Official Website of The ICNA

posters2022

Details
Home
Hits: 2840

Submission IDConfirmedRegisteredDateStreamInternational ChairTurkish ChairpresentingauthorpresentingauthoremailTitleeposterdateposterstreamcontactauthorcontactauthoremail
675NoNoEsra Özpınardr.esraozpinar@gmail.comAn overview of drug-resistant epilepsies based on advances in genetics: a cohort studyBetül Kılıçbetulklc82@gmail.com
607YesNoAchmad Rafliachmad.rafli@gmail.com"Subacute Sclerosing Panencephalitis in Children: A Case Series in Dr. Cipto Mangunkusumo Tertiary General Hospital Jakarta Indonesia"Achmad Rafliachmad.rafli@gmail.com
635YesNo4th Oct 2022Epilepsy: Treatment 3 – ASM/ Dietary TreatmentsJ SahuAchmad Rafliachmad.rafli@gmail.comModified Atkins Diet for the Treatment of Refractory Epilepsy in Children: A Pilot Study from IndonesiaAchmad Rafliachmad.rafli@gmail.com
681YesNo4th Oct 2022Epilepsy: Genetics 3L LagaeAsli Kübra Ataseverakubrat@gmail.comNovel ANKRD11 gene mutation in an individual with a phenotype of KBG syndrome presenting like West syndromeAsli Kübra Ataseverakubrat@gmail.com
375YesNo6th Oct 2022Education"Jorge Vidaurre US"Alexandra Santana Almansaalexandra.santanaalmansa@childrens.harvard.eduConstruction of an introductory curriculum for new child neurology and neurodevelopmental disabilities traineesAlexandra Santana Almansaalexandra.santanaalmansa@childrens.harvard.edu
324YesNo6th Oct 2022"Metabolic 5 Neurodegenerative diseases (NBIAs metabolic causes of stroke CDG NCLs NKH"Suvasini Sharma IndiaAmi Shahami.en1neuro@gmail.comFatty Acid Hydroxylase associated Neurodegeneration (FAHN) – A case report from India highlighting its heterogenous nature.Ami Shahami.en1neuro@gmail.com
463YesNo6th Oct 2022Metabolic 3 Mitochondrial disorders II: Etiologies and mechanismsSaskia Wortmann NetherlandsAmi Shahami.en1neuro@gmail.comThiamine Pyrophosphokinase Deficiency in Indian origin Siblings - Expanding the phenotypeAmi Shahami.en1neuro@gmail.com
290YesNo5th Oct 2022Spasticity and ataxiaC CatsmanAmita Moirangthemamis.72000@gmail.comNeurodegeneration with brain iron accumulation in 18 Indian families: a case series highlighting phenotypic and genotypic diversityAmita Moirangthemamis.72000@gmail.com
666YesNo4th Oct 2022Epilepsy: Status epilepticus and MiscellaneousT LoddenkemperAmna Al Futaisiamnaf@squ.edu.omChildhood status epilepticus in children of 1-12 years of age SQUH: demographics and outcome of treatmentAmna Al Futaisiamnaf@squ.edu.om
372YesNoAndrew Heyandrew.hey@louisville.eduReactivation of HSV-1 Encephalitis in an Infant Within One-Month of Completing Acyclovir Treatment: A Case StudyAndrew Heyandrew.hey@louisville.edu
231YesNo4th Oct 2022Epilepsy: Genetics 2N SpecchioAna Carolina Coananghelescu.cristina@gmail.comClinical predictors of positive genetic investigation of the developmental and epileptic encephalopathiesMaria Benevidesbenevidesmarialuiza@gmail.com
447YesNo6th Oct 2022Neuroradiology 2"Kshitij Mankand UK"Anish Ainapureanish.ainapure1@gmail.comBasal ganglia germinoma in an adolescent: A case reportAnish Ainapureanish.ainapure1@gmail.com
451YesNo6th Oct 2022Metabolic 2 Mitochondrial disorders I : clinical phenotypes and tx"Rita Horvath UK"Anish Ainapureanish.ainapure1@gmail.comProgressive Mitochondrial Leukoencephalopathy in a one and half year-old boy: A Case ReportAnish Ainapureanish.ainapure1@gmail.com
