Oct 2022 | Education | "Jorge Vidaurre | US" | Zeinab Kone | inakone82@yahoo.fr | The challenges of training in Child Neurology in West Africa countries | Zeinab Kone | inakone82@yahoo.fr | |||||||
85 | No | No | 6th Oct 2022 | Cerebral palsy 2- Management; current and future | "Antigone Papavasiliou | Greece" | Indrasish Ray Chaudhuri | indrasishraychaudhuri162@gmail.com | An unusual cause of torticollis in childhood | Indrasish Ray Chaudhuri | indrasishraychaudhuri162@gmail.com | |||||||
56 | No | No | 4th Oct 2022 | ASD/NDD/ADHD 1 ASD genetic / biomarkers / | Chahnez Triki | Ingrid Tein | ingtein@sympatico.ca | Identification of candidate genetic susceptibility variants in the carnitine (Cn) transporter and carnitine biosynthesis gene families in Autism Spectrum Disorder: A novel precision medicine target | Ingrid Tein | ingtein@sympatico.ca | ||||||||
317 | No | No | 6th Oct 2022 | Neuroradiology 1 | "Manohar Schroff | Canada" | Dasaratha Ramaiah Jinka | jdashrath86@gmail.com | Clinico-Etiological Spectrum of Children with Bilateral Basal ganglia lesions: An Observational Study from A Tertiary Care Centre | Lokesh Lingappa | siriloki@gmail.com | |||||||
622 | No | No | 5th Oct 2022 | Molecular genetics | T Sultan | Jee Min Kim | jee.raphaela.kim@gmail.com | Complete Penetrance but Different Phenotypes in a Korean Family with Maternal Interstitial Duplication at 15q11.2-q13.1: A Case Report | Jee Min Kim | jee.raphaela.kim@gmail.com | ||||||||
551 | No | No | 6th Oct 2022 | Neuroradiology 3 | "Ajay Taranath | Australia" | Jessica Ringshaw | jess.ringshaw@uct.ac.za | Effects of maternal and early-life anaemia on child brain development: a South African birth cohort study | Jessica Ringshaw | jess.ringshaw@uct.ac.za | |||||||
261 | No | No | 4th Oct 2022 | "Epilepsy: Syndromes 2 – IESS | Dravet | HHE | EMAS" | E Wirrell | Peifang Jiang | jiangpeifang@zju.edu.cn | Treatments and Seizure Outcome of 327 Patients with Infantile Spasms: A Retrospective Analysis | Peifang Jiang | jiangpeifang@zju.edu.cn | |||||
603 | No | No | 4th Oct 2022 | Epilepsy: Investigations | P Madaan | Jithangi Wanigasinghe | jithangi@gmail.com | Maturation of the auditory evoke potentials with age: data from a pilot study | Jithangi Wanigasinghe | jithangi@gmail.com | ||||||||
420 | No | No | 4th Oct 2022 | Epilepsy: Genetics 3 | L Lagae | Linjie Jiang | JJJLJ2020@163.com | Features of a male with MACF1 mutation suffered from West syndrome:a case report and literature review | Linjie Jiang | JJJLJ2020@163.com | ||||||||
200 | No | No | 5th Oct 2022 | "CNS Malformations | NGS" | A Narayan | Jehan Suleiman | jsuleiman10@gmail.com | Posterior fossa malformations in TASP1-related disorder (Suleiman-El-Hattab Syndrome) | Jehan Suleiman | jsuleiman10@gmail.com | |||||||
177 | No | No | 6th Oct 2022 | Headache 1 | "Ken Mack | US" | Juliana Da Silva Cardoso | julianapsilvacardoso@gmail.com | Primary headache with onset in childhood and adolescence: natural history and prognostic factors in a Portuguese population | Juliana Da Silva Cardoso | julianapsilvacardoso@gmail.com | |||||||
436 | No | No | 4th Oct 2022 | ASD/NDD/ADHD 3 NDD / ID | Charuta Joshi | Karthika Ajit Valaparambil | karthikaajitv@gmail.com | CLINICAL UTILITY OF NEXT GENERATION SEQUENCING IN NEURODEVELOPMENTAL DISORDERS —EXPERIENCE FROM A TERTIARY CARE CENTRE | Karthika Ajit Valaparambil | karthikaajitv@gmail.com | ||||||||
629 | No | No | 4th Oct 2022 | Epilepsy: Outcomes and Epidemiology | E Kija | Brahmini Korrai | kbrahmini49@gmail.com | Predicting seizure recurrence risk in pediatric epilepsy patients who are seizure free and stopped Anti-Epileptic Drugs | Brahmini Korrai | kbrahmini49@gmail.com | ||||||||
68 | No | No | 6th Oct 2022 | "Cerebral palsy 1- Evaluation: clinic | neurophysiologic" | "Catherine Arnaud | France" | Khaled Ashour | khaled3shour77@gmail.com | Establishment of High-Risk Infant Follow up Clinic for Implementation of Early Diagnosis of Cerebral Palsy Guidelines | Khaled Ashour | khaled3shour77@gmail.com | ||||||
758 | No | No | 4th Oct 2022 | Epilepsy: Investigations | P Madaan | Kun-long Hung | klhung@ms10.hinet.net | NEXT GENERATION WHOLE EXOME SEQUENCING IN THE GENETIC DIAGNOSIS OF DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY | Kun-long Hung | klhung@ms10.hinet.net | ||||||||
481 | No | No | 5th Oct 2022 | Neuroimmunology 2 Antibody mediated disorders / monophasic demyel disorder | Banu Anlar | Konika Bansal | konikabansal2@gmail.com | Clinico-radiological spectrum of MOG antibody associated disorder (MOGAD) in Pediatric population. | Konika Bansal | konikabansal2@gmail.com | ||||||||
370 | No | No | 5th Oct 2022 | SMA | N Chrestian | Katarzyna Kotulska | kotulska.jozwiak@gmail.com | "Safety | tolerability and efficacy of widely available nusinersen program in children with Spinal Muscular Atrophy." | Katarzyna Kotulska | kotulska.jozwiak@gmail.com | |||||||
502 | No | No | 6th Oct 2022 | "Metabolic 5 Neurodegenerative diseases (NBIAs | metabolic causes of stroke | CDG | NCLs | NKH" | Suvasini Sharma India | Roshan Koul | Koulroshan@gmail.com | EEG and ONSD in management of hepatic encephalopathy: additional role of EEG in prognosis | Roshan Koul | Koulroshan@gmail.com | ||||
769 | No | No | 6th Oct 2022 | "Tuberous sclerosis | Radiology" | K Aydın | Ichraf Kraoua | kraoua_ichraf@yahoo.fr | Clinical and genetic study of leukodystrophies in Tunisian cohort | Thouraya Ben Younes | bythouraya@yahoo.fr | |||||||
477 | No | No | 6th Oct 2022 | Education | "Jorge Vidaurre | US" | Tina Krysiak | KrysiakT@childrensdayton.org | Title: Measuring Transition Readiness in Adolescents with Epilepsy: Opportunities and Challenges | Tina Krysiak | KrysiakT@childrensdayton.org | |||||||
499 | No | No | 4th Oct 2022 | Neonatal 1: Neonatal seizures and EEG | Hannah Glass | Fatma Kusgoz | kusgozfatma@gmail.com | Levetiracetam as mono-and polytherapy in the treatment of neonatal-onset seizures | Pinar Gencpinar | pinargencpinar@gmail.com | ||||||||
530 | No | No | 6th Oct 2022 | CNS Infections 1 Covid-related | "Charles Newton | Kenya" | Young Jun Ko | kyjmillenium@naver.com | Changes in the patient number of viral infections and febrile seizure before and after the COVID-19 pandemic | Soo Ahn Chae | kidbrain@cau.ac.kr | |||||||
239 | No | No | 5th Oct 2022 | "CNS Malformations | NGS" | A Narayan | Leman Tekin Orgun | lemantekin15@yahoo.com | A pediatric case with primary familial brain calcification due to a homozygous variant on the JAM2 gene | İlknur Erol | ilknur_erol@yahoo.com | |||||||
246 | No | No | 6th Oct 2022 | Metabolic 2 Mitochondrial disorders I : clinical phenotypes and tx | "Rita Horvath | UK" | Leman Tekin Orgun | lemantekin15@yahoo.com | Two siblings with combined oxidative phosphorylation defect 11 with a novel mutation in the RMND1 gene | İlknur Erol | ilknur_erol@yahoo.com | |||||||
766 | No | No | 4th Oct 2022 | Epilepsy: Genetics 1 | S Perry | Leman Tekin Orgun | lemantekin15@yahoo.com | Pyridoxine Dependent Epilepsy with ALDH7A1 Mutation: Clinical Spectrum and Outcome in A Multicenter Study Cohort From Turkey | Leman Tekin Orgun | lemantekin15@yahoo.com | ||||||||
404 | No | No | 4th Oct 2022 | Epilepsy: Genetics 2 | N Specchio | Xiao Li | Lexiecqmu@hotmail.com | Focal cortical dysplasia type II related to a new pathogenic gene-RAB6B | Yuwu Jiang | jiangyw@263.net | ||||||||
533 | No | No | 5th Oct 2022 | Peripheral nerve | D Selcen | Xiaomei Zhu | lisymei@126.com | Nusinersen safety and effects in children with spinal muscular atrophy: a single center experience | Wenhui Li | wenhuili@fudan.edu.cn | ||||||||
409 | No | No | 5th Oct 2022 | Muscular dystrophy | Y Nevo | Yi-dan Liu | liuyidan322@163.com | Uniparental disomy unmasks a homozygous mutation of POMGNT1 in a case of muscle-eye-brain disease | Yi-dan Liu | liuyidan322@163.com | ||||||||
147 | No | No | 6th Oct 2022 | Metabolic 2 Mitochondrial disorders I : clinical phenotypes and tx | "Rita Horvath | UK" | Asburce Olgac | mabolgac@yahoo.com | A case of mitochondrial depletion syndrome type 13 due to a FBXL4 variant | Asburce Olgac | mabolgac@yahoo.com | |||||||
440 | No | No | 4th Oct 2022 | "Epilepsy: DEEs | TSC | RETT and Comorbidities" | Y Jiang | Madhavi Shelke | madhavishelke@yahoo.com | Genetic spectrum of Developmental and Epileptic Encephalopathies | Madhavi Shelke | madhavishelke@yahoo.com | ||||||
89 | No | No | 6th Oct 2022 | Neuroradiology 1 | "Manohar Schroff | Canada" | Kanij Fatema | mailmonami@gmail.com | Pediatric Moya Moya Disease: Clinical and Radio-Angiographic characteristics- A study from a Tertiary care center in Bangladesh | Kanij Fatema | mailmonami@gmail.com | |||||||
98 | No | No | 5th Oct 2022 | Genetics and epilepsy I | W Hakami | Kanij Fatema | mailmonami@gmail.com | Gene Panel Testing in children with Early Onset Epileptic Encephalopathies : A study in a Tertiary car center in Bangladesh | Kanij Fatema | mailmonami@gmail.com | ||||||||
464 | No | No | 5th Oct 2022 | Neuroimmunology 2 Antibody mediated disorders / monophasic demyel disorder | Banu Anlar | Maria Shumilina | maria_shumilina@yahoo.com | GAD antibody-spectrum disorders: case report | Maria Shumilina | maria_shumilina@yahoo.com | ||||||||
558 | No | No | 6th Oct 2022 | Headache 1 | "Ken Mack | US" | Maria Vu | maria.vu@sickkids.ca | "Vascular Endothelial Dysfunction | Cognition and Stroke in Early Life Study (VECSELS)" | Maria Vu | maria.vu@sickkids.ca | ||||||
634 | No | No | 5th Oct 2022 | "Neuropathy | GBS | and CMS" | C Bönnemann | Sibğatullah Ali Orak | maviihsan@gmail.com | Two Cases With Typical GBS And Rare GBS Variant Associated With Covid-19 | Sibğatullah Ali Orak | maviihsan@gmail.com | ||||||
311 | No | No | 5th Oct 2022 | General II | M Sönmez | Wahed | mawahed.rangpur@gmail.com | Prematurity and Postnatal Neurological Sequelae | Wahed | mawahed.rangpur@gmail.com | ||||||||
312 | No | No | 6th Oct 2022 | "Cerebral palsy 1- Evaluation: clinic | neurophysiologic" | "Catherine Arnaud | France" | Wahed Wahed | mawahed.rangpur@gmail.com | Wasting Syndrome is a predictor of early death in Spastic Cerebral Palsy | Wahed Wahed | mawahed.rangpur@gmail.com | ||||||
62 | No | No | 5th Oct 2022 | Neuromuscular 1 | H Lochmüller | Duygu Yılmaz | md.duyguyilmaz@gmail.com | Congenital myotonic dystrophy: a retrospective study of a single center | Haluk Topaloglu | htopalog@hacettepe.edu.tr | ||||||||
93 | No | No | 6th Oct 2022 | Metabolic 3 Mitochondrial disorders II: Etiologies and mechanisms | Saskia Wortmann Netherlands | Ayse Yasemin Celik | mdayasminc@gmail.com | "Solving a puzzle: An infant with developmental delay | epileptic spasms | and petechiae" | Ayse Yasemin Celik | mdayasminc@gmail.com | ||||||
70 | No | No | 4th Oct 2022 | ASD/NDD/ADHD 1 ASD genetic / biomarkers / | Chahnez Triki | Nagwa Meguid | meguidna@yahoo.com | Effect of oxidative stress and Glutathione on telomere length in a population of Egyptian autistic children | Nagwa Meguid | meguidna@yahoo.com | ||||||||
693 | No | No | 6th Oct 2022 | Cerebral palsy 2- Management; current and future | "Antigone Papavasiliou | Greece" | Mehmet Akif Kılıç | mehmetakifkilic1@istanbul.edu.tr | Relationship between MRI patterns and refractory epilepsy in children with cerebral palsy: Cross-sectional study from a tertiary center | Mehmet Akif Kılıç | mehmetakifkilic1@istanbul.edu.tr | |||||||
715 | No | No | 6th Oct 2022 | Metabolic 3 Mitochondrial disorders II: Etiologies and mechanisms | Saskia Wortmann Netherlands | Mehmet Palaz | mehmetpalaz_md@hotmail.com | Ventricular septation on MRI could be diagnostic clue for PDH: Two case reports | Mehmet Palaz | mehmetpalaz_md@hotmail.com | ||||||||
719 | No | No | 6th Oct 2022 | Metabolic 3 Mitochondrial disorders II: Etiologies and mechanisms | Saskia Wortmann Netherlands | Mehmet Palaz | mehmetpalaz_md@hotmail.com | Can leukodystrophy be reversible? a LTBL case report | Mehmet Palaz | mehmetpalaz_md@hotmail.com | ||||||||
500 | No | No | 5th Oct 2022 | Peripheral nerve | D Selcen | Biljana Mitrevska | mitrevskabiljana@hotmail.com | Funccional testing and rehabilitation of spinal muscular atrophy patients | Biljana Mitrevska | mitrevskabiljana@hotmail.com | ||||||||
462 | No | No | 4th Oct 2022 | ASD/NDD/ADHD 3 NDD / ID | Charuta Joshi | F. Müjgan Sonmez | mjgsonmez@yahoo.com | TRAPPC9-related intellectual disability: report of two new cases | Eyyüp Üçtepe | eyupsvs@hotmail.com | ||||||||
161 | No | No | 4th Oct 2022 | Epilepsy: Treatment 1 – ASMs | B Sanchez-Gan | Mohammad Barzegar | mm_barzegar@yahoo.com | The efficacy of Everolimus onTSC associated drug resistant epilepsy | Mohammad Barzegar | mm_barzegar@yahoo.com | ||||||||
638 | No | No | 6th Oct 2022 | Education | "Jorge Vidaurre | US" | Michael E. Msall | mmsall@peds.bsd.uchicago.edu | Children’s Medical Home in China (CHMC) – Promoting Early Development of Chinese Children | Michael E. Msall | mmsall@peds.bsd.uchicago.edu | |||||||
272 | No | No | 5th Oct 2022 | Spasticity and ataxia | C Catsman | Muhammad Mahajnah | mohamedm@hymc.gov.il | The neuronal ceroid lipofuscinoses type 8 (CLN8) gene mutations: A new compound heterozygous case and the protein's bioinformatic analyses | Muhammad Mahajnah | mohamedm@hymc.gov.il | ||||||||