454YesNo6th Oct 2022"Movement 3 Ataxias opsoclonus myoclonus and covid 19 impact""Russell Dale Australia"Anish Ainapureanish.ainapure1@gmail.comAutosomal recessive spastic ataxia of Charlevoix–Saguenay : Two case reportsAnish Ainapureanish.ainapure1@gmail.com
441YesNo6th Oct 2022"Movement 2 Dystonia Parkinsons tremor and epidemiology""Jon Mink US"Ayşe Nur Coşkunanurcoskun@gmail.comA Case of Childhood Onset Dystonia Due to KMT2B Gene MutationAyşe Nur Coşkunanurcoskun@gmail.com
461YesNoAreeba Wasimareeba.wasim2@gmail.com"VARIATIONS IN CLINICAL PRESENTATION NEUROIMAGING AND ELECTROENCEPHALOGRAPHIC PATTERNS OF SUBACUTE SCLEROSING PANENCEPHALITIS"Areeba Wasimareeba.wasim2@gmail.com
298YesNo6th Oct 2022"Metabolic 5 Neurodegenerative diseases (NBIAs metabolic causes of stroke CDG NCLs NKH"Suvasini Sharma IndiaAyşe Aksoyaysechild@gmail.comA Mutation in Neurodegeneration with Brain Iron Accumulation – Two BrothersSeren Aydinserenaydin5228@gmail.com
550YesNo4th Oct 2022Epilepsy: InvestigationsP MadaanAysen Gokaysenngok@gmail.comCases with Seizures During Routine Video Electroencephalography: Clinical and Electroencephalographic CharacteristicsAysen Gokaysenngok@gmail.com
711YesNo6th Oct 2022Metabolic 6 Defects of bioenergetic and intermediary metabIngrid Tein CanadaSachendra Badalbadalsachendra@yahoo.comChylous blood in an infant with febrile encephalopathy: Clues to metabolic etiology (Very Long Chain Acyl CoA Dehydrogenase Deficiency)Sachendra Badalbadalsachendra@yahoo.com
717YesNo6th Oct 2022Neuroradiology 2"Kshitij Mankand UK"Sachendra Badalbadalsachendra@yahoo.comIntracranial haemorrhage in two infant siblings: hereditary or acquired?Sachendra Badalbadalsachendra@yahoo.com
721YesNo6th Oct 2022Neuroradiology 3"Ajay Taranath Australia"Sachendra Badalbadalsachendra@yahoo.comParoxysmal sympathetic hyperactivity in a child with High Grade Glioma post resection surgery.Sachendra Badalbadalsachendra@yahoo.com
401YesNo5th Oct 2022General IIM SönmezBushra Alattasbalattas@seha.aeDiagnostic yield of Whole Exome and Whole Genome Sequencing in pediatric neurological disorders. A UAE Tertiary hospital experienceBushra Alattasbalattas@seha.ae
308YesNo4th Oct 2022"Epilepsy: Neuroimaging Surgery and Basic Science"C AkmanBilal Berke Ayvazbilalberke.ayvaz@ogr.iuc.edu.trComparison of 3D Printing Techniques with Patient-Specific Models for Epilepsy SurgeryBilal Berke Ayvazbilalberke.ayvaz@ogr.iuc.edu.tr
388YesNo6th Oct 2022Metabolic 2 Mitochondrial disorders I : clinical phenotypes and tx"Rita Horvath UK"Dan Sunbloveriver@163.comEfficacy and Safety of the Ketogenic Diet for Mitochondrial Disease with Epilepsy: A Prospective Controlled StudyDan Sunbloveriver@163.com
210YesNo5th Oct 2022General IJ VajsarBita Poorshiribpskam@yahoo.comThe Co-existence of Phenylketonuria and Myasthenia Gravis: A CaseReportBita Poorshiribpskam@yahoo.com
724YesNo6th Oct 2022Neuroradiology 2"Kshitij Mankand UK"Burçin Şanlıdağburcinsanlidag@yahoo.comIntracranial cysts in pediatric age group: Incidental or developmental?Burçin Şanlıdağburcinsanlidag@yahoo.com
292YesNo6th Oct 2022Metabolic 1 Clinical phenotypes"Brahim Tabarki KSA"Cemile Busra Olculubusra.olculu@ege.edu.trA Rare Cause of Developmental Epileptic Encephalopathy: D-Bifunctional Protein Deficiency with a Novel Pathogenic VariantCemile Busra Olculubusra.olculu@ege.edu.tr
625YesNo6th Oct 2022Headache 1"Ken Mack US"Cemile Busra Olculubusra.olculu@ege.edu.trPseudotumor cerebri in childhood: a new vision to clinical spectrum and predictors for visual outcomeCemile Busra Olculubusra.olculu@ege.edu.tr
181YesNo6th Oct 2022Headache 1"Ken Mack US"Çağatay Günaycagataygunaymd@gmail.comRecurrent Painful Ophthalmoplegic Neuropathy: Report of the Two New Pediatric CasesÇağatay Günaycagataygunaymd@gmail.com
182YesNo4th Oct 2022"Epilepsy: Syndromes 1 – Self-limited EE/DEE-SWAS"C JoshiÇağatay Günaycagataygunaymd@gmail.comThe fate of spikes in self-limited epilepsy with centrotemporal spikes: Are clinical and baseline EEG features effective?Çağatay Günaycagataygunaymd@gmail.com
548YesNo6th Oct 2022CNS Infections 1 Covid-related"Charles Newton Kenya"Çiğdem Genç Selcigdemsel@yahoo.comA Rare Neurological Manifestation of Coronavirus Disease 2019 (COVID-19) in a Single Reference Center: Ramsay Hunt SyndromeÇiğdem Genç Selcigdemsel@yahoo.com
673YesNo6th Oct 2022"Movement 3 Ataxias opsoclonus myoclonus and covid 19 impact""Russell Dale Australia"Çi̇si̇l Çerçi̇ Kuburcisilcerci@gmail.comA study in a Turkish family with ataxia and points to MTCL1 as a candidate gene for autosomal dominant cerebellar ataxiaÇi̇si̇l Çerçi̇ Kuburcisilcerci@gmail.com
376YesNo5th Oct 2022"CNS Malformations NGS"A NarayanChew Thye Choongctfan88@gmail.comFilamin A associated periventricular nodular heterotopia presenting with mutismChew Thye Choongctfan88@gmail.com
527YesNo5th Oct 2022General IJ VajsarDuygu Aykold_aykol@hotmail.com"Electromyography in Pediatric Population A Single Center Experience"Duygu Aykold_aykol@hotmail.com
248YesNo4th Oct 2022Epilepsy: Semiology and ClinicalH CrossDeniz Menderesdenizkrgn@gmail.comHand Postures and Localization Value in Patients at Video EEG MonitorizationDeniz Menderesdenizkrgn@gmail.com
304YesNo6th Oct 2022Headache/Stroke 2"Mahendra MoharirCanada"Dhanalakshmi AngappanDhanalakshmivj@gmail.com"Stroke secondary to thoracic outlet syndrome treated successfully with thrombolytics and thrombectomy in a teenager: a case report"Dhanalakshmi AngappanDhanalakshmivj@gmail.com
663YesNo6th Oct 2022Headache/Stroke 3"Mubeen Rafay Canada"Sarolta Dobnerdobnersara@gmail.comA retrospective study of central nervous system vasculitis patientsZoltán Liptaizliptai@gmail.com
466YesNo4th Oct 2022Epilepsy: Outcomes and EpidemiologyE KijaNicholas Oderodocodero@gmail.comRisk Factors for Seizure Recurrence After Initial Withdrawal of Anti-Seizure Medication in Childhood EpilepsyNicholas Oderodocodero@gmail.com
339YesNo4th Oct 2022Epilepsy: Treatment 2 – ASMsRamachandran NairMahmut Aslandr_mahmut_21@hotmail.comEffectiveness of zonisamide in childhood refractory epilepsyMahmut Aslandr_mahmut_21@hotmail.com
475YesNo4th Oct 2022"Epilepsy: Syndromes 1 – Self-limited EE/DEE-SWAS"C JoshiSibel Oz Yildizdr_sibeloz@hotmail.comElectrical status epilepticus during sleep: A study of 67 patientsSibel Oz Yildizdr_sibeloz@hotmail.com
720YesNo5th Oct 2022Molecular geneticsT SultanAyten Güleçdr.aytengulec@gmail.com"National Based Retrospective Study on the Evaluation of Clinical Laboratory and Imaging Research of Angelman Syndrome- Turkey's Multicenter Study"Ayten Güleçdr.aytengulec@gmail.com
296YesNo4th Oct 2022Epilepsy: Treatment 1 – ASMsB Sanchez-GanEbru Arhandr.elif.ksglyldrm@gmail.comReversible Leigh’s-like brain abnormalities with Vigabatrin: A Case SeriesRamesh Konankirameshkonanki@gmail.com