539 | No | No | 6th Oct 2022 | Headache/Stroke 2 | "Mahendra Moharir | Canada" | Moran Hausman-kedem | moranhk@gmail.com | Sleep-related difficulties and decreased sleep quality among adolescents with idiopathic intracranial hypertension | Moran Hausman-kedem | moranhk@gmail.com | |||||||
754 | No | No | 4th Oct 2022 | Epilepsy: Status epilepticus and Miscellaneous | T Loddenkemper | Müge Ayanoğlu | mugeayanoglu_05@hotmail.com | Assessment of the knowledge level of physicians regarding the management of acute seizures in children and adolescents | Müge Ayanoğlu | mugeayanoglu_05@hotmail.com | ||||||||
307 | No | No | 5th Oct 2022 | Muscular dystrophy | Y Nevo | Bakhytkul Myrzaliyeva | myrzaliyeva@gmail.com | "Diagnostics | clinical and genetic characteristics of Duchenne muscular dystrophy in Kazakhstan" | Bakhytkul Myrzaliyeva | myrzaliyeva@gmail.com | |||||||
771 | No | No | 4th Oct 2022 | ASD/NDD/ADHD 2 ASD assessments / management / Rett syndrome / high risk infants | Antigone Papavasiliou | Naama Yosha-orpaz | naamaorpaz@gmail.com | A Protocol for Evaluation and Treatment of Children with Autistic/Psychotic Regression | Naama Yosha-orpaz | naamaorpaz@gmail.com | ||||||||
537 | No | No | 6th Oct 2022 | Cerebral palsy 2- Management; current and future | "Antigone Papavasiliou | Greece" | Zhao-qing Lin | naeun.tw@gmail.com | "Erythropoietin for Hypoxic-Ischemic Encephalopathy: A Follow up Study in New Taipei City | Taiwan" | Zhao-qing Lin | naeun.tw@gmail.com | ||||||
617 | No | No | 4th Oct 2022 | Epilepsy: Semiology and Clinical | H Cross | Eiji Nakagawa | nakagawa@ncnp.go.jp | Evaluation of periodic slow head nodding seizure | Eiji Nakagawa | nakagawa@ncnp.go.jp | ||||||||
270 | No | No | 6th Oct 2022 | "Cerebral palsy 1- Evaluation: clinic | neurophysiologic" | "Catherine Arnaud | France" | Nargiz Aliyeva | nargis.asadova@gmail.com | General Movements Assessment in Term Newborns with Moderate Hyperbilirubinemia | Nargiz Aliyeva | nargis.asadova@gmail.com | ||||||
470 | No | No | 6th Oct 2022 | Neuroradiology 2 | "Kshitij Mankand | UK" | Natalia Bronina | Nata-dim@mail.ru | Posterior reversible encephalopathy syndrome in children with malignances | Natalia Bronina | Nata-dim@mail.ru | |||||||
348 | No | No | 4th Oct 2022 | Epilepsy: Genetics 2 | N Specchio | Nuriye Ayca Gul | naycagul@gmail.com | Case report: Potassium sodium-activated channel subfamily T member 1 gene mutation related epilepsy. | Nuriye Ayca Gul | naycagul@gmail.com | ||||||||
310 | No | No | 5th Oct 2022 | Muscular dystrophy | Y Nevo | Nidheesh Chencheri | NCChencheri@ajch.ae | Clinical Experience of gene replacement therapy in children with Spinal Muscular Atrophy: A single center retrospective study of 25 children | Nidheesh Chencheri | NCChencheri@ajch.ae | ||||||||
64 | No | No | 4th Oct 2022 | Epilepsy: Investigations | P Madaan | Nebal Waill Saadi | nebalpedneu2013@gmail.com | Seroprevalence of Anti- N-methyl-D-aspartate receptor antibodies in children with seizures of unknown cause | Nebal Waill Saadi | nebalpedneu2013@gmail.com | ||||||||
289 | No | No | 5th Oct 2022 | Neuroimmunology 2 Antibody mediated disorders / monophasic demyel disorder | Banu Anlar | Nefise Arıbaş Öz | nefisearibas@hotmail.com | A Rare Complication of COVID-19 in a Pediatric Patient; Acute Transverse Myelitis | Nefise Arıbaş Öz | nefisearibas@hotmail.com | ||||||||
578 | No | No | 5th Oct 2022 | Genetics and epilepsy II | Ramachandran Nair | Neil Atkinson | neil.atkinson@nhs.net | Clinical and genetic features of acute deterioration with resulting neurological regression in children with Dravet Syndrome | Neil Atkinson | neil.atkinson@nhs.net | ||||||||
415 | No | No | Nezir Özgün | nezirozgun@hotmail.com | 12-Year Surveillance Results of Acute Flask Paralysis Cases in Southeast Turkey and the Effect of Refugee Movements on Surveillance Results | Nezir Özgün | nezirozgun@hotmail.com | |||||||||||
596 | No | No | 6th Oct 2022 | "Metabolic 5 Neurodegenerative diseases (NBIAs | metabolic causes of stroke | CDG | NCLs | NKH" | Suvasini Sharma India | Nicolas Abreu | nicolas.abreu@nyulangone.org | Clarifying missense variants of uncertain significance in CLN6 Batten disease through the use of skin biopsy – a case report | Nicolas Abreu | nicolas.abreu@nyulangone.org | ||||
188 | No | No | 5th Oct 2022 | Neuroimmunology 1 Demyelinating / MS related | Russell Dale | Nihal Yıldız | nihalyildiz661@gmail.com | Evaluation of the Risk Factors for Developing Demyelinating Disease after Optic Neuritis in Children: A Single Center Experience | Sevim Şahin | sevimsahin1@yahoo.com | ||||||||
354 | No | No | 6th Oct 2022 | "Tuberous sclerosis | Radiology" | K Aydın | Nihal Yıldız | nihalyildiz661@gmail.com | Ketogenic Diet Therapy for Drug-resistant Epilepsy and Cognitive Impairment in Children with Tuberous Sclerosis Complex | Jianxiang Liao | liaojianxiang@vip.sina.com | |||||||
687 | No | No | 5th Oct 2022 | Neuroimmunology 1 Demyelinating / MS related | Russell Dale | Nihal Yıldız | nihalyildiz661@gmail.com | Effects of Oleuropein on Systemic Lipopolysaccharide-Induced Neuroinflammation in Rats | Sevim Şahin | sevimsahin1@yahoo.com | ||||||||
563 | No | No | 5th Oct 2022 | Neuroimmunology 1 Demyelinating / MS related | Russell Dale | Nisreen Bader | nisreen_bader2006@hotmail.com | Successful management of Pediatric-onset Multiple sclerosis with Ocrelizumab | Nisreen Bader | nisreen_bader2006@hotmail.com | ||||||||
226 | No | No | 5th Oct 2022 | "İon channel myopathy | and metabolic" | R Horvath | Nouha Bouayed Abdelmoula | nouha_abdelmoulabouayed@yahoo.fr | Myotonia congenita associated to multiple sclerosis in a Tunisian family | Nouha Bouayed Abdelmoula | nouha_abdelmoulabouayed@yahoo.fr | |||||||
228 | No | No | 5th Oct 2022 | "Neuropathy | GBS | and CMS" | C Bönnemann | Nouha Bouayed Abdelmoula | nouha_abdelmoulabouayed@yahoo.fr | Preconceptional diagnosis for giant axonal neuropathy before wedding engagement decision | Nouha Bouayed Abdelmoula | nouha_abdelmoulabouayed@yahoo.fr | ||||||
664 | No | No | 5th Oct 2022 | Neuromuscular 1 | H Lochmüller | Nurşah Yeniay Süt | nursah_ny@hotmail.com | A rare manifestation of pediatric CIDP: hypoglossal nerve involvement | Nurşah Yeniay Süt | nursah_ny@hotmail.com | ||||||||
90 | No | No | 4th Oct 2022 | Epilepsy: Outcomes and Epidemiology | E Kija | Amarachukwu Okafor | okaforamara2@gmail.com | Predisposing factors to childhood Epilepsy at the Federal Medical Centre Umuahia Nigeria | Amarachukwu Okafor | okaforamara2@gmail.com | ||||||||
722 | No | No | Olgay Bildik | olgaybildik@hotmail.com | The Rare Central Nervous System Findings in Pediatric SARS-COV-2 Patients | Olgay Bildik | olgaybildik@hotmail.com | |||||||||||
352 | No | No | 5th Oct 2022 | Neuroimmunology 3 Autoimmune encephalitis plus | Silvia Tenenbaum | Liu Liu | osier0615xw@zju.edu.cn | Paediatric anti-gamma aminobutyric acid-B receptor encephalitis with benign prognosis | Feng Gao | epilepsy@zju.edu.cn | ||||||||
428 | No | No | 5th Oct 2022 | Genetics and epilepsy II | Ramachandran Nair | Liu Liu | osier0615xw@zju.edu.cn | Clinical and genetic characteristics of PCDH19-related epilepsy syndromes:differences between East-Asians and European-Americans | Feng Gao | epilepsy@zju.edu.cn | ||||||||
424 | No | No | 5th Oct 2022 | Muscular dystrophy | Y Nevo | Özgen Hür | ozgenozyazicioglu@yahoo.com | "A rare phenotype of congenital muscular dystrophy: 'Muscular dystrophy-dystroglycanopathy type B | 1'" | Özgen Hür | ozgenozyazicioglu@yahoo.com | |||||||
513 | No | No | 6th Oct 2022 | "Movement 3 Ataxias | opsoclonus myoclonus and covid 19 impact" | "Russell Dale | Australia" | Özge Tanıdır Artan | ozgetanidir@hotmail.com | Ataxia oculomotor apraxia type 4 due to a pathogenic variant in PNKP gene | Özge Tanıdır Artan | ozgetanidir@hotmail.com | ||||||
557 | No | No | 4th Oct 2022 | "Epilepsy: Syndromes 1 – Self-limited | EE/DEE-SWAS" | C Joshi | Özge Tanıdır Artan | ozgetanidir@hotmail.com | Heart Rate Variability in Childhood Benign Rolandic Epilepsy | Özge Tanıdır Artan | ozgetanidir@hotmail.com | |||||||
221 | No | No | 5th Oct 2022 | Neuroimmunology 3 Autoimmune encephalitis plus | Silvia Tenenbaum | Merve Öztürk | ozturk_merve@hotmail.com | Efficacy of Rituximab Treatment in Rasmussen’s Encephalitis | Merve Öztürk | ozturk_merve@hotmail.com | ||||||||
222 | No | No | 4th Oct 2022 | Epilepsy: Status epilepticus and Miscellaneous | T Loddenkemper | Merve Öztürk | ozturk_merve@hotmail.com | Leuprolide Acetate Induced Non-convulsive Status Epilepticus: Case Report | Merve Öztürk | ozturk_merve@hotmail.com | ||||||||
80 | No | No | 5th Oct 2022 | General I | J Vajsar | Elif Perihan Öncel | peri_elif@hotmail.com | A case of CAV3 caveolinopathy / channelopathy with familial absence epilepsy and distal myoneuronopathy extending the clinical spectrum | Elif Perihan Öncel | peri_elif@hotmail.com | ||||||||
81 | No | No | 5th Oct 2022 | General I | J Vajsar | Elif Perihan Öncel | peri_elif@hotmail.com | The first Turkish case with early-juvenile-onset recessive distal titinopathy and the first case with prominent neurogenic involvement | Elif Perihan Öncel | peri_elif@hotmail.com | ||||||||
82 | No | No | 5th Oct 2022 | General I | J Vajsar | Elif Perihan Öncel | peri_elif@hotmail.com | First Turkish case with MICU1 mutation-related myopathy and extrapyramidal findings | Elif Perihan Öncel | peri_elif@hotmail.com | ||||||||
291 | No | No | 6th Oct 2022 | "Movement 2 Dystonia | Parkinsons | tremor and epidemiology" | "Jon Mink | US" | Elif Perihan Öncel | peri_elif@hotmail.com | A novel combined heterozygous mutation in the PLA2G6 gene associated with early-onset Parkinson’s disease | Şeyda Beşen | seydabesen2000@gmail.com | |||||
353 | No | No | 6th Oct 2022 | Metabolic 6 Defects of bioenergetic and intermediary metab | Ingrid Tein Canada | Elif Perihan Öncel | peri_elif@hotmail.com | SLC2A1 mutations associated Glucose Transport Type 1 Deficiency Syndrome: A Single Center Case Series | Elif Perihan Öncel | peri_elif@hotmail.com | ||||||||
583 | No | No | 5th Oct 2022 | Genetics and epilepsy II | Ramachandran Nair | Elif Perihan Öncel | peri_elif@hotmail.com | First Turkish case with UNC80 deficiency | İlknur Erol | ilknur_erol@yahooo.com | ||||||||
759 | No | No | 5th Oct 2022 | Genetics and epilepsy II | Ramachandran Nair | Elif Perihan Öncel | peri_elif@hotmail.com | "Evaluation of genetic | electrophysiological and clinical characteristics of patients followed up with the diagnosis of Developmental Epileptic Encephalopathy: A single center experience" | Elif Perihan Öncel | peri_elif@hotmail.com | |||||||
752 | No | No | 4th Oct 2022 | Epilepsy: Genetics 1 | S Perry | Ebru Arhan | petekarhan@yahoo.com.tr | Whole Exome Sequencing Results of 101 Epilepsy-Related Patients | Emriye Ferda Perçin | ferdaep@yahoo.com | ||||||||
86 | No | No | 6th Oct 2022 | "Movement 3 Ataxias | opsoclonus myoclonus and covid 19 impact" | "Russell Dale | Australia" | Pinar Yavuz | pinaryavuz@hacettepe.edu.tr | Neurological and immunological phenotypes in Ataxia Telangiectasia | Pinar Yavuz | pinaryavuz@hacettepe.edu.tr | ||||||
738 | No | No | 4th Oct 2022 | Neonatal 2: Neonatal neurology – other | Lakshmi | Prajakta Ghatage | prajaktaghatage38@gmail.com | To study the most efficacious drug combination for drug resistant NHBI cases. | Prajakta Ghatage | prajaktaghatage38@gmail.com | ||||||||
503 | No | No | 6th Oct 2022 | "Metabolic 5 Neurodegenerative diseases (NBIAs | metabolic causes of stroke | CDG | NCLs | NKH" | Suvasini Sharma India | Prashant Utage | prashant.utage1@gmail.com | Congenital disorder of glycosylation : clinical case study of patients harboring pathogenic mutations in phosphomannomutase 2 gene (PMM2-CDG) | Umesh Umesh Bhammarkar | dr_umeshbh@yahoo.co.in | ||||
163 | No | No | 5th Oct 2022 | Treatment | F Muntoni | Panayiota Trifillis | ptrifillis@ptcbio.com | Comparison of timed function test results in nmDMD patients receiving ataluren: STRIDE Registry vs phase 3 clinical trial | Panayiota Trifillis | ptrifillis@ptcbio.com | ||||||||
164 | No | No | 5th Oct 2022 | Treatment | F Muntoni | Panayiota Trifillis | ptrifillis@ptcbio.com | Comparing the change in 6-minute walk distance in nmDMD patients receiving ataluren: STRIDE Registry compared with phase 3 clinical trial | Panayiota Trifillis | ptrifillis@ptcbio.com | ||||||||
170 | No | No | 5th Oct 2022 | Treatment | F Muntoni | Panayiota Trifillis | ptrifillis@ptcbio.com | Comparison of North Star Ambulatory Assessment score change in nmDMD patients receiving ataluren: STRIDE Registry vs phase 3 clinical trial | Panayiota Trifillis | ptrifillis@ptcbio.com | ||||||||
300 | No | No | 6th Oct 2022 | "Movement 1 Chorea | dyskinesias | tremor | spasms & tx" | "Biju Hameed | UK" | Qiao Hu | qiaohu1989@163.com | Early-onset spontaneously relieved spasms of infancy in sleep: electroclinical characteristics and differential diagnoses | Shuang Liao | shuangliao20211123@163.com | ||||
418 | No | No | 4th Oct 2022 | Neonatal 1: Neonatal seizures and EEG | Hannah Glass | Şeyda Beşen | rameshkonanki@gmail.com | Neonatal-onset epilepsy: Clinico-etiological spectrum and developmental outcomes | Prasanthi Aripirala | mimu2010@gmail.com | ||||||||