632YesNo4th Oct 2022Epilepsy: Treatment 3 – ASM/ Dietary TreatmentsJ SahuEsra Özpınardr.esraozpinar@gmail.comKetogenic diet treatment success in our two patients with epilepsy of infancy with migrating focal seizuresBetül Kılıçbetulklc82@gmail.com
672YesNo4th Oct 2022Epilepsy: Genetics 3L LagaeEsra Özpınardr.esraozpinar@gmail.com"Epileptic encephalopathy visual impairment and developmental retardation: CDKL5 deficiency disorder"Betül Kılıçbetulklc82@gmail.com
278YesNo6th Oct 2022Headache/Stroke 2"Mahendra MoharirCanada"Gülnur Esenülküdr.gesenulku@gmail.comUnilateral internal carotid artery and middle cerebral artery thrombosis in a pediatric patient with mildly symptomatic COVID-19: Case report and literature reviewGülnur Esenülküdr.gesenulku@gmail.com
718YesNo6th Oct 2022Headache/Stroke 3"Mubeen Rafay Canada"Gülnur Esenülküdr.gesenulku@gmail.comDoes the presence of Friedman criteria always spesific for pseudotumor cerebri?Gülnur Esenülküdr.gesenulku@gmail.com
316YesNo4th Oct 2022"Epilepsy: Neuroimaging Surgery and Basic Science"C AkmanHilal Altasdr.hilalaltas@gmail.comIs There a Relation Between Hippocampal Measurements and Childhood Idiopathic Generalized Epilepsy?Hilal Altasdr.hilalaltas@gmail.com
457YesNo4th Oct 2022Epilepsy: Genetics 3L LagaeMerve Hilal Doludr.mervehilal@hotmail.comA Rare Cause of Developmental Epileptic Encephalopathy; UBA5 Gene MutationMerve Hilal Doludr.mervehilal@hotmail.com
269YesNo6th Oct 2022Headache 1"Ken Mack US"Müge Baykandr.mugebaykan@gmail.comASSESSMENT OF CHILDHOOD HEADACHES: A SINGLE CENTER EXPERIENCEMüge Baykandr.mugebaykan@gmail.com
453YesNo5th Oct 2022Molecular geneticsT SultanMüge Baykandr.mugebaykan@gmail.comDuplication 9 p Syndrome; Case ReportMüge Baykandr.mugebaykan@gmail.com
567YesNo6th Oct 2022Headache/Stroke 2"Mahendra MoharirCanada"Payal Shahdr.payalshah@gmail.comPOSTERIOR CIRCULATION ARTERIAL ISCHEMIC STROKE IN CHILDRENPayal Shahdr.payalshah@gmail.com
593YesNo6th Oct 2022Metabolic 6 Defects of bioenergetic and intermediary metabIngrid Tein CanadaAmi Shahdrami.rajesh.shah@gmail.comFuel for Thought – Case series of Beta-Ketothiolase patients presenting with metabolic encephalopathyAmi Shahdrami.rajesh.shah@gmail.com
332YesNo4th Oct 2022Epilepsy: Genetics 3L LagaeCanan Üstündrcananustun@hotmail.comTwo Cases of ACTL6B Mutation-Associated Epileptic EncephalopathyCanan Üstündrcananustun@hotmail.com
338YesNo4th Oct 2022Epilepsy: Genetics 2N SpecchioCanan Üstündrcananustun@hotmail.comCDKL5 Mutation-Associated Epileptic Encephalopathy CaseCanan Üstündrcananustun@hotmail.com
342YesNo4th Oct 2022Epilepsy: Genetics 2N SpecchioCanan Üstündrcananustun@hotmail.comA Case of Dup15q Syndrome Presenting with WEST SyndromeCanan Üstündrcananustun@hotmail.com
216YesNo4th Oct 2022Epilepsy: Genetics 2N SpecchioEmine Tekindreminetekin@yahoo.com"A case with developmental delay resistant epilepsy and invuluntary movements diagnosed as SCN8A mutation"Emine Tekindreminetekin@yahoo.com
230YesNo5th Oct 2022Genetics and epilepsy IW HakamiGül Yüceldrgulyucel@hotmail.comNovel Mutations in AP3B2 Gene Cause an Early Onset Developmental and Epileptic Encephalopathy: A Rare Clinical EntityGül Yüceldrgulyucel@hotmail.com
355YesNo4th Oct 2022Epilepsy: Treatment 2 – ASMsRamachandran NairHilal Aydindrhilalaydin@gmail.comThe Effect Of Levetiracetam Therapy On Electrocardiography ParametersHilal Aydindrhilalaydin@gmail.com
303YesNo4th Oct 2022"Epilepsy: Syndromes 2 – IESS Dravet HHE EMAS"E WirrellMahesh Kamatedrmaheshkamate@gmail.comIdiopathic Hemiconvulsion Hemiplegia Epilepsy (IHHE) in an 8 yr old boyMahesh Kamatedrmaheshkamate@gmail.com
505YesNo6th Oct 2022"Metabolic 5 Neurodegenerative diseases (NBIAs metabolic causes of stroke CDG NCLs NKH"Suvasini Sharma IndiaMahesh Kamatedrmaheshkamate@gmail.comAtypical presentation of PLAN-associated NBIAMahesh Kamatedrmaheshkamate@gmail.com
207YesNo5th Oct 2022Genetics and epilepsy IW HakamiÖzlem Özsoydrozlemozsoypediatri@gmail.com"CASE REPORT: DOCK7 MUTATION AS A RARE CAUSE OF EPILEPTIC ENCEPHALOPATHY WITH CORTICAL BLINDNESS DYSMORPHIC FINDINGS"Özlem Özsoydrozlemozsoypediatri@gmail.com
735YesNo4th Oct 2022Epilepsy: Treatment 1 – ASMsB Sanchez-GanPinar Ozkan Kartdrpinar_ozkan@yahoo.comEvaluation of Efficacy and Tolerability of Lacosamide in Children with Drug-Resistant Epilepsy: A Multicenter Cohort StudyPinar Ozkan Kartdrpinar_ozkan@yahoo.com
744YesNo4th Oct 2022"Epilepsy: Syndromes 2 – IESS Dravet HHE EMAS"E WirrellPi̇nar Ozkan Kartdrpinar_ozkan@yahoo.comThe Role of Genetic Factors in Electroclinic and Therapeutic Effectiveness in Children with Dravet Syndrome: A Multi-Center Cohort StudyPi̇nar Ozkan Kartdrpinar_ozkan@yahoo.com
743YesNo4th Oct 2022Epilepsy: Status epilepticus and MiscellaneousT LoddenkemperRamya Bandidrramyabandi@gmail.com"Clinical spectrum treatment response and outcomes in children with Febrile Infection Related Epilepsy Syndrome (FIRES) : A case series from India"Ramesh Konankirameshkonanki@gmail.com
487YesNo6th Oct 2022CNS Infections 1 Covid-related"Charles Newton Kenya"Rekha Mittaldrrekhamittal2008@gmail.comProfile of Neurological manifestations of Covid 19 in a Pediatric hospital in DelhiRekha Mittaldrrekhamittal2008@gmail.com
682YesNo5th Oct 2022General IJ VajsarYavuz Sayardrsayar3@hotmail.comA case of TUBGCP2-associated tubulinopathy with a novel missense variantMiraç Yıldırımmiracyildirim81@hotmail.com
685YesNoYavuz Sayardrsayar3@hotmail.comA case of posttransplant acute limbic encephalitis associated with human herpesvirus-6Miraç Yıldırımmiracyildirim81@hotmail.com
740YesNo6th Oct 2022CNS Infections 1 Covid-related"Charles Newton Kenya"Yavuz Sayardrsayar3@hotmail.comA case of acute ophthalmoplegia presenting after multisystem inflammatory syndrome in children (MIS-C)Miraç Yıldırımmiracyildirim81@hotmail.com
739YesNo4th Oct 2022"Epilepsy: DEEs TSC RETT and Comorbidities"Y JiangSeda Kanmazdrsedakanmaz@gmail.comDevelopmental Epileptic Encephalopathies in A National Cohort Study (Turkish EPISTEP -1): A Step-based Approachment for Etiologic DiagnosisSeda Kanmazdrsedakanmaz@gmail.com
384YesNo6th Oct 2022"Movement 2 Dystonia Parkinsons tremor and epidemiology""Jon Mink US"Serdar Saritasdrserdarsaritas@gmail.comA case of dopa responsive dystonia due to compound heterozygous TH gene mutation in a Turkish Girl.Serdar Saritasdrserdarsaritas@gmail.com
726YesNo5th Oct 2022Spasticity and ataxiaC CatsmanSüleyman Şahindrsulimen2003@hotmail.comRare dual diagnoses in an infant: Aicardi-Goutieres and Moyamoya SyndromesSüleyman Şahindrsulimen2003@hotmail.com
665YesNo4th Oct 2022"Epilepsy: Syndromes 1 – Self-limited EE/DEE-SWAS"C JoshiEmine Tekinemine.tekin@giresun.edu.trResearch of autoimmunity clues in electrical status epilepticus (ESES) during sleepTurgay Cokyamandrturgay@comu.edu.tr