444 | No | No | 5th Oct 2022 | SMA | N Chrestian | Ramesh Konanki | rameshkonanki@gmail.com | Spinal muscular atrophy with lower extremity-predominant (SMA-LED) | Ramesh Konanki | rameshkonanki@gmail.com | ||||||||
469 | No | No | 6th Oct 2022 | Education | "Jorge Vidaurre | US" | Ryan Sauer | rasa238@uky.edu | Making it Home on Time: Improving Child Neurology Inpatient Discharge Timing | Ryan Sauer | rasa238@uky.edu | |||||||
283 | No | No | 4th Oct 2022 | Neonatal 1: Neonatal seizures and EEG | Hannah Glass | Recep Kamil Kilic | recepkamil09@hotmail.com | NEONATAL EEG: IMPORTANCE AND UTILITY IN DIFFERANTIAL DIAGNOSIS and PROGNOSIS | Recep Kamil Kilic | recepkamil09@hotmail.com | ||||||||
373 | No | No | 4th Oct 2022 | Neonatal 2: Neonatal neurology – other | Lakshmi | Recep Kamil Kilic | recepkamil09@hotmail.com | THE RELATİONSHİP BETWEEN FİRST TRİMESTER MATERNAL SERUM PAPP-A LEVEL AND POSTNATAL NEUROLOGİCAL DEVELOPMENT LEVEL | Recep Kamil Kilic | recepkamil09@hotmail.com | ||||||||
654 | No | No | 5th Oct 2022 | "Neuropathy | GBS | and CMS" | C Bönnemann | Recep Kamil Kilic | recepkamil09@hotmail.com | PERONEAL NERVE PALSY DUE TO OSTEOCHONDROMA OF THE FİBULAR HEAD: A RARE CAUSE OF FOOT DROP | Recep Kamil Kilic | recepkamil09@hotmail.com | ||||||
655 | No | No | Recep Kamil Kilic | recepkamil09@hotmail.com | COVID-19 RELATED ADEM AND LONGITUDINAL EXTENSIVE TRANSVERSE MYELITIS WITH ACUTE ADENOVIRUS CO-INFECTION IN A NINE-YEAR-OLD CHILD | Recep Kamil Kilic | recepkamil09@hotmail.com | |||||||||||
116 | No | No | 6th Oct 2022 | Neuroradiology 1 | "Manohar Schroff | Canada" | Robert Hendeson | robert.henderson2@health.wa.gov.au | A Pictorial Review of Paediatric Histiocytic Disorders in the Head and Neck | Robert Hendeson | robert.henderson2@health.wa.gov.au | |||||||
536 | No | No | 4th Oct 2022 | Epilepsy: Treatment 2 – ASMs | Ramachandran Nair | Sait Acik | saitopen@yahoo.com | "Clobazam Experience in Childhood Epilepsy from a Tertiary Center | Turkey" | Sait Acik | saitopen@yahoo.com | |||||||
661 | No | No | 5th Oct 2022 | General II | M Sönmez | Saleel Ramesh Chandratre | saleel.chandratre@gmail.com | ERCC5 novel missense mutation causing developmental delay and spasticity | Saleel Ramesh Chandratre | saleel.chandratre@gmail.com | ||||||||
256 | No | No | 6th Oct 2022 | Metabolic 4 Therapeutic approaches | Samantha Marin Canada | Salih Akbaş | salihakbas89@gmail.com | Efficacy and Safety of Cerliponase Alpha Therapy in Neuronal Ceroid Lipofuscinosis Type 2 | Salih Akbaş | salihakbas89@gmail.com | ||||||||
257 | No | No | 4th Oct 2022 | Epilepsy: Semiology and Clinical | H Cross | Salih Akbaş | salihakbas89@gmail.com | "Childhood Frontal Lobe Epilepsies: Etiology | Classification | and EEG Findings" | Salih Akbaş | salihakbas89@gmail.com | ||||||
777 | No | No | 5th Oct 2022 | Peripheral nerve | D Selcen | Salih Akbaş | salihakbas89@gmail.com | PRIDOSTIGMIN TREATMENT IN X-LINKED MYOTBULAR MYOPATHY | Salih Akbaş | salihakbas89@gmail.com | ||||||||
442 | No | No | 4th Oct 2022 | Epilepsy: Semiology and Clinical | H Cross | Sanem Yilmaz | sanem.yilmaz@ege.edu.tr | Intractable epilepsy due to cerebellar ganglioneural hamartoma: Evidence for seizures originating from cerebellum | Sanem Yilmaz | sanem.yilmaz@ege.edu.tr | ||||||||
157 | No | No | 5th Oct 2022 | General II | M Sönmez | Sarafroz Fayzullaeva | sarafrozerkinova@gmail.com | Linear scleroderma as one of the manifestations of collagenosis | Sarafroz Fayzullaeva | sarafrozerkinova@gmail.com | ||||||||
330 | No | No | 6th Oct 2022 | Metabolic 6 Defects of bioenergetic and intermediary metab | Ingrid Tein Canada | Esra Sarigecili | sarigeciliesra@gmail.com | A RARE GLUT 1 DEFICIENCY SYNDROME PRESENTING WITH SPEECH DELAY | Esra Sarigecili | sarigeciliesra@gmail.com | ||||||||
657 | No | No | 4th Oct 2022 | ASD/NDD/ADHD 4 ADHD and Behav / syndromes / LD | Pratibha Singhi | Saurodip Maity | saurodipcmc@gmail.com | STUDY TO DETERMINE SENSORY PROCESSING DYSFUNCTION IN CHILDREN WITH ATTENTION DEFICIT HYPERACTIVITY DISORDER | Saurodip Maity | saurodipcmc@gmail.com | ||||||||
295 | No | No | 4th Oct 2022 | ASD/NDD/ADHD 2 ASD assessments / management / Rett syndrome / high risk infants | Antigone Papavasiliou | Selin Akyüz Oktay | selinakyuz93@gmail.com | "Evaluation of Psychomotor | Behavioral and Sensory Development in Hypoxic Ischemic Encephalopathy Patients" | Selin Akyüz Oktay | selinakyuz93@gmail.com | |||||||
61 | No | No | 5th Oct 2022 | Neuroimmunology 1 Demyelinating / MS related | Russell Dale | Semra Saygi | semra_saygi@yahoo.com | High-efficacy treatment for aggressive pediatric Multiple Sclerosis | Maria Shumilina | MARIA_SHUMILINA@YAHOO.COM | ||||||||
602 | No | No | 6th Oct 2022 | CNS Infections 1 Covid-related | "Charles Newton | Kenya" | Semra Saygi | semra_saygi@yahoo.com | COVID-19-associated Retrobulbar Neuritis In A Child | Semra Saygi | semra_saygi@yahoo.com | |||||||
614 | No | No | 4th Oct 2022 | Epilepsy: Semiology and Clinical | H Cross | Semra Saygi | semra_saygi@yahoo.com | Vermian dysplasia and lipoma in a child with headache and epileptic seizure | Senay Demir | drsenaydemir@hotmail.com | ||||||||
615 | No | No | 6th Oct 2022 | Neuroradiology 3 | "Ajay Taranath | Australia" | Semra Saygi | semra_saygi@yahoo.com | Posterior periventricular extensive diffusion restriction in a 17 years old boy after cardiopulmonary resuscitation | Senay Demir | drsenaydemir@hotmail.com | |||||||
639 | No | No | 5th Oct 2022 | Neuroimmunology 1 Demyelinating / MS related | Russell Dale | Semra Saygi | semra_saygi@yahoo.com | Optic Neuritis And Pseudotumor Cerebri Co-Existence İn A Patient With A Recent COVID-19 Infection | Semra Saygi | semra_saygi@yahoo.com | ||||||||
642 | No | No | 6th Oct 2022 | Metabolic 1 Clinical phenotypes | "Brahim Tabarki | KSA" | Semra Saygi | semra_saygi@yahoo.com | A Rare Case Of Mucopolysaccharidosis Type VI (Maroteaux–Lamy Syndrome) | Semra Saygi | semra_saygi@yahoo.com | |||||||
645 | No | No | 5th Oct 2022 | "Neuropathy | GBS | and CMS" | C Bönnemann | Semra Saygi | semra_saygi@yahoo.com | Facial Nerve Venous Malformation Presenting As Bell's Palsy | Semra Saygi | semra_saygi@yahoo.com | ||||||
142 | No | No | 4th Oct 2022 | Epilepsy: Genetics 2 | N Specchio | Senem Ayca | senemkaleci85@gmail.com | Early infantile epileptic encephalopathy (Ohtahara Syndrome): A case report with STXBP1 mutation | Senem Ayca | senemkaleci85@gmail.com | ||||||||
178 | No | No | 5th Oct 2022 | Spasticity and ataxia | C Catsman | Senem Ayça | senemkaleci85@gmail.com | "A case of a ADPRHL2 Mutation; Neurodegeneration with Developmental Delay | Ataxia | and Axonal Neuropathy" | Senem Ayça | senemkaleci85@gmail.com | ||||||
640 | No | No | 5th Oct 2022 | Muscular dystrophy | Y Nevo | Senem Ayça | senemkaleci85@gmail.com | A case of Emery Dreifuss Muscular Dystrophy with SYNE1 and SYNE2 mutations and white matter involvement | Senem Ayça | senemkaleci85@gmail.com | ||||||||
264 | No | No | 6th Oct 2022 | "Movement 1 Chorea | dyskinesias | tremor | spasms & tx" | "Biju Hameed | UK" | Seren Aydin | serenaydin5228@gmail.com | Hereditary Spastic Paraparesis Type 55: A Case Report | Seren Aydin | serenaydin5228@gmail.com | ||||
113 | No | No | 4th Oct 2022 | Epilepsy: Semiology and Clinical | H Cross | Sevgi Yimenicioglu | sevgifahri@yahoo.com | Opercular syndrome due to Herpes Encephalitis | Sevgi Yimenicioglu | sevgifahri@yahoo.com | ||||||||
84 | No | No | 5th Oct 2022 | Spasticity and ataxia | C Catsman | Şeyda Beşen | seydabesen2000@gmail.com | The first case of spastic ataxia type 4 associated with heterozygous mutations in MTPAP gene | İlknur Erol | ilknur_erol@yahoo.com | ||||||||
240 | No | No | 5th Oct 2022 | General neurogenetics II | A R Tavasoli | Şeyda Beşen | seydabesen2000@gmail.com | The First Turkish case with HIVEP2-related intellectual disability | İlknur Erol | ilknur_erol@yahoo.com | ||||||||
244 | No | No | 5th Oct 2022 | General neurogenetics II | A R Tavasoli | Şeyda Beşen | seydabesen2000@gmail.com | Is pyridoxine effective in the treatment of hyperphosphatasia with mental retardation syndrome type 4: Single center experience | Şeyda Beşen | seydabesen2000@gmail.com | ||||||||
245 | No | No | 5th Oct 2022 | General neurogenetics II | A R Tavasoli | Şeyda Beşen | seydabesen2000@gmail.com | The first siblings with TRAPPC6B mutation | İlknur Erol | ilknur_erol@yahoo.com | ||||||||
247 | No | No | 5th Oct 2022 | General neurogenetics II | A R Tavasoli | Şeyda Beşen | seydabesen2000@gmail.com | Two Turkish siblings with intellectual disability associated with TUSC3 mutation | İlknur Erol | ilknur_erol@yahoo.com | ||||||||
765 | No | No | 5th Oct 2022 | Spasticity and ataxia | C Catsman | Şeyda Beşen | seydabesen2000@gmail.com | Children with genetically confirmed Hereditary Spastic Paraplegia (HSP): A case series from Eastern Mediterranean Region of Turkey | Şeyda Beşen | seydabesen2000@gmail.com | ||||||||
507 | No | No | 4th Oct 2022 | ASD/NDD/ADHD 4 ADHD and Behav / syndromes / LD | Pratibha Singhi | Sheffali Gulati | sheffaligulati@gmail.com | Spectrum of co-morbidities and psychopathology in children with Attention-deficit hyperactivity disorder (ADHD): A retrospective study | Sheffali Gulati | sheffaligulati@gmail.com | ||||||||
534 | No | No | 4th Oct 2022 | ASD/NDD/ADHD 4 ADHD and Behav / syndromes / LD | Pratibha Singhi | Sheffali Gulati | sheffaligulati@gmail.com | The spectrum of specific learning disability and associated co-morbidities in children at a tertiary care center: A retrospective study. | Sheffali Gulati | sheffaligulati@gmail.com | ||||||||
568 | No | No | 4th Oct 2022 | ASD/NDD/ADHD 1 ASD genetic / biomarkers / | Chahnez Triki | Sheffali Gulati | sheffaligulati@gmail.com | The Spectrum of Co-morbidities in children with ASD (Autism Spectrum Disorder): a retrospective study | Sheffali Gulati | sheffaligulati@gmail.com | ||||||||
580 | No | No | 4th Oct 2022 | ASD/NDD/ADHD 1 ASD genetic / biomarkers / | Chahnez Triki | Sheffali Gulati | sheffaligulati@gmail.com | Biomarkers in children with Autism: A case control Study | Sheffali Gulati | sheffaligulati@gmail.com | ||||||||
529 | No | No | Sheffali Gulati | sheffaligulati1@gmail.com | Clinico-etiological profile of Acute Encephalitic syndrome from Northern India | Sheffali Gulati | sheffaligulati1@gmail.com | |||||||||||
542 | No | No | 4th Oct 2022 | Epilepsy: Treatment 3 – ASM/ Dietary Treatments | J Sahu | Sheffali Gulati | sheffaligulati1@gmail.com | Children with Tuberous Sclerosis Complex (TSC) on Ketogenic diet therapies: Outcome of a retrospective cohort | Sheffali Gulati | sheffaligulati1@gmail.com | ||||||||
560 | No | No | 4th Oct 2022 | Epilepsy: Treatment 3 – ASM/ Dietary Treatments | J Sahu | Sheffali Gulati | sheffaligulati1@gmail.com | Efficacy of Ketogenic Diet therapies in Lennox Gastaut Syndrome: A Prospective Cohort Study | Sheffali Gulati | sheffaligulati1@gmail.com | ||||||||
647 | No | No | 5th Oct 2022 | Peripheral nerve | D Selcen | Sheffali Gulati | sheffaligulati1@gmail.com | Spinal Muscular Atrophy - Emerging therapies: Experience from a tertiary care hospital | Sheffali Gulati | sheffaligulati1@gmail.com | ||||||||
756 | No | No | 6th Oct 2022 | Headache/Stroke 3 | "Mubeen Rafay | Canada" | Shikha Jain | shikha.5dec@gmail.com | mineralising angiopathy presenting as stroke | Shikha Jain | shikha.5dec@gmail.com | |||||||
764 | No | No | 6th Oct 2022 | Neuroradiology 1 | "Manohar Schroff | Canada" | Shikha Jain | shikha.5dec@gmail.com | clinical and radiological profile of focal cortical dysplasia in children | Shikha Jain | shikha.5dec@gmail.com | |||||||
540 | No | No | Shreya Gandhi | shreyagandhi317@gmail.com | Neuro-tuberculosis in COVID: Our experience | Shreya Gandhi | shreyagandhi317@gmail.com | |||||||||||
504 | No | No | 6th Oct 2022 | Neuroradiology 2 | "Kshitij Mankand | UK" | Shubham Kaudinya | shubham.kaudinya@gmail.com | Neurological manifestations of lympho-haematopoietic malignancies | Shubham Kaudinya | shubham.kaudinya@gmail.com | |||||||
509 | No | No | 5th Oct 2022 | Neuroimmunology 2 Antibody mediated disorders / monophasic demyel disorder | Banu Anlar | Shubham Kaudinya | shubham.kaudinya@gmail.com | RISING SURGE OF SUBACUTE SCLEROSING PANENCEPHALITIS IN PANDEMIC ERA | Shubham Kaudinya | shubham.kaudinya@gmail.com | ||||||||
510 | No | No | 5th Oct 2022 | Neuroimmunology 3 Autoimmune encephalitis plus | Silvia Tenenbaum | Shubham Kaudinya | shubham.kaudinya@gmail.com | CLINICAL PROFILE OF AUTOIMMUNE ENCEPHALITIS IN WESTERN INDIA | Shubham Kaudinya | shubham.kaudinya@gmail.com | ||||||||
140 | No | No | 5th Oct 2022 | Muscular dystrophy | Y Nevo | Siddharth Shah | sidh909@hotmail.com | A Novel Founder Mutation in the SGCB Gene Causes Severe Form of Limb Girdle Muscular Dystrophy (LGMD) 2E in Sathwara Community | Siddharth Shah | sidh909@hotmail.com | ||||||||
549 | No | No | 6th Oct 2022 | "Cerebral palsy 1- Evaluation: clinic | neurophysiologic" | "Catherine Arnaud | France" | Siddharth Shah | sidh909@hotmail.com | A Retrospective Case Series of Indian Children With Homozygous RNASEH2B Mutations Presenting As ‘Cerebral Palsy’ Mimic | Siddharth Shah | sidh909@hotmail.com | ||||||
528 | No | No | 6th Oct 2022 | "Movement 3 Ataxias | opsoclonus myoclonus and covid 19 impact" | "Russell Dale | Australia" | Sihem Ben Nsir | sihambn@yahoo.fr | Hereditary cerebellar ataxias: descriptive study of a hospital cohort | Sihem Ben Nsir | sihambn@yahoo.fr | ||||||
559 | No | No | 6th Oct 2022 | Neuroradiology 1 | "Manohar Schroff | Canada" | Sindhura P | sindhupappula84@gmail.com | CLINICAL PROFILE OF CONGENITAL MALFORMATIONS OF NERVOUS SYSTEM - IS IT STILL AN ICEBERG??? | Sindhura P | sindhupappula84@gmail.com | |||||||
495 | No | No | 4th Oct 2022 | Epilepsy: Treatment 2 – ASMs | Ramachandran Nair | Lokesh Lingappa | siriloki@gmail.com | Permampenel in Refractory Epilepsy - Investigator initiated study | Lokesh Lingappa | siriloki@gmail.com | ||||||||
579 | No | No | 4th Oct 2022 | ASD/NDD/ADHD 3 NDD / ID | Charuta Joshi | Aleya Remtulla | sisaleya@gmail.com | Neuroimaging for children with Neurodevelopmental Disorders (NDDs) in the African Population | Aleya Remtulla | sisaleya@gmail.com | ||||||||
432 | No | No | 5th Oct 2022 | SMA | N Chrestian | Sophelia Hoi-shan Chan | sophehs@hku.hk | Bone Health in Children with Spinal Muscular Atrophy | Joanna Yuet-ling Tung | tyl404@ha.org.hk | ||||||||
371 | No | No | 5th Oct 2022 | Muscular dystrophy | Y Nevo | Didem Soydemir | soydemirdidem8@gmail.com | GENETIC LANDSCAPE OF CONGENITAL MUSCULAR DYSTROPHIES(CMD) FROM CENTRAL AEGEAN PART OF TURKEY | Didem Soydemir | soydemirdidem8@gmail.com | ||||||||
241 | No | No | 5th Oct 2022 | General I | J Vajsar | Serkan Kirik | srknkrk@hotmail.com | CLINICAL FEATURES OF PEDIATRIC ACUTE RHABDOMYOLYSIS | Serkan Kirik | srknkrk@hotmail.com | ||||||||
374 | No | No | 5th Oct 2022 | Neurogenetics practice | T Lerman-Sagie | Sergio Rosemberg | srosem@uol.com.br | Progressive encephalopathy due to SLC1A4 mutations in two non Ashkenazi Brazilian siblings. | Sergio Rosemberg | srosem@uol.com.br | ||||||||
377 | No | No | 4th Oct 2022 | ASD/NDD/ADHD 2 ASD assessments / management / Rett syndrome / high risk infants | Antigone Papavasiliou | Soumya Sundaram | ssdr.soumya@gmail.com | Broad Autism Phenotype Questionnaire— Translation and Validation in a South Indian language followed by pilot study | Soumya Sundaram | ssdr.soumya@gmail.com | ||||||||
394 | No | No | 5th Oct 2022 | Neuroimmunology 2 Antibody mediated disorders / monophasic demyel disorder | Banu Anlar | Sedef Terzioğlu Öztürk | ssedef_88@hotmail.com | Acute transverse myelitis related to BNT162b2 vaccine in a teenage girl | Sedef Terzioğlu Öztürk | ssedef_88@hotmail.com | ||||||||
455 | No | No | 6th Oct 2022 | Headache/Stroke 2 | "Mahendra Moharir | Canada" | Sedef Terzioğlu Öztürk | ssedef_88@hotmail.com | AN ATYPİCAL CASE OF POST VARİCELLA STROKE İN A CHİLD ASSOCİATED WİTH HYPERHOMOCYSTEİNEMİA AND MTHFR A1298C MUTATİON | Sedef Terzioğlu Öztürk | ssedef_88@hotmail.com | |||||||
497 | No | No | 5th Oct 2022 | General neurogenetics I | AR Zamani | Sedef Terzioğlu Öztürk | ssedef_88@hotmail.com | "DE NOVO MUTATION IN SETD1B IS ASSOCİATED WITH INTELLECTUAL DISABILITY | EPILEPSY | AND AUTISTIC BEHAVIOR" | Sedef Terzioğlu Öztürk | ssedef_88@hotmail.com | ||||||
573 | No | No | 4th Oct 2022 | Epilepsy: Treatment 3 – ASM/ Dietary Treatments | J Sahu | Suvasini Sharma | suvasini.sharma@sickkids.ca | Effect of concurrent anti-seizure medications on the efficacy of the ketogenic diet in children with epilepsy | Suvasini Sharma | suvasini.sharma@sickkids.ca | ||||||||
67 | No | No | 4th Oct 2022 | "Epilepsy: Syndromes 1 – Self-limited | EE/DEE-SWAS" | C Joshi | Sviatlana Kulikova | sviatlana.kulikova@gmail.com | Polymicrogyria and epilepsy with continuous spike-wave during sleep in pediatric patients | Sviatlana Kulikova | sviatlana.kulikova@gmail.com | |||||||
393 | No | No | 5th Oct 2022 | Genetics and epilepsy I | W Hakami | Dandan Tan | tandandan18@163.com | Clinical and genetic study of rare cases with coexistence of dual genetic diagnoses | Hui Xiong | xh_bjbj@163.com | ||||||||
137 | No | No | 4th Oct 2022 | ASD/NDD/ADHD 2 ASD assessments / management / Rett syndrome / high risk infants | Antigone Papavasiliou | Telma Dagmar Oberg | telmaoberg@hotmail.com | Performance of Physiotherapy Through Early Stimulation in High Risk Babies. Experience Report on the Insertion of this Elective Internship Program for Physiotherapy Students | Regina Turolla De Souza | reginaturolla@yahoo.com.br | ||||||||
108 | No | No | 4th Oct 2022 | ASD/NDD/ADHD 1 ASD genetic / biomarkers / | Chahnez Triki | Hiromi Wada | terrence_thomas@me.com | Acoustic alterations of ultrasonic vocalization in the autism model mice (duplication of 15 q11-13) upon maternal isolation | Hiromi Wada | wada@let.hokudai.ac.jp | ||||||||
156 | No | No | 5th Oct 2022 | Neuroimmunology 3 Autoimmune encephalitis plus | Silvia Tenenbaum | Terrence Thomas | terrence_thomas@me.com | Acute necrotizing encephalopathy (ANE) is a feature of dengue virus encephalitis | Terrence Thomas | terrence_thomas@me.com | ||||||||
100 | No | No | 5th Oct 2022 | Genetics and epilepsy I | W Hakami | Thomas Murray | thomas.murray@nationwidechildrens.org | A case report of sequential seizure semiology as a sign of genetic etiology | Thomas Murray | thomas.murray@nationwidechildrens.org | ||||||||
152 | No | No | 6th Oct 2022 | Metabolic 4 Therapeutic approaches | Samantha Marin Canada | Tuna Koca | tkoca@ptcbio.com | Eladocagene Exuparvovec Gene Therapy Improves Motor Development in Patients With Aromatic L-Amino Acid Decarboxylase Deficiency | Panayiota Trifillis | ptrifillis@ptcbio.com | ||||||||
153 | No | No | 6th Oct 2022 | Metabolic 4 Therapeutic approaches | Samantha Marin Canada | Tuna Koca | tkoca@ptcbio.com | Eladocagene Exuparvovec Improves Body Weight and Reduces Respiratory Infections in Patients With Aromatic L-Amino Acid Decarboxylase Deficiency | Panayiota Trifillis | ptrifillis@ptcbio.com | ||||||||
154 | No | No | 6th Oct 2022 | Metabolic 4 Therapeutic approaches | Samantha Marin Canada | Tuna Koca | tkoca@ptcbio.com | Gene Therapy With Eladocagene Exuparvovec Improves Cognition and Language in Patients With Aromatic L-Amino Acid Decarboxylase Deficiency | Panayiota Trifillis | ptrifillis@ptcbio.com | ||||||||
609 | No | No | 4th Oct 2022 | ASD/NDD/ADHD 1 ASD genetic / biomarkers / | Chahnez Triki | Tuğçe Aksu Uzunhan | tugceuzunhan@yahoo.com | Macrocephaly/autism syndrome exhibits neuroradiological abnormalities including Arnold-Chiari syndrome type I: Clinico-radiological spectrum of a PTEN-opathy | Tuğçe Aksu Uzunhan | tugceuzunhan@yahoo.com | ||||||||
184 | No | No | 5th Oct 2022 | Treatment | F Muntoni | Michael Kwan Leung Yu | u3005180@connect.hku.hk | COVID-19 Vaccine Hesitancy Among Neuromuscular Disorder Children and Adolescents | Michael Kwan Leung Yu | u3005180@connect.hku.hk | ||||||||
262 | No | No | 5th Oct 2022 | Treatment | F Muntoni | Michael Kwan Leung Yu | u3005180@connect.hku.hk | Impact of COVID-19 pandemic on healthcare utilitsation and psychosocial well-being of children with neuromuscular disorder | Michael Kwan Leung Yu | u3005180@connect.hku.hk | ||||||||
459 | No | No | 6th Oct 2022 | Cerebral palsy 2- Management; current and future | "Antigone Papavasiliou | Greece" | Madina Taghiyeva | vagabova_medina@yahoo.com | Features of epilepsy drug therapy in children with cerebral palsy | Madina Taghiyeva | vagabova_medina@yahoo.com | |||||||
249 | No | No | 5th Oct 2022 | SMA | N Chrestian | Vivek Mundada | vbmundada@gmail.com | Onasemnogene abeparvovec for Spinal Muscular Atrophy: Experience from one center in the United Arab Emirates | Vivek Mundada | vbmundada@gmail.com | ||||||||
159 | No | No | 5th Oct 2022 | "CNS Malformations | NGS" | A Narayan | Vinodh Narayanan | vnarayanan@tgen.org | Prevention of Inherited Genetic Disease using WGS (whole genome sequencing) | Vinodh Narayanan | vnarayanan@tgen.org | |||||||
186 | No | No | 4th Oct 2022 | ASD/NDD/ADHD 2 ASD assessments / management / Rett syndrome / high risk infants | Antigone Papavasiliou | Taras Voloshyn | voloshynt@yandex.ru | New ways of treatment for childhood autism: are we moving in the right direction? | Taras Voloshyn | voloshynt@yandex.ru | ||||||||
674 | No | No | 5th Oct 2022 | General II | M Sönmez | Wafa Bouchaala | wafabouchaala85@gmail.com | Clinical evolution in patients with autosomal recessive limb-girdle muscular dystrophy (LGMDR5): A Tunisian cohort | Wafa Bouchaala | wafabouchaala85@gmail.com | ||||||||
203 | No | No | 5th Oct 2022 | Neurogenetics practice | T Lerman-Sagie | Xiaofan Yang | xiaofan.yang@sdu.edu.cn | Social deficits and cerebellar degeneration in Purkinje cell Scn8a knockout mice | Xiaofan Yang | xiaofan.yang@sdu.edu.cn | ||||||||
195 | No | No | 6th Oct 2022 | Neuroradiology 1 | "Manohar Schroff | Canada" | Xuemei Wu | xmwu@jlu.edu.cn | Risk factors and prognosis of spinal cord injury without radiological abnormality in children in China | Xuemei Wu | xmwu@jlu.edu.cn | |||||||
714 | No | No | 4th Oct 2022 | Epilepsy: Investigations | P Madaan | Yael Michaeli Yossef | yaelyos@gmail.com | Home-EEG long term monitoring versus in house long term EEG monitoring | Yael Michaeli Yossef | yaelyos@gmail.com | ||||||||
201 | No | No | 4th Oct 2022 | "Epilepsy: Syndromes 2 – IESS | Dravet | HHE | EMAS" | E Wirrell | Guang Yang | yangg301@sina.com | Assessing risk for relapse among children with infantile spasms using the BASED score | Guang Yang | yangg301@sina.com | |||||
274 | No | No | 4th Oct 2022 | ASD/NDD/ADHD 4 ADHD and Behav / syndromes / LD | Pratibha Singhi | Jian Yang | yangjian1306@sina.com | Response Inhibition in Children with Different Subtypes/Presentations of Attention deficit hyperactivity disorder: a Near-infrared Spectroscopy Study | Jian Yang | yangjian1306@sina.com | ||||||||
329 | No | No | 4th Oct 2022 | ASD/NDD/ADHD 4 ADHD and Behav / syndromes / LD | Pratibha Singhi | Jian Yang | yangjian1306@sina.com | Exploration of serum B vitamin levels in children with ADHD and their correlation with clinical symptoms | Fan Zhang | cmufanzhang@163.com | ||||||||
727 | No | No | 4th Oct 2022 | Epilepsy: Treatment 3 – ASM/ Dietary Treatments | J Sahu | Yasemin Topcu | yasemintopcu35@gmail.com | Efficiency of Rufinamide as add-on Treatment of Drug Resistant Generalized and Focal Epilepsies: One center | Yasemin Topcu | yasemintopcu35@gmail.com | ||||||||
608 | No | No | 5th Oct 2022 | Neuromuscular 1 | H Lochmüller | Yavuz Ataş | yavuzatas23@gmail.com | The Utility of Prognostic Models in Pediatric Guillain Barre Syndrome : A Regional Cohort Study-EGE | Yavuz Ataş | yavuzatas23@gmail.com | ||||||||
729 | No | No | 4th Oct 2022 | ASD/NDD/ADHD 4 ADHD and Behav / syndromes / LD | Pratibha Singhi | Yeliz Engindereli | yeliz.engindereli@neu.edu.tr | Co-morbid psychiatric disorders in patients with arachnoid cyst: A case series | Burçin Şanlıdağ | burcinsanlidag@yahoo.com | ||||||||
628 | No | No | 4th Oct 2022 | Epilepsy: Genetics 3 | L Lagae | Yi̇ğithan Güzin | yguzin@hotmail.com | Clinical Evaluation of Childhood Rare Genetic Epilepsies; Multicentric collaboration study | Yi̇ğithan Güzin | yguzin@hotmail.com | ||||||||
637 | No | No | 4th Oct 2022 | Epilepsy: Treatment 3 – ASM/ Dietary Treatments | J Sahu | Yiğithan Güzin | yguzin@hotmail.com | Kidney Stone Formation İn Children Receiving Ketogenic Diet Therapy | Yiğithan Güzin | yguzin@hotmail.com | ||||||||
286 | No | No | 6th Oct 2022 | Headache/Stroke 2 | "Mahendra Moharir | Canada" | Ziyodakhon Abduyaminova | z.saidazizova@gmail.com | «Risk factors of the stroke in early age children» | Ziyodakhon Abduyaminova | z.saidazizova@gmail.com | |||||||
328 | No | No | 6th Oct 2022 | Metabolic 1 Clinical phenotypes | "Brahim Tabarki | KSA" | Zahra Rezaei | zahra.rezaii84@gmail.com | Cystic Leukoencephalopathy; a confusing neuroimaging feature! | Zahra Rezaei | zahra.rezaii84@gmail.com | |||||||
197 | No | No | 5th Oct 2022 | Molecular genetics | T Sultan | Gang Zhang | zhanggangnjmu@126.com | Identification of 1q21.1 Microduplication in a family | Gang Zhang | zhanggangnjmu@126.com | ||||||||
214 | No | No | 5th Oct 2022 | General neurogenetics I | AR Zamani | Yunjian Zhang | zhangyunjian2008@sina.com | Analysis of clinical features and genetic variants among patients with SLC6A1 mutations | Yunjian Zhang | zhangyunjian2008@sina.com | ||||||||
483 | No | No | 5th Oct 2022 | General I | J Vajsar | Zhuldyz Nukebayeva | zhuldyz_nm@mail.ru | Clinical case of acromicric dysplasia syndrome (ACMICD-syndrome) | Zhuldyz Nukebayeva | zhuldyz_nm@mail.ru | ||||||||
53 | No | No | 5th Oct 2022 | Molecular genetics | T Sultan | TBC | zouliping21@hotmail.com | SLC25A12 as a new candidate for febrile seizures: a case-control association study | Li-ping Zou | zouliping21@hotmail.com | ||||||||
54 | No | No | 6th Oct 2022 | "Tuberous sclerosis | Radiology" | K Aydın | TBC | zouliping21@hotmail.com | Long-term prognosis of neurological system in tuberous sclerosis complex with neonatal onset epilepsy | Li-ping Zou | zouliping21@hotmail.com | |||||||
66 | No | No | 6th Oct 2022 | Metabolic 6 Defects of bioenergetic and intermediary metab | Ingrid Tein Canada | TBC | dr.iramjaved@gmail.com | Clinical profile and outcome of 6 patients with Biotinidase deficeince: An experience from a tertiary care hospital of Pakistan | Dr.iram Javed | dr.iramjaved@gmail.com | ||||||||