591YesNo6th Oct 2022"Metabolic 5 Neurodegenerative diseases (NBIAs metabolic causes of stroke CDG NCLs NKH"Suvasini Sharma IndiaFatema Al Amranifatemaamrani@gmail.comAutosomal recessive NOTCH3-related leukodystrophy in two siblings and review of the literatureFatema Al Amranifatemaamrani@gmail.com
277YesNo6th Oct 2022Headache 1"Ken Mack US"Fatih Mehmet Akif Özdemi̇rfatihmehmetakif@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 Özdemi̇rfatihmehmetakif@hotmail.com
630YesNo5th Oct 2022Genetics and epilepsy IIRamachandran NairFatma Hancifatmah.arslan@gmail.comA Photosensitivite Trichothiodystrophy Patient With A Mutation in ERCC2 GeneFatma Hancifatmah.arslan@gmail.com
706YesNo4th Oct 2022Epilepsy: Genetics 3L LagaeFlorinela Gisela Rotaruflorirotaru9@gmail.comClinical features of KCNQ2 mutation in a Romanian familyFlorinela Gisela Rotaruflorirotaru9@gmail.com
223YesNo4th Oct 2022"Epilepsy: Syndromes 1 – Self-limited EE/DEE-SWAS"C JoshiZhijie Zhangflyzoe423@sjtu.edu.cnImmune mechanism in Benign Epilepsy with Centrotempral SpikesLing Lililing@xinhuamed.com.cn
659YesNoFranzina Coutinhofranzina.research@gmail.comThe Enabling Inclusion (EI) App: A story from Rural South India about COVID-19 and digital technoFranzina Coutinhofranzina.research@gmail.com
669YesNoFranzina Coutinhofranzina.research@gmail.comHealth coaching and COVID-19: Parent reports from IndiaFranzina Coutinhofranzina.research@gmail.com
688YesNo6th Oct 2022Education"Jorge Vidaurre US"Franzina Coutinhofranzina.research@gmail.comEarly Intervention app and Digital technology: Bridging the rehabilitation service gap in IndiaFranzina Coutinhofranzina.research@gmail.com
209YesNo4th Oct 2022Epilepsy: Treatment 1 – ASMsB Sanchez-GanGamze Sarıkaya Uzangamzeuzan36@gmail.comLevetiracetam Monotherapy For The Treatment Of Febrile and Febrile Induced SeizuresGamze Sarıkaya Uzangamzeuzan36@gmail.com
350YesNo5th Oct 2022Neurogenetics practiceT Lerman-SagieGamze Sarıkaya Uzangamzeuzan36@gmail.comPontocerebellar Hypoplasia Associated With TTC 1 Mutation: Case SeriesGamze Sarıkaya Uzangamzeuzan36@gmail.com
649YesNo4th Oct 2022"Epilepsy: Neuroimaging Surgery and Basic Science"C AkmanGautam Kamilagautamkamila7@gmail.comNon-dominant hemisphere is more excitable compared to dominant hemispherePrashant Jauharipjauhari0@gmail.com
340YesNo6th Oct 2022Metabolic 3 Mitochondrial disorders II: Etiologies and mechanismsSaskia Wortmann NetherlandsGülbahar Kurt Bayirgulbaharkurtbayir@gmail.comMutations of The E3 Beta Subunit of The Pyruvate Dehydrogenase (PDH) Complex Gene: A Case ReportGülbahar Kurt Bayirgulbaharkurtbayir@gmail.com
341YesNo6th Oct 2022Metabolic 3 Mitochondrial disorders II: Etiologies and mechanismsSaskia Wortmann NetherlandsGülbahar Kurt Bayirgulbaharkurtbayir@gmail.comTwo Different Phenotypes Caused by Mutation in the EARS2 Gene in Two SiblingsGülbahar Kurt Bayirgulbaharkurtbayir@gmail.com
343YesNo5th Oct 2022General neurogenetics IIA R TavasoliGülbahar Kurt Bayirgulbaharkurtbayir@gmail.comA Case of OTUD6B-Related DisorderGülbahar Kurt Bayirgulbaharkurtbayir@gmail.com
610YesNo6th Oct 2022CNS Infections 1 Covid-related"Charles Newton Kenya"Gülcan Akyüzgulcan.akyuz@hotmail.comMOG ANTIBODY- ASSOCIATED ENCEPHALITIS SECONDER TO COVID 19Gülcan Akyüzgulcan.akyuz@hotmail.com
496YesNo6th Oct 2022Headache/Stroke 2"Mahendra MoharirCanada"Gunce Basarirguncebasarir@gmail.comAmbulatory blood pressure monitoring in children diagnosed with primary headachePinar Gencpinarpinargencpinar@gmail.com