196 | No | No | 4th Oct 2022 | "Epilepsy: Neuroimaging | Surgery and Basic Science" | C Akman | TBC | xmwu@jlu.edu.cn | Dynamic changes of cytoskeleton in epileptic mice | Xuemei Wu | xmwu@jlu.edu.cn | |||||||
271 | No | No | 5th Oct 2022 | "Neuropathy | GBS | and CMS" | C Bönnemann | TBC | drrenusuthar@gmail.com | Congenital Myasthenia Syndrome: Correlation between clinical features and genetics from North India | Renu Suthar | drrenusuthar@gmail.com | ||||||
333 | No | No | 4th Oct 2022 | Epilepsy: Treatment 3 – ASM/ Dietary Treatments | J Sahu | TBC | liaojianxiang@vip.sina.com | The ketogenic diet for Dravet syndrome: a multi-center retrospective study | Jianxiang Liao | liaojianxiang@vip.sina.com | ||||||||
566 | No | No | 5th Oct 2022 | Muscular dystrophy | Y Nevo | Ichraf Kraoua | bythouraya@yahoo.fr | Gamma-sarcoglycanopathy (LGMDR5): clinical and genetic study of a pediatric Tunisian cohort | Thouraya Ben Younes | bythouraya@yahoo.fr | ||||||||
775 | No | No | 5th Oct 2022 | "Neuropathy | GBS | and CMS" | C Bönnemann | TBC | rjnipek@hotmail.com | Four Different Types of Cases with Charcot-Marie-Tooth Axonal Involvement | Rojan İpek | rjnipek@hotmail.com |
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Visa Requirements
You may need a visa to enter Türkiye if you arrive by plane. This can easily be checked via https://www.mfa.gov.tr/visa-information-for-foreigners.en.mfa. Please note that a visa needs to be obtained prior to arrival. You can either acquire your visa from a local Turkish embassy or consulate or alternatively obtain it easily via an online application form.
Delegates are able to request and official letter of invitation here at https://icnapedia.org/icnc-registration/letter-of-invitation-icnc2022
Transport in Antalya
Major cities in Türkiye, including Istanbul and Antalya, have a good quality public transport system. Many taxis are available at the airport, or you can arrange your private hotel transfer via SOLO Events (Phone Number: +90 2122790020 / E-Mail: accommodation_icnc2022@soloevent.net)
The distance between Antalya Airport and Sueno Hotel is 30km. It takes approximately 40-45 minutes by taxi and minibus.
Electricity
Türkiye operates on 220 volts, 50 Hz and uses round European style plugs.
Weather in Antalya
The area around the city is known as the Turkish Riviera for a good reason. It experiences a typical Mediterranean climate throughout the year, with hot and dry summers and mild rainy winters. Antalya on average experiences around 300 sunny days every year. Expect a warm October in Antalya during the congress, but be prepared for occasional rain falls.
Credit Card Transactions
All major credit card providers (such as Mastercard, VISA and AmEx) are widely accepted. Please check additional fees before your transaction.
Covid-19 Situation in Turkey
As of June 1, 2022, almost all of the measures have been canceled. This means:
- There is no requirement of vaccination certificate and/or PCR or antigen tests before entering Türkiye.
- Wearing a mask on international flights to Türkiye is at the passenger’s discretion.
- Mask requirements on international flights from Türkiye depend upon the regulations set by the destination country.
Please note that wearing a mask is only mandatory in hospitals. We encourage you to carry your masks with you in case you don’t feel comfortable. Many Turkish citizens are still wearing masks while in public. Please consult your airline’s website before your travel for any updates on Covid-19 measures. Should the Covid-19 situation change, the necessary precautions will be taken both in public areas as at the congress venue.
Safety in Antalya
Antalya, being the tourism capital of Türkiye and the region, is one of the safest travel destinations in the world. Many travelers comment on the friendliness and hospitality of the Turkish people. Türkiye is not only friendly, it is, in many ways, as safe as North America and Western Europe with one of the lowest police-recorded offences (criminal acts) rates in Europe.
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Invited speakers who are unable to travel and have requested to pre-record their talks
- Adam Kirton (Plenary speaker; Alberta, Canada)
Plenary Session: 08:00-08:45 Thursday 6 October
Parallel Symposia: 10:00-12:00 Friday 7 October (Neuronal Plasticity) - Bernard Dan (Belgium) - Files received
- Mubeen Rafay (Manitoba) - Files received
Parallel Symposia: 10:00-12:00 Wed 5 October (Paediatric Stroke) - Samantha Marin - Files received
Parallel Symposia: 10:00-12:00 Wed 5 October (Neurometabolic) - Tobias Loddenkemper (Boston) - Files Received
Controversies: 17:30-18:30 Tue 4 October - Audrey Foster-Barber (San Francisco)
07:00-08:00 Thu 6 Oct - Rise & Shine Seminar (Neuropalliative care) - Peter sidgwick
07:00-08:00 Thu 6 Oct - Rise & Shine Seminar (Neuropalliative care) - Howard Goodkin
- Parallel Symposia: 10:00-12:00 Fri 7 October (Status epilepticus)
- Matthis Synofzik (Germany)
Parallel Symposia: 10:00-12:00 Tue 4 October (Orphans without borders) - Timothy Yu (US)
Parallel Symposia: 10:00-12:00 Tue 4 October (Orphans without borders)
Speakers who are not attending
Manju Kurian
Martino
Richard Edwards
Francesco Pisani
Parallel Symposia: 10:00-12:00 Thu 6 October (Epilepsy networks: seizures, surgery and neuronal plasticity)
Victoria Ruiz (Uruguay)
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Individuals requiring an official Letter of Invitation can request one here. The Letter of Invitation does not financially obligate the Congress organisers in any way. All expenses incurred in relation to the Congress are the sole responsibility of the attendee.
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North America
Archana Patel
Biosketch
From the earliest stages of my career, I have been committed to improving access to appropriate neurologic care for children in resource-constrained regions. As a pediatric neurologist and epileptologist at Boston Children’s Hospital, I lead our department’s global health efforts, including trainee education focused on global perspectives of pediatric neurologic conditions and how to work effectively and ethically in limited resource regions. For over a decade, I have worked in Africa, currently spending over 4 months in the region annually focused on: (1) clinical neurology education and infrastructure development in Rwanda and Zambia, and (2) collaborative clinical research focused on early identification and management of children with epilepsy.
In Zambia, I have been deeply involved in training the first Zambian child neurologists, teaching neurology to pediatric residents and non-specialists across the country and promoting epilepsy advocacy through community health worker initiatives. Through the Human Resources for Health Program in Rwanda, I developed and implemented a child neurology curriculum for pediatric trainees, and continue to provide clinical, education, and research support for young pediatricians as a visiting consultant, with a focus on nurturing interest in our field as the country currently has no child neurologist. My current research is focused on identifying predictive factors for post-malaria epilepsy, with the goal of improving early identification of epilepsy in the highest risk children.
I am active in the global neurology community through several mechanisms that allow me to promote practice and policy change focused on health equity and access to care. I have served as an active consultant with the World Health Organization since 2015. I also serve on the Lancet Commission on Epilepsy; the International League Against Epilepsy’s Commission on Medical Therapies, including as Chair of the Task Force on Access to Medications; and most recently, joined the JICNA editorial board.
Vision
The ICNA’s focus on providing education and research opportunities for child neurologists globally with consideration of perspectives from all regions is central to my own career mission. Having seen the impact of child neurology exposure on places where subspecialty expertise is scarce, I have a strong understanding of the needs and potential for improvement in these regions. In Zambia, the field is exponentially growing since graduation of the first local neurologists; in Rwanda, there has been significant improvement in caring for children with neurologic needs with inclusion of neurology education in the pediatric curriculum.
My experiences have highlighted the importance of bidirectional educational exchanges. Should I be elected to the board, I would work to continue to promote such exchanges through several avenues: (1) increasing opportunities for child neurologists from LMIC to see advanced diagnostics and treatments available in resource-rich countries for both experience as well as drive vision for advancing care locally; (2) fostering partnerships with pediatric associations in countries without child neurologists to provide both deeply needed clinical expertise and exposure and training opportunities for local clinicians; (3) expanding opportunities for trainees from high resourced countries to gain direct experience on the impact of resource limitations on children with neurological diseases and to encourage the consideration of global perspectives in research and development of policy and practice parameters; and (4) promoting and advocating for increased investment in research exchanges between higher and lower resourced regions which demonstrate principles of strong and fair partnerships, including building sustainable clinical and research capacity on the ground.
By assuring that these global clinical and research initiatives are appropriately collaborative and respectful of local healthcare needs and priorities, we can continue toward the important goal of achieving equity in child health.
Charuta Joshi
Biosketch
Biosketch
Dr Charuta Joshi is board certified in pediatric neurology in both Canada and the United States, clinical neurophysiology (Canada) and epilepsy (United States). She graduated medical school from Grant Medical College, Mumbai in 1995 with high honors. She did her pediatric neurology training in New York Presbyterian Hospital and clinical neurophysiology fellowship at Childrens Hospital Michigan. This was followed by seven years in Canada where she practiced pediatric neurology/ epilepsy at the University of Manitoba, Childrens Hospital Winnipeg before returning to the United States. She is presently a Professor in Pediatric Neurology at University of Texas Southwestern, School of Medicine, Childrens Medical Centre Dallas and holds the Dr Roy D. and Ragan S Distinguished Chair in Pediatric Epilepsy.
She is the Program Director of Advanced EEG and Epilepsy Research Fellowship. She has worked in resource rich as well as resource limited countries and is interested in global health, developmental and epileptic encephalopathies, surgical and non -surgical therapy (ketogenic diet, neuromodulation) of medically intractable epilepsies.
She spoke at ICNA in 2018 (Mumbai) as co-chair of a parallel symposium on infantile spasms. In 2020 (San Diego), she co-chaired a symposium on telemedicine and global heath. In 2022 (Antalya Turkey), she will chair a breakfast symposium on EMAS. She has been an invited speaker for the Epilepsy Colloquium (India 2020- converted to zoom due to COVID), Brain Hour at the McMaster University and at local, regional and national educational congresses.
Dr Joshi is passionate about teaching and has received several awards for teaching(medical student and resident level). She wishes to teach globally. She has participated in the ICNTN webinar and serves on the international affairs committee of the Child Neurology Society. She has started discussions with Dr Edward Kija regarding setting up a curriculum for teaching in Tanzania.
Vision
Vision
I finished medical training in Mumbai – Grant Medical College -batch of 1989 and am board certified in pediatric neurology (Canada and USA), clinical neurophysiology (Canada), and epilepsy (USA). My main interests are in global health, developmental and epileptic encephalopathies, surgical and non -surgical therapy (ketogenic diet, neuromodulation) of medically intractable epilepsies. I have seen the scope of medical practice in both resource rich and resource poor areas of the world. While there are factors that cannot be changed in how medicine is practiced, I feel that increasing knowledge has the power to change attitudes and finally change practice of whichever field one might be in.
My goal is to take another step in the right direction for the global population of children with epilepsy through greater participation in ICNA. This could be achieved through greater number of seminars/ lectures done online. The seminars could either be directed towards specialists or towards generalists and the hope is that case-based teaching will help the general care of epilepsy patients in areas where the ratio of the patient to doctor is very low. During COVID lockdown, I was bolstered by the educational content on websites like AES and ILAE and hope that I can contribute to enriching the same for ICNA.