570YesNo6th Oct 2022Metabolic 6 Defects of bioenergetic and intermediary metabIngrid Tein CanadaGunjan Didwalgunjan276@gmail.com"Clinical Biochemical and Genetic analysis of 6 North Indian families: Biotinidase deficiency in 86% of the children"Gunjan Didwalgunjan276@gmail.com
543YesNo6th Oct 2022Metabolic 4 Therapeutic approachesSamantha Marin CanadaGurdeep Sekhongurdeep.sekhon@gosh.nhs.ukUridine-responsive epileptic encephalopathy: precision treatment across the age spectrumGurdeep Sekhongurdeep.sekhon@gosh.nhs.uk
694YesNoWen-xiong Chengzchcwx@126.comClinical analysis of 26 children with recurrent bacterial meningitisWen-xiong Chengzchcwx@126.com
612YesNo4th Oct 2022"Epilepsy: DEEs TSC RETT and Comorbidities"Y JiangHakan Ercelebihakanerc@hotmail.comApplication of a Recently Proposed Semiological Classification to Psychogenic Nonepileptic Seizures in ChildrenHakan Ercelebihakanerc@hotmail.com
778YesNo6th Oct 2022Metabolic 3 Mitochondrial disorders II: Etiologies and mechanismsSaskia Wortmann Netherlandsİsmail Hakkı Akbeyazhakkiakbeyaz@gmail.comA CHALLENGING CASE: WERNICKE ENCEPAHALOPATHY AFTER GASTRIC SLEEVE SURGERYİsmail Hakkı Akbeyazhakkiakbeyaz@gmail.com
263YesNo4th Oct 2022"Epilepsy: Neuroimaging Surgery and Basic Science"C AkmanHale Atalay Celikhale.atalay@gmail.comAcute encephalopathy with biphasic seizures and late reduced diffusion (AESD); 2 different clinical outcomeHale Atalay Celikhale.atalay@gmail.com
365YesNo6th Oct 2022Metabolic 3 Mitochondrial disorders II: Etiologies and mechanismsSaskia Wortmann NetherlandsHale Atalay Celikhale.atalay@gmail.comA Rare Mitochondrial disease; Naxe Gene MutationHale Atalay Celikhale.atalay@gmail.com
446YesNo6th Oct 2022"Metabolic 5 Neurodegenerative diseases (NBIAs metabolic causes of stroke CDG NCLs NKH"Suvasini Sharma IndiaHale Atalay Celi̇khale.atalay@gmail.comMetabolic Stroke; A Rare Clinical Condition of Glycerol Kinase DeficiencyHale Atalay Celi̇khale.atalay@gmail.com
334YesNo6th Oct 2022Metabolic 1 Clinical phenotypes"Brahim Tabarki KSA"Harshuti Shahharshuti@yahoo.co.inGenotypic phenotypic charecteristics of galactosemia in postneonatal age in western IndiaHarshuti Shahharshuti@yahoo.co.in
337YesNo6th Oct 2022Metabolic 4 Therapeutic approachesSamantha Marin CanadaHarshuti Shahharshuti@yahoo.co.inStudy of 15 patients with early infantile neurometabolic epileptic encephalopathy-treatable etiologiesHarshuti Shahharshuti@yahoo.co.in
660YesNo5th Oct 2022General neurogenetics IAR ZamaniHossein FarshadmoghadamHossein772000@yahoo.comStudy of clinical and genetic characteristics of limb-girdle muscular dystrophy in Iranian patientsHossein FarshadmoghadamHossein772000@yahoo.com
767YesNo6th Oct 2022Neuroradiology 1"Manohar Schroff Canada"Hülya Maraş Gençhulyamaras@gmail.comTwo cases with Pontine Tegmental Cap Dysplasia: a rare hindbrain anomaly which may be misdiagnosed as Moebius SequenceHülya Maraş Gençhulyamaras@gmail.com
398YesNo4th Oct 2022Epilepsy: Treatment 2 – ASMsRamachandran NairHuriye Cetinhuriyeecetin@gmail.com"Relationship Between Valproic Acid Hepatosteatosis and Serum Betatrophin Levels"Turgay Cokyamandrturgay@comu.edu.tr
287YesNo6th Oct 2022"Movement 1 Chorea dyskinesias tremor spasms & tx""Biju Hameed UK"Hüseyin Pürhuseyinpur@gmail.com"CLINICAL EVALUATION OF CHILDREN DIAGNOSED WITH SYDENHAM CHOREA SINGLE CENTER EXPERIENCE"Hüseyin Pürhuseyinpur@gmail.com