I would like to run for the position of treasurer along with my application to the executive board because I believe that sitting at the same table will allow greater participation and would also allow me to use my time more wisely due to the advice received from other members of the board. My work as a treasurer will be geared to towards assuring that ICNA remains financially stable to allow further growth in its activities to promote care for children with neurological disabilities worldwide.
Elaine Wirrell
Biosketch
Biosketch
Dr. Wirrell completed her medical school at the University of British Columbia, followed by a residency in Child Neurology at Dalhousie University. She is currently the Director of Pediatric Epilepsy at Mayo Clinic in Rochester Minnesota. Dr. Wirrell has served as an ICNA Board member since 2018 and is Chair of the ICNA Research Committee. She is also the former Co-Chair of the Nosology and Definitions Task Force of the ILAE, and currently serves on both the Pediatrics and Surgical Therapies Commissions and the Terminology and the SNOMED Task Forces. She is Co-Editor-in-Chief of Epilepsy.com, the public education website for the Epilepsy Foundation of America.
Dr. Wirrell has a keen interest in Neurology Education and served as the Vice-Chair of the Neurology Examination Committee of the Royal College of Physicians and Surgeons of Canada from 2009-14. She currently is the Program Director of the Child and Adolescent Neurology Residency at Mayo Clinic as well as Co-Chair of the Pellock Epilepsy Symposium, an educational program offered to all North American final year Child Neurology trainees through the Child Neurology Society. Her research interests include optimizing care for children with Developmental and Epileptic Encephalopathies, epidemiology of epilepsy and co-morbidities of pediatric epilepsy and she has published over 230 peer-reviewed articles and numerous book chapters. She has been the recipient of several awards including the AES Kiffin Penry award for Excellence in Epilepsy Care and the Mayo Clinic Distinguished Clinician award.
Vision
Vision
I have had the privilege of serving on the Executive Board of ICNA since 2018 representing North America. During this time, I have chaired the ICNA Research Committee, served on the Finance and Nominations committees as well as the Scientific Committees for the 2020 and 2022 ICNA Meetings. I have a keen interest in enhancing collaboration between members of the international child neurology community and have had the privilege of visiting child colleagues in many regions of the globe. This alliance has allowed me to gain valuable insight on global delivery of care to children with neurological disorders, as well as opportunities to enhance collaboration for education and research amongst child neurology providers. My goals for the ICNA:
- Continue the efforts of ICNA to advance child neurology globally, to optimize clinical care of all children with neurological disease, regardless of socioeconomic status or region of residence. This work will involve continued partnering with representatives of other national and international child neurology organizations and health agencies to work towards this goal.
- Support education in child neurology globally, and in particular in resource-limited regions.
- Enhance international collaboration of child neurologists in practice-changing research to reduce burden of disease and enhance quality of life for children impacted by neurological disorders.
The COVID pandemic has challenged our traditional models of care delivery as well as education and research collaboration. ICNA has responded to this challenge by building outstanding educational and research content on ICNApedia, with key input from our junior members (FLICNA), which is readily accessible online to all members. Our Research committee has created on-line content on how to do research and designed a Research Methodology course, to be offered to attendees of the upcoming ICNA meeting in Antalya. We anticipate this work will facilitate international collaboration in child neurology research.
I would be honored to continue to serve on the ICNA Board.
Hannah Glass
Biosketch
Biosketch
Dr. Hannah Glass, MDCM, MAS (https://profiles.ucsf.edu/hannah.glass) is a Professor of Neurology, Pediatrics, and Epidemiology & Biostatistics at the University of California, San Francisco, where she leads clinical, research, and education programs in Neonatal Neurology. She is the founding co-director of the Neurointensive Care Nursery (NICN), and Director of Neonatal Critical Care Services at the UCSF Benioff Children's Hospital, as well as the director of the Neonatal Neurology Fellowship Program. Dr. Glass leads a robust research program that has received funding from the NIH, Patient Centered Outcomes Research Institute, March of Dimes, Cerebral Palsy Alliance, and the Pediatric Epilepsy Research Foundation to conduct research that uses advanced imaging and brain monitoring to predict outcomes following newborn brain injury.
She is co-PI of the Neonatal Seizure Registry (https://neonatalseizureregistry.ucsf.edu/), a ninecenter collaborative that has studied diagnosis, treatment, and outcomes of seizures in more than 1000 newborns since 2012. Dr. Glass earned a medical degree at McGill University in Montreal, Canada, and completed pediatrics training, a child neurology residency, and chief residency at the University of Calgary. She trained in Neonatal Neurology and earned a master's degree in clinical research at UCSF. She lives with her husband, six-year-old son and nine-year-old dog in beautiful Lafayette, California. When not working, she enjoys reading, hiking, and travel.
Vision
Vision
There have been rapid advances in neurological care for children over the last decade, including genetic testing, detailed brain imaging, and specialized treatments for rare diseases. Yet many countries around the world lack access to these tools and specialized treatments. As a result, there are growing inequities in the way we understand local frequency, manifestations, and treatment options for important neurological conditions that affect children around the world. As a member of the Executive Board for the ICNA, my overarching goal would be to reduce inequity in the treatment and outcomes of neurological conditions that affect children around the world through education and support for local research programming. To achieve this goal, my primary approach would be to work with the international Scientific Committee to better understand the educational needs of the society members and help plan meetings with strong content to address those needs.
Jonathan Mink
Biosketch
Jonathan W. Mink, MD PhD is Professor of Neurology, Neuroscience, and Pediatrics at the University of Rochester (NY) where he is the Frederick A. Horner, MD Distinguished Professor in Pediatric Neurology and Chief of Child Neurology. He has an research program that focuses on 1) understanding the control of movement and mechanisms of movement disorders due to basal ganglia disease and 2) therapy development for the Neuronal Ceroid Lipofuscinoses (Batten Diseases). Clinically, he specializes in pediatric movement disorders with special interests in dystonia and Tourette Syndrome and in childhood-onset neurodegenerative disease. He is former President of the Child Neurology Society (CNS) and was the Chair of the Scientific Planning Committee for the joint meeting the CNS and ICNA in 2020. Dr. Mink is a former Associate Editor of Neurology and currently serves on the Editorial Boards of Pediatric Neurology, Neurology, and the Journal of the International Child Neurology Society.
Vision
I have been a member of the ICNA since 2004 and have participated actively in the ICNCs since then. I have had the privilege to serve on the ICNA Executive Board since 2014 and Chaired the Constitution and Bylaws Committee from 2014 – 2018. During that time, the ICNA has grown substantially and I have had the pleasure of participating in a number of educational programs in low- and middle-resource settings. This, to me, is the most important mission of the ICNA. The impact of the COVID-19 pandemic has been to limit the opportunities for in-person educational programs, but the use of technology has allowed us to reimagine how these programs can occur virtually.
My vision for the ICNA in the next 4 years is to capitalize on more widespread use of video technology to foster the expansion of the ICNA community in the areas of education, clinical consultation, and research. The historical priorities of providing opportunities in low- and middle-resource settings and to younger members of our profession are my priorities as well. As a member of the 2022-2026 Executive Board, I would leverage my prior experiences in these areas and work with my colleagues to develop and expand opportunities in the areas of education and research. In particular, working to develop a platform for consultation and sharing of expertise on children with complex movement disorders will be a priority aim.
Jorge Vidaurre
Biosketch
Jorge Vidaurre MD, FAES, FACNS
Director, Pediatric Clinical Neurophysiology
Program Director EEG laboratory
Nationwide Children’s Hospital - The Ohio State University
Dr. Vidaurre currently serves as Director of the Pediatric Clinical Neurophysiology Program and EEG Laboratory at Nationwide Children's Hospital - The Ohio State University Medical Center. He is the Chair of “International Affairs Committee” for the Child Neurology Society (CNS), Chair for the “Education Task Force” from the International League Against Epilepsy (ILAE)” and “International Education Advisor” for the International Child Neurology Association (ICNA).
Dr. Vidaurre actively serves in multiple national and international societies. His activities include: Chair of the “Global Health, Special Interest Group (SIG)” at the American Epilepsy Society (AES), Regional leader for Latin America, from ILAE “Global Task Force” and member of the “Executive Board and Education Committee” at the Ibero-American Child Neurology Association (AINP). He participates in the “Professional Development Mentorship Program” at the American Clinical Neurophysiology Society (ACNS) and “Fellow-Mentor Program” from AES. He also served as member of the AES “Scientific Program Committee” and ACNS “International”, “Clinical Research Committee”.
Dr. Vidaurre is board certified in Neurology with Special Qualifications in Child Neurology, Clinical Neurophysiology and Epilepsy. He completed his neurology training at State University of New York (SUNY) and epilepsy training at Montefiore Medical Center, Albert Einstein College of Medicine. After finishing his fellowship, he returned to Latin America and worked in El Salvador for three years, before accepting his current position at Nationwide Children’s Hospital. As a member of the “ILAE North American Commission”, he collaborated in the implementation of epilepsy surgical programs in El Salvador and continues to work in this project.
Dr. Vidaurre is greatly involved in work related to international outreach collaborative programs in the field of pediatric neurology and epilepsy. He has extensive experience in the planning of educational and training programs in poor- resource regions, fostering collaborative efforts between multiple national and international societies. He works with local leaders in different regions including Latin America, Caribbean, Africa, and Asia. He has organized numerous local and regional international symposia in different countries and joined collaborative efforts directed at building infrastructure, such as, establishment of EEG laboratories, donations of EEG machines and training of EEG technicians in low -income countries. As chair of the ILAE Education Task Force, he is working on a practical, interactive, basic EEG curriculum to be used in resource limited countries.
Dr. Vidaurre is the recipient of the 2022 “Arnold P. Gold Foundation Humanism award” form CNS. He has authored and published multiple peer-reviewed journal articles and book chapters. His research interests and publications are in the field of pediatric epilepsy, epileptic encephalopathies, quality improvement in status epilepticus, and global health. He is an advisor for the international National Institute of Health (NIH) grant “Center without walls grant on antiepileptogenesis in traumatic brain injury”.
Vision
Future Vision
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Encourage active participation of young leaders from different world regions, especially low-income countries, in the planning of educational programs directed to improve the practice of child neurology in poor-resource areas.
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Support specific educational and training programs (These programs include local/regional symposia and training workshops) based on local need assessment.
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Stimulating research that is of benefit for resource-limited region. This includes fostering programs directed to mentor and support young investigators, especially researchers working in low-medium income countries
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Strengthen collaborative efforts between ICNA , CNS to increase the number of educational programs and develop long term- self-sustainable international outreach programs and facilitate collaborative efforts with other local, regional, and international societies, such as International League Against Epilepsy (ILAE).
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Facilitate building of infrastructure needed in poor resource areas, throughout collaboration between societies, academic institutions and nonprofit organizations
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Creation of new initiatives to support training of primary care providers, working in regions with limited or no access to properly trained child neurologist and creating practice guidelines, which are applicable to the specific regions and can facilitate neurological care.
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Continue to build online resources which can be used by members seeking educational material and websites that facilitate communication between members and local leaders
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Develop collaborations with large academic medical centers, involved in training of child neurologists in poor-resource regions by strengthening their infrastructure and providing support with ongoing programs.
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Promote collaboration of academic centers in high income countries to support training in poor resource settings
Karen Skjei
Biosketch
Karen L. Skjei, M.D. was inspired to pursue a career in medicine after witnessing the impact of limited access to medical care during her 2 years in the U.S. Peace Corps in the Dominican Republic. She attended medical school at the University of California, San Francisco, followed by a pediatric neurology residency at the Mayo Clinic in Minnesota. She then completed a 2-year fellowship in Clinical Neurophysiology/Epilepsy at the Children's Hospital of Philadelphia. She is active in health disparities research and founded/leads the Health Equity Committee of the Pediatric Epilepsy Research Consortium.
After serving in academic leadership positions for 10 years, Dr. Skjei chose to combat health disparities directly by setting up the first pediatric epilepsy practice in El Paso, Texas, a city of 850,000 with a single pediatric neurologist. Internationally she has given lectures in English and Spanish at regional education conferences organized by ICNA, the American Epilepsy Society and the American Academy of Neurology in Ecuador, Paraguay, India and the Sudan. She has been editor of the ICNA Journal Watch since its inception in 2019 and now serves as editor of the Journal Watch section of JICNA. She has been an active participant in Executive Board meetings for the past 2 years.
Dr. Skjei is a fellow of the AES and has published more than a dozen peer-reviewed articles and book chapters. She’s won major awards throughout her career including the UCSF Chancellor’s Award for Public Service, the Mayo Brother’s Distinguished Fellows Award at Mayo, and the Tower Award for Outstanding Faculty at the University of Texas-Austin. She founded the Epilepsy Fellowship at the University of Texas and has garnered several teaching awards. Her passion has inspired many trainees to pursue pediatric neurology and pediatric epilepsy and she continues to mentor trainee from the undergraduate level through fellowship.
Vision
There are great disparities in Pediatric Neurology training and specialty care across the globe. Through its international reach, ICNA is positioned to ameliorate some of these disparities. I believe ICNA’s priorities in the coming years should include:
1) Improving our understanding of the needs of our membership. This can be accomplished through a biannual membership renewal survey which I suggested at the most recent Executive Board Meeting and which was approved by the Board.
2) Focusing our educational efforts on practice-changing discoveries. I have assisted in this through the educational lectures I have given in India, the Sudan, and Latin America, and through founding an organized ICNA Journal Watch, which has now been incorporated as a section in JICNA
3) Promoting international networking so that we can assist each other on an individual scale. This is accomplished through our biannual meetings and through sub-organizations such as FLICNA and the ICNA committees. I believe this can be aided by providing opportunities to a broader pool of interested members to be actively involved in ICNA committees, ICNApaedia and other ICNA activities. These members and their areas of interest and talent will be identified through the biannual membership survey.
4) Expanding the reach of our communal knowledge through virtual Pediatric Neurology training and other in-person and online educational opportunities.
Phillip Pearl
Biosketch
Phillip L. Pearl, M.D. is Director of Epilepsy and Clinical Neurophysiology at Boston Children’s Hospital and William G. Lennox Chair and Professor of Neurology at Harvard Medical School. Dr. Pearl, originally from Baltimore, attended Johns Hopkins University and Peabody Conservatory of Music and University of Maryland School of Medicine. He took his residency at Baylor College of Medicine in Houston and fellowship at Boston Children’s Hospital. He was Division Chief of Neurology at Children’s National Medical Center, Director of Neurology Education Programs, and Professor of Neurology, Pediatrics, and Music at the George Washington University School of Medicine until returning to Boston in January 2014. Dr. Pearl also is a faculty member of the Music and Health Institute at the Berklee College of Music in Boston.
Dr. Pearl served on the Neurology RRC of the ACGME for six years and was a principal author of the revised program requirements for training in child neurology in the US as well as for the epilepsy fellowship. He has been a member of examination writing committees of the ABPN for 20 years and served as an oral board examiner over 20 times.
His major research interest is inherited metabolic epilepsies with specific focus on disorders of GABA metabolism. His book, Inherited Metabolic Epilepsies, had a second edition published in 2018. He is an editor of Swaiman’s Pediatric Neurology. Dr. Pearl is Past President of the Professors of Child Neurology and the immediate Past President of the Child Neurology Society. He has authored over 220 peer-reviewed manuscripts and over 150 chapters and reviews, written or edited five books including one translated into Chinese and another into Japanese, and produced two musical CDs, the first of which debuted at Georgetown’s Blues Alley and supports the care of indigent children in the capital city, Washington, D.C.
Vision
On one hand, it was jarring to have had the “pandemic presidency” of the Child Neurology Society (CNS). Having looked forward to leading the CNS into the long anticipated 2020 combined meeting with ICNA, and then our 50th Anniversary 2021 meeting, we were instead thrust with rapid fire and unprecedented needs, e.g. changing the standard of care for infantile spasms, assembling telemedicine toolkits, responding to crises in institutional racism.
On the other hand, what was inspiring above all was to work with Jo Wilmshurst and Pratibha Singhi in organizing the ICNA-CNS conference, a true albeit virtual success that required rapid implementation of a unique e- format. Furthermore, I developed more connections with international colleagues, with an especially important new group consisting of the presidents of child neurology societies across the globe. I have had meaningful international experiences previously, from working in Romanian orphanages during the 1990s, including establishing an epilepsy clinic in an orphanage in Siret, Romania and bringing children to the US for care before a moratorium was placed there on international adoptions, to wonderful visits and lecturing at conferences throughout Europe, Asia, the Middle East, and South America.
These international experiences, now facilitated by our new electronic means to meet and communicate, have been eye opening and enlightening. While I hope the input of the Child Neurology Society and my experiences will be helpful to ICNA, it is me that has truly benefitted from widening my horizons and working on behalf of pediatric neurology globally to enhance our discipline and improve conditions for all of our practitioners and investigators and, above all, our mutual patients and their families. The current pandemic only proves our interdependence. It would be a special pleasure and honor to join the ICNA board and continue to work on behalf of pediatric neurology worldwide.
Rajesh RamachandranNair
Biosketch
Rajesh Ramachandran Nair, MD,FRCP, FRCPCH,FRCPC is an Associate Professor at McMaster University and the Director of the Comprehensive Pediatric Epilepsy Program (CPEP) at McMaster Children’s Hospital (MCH), Canada.
Dr Ramachandran Nair is the Co-Program Director of the International Child Neurology Teaching Network (ICNTN) of the ICNA. He initiated the ICNTN grandrounds in early 2021, providing the membership with the oppurtunity to interect with experts in child neurology worldwide. Dr Ramachandran Nair and team is develeoping a comprehensive learning module based certificate program in Pediatric Neurology. Dr. Ramachandran Nair leads the creation of the epilepsy module. His team will be presenting a symposium on ICNTN at the ICNC 2022, Turkey.
In 2020, Dr. Ramachandran Nair established the Canadian Epilepsy Teaching Network (CETN) the Canadian league Against Epilepsy (CLAE0.. In addition to monthly webinars CETN also started an EEG teaching course for neurology trainees. Dr. Ramachandran Nair started the weekly McMaster Pediatric Neurology Rounds “Brain Hour” in 2007, which are now attended (virtually) by an international audience. In 2012, he helped to develop the accredited EEG training program for EEG technologists. In 2017, he was awarded the McMaster Pediatric Neurology teaching award. Dr. Ramachandran Nair started the first epilepsy monitoring unit (EMU) at MCH in 2008, and developed CPEP in 2014. He was an active member of the Provincial Epilepsy Task Force.
Dr Ramachandran Nair was the co-Chair of the committee that drafted the Provincial Guidelines for the Management of Epilepsy. He was an invited member of the SUDEP Task Force of the AES, and a board member of the Canadian Association of Child Neurologists (3 years) He is a member of the scientific program committee of the AES. He is funded by the Ontario Brain Institute, Hamilton Health Sciences Foundation, Innovation Fund of the Academic Health Sciences by the Ministry of Health, and SUDEP Aware. To date he has authored over 50 peer reviewed journal articles, 4 book chapters and numerous conference abstracts. His publications on SUDEP communication with patients are widely cited by healthcare professionals, in conferences and in professional guidelines about SUDEP.
Vision
ICNA should continue to function as the primary global professional organization of child neurology clinicians that advocates and facilitates quality, comprehensive and optimal clinical care for children with neurological diseases worldwide at the right time and at the right place. This can be achieved through fruitful collaboration with regional child neurology professional organizations, global membership campaign, and working with child neurology patient advocacy groups. As the co-program director of ICNA’s Child Neurology Teaching Network (ICNTN), my major goal will be around education.
- Enhance the work of International Child Neurology Teaching Network (ICNTN) through better visibility and quality work using modern technology.
- Timely completion of the all the modules of ICNTN ICNA child neurology e-learning modules
- Facilitate translation of e-learning modules to major languages.
- Providing the e-learning modules at reduced fee to professionals from low-income regions.
- Working with national and regional child neurology training institutions and Universities to encourage trainees to adopt the ICNTN ICNA Child Neurology teaching modules as part of their curriculum.
- Provide more opportunities for young child Neurologists in ICNA education and policy working groups.
- Create a framework for international trainee exchange programs, and national and international mentorship program.
South/Central America
Ana Carolina Coan
Biosketch
Dr. Ana Carolina Coan is Associated Professor of Child Neurology of the Department of Neurology of the Campinas University – Unicamp, Campinas, Brazil. Dr. Coan is author of over 71 peer-reviewed original articles and reviews. Since 2000, she developed her research at the Neuroimaging Laboratory at UNICAMP focusing at the use of structural and functional MRI for the identification of biomarkers associated epilepsies phenotypes. Her studies described the network of cerebral gray and white matter abnormalities in distinct phenotypes of epilepsies.
Dr. Coan also studied the use of multimodal neuroimaging to improve the noninvasive pre-surgical evaluation of individuals with pharmacoresistant epilepsies and how they can accelerate and diminish the costs of this evaluation. Her current research focuses on the association of clinical phenotypes and brain structural and functional abnormalities of different epileptic syndromes and their impact on brain development. At Unicamp, she is involved in teaching both undergraduates, residents and post-graduates. She supervised 9 master and doctoral thesis. She supervise the general child neurology and epilepsy outpatient clinics as well as the pediatric video-EEG and epilepsy surgery program of the Clinical Hospital of Unicamp. She has dedicated to translating and teaching PET (Pediatric Epilepsy Training) courses in Brazil.
Dr. Coan is an associated researcher of the Brazilian Institute of Neuroscience and Neurotechnlogy - BRAINN. She is currently the vice president of the Brazilian Society of Child Neurology (SBNI) and the representative of child neurology of the Education Commission of the Brazilian Academy of Neurology (ABN). She is also member of the Executive Board of the International Child Neurology Association (ICNA).
Vision
My vision is that ICNA should be a reference for worldwide education of pediatric neurologists as well as a society engaged in contributing to achieve high quality, efficient and humanistic health care services for children and adolescents according to the specific needs of each country. I believe I can contribute to maintain and expand the important work of ICNA worldwide. I believe ICNA should guarantee continuous worldwide education of pediatric neurologists according to the reality and needs of each different country. This educational approach was significantly expanded with the improvement of online contents in the last two years. I believe I can contribute to improve the access to the educational content for the Latin America and other countries of Portuguese languages.
The translation and teaching o PET (Paediatric Epilepsy Training) is an example of success in this area. By removing the language barrier, the PET course was accessible to different countries in the South America and Africa. A second important role of ICNA in my view is to contribute to advance research in different areas of child neurology. Through proposals such as the Connectome project ICNA can help to improve multicenter studies initiatives.
The Connectome project it could be expanded through partnerships and possible funding from national societies. As a professor of one of the most important Brazilian universities, I have access to government personal and it also puts me in contact with healthy professionals of the different facilities in Brazil. Being a university professor also facilitates my contact with international professionals. I have been working with different international consortiums of child epilepsy education, including an online Latin American course for primary physicians.
West Asia
Anaita Hegde
Biosketch
Dr Anaita Udwadia-Hegde, Pediatric Neurologist, Mumbai, India. -Director of Neurosciences, SRCC Narayana Children’s Hospital & Honorary Consultant at the Jaslok Hospital & Research Centre & Wadia Children’s Hospital. -President of the Association of Child Neurology-India (AOCN-India)2021-2023. -Elected, Executive Board Member of the International Child Neurology Association, ICNA, 2018-2022, Lead of Education.
- Jt Organising Secretary, International Child Neurology Congress, Mumbai, 2018.
- Post graduate teacher, over 25 years
- Guide and mentor, Pediatric Neurology Fellowship program, over 16 years.
In the 4 years with ICNA, learnt alot regards the situation & needs of child neurology in different regions of the world. We have helped support with personnel, ideas, funds and or collaboration, national child neurology bodies and passionate professionals keen to improve the situation in their country.
Helped conceive the Global Regional Initiative Program -GRIP, a collaborative effort to upskill child neurology worldwide. Here ICNA with other international child neurology associations such as CNS, EPNS, etc plan to fund & support an upskilling regional project for 2 years.
The ICNA educational activities, inspite of COVID have been amazing. Numerous National associations have been endorsed by ICNA. Cross continent teaching programs and the ICNTN has been a run-away success.
As President of the AOCN-India, have created active verticals with a thrust on education, research, advocacy, outreach, finance, website and offbeat. Focus is to connect, empower, increase and enhance the child neurology fraternity in our country.
But my passion, is my work in rural Maharashtra. Founded the Rural Child Neurology Program, in 2010. Conduct camps quarterly. We treat, give holistic, multidisciplinary & nutritional care to over 800 children with neurological problems at each camp, & focus on parent education. During COVID, we were able to support the children with medication and virtual consults. I do believe that corrective measures in the critical first few years of a child’s development, have maximum benefits on mental and developmental growth
Vision
Having completed a term on the Executive board, I have had the opportunity to learn and see how the ICNA works in all regions of the world. As Lead of Education, ICNA, the pandemic made us move from conventional academic programs to the beauty of the virtual world. Change in educational methods, structure, platforms, has made us all closer, connected and made travel dispensable in the pursuit of education.
- I hope to enhance the educational activities already conducted by regional national bodies, international conferences, the very successful ICNTN & FLICNA sessions. We will continue the programs with the aim to reach all corners of the world.
- I would like to see the GRIP program (Global Regional Initiative Program)come to fruition and thus help different regions of the developing world to a solid 2year supported program, from ICNA & other international child neurology partners eg CNS, EPNS etc. They can avail of this program for any emergent need in their region eg: training of first few child neurologist in their country, establishing an epilepsy surgery program, metabolic lab, research project etc.
- Collaborating with other child neurology bodies to facilitate cross continental training for both students in developed and developing countries. There is much to be learned on both sides.
- Creating a role for ICNA as a body to promote the number of child neurology members worldwide. Creating awareness at international and local levels, support training programs, eg: fellowships, funds, collaboration, and help with practice parameters.
- In creating advocacy statements in support of correct child care, against wrong or misinformed practices and to guide the parent body towards correct developmental concerns.
- Multinational, multicentric research activities to combine knowledge for better science.
- Giving a more global and multicultural feel to the practice of child neurology worldwide.
HasanTekgül
Biosketch
Dr. Hasan Tekgül was born in Gümülcine-Greece, in 1964. He migrated with his family to the west part of Turkey, Izmir, in 1974. Dr. H. Tekgül graduated from the University of Ege, Izmir, Turkey in 1986. Dr. Tekgül began his career in pediatrics in 1992, then as a pediatric neurologist in 1994, and as an associate professor in 1998. In 2000, he was awarded a grant by the Turkish Scientific Research Council, Research Fellowship at Harvard University. He studied neonatal neurology with Joseph Volpe and neonatal EEG with Gregory Holmes and Blaise Bourgeois between 2000-2002 at Children’s Hospital Boston.
Dr. Tekgül also spent three months in Cleveland Clinics, Ohio, for a three-month EEG course. He returned in 2002 to set up a pediatric clinical neurophysiology lab for the comprehensive diagnostic evaluation and treatment of children and adolescents with epilepsy at Ege University Hospital. Dr. Hasan Tekgül took up the position as Professor of Pediatric Neurology at the University of Ege, in 2003. His clinical sub-specialties are Neonatal Neurology, Developmental Neurology, Pediatric Epilepsy, and Pediatric Clinical Neurophysiology (EEG Monitoring, EMG, and Transcranial Magnetic Stimulation-TMS). He has designed and tested a reduced electrode EEG montage for neonatal EEG monitoring. He has also contributed to seminal research on biomarkers of epileptogenesis and neuronal plasticity in the developing brain with TMS. His current projects include genetic characterization of developmental epileptic encephalopathies, new EEG modalities for neonatal seizures in neonatal intensive care units.
Dr. Hasan Tekgül has 166 original research publications (103 in international journals and 63 national journals) and numerous book chapters. He has presented her research at international meetings but also supports global educational programs, with a particular focus on national EEG courses ( basic EEG: 12, and advanced EEG:11) and EMG courses.
Current Position:
- Pediatric Neurologist / Epileptologist Consultant Head, Department of Pediatric Neurology, Ege Children’s Hospital, Izmir, Turkey,
- Clinical Professor Ege University Medical Faculty, Izmir, Turkey
Other Relevant Positions:
- Turkish Child Neurology Society Vice President
- An Active Member of the International Child Neurology Association (ICNA)
- Antalya 2022 ICNC Chairman and Scientific Committee Member
- The European Pediatric Neurology Society is an active member.
- The Asian-Oceanian Child Neurology Association is an active member.
- Reviewer for a number of journals.
- Turkish Scientific and Research Council (TUBTAK) reviewer
Conflict of Interest I have provided consulting services to UCB, Sanofi, Novartis, Nutricia, Abbot, and Nestle. I received lecture fees and professional travel accommodations from UCB, Sanofi, Novartis, Nutricia, Abbot, and Nestle.
Vision
ICNA is a golden synapsis between health professionals to advance knowledge, education, facilitation, and sharing resources in field of neuroscience and reach children across the world.
I have been a member of ICNA since 2005 and have attended ICNA meetings. I have worked over the past fifteen years to establish international collaborations. I have trained residents and fellows from Cyprus, Azerbaijan, and Iran.
I have attended four educational meetings as an ICNA speaker: Colombus, Sri Lanka (22-23 March 2014), Tebrise, Iran (13-15 Sep 2016), Cox-Bazar, Bangladesh (5-6 November, 20016), Chennai, India (Jan 2016).
I actively work in clinical and laboratory research on neonatal neurology, pediatric epilepsy, and pediatric clinical neurophysiology. I would like to share and contribute to the education of junior child neurologists. I can be actively involved in educational exchange programs, symposiums, workshops.
It would be an honor to be a member of the Executive Board of ICNA. If I have been nominated and elected to the EB of ICNA, I can contribute to international education activities and congresses.
Rekha Mittal
Biosketch
Dr Rekha Mittal Additional Director ( Pediatric Neurology)
Madhukar Rainbow Children’s Hospital, New Delhi – 110017
Ph: 9958870028, Email: drrekhamittal2008@gmail.com
Professional experience
1988: Completed two years in - service training (from the Army ) in Pediatric Neurology from All India Institute of Medical Sciences, Delhi , in 1998.
1988-2010 : Worked as Pediatrician and later Pediatric Neurologist in Armed Forces, India.
Subsequently, practiced Pediatric Neurology in diverse medical set ups in different cities across India – from basic medical centres to the advanced Army Hospital Research and Referral, New Delhi.
2010 - present: Worked in different superspeciality hospitals in New Delhi. Presently with the Madhukar Rainbow Children’s Hospital, New Delhi, where I also see children from different countries, including the middle east, Africa, and Asia, and have some insight into challenges in Pediatric Neurology in these countries.
Social work
Ran a charitable centre for 5 years, where Pediatric Neurology services were provided free of cost to children from economically weaker families.
Organisational experience
A. Association of Child Neurology (AOCN):
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Was one of the seven founding members of the AOCN, and subsequently, Secretary and President of the AOCN.
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Was secretary/chairperson in the organization of 3 National Conferences of the AOCN
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Initiated /organized and was part of, many educational activities of the AOCN like Continuing Medical Education/ similar programs.
During the Covid pandemic, which happened when I was president of AOCN, academic activities were continued online, with masterclasses, short courses, lectures for Pediatric / Pediatric Neurology Residents, General Pediatricians and Pediatric Neurologists.
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Convened 3 important consensus statements for India : • Social and Legal Aspects of Childhood Epilepsy • Diagnosis and Management of Febrile Seizures • Diagnosis and Management of West Syndrome
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As President, I was successful in getting approval from the National Board of Examinations in Medical Sciences (Government of India), for Pediatric Neurology as a subject for awarding a degree in this subject ( equivalent DM )
I have experience in practice of Pediatric Neurology under diverse medical setups and populations, and also organisational experience and success in different activities at a National Level in India.
Vision
1. Pediatric Neurology UPSKILLING AT EVERY LEVEL : from the ground upwards to the sky is the limit, can be achieved; it is the key for resource development.
The ICNA is a prestigious world body to which Pediatric Neurologists the world over seek membership and follow. As such, the body already has a leadership role in multiple areas of education, practice, advocacy and encouraging and awarding research in Pediatric Neurology at different levels. However, a footprint into Pediatric Neurology practice at the grassroots level can be expanded, in best interest of children requiring Pediatric Neurology services.
In a majority of developing countries with limited resources, the pediatric neurology practice is mostly by General Pediatricians. The Zimbabwe story on the ICNA website ( https://icnapedia.org/icna-zimbabwe-appeal ) is not limited to Zimbabwe; it is still the story of most countries.
The way forward would be :
- Pediatric Neurology for Pediatricians : ICNA could have a greater role in improving knowledge and academic programs by partnering with local Pediatric / Pediatric Neurology bodies in different countries and regions.
- Training and teaching modules for Pediatric residents in certain key areas ( Epilepsy, Developmental disorders, Neuroinfections, clinical examinations). The making of a good Pediatric Neurologist , as well as inculcating good Neurology practice starts in Pediatric MD residency. Residents doing MD often find Pediatric Neurology challenging. Hopefully, this will spark more interest in the subject in the brightest minds.
- Short term courses for paramedical workers in certain focussed areas can be designed (eg Epilepsy counselling, Autism counsellors, Neuromuscular disorder counsellors). This can be modified according to regions in partnership with local bodies, to adjust for regional differences.
- The network of Pediatric Neurologists around the world could be motivated to volunteer for this activity.
2. Development of ICNA consensus statements/ guidelines on common neurological disorders for practice at differing levels of healthcare.
3. Recognition of Pediatric Neurology services by individuals in this field, beyond research. This would encourage Humanism and innovation in practice of Pediatric Neurology.
Shaheen Akhter
Biosketch
Prof Akhter is the Professor of Paediatric Neurology and Dean, Faculty of Paediatrics at Bangabandhu Sheikh Mujib Medical University (BSMMU), the only medical university in Bangladesh. She has been working for more than 22 years in Paediatric Neurology, Neurodevelopment, and Autism. She has taken an active role in developing and implementing the 'Paediatric Neurology and Neurodevelopment Residency Course' at BSMMU. She is actively engaged in patient management alongside clinical research and teaching commitments.
Prof Akhter is the Founder-Director of the Institute of Paediatric Neurodisorder and Autism (IPNA). IPNA is a pioneer institute that operates at the national level, providing comprehensive and tertiary-level services to children with neurodevelopmental disorders and autism. IPNA aims to consolidate research initiatives at the national and international level and organize national and international seminars and workshops to disseminate disability/autism-related knowledge and other essential skills to doctors, teachers, and parents. It also runs a model 'School for Children with Autism' by autism-expert teachers and their team, involving parents in managing children with disabilities. IPNA regularly organizes national and international training and seminars for paediatric neurologists, paediatricians, and other health professionals.
She is an active member of ICNA and, as IPNA head, she and her team had organized a two-day-long "ICNA Educational Meeting" at Cox's Bazar, Bangladesh, in 2016. The event hosted internationally reputed child neurology and child development scholars and focused on exchanging knowledge and best practices in Autism, Epilepsy, Movement Disorder, child development, CNS Infections, Cerebral Palsy Neurometabolism, and Neurodegenerative disorders.
Prof Akhter has also been working with the Bangladesh Non-communicable Disease Control Programme to develop tools for screening neurodevelopmental problems and ASD for community field workers in health care. Prof. Shaheen does not have any conflicts of interest to disclose.
Vision
During the pandemic, the ICNA’s continued role in creating a knowledge environment by providing education and training and engaging in research and advocacy was hugely beneficial for paediatric neurologists worldwide. We especially felt its positive impact in Bangladesh during the prolonged and continued lockdowns. I believe it is vital to build on these close connections and forge a deeper relationship based on learning and knowledge-sharing. I believe we can offer a unique perspective: of medical practitioners dealing with a vast number of healthcare seekers in low-resource settings.
More and more research is being conducted locally based on this context, especially since there are still certain infectious diseases that prevail in developing countries like Bangladesh, which struggle with providing care to a significant population with limited means. In Bangladesh, paediatric neurology is still a relatively new sub-specialty, but more and more doctors specialise in it. Integrating such understandings into a platform as huge as ICNA can enrich us in Bangladesh and bring diverse critical perspectives into the ICNA itself. Such representations can make crucial contributions to an ever-growing and increasingly diverse association in an ever globalizing and integrating world. Now more than ever, we need to improve systems to respond adeptly to the challenges children living with a neurologic condition face.
We need to work harder to create inclusive opportunities for all children and families to access and receive the quality of care they deserve. In this, each of us in the child neurology community has a role to play, and ICNA is already an integral actor in fulfilling this responsibility and disseminating scientific knowledge to empower regional healthcare delivery. I am committed to being a part of this journey and working to improve the lives of children with neurological disorders and neurodisability as a part of this worldwide neurology community.
Sheffali Gulati
Biosketch
Professor Sheffali Gulati: trained/working at All India Institute of Medical Sciences, New Delhi. Part of the team which started first DM Pediatric Neurology Program in South Asia (2004), Program Director (2008-). Contributed towards establishing Pediatric Neurology programs across India/SAARC countries.
Over 25 years experience, has developed Pediatric Neurology in India as a specialty- academics, clinical care, patient empowerment, research, advocacy and public health domains. National/International awards(Over 25)- First India recipient, Sheila Wallace Award(ICNA)2014, National Award for Science & Technology communication 2021; Fellowship Award, McGill University 2006,ICNA 2010. Fellow, Royal College of Pediatrics and Child Health, UK; Fellow, National Academy of Medical Sciences/Indian Academy of Pediatrics/International Medical Science Academy.
Envisioned, conceptualized and heading Centre of Excellence and Advanced Research for Childhood Neurodevelopmental Disorders (2017-): high quality care, high end research, education hub(www.pedneuroaiims.org), National registry and National Child Neurology telehelpline/ consultation (24X7; toll free) .
Over 365 research publications (NEJM, JAMA pediatrics), Citations: 5094; h-Index 34; i10-index 125; Highest IF: 91.245, Maximum citations:316.Research projects leading to innovations/advocacy (NIH/Autism speaks/MRC,UK/ AIIMS-UCL): Neurodevelopmental disorders including Screening/Diagnostic Instruments(National programs; Mobile app PedneuroaiimsDiagnostics: google/ios) Drug refractory epilepsy including dietary therapies, Autism spectrum disorders, Cerebral palsy, SLD, Neuromuscular disorders/neurorehabilitation
Scientific associations International Society for Autism Research-Global Senior Leader (2021-); Association of Child Neurology, India- Founder member (2002); President elect (2023-2025); Academy of Paediatric Neurology, Indian Academy of Paediatrics- Chairperson (2021); National Convenor-Guidelines (2022), Indian Epilepsy Society(National body of ILAE): Co-convenor Paediatric section; Executive Board Member; Indian Academy of Neurology- Curriculum review / Guidelines development committee Member, Advisory board, ICNC 2018; Member, Advisory Board, ICNTN; Coordinator, Neurodevelopmental disorders module, organized “PediatricNeurogenomics” webinar series with ICNTN collaboration.
Has been instrumental in transforming care for children with neurodevelopmental disorders across India and her contributions in the field of epilepsy, autism and other neurodevelopmental disorders are unmatched CV summary: https://drive.google.com/file/d/12q3y8JIYWazVSCxrUc74rB60C4t7jWv9/view?usp=sharing
Vision
My vision for ICNA is for it to be a premier association for paediatric neurologists globally promoting the highest quality patient centered care for children with neurological disorders and neuro-disability and supporting the professional development of the members.
The association should focus on the trinity of clinical care, academics and research and to
- Promote advocacy and commit itself to the better care of children and families through joint collaborative work with the National/regional neurological societies, national governments and NGOs.
- Promote evidence-based medicine, and best education for both families and professionals, through adoption of modern technology to surmount barriers to health care in culturally/linguistically diverse settings in both patient/ practitioner populations.
- Equip child neurologists with the tools, skills and knowledge to be the best qualified health professional through innovative approaches in education and lifelong learning especially in resource limited countries.
- Provide members with platforms for improved networking, communication, coaching & mentoring opportunities to help advance their career goals.
- Lead and guide, how we adapt and respond to evolving changes in the post-COVID era, in supporting members to remain resilient, work together and help deal with local/regional/global issues.
- Use of a comprehensive registry may be helpful in many ways including creating a database and improving the clinical practice as per SOPs developed.
- Contribute to the development of assessment, training and recruitment strategy, creating and maintaining an efficient world-class training system that engages and prepares students to be globally competitive and to foster the future generation of child neurologists with a special focus on LMICs.
- Facilitate capacity building of research institutions for education, research and international co-operation to develop an effective international research system and foster local, regional, national and international collaborations. We should be fostering interactive, dynamic and more collegial relationship.
Viraj Sanghi
Biosketch
Viraj Sanghi is a consultant paediatric neurologist at the SRCC Children’s Hospital and the KEM hospital and GS Medical College in Mumbai with a keen interest in paediatric stroke, neuromuscular disorders and palliative care.
He received his MBBS and MD degrees from Grant Medical College in Mumbai, India and subsequently received the Diplomate of the National Board in Neurology in 2002. He went on to obtain his fellowship in Paediatric Neurology from SickKids, Toronto. Recently he completed certification in Palliative care from Harvard Medical School, Boston.
Over the past 22 years he has been passionate about and closely involved in ethical and holistic care as well as rehabilitation of children and currently serves the Rehabilitation committee as well as the Ethics committees at the SRCC Children’s Hospital in Mumbai. He is also instrumental in establishing the Family Centred Care programme and setting up a paediatric Palliative Care programme at the hospital. He is an enthusiastic teacher and has conducted several education programmes for fellows, residents, neurologists, community paediatricians and other healthcare workers. Additionally, he has also uses his administrative skills to organize and serves as faculty in several Regional, National and International conferences including the ICNC 2018 which was held in Mumbai. As a Trustee of Neurology Foundation, a charitable organization based in Mumbai, he is involved in fund raising and philanthropic activities for the underprivileged sector of society. He is currently on the ICNA Executive Board and is committed to serving the organization to help achieve its mission and goals.
In his spare time, away from the hospital and his work, Viraj enjoys spending time with his wife and two daughters, adorable black Labrador, reading, working out and watching Netflix! He is an avid traveler and loves to explore different cultures and cuisines across the globe.
Vision
ICNA is a global community of individuals who share the philosophy of providing high quality neurological healthcare for children from all regions of the world. We come together on a common platform with the intent of decreasing the burden of disease. Towards this common goal we must strive to achieve the following:
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Grow the paediatric neurology workforce, especially in resource limited regions, with an unwavering commitment to excellence in education. We must continue to provide cutting-edge academic programs that promote the intellectual and ethical growth of students, residents and fellows through in-person as well as online models of academic programmes.
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Expand and support paediatric neuroscience Research and encourage and support young researchers in this regard.
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Develop standardized protocols and clinical algorithms that can promote highest levels of care and yet be applicable to those with limited financial means.
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Provide a network that allows for free exchange of ideas and communication towards the promotion of high quality patient care and better outcomes. This would include mentorship programmes for residents and neurologists in early stages of their careers to help foster a sense of support.
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Attain financial growth and sustainability for the organisation and yet continue to provide low cost resources for those regions that need financial support.
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Continue the development and promotion of JICNA and other educational activities already in place.
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Advocate for patients and care givers with policymakers and form partnerships with other societies, the government and community.
8.Uphold the values, ethics and integrity of ICNA and integrate professional education with humanistic, scientific and social learning.
I remain committed to the core principles of ICNA and would be honoured to continue to serve the board.
Vrajesh Udani
Biosketch
Vrajesh Udani completed his medical training at the prestigious Grant Medical college Mumbai, India with honours. He trained in Child Neurology and Clinical Neurophysiology at the State University of New York, Brooklyn. After board certification he returned to Mumbai and set up one of the first Child Neurology services in India at the PD Hinduja National Hospital. A sabbatical year at the Miami Children’s Hospital enabled him to set up an active epilepsy surgery program. He further started an active teaching program at two public teaching institutions. Several child neurologists have trained under him in India.
His clinical and research interests have spanned several areas. He was part of the first international RCT studying the use of interferon in SSPE. He co-authored original clinical and genetic descriptions of MLC with subcortical cysts and PKAN in the Agrawal community in India. The link between infantile epilepsy and neonatal hypoglycemic brain injury was explored and has emerged as one of the commonest etiologies of drug-resistant epilepsy in the developing world. Long-term outcome studies in drug resistant epilepsy and autistic spectrum disorders have highlighted what happens in resource-poor setting. Recent research interests have been autoimmune encephalitis and MOG associated disorders.
He has published > 80 papers in peer-reviewed journals and 25 chapters in textbooks. He has served on expert consensus groups including the ILAE Pediatric Epilepsy Surgery task force and the ILAE Nosology Commission Syndrome Definitions.
He was the organizing chairperson of the International Child Neurology Congress in Mumbai in 2018 which was rated highly by most members. He is a member on the ICNA nominating committee for the last 4 years. He has served the Indian neurology community as President of the Association of Child Neurology-India and Chairman of the Pediatric Neurology subsection of the Indian Academy of Neurology.
He has lectured extensively in national and international meetings and given several prestigious orations.
A few initial thoughts about the state of world child neurology and what my goals would be if elected to the executive board
1) Though the burden of childhood neurological disease is high in the developing world, access to even basic child neurologic services is sorely lacking. This is primarily due to the lack of organized training in many parts of the world. The ICNA has been fairly successful in the continuing medical educational activities tried with regular physical and online teaching programs but a lot more needs to be done.
2) We probably have the highest numbers of rare disorders in child neurology. This makes it a challenge to study these diseases. We need international registries to be set up so to help increase our collective knowledge which would help our patients in the long run.
3) Access to advanced testing is a still a major hurdle in diagnosing rare disorders in many parts of the world due to cost / availability issues.
4) Finally novel therapies are rapidly gaining ground in different disorders. However, these are extraordinarily expensive and out of reach for most of the world. The ICNA is in a unique position in bridging these gaps with its reach across the world and its rapidly expanding membership.
I propose to help
1) Expand educational initiatives in parts of the world needing them most using not only world-renowned speakers but local experts as well
2) Establish registries to help study the epidemiology & natural history of rare disorders
3) Make available lists of where advanced genetic /immunologic tests can be done at reasonable rates
4) Use the good offices of ICNA to lobby the pharmaceutical industry to reduce costs and increase access to expensive medications
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