676YesNo6th Oct 2022"Movement 2 Dystonia Parkinsons tremor and epidemiology""Jon Mink US"Çiğdem İlter Uçariltercigdem@gmail.comHolmes tremor associated with two different etiologiesMiraç Yıldırımmiracyildirim81@hotmail.com
677YesNo6th Oct 2022"Movement 3 Ataxias opsoclonus myoclonus and covid 19 impact""Russell Dale Australia"Çiğdem İlter Uçariltercigdem@gmail.comAcute cerebellitis associated with juvenile idiopathic arthritisMiraç Yıldırımmiracyildirim81@hotmail.com
692YesNo6th Oct 2022Education"Jorge Vidaurre US"Ipek Tekcicekipekt08@gmail.comA pilot study on the opinions of future doctors about child neurologyEsra Serdarogluesra.serdaroglu@gmail.com
686YesNo4th Oct 2022Epilepsy: Outcomes and EpidemiologyE KijaIrmak Simsekirmaksimsek@gmail.comEpilepsy prevalence and trends in antiepileptic medication use among children in Turkey between 2015-2020Irmak Simsekirmaksimsek@gmail.com
361YesNo5th Oct 2022General neurogenetics IIA R TavasoliIrmak Erdoğanirmkerdgn@gmail.comA report of a rare syndrom: Alazami SyndromIrmak Erdoğanirmkerdgn@gmail.com
172YesNo6th Oct 2022"Movement 2 Dystonia Parkinsons tremor and epidemiology""Jon Mink US"Jo-anna Allenjallen@ptcbio.comA Mobile Domiciliary Phlebotomy Service to Support Patients With Rare Disease and Screening Study Recruitment in the UKJo-anna Allenjallen@ptcbio.com
258YesNo4th Oct 2022Epilepsy: Genetics 2N SpecchioJohanna De Luca-ramirezjdeluca20@stu.psm.eduEpileptic Encephalopathy Secondary to Homozygous TBC1 Domain-Containing Kinase (TBCK) Mutation in Four Patients of Puerto Rican DescentOrlando Torresorlandotorres@psm.edu
320YesNo6th Oct 2022Metabolic 2 Mitochondrial disorders I : clinical phenotypes and tx"Rita Horvath UK"Jorge Vidaurrejorge.vidaurre@nationwidechildrens.orgKetamine: An effective and safe treatment for patients with MELAS and refractory status epilepticusEzgi Saylamezgi.saylam@nationwidechildrens.org
321YesNo4th Oct 2022Epilepsy: Status epilepticus and MiscellaneousT LoddenkemperJaveria Razajra_28@hotmail.comOUTCOME OF REFRACTORY STATUS EPILEPTICUS IN CHILDRENJaveria Razajra_28@hotmail.com
423YesNo6th Oct 2022CNS Infections 1 Covid-related"Charles Newton Kenya"Javeria Alvijra_28@hotmail.comPost COVID anti-NMDAR Encephalitis in an adolescent girlJaveria Alvijra_28@hotmail.com
430YesNo5th Oct 2022"CNS Malformations NGS"A NarayanJaveria Alvijra_28@hotmail.com"PSEUDO-TORCH- A rare mutation causing global development delay microcephaly and extensive band like brain calcification"Javeria Alvijra_28@hotmail.com
63YesNo6th Oct 2022Metabolic 1 Clinical phenotypes"Brahim Tabarki KSA"Judy Pipo-devezajudepipo@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 Teiningtein@sympatico.ca
770YesNo4th Oct 2022Epilepsy: Outcomes and EpidemiologyE KijaKavita Srivastavakavisri1970@gmail.comClinical profile and short term seizure outcome in children with Genetic Generalized EpilepsiesKavita Srivastavakavisri1970@gmail.com
774YesNo4th Oct 2022Epilepsy: Treatment 1 – ASMsB Sanchez-GanKavita Srivastavakavisri1970@gmail.com"Effect of antiseizure medications on calcium profile thyroid profile and bone mineral density in children"Kavita Srivastavakavisri1970@gmail.com
252YesNo5th Oct 2022General neurogenetics IAR ZamaniKursat Bora Carmankbcarman@gmail.comEvaluation of MicroRNAs in Pediatric EpilepsyKursat Bora Carmankbcarman@gmail.com
253YesNo6th Oct 2022Headache 1"Ken Mack US"Kursat Bora Carmankbcarman@gmail.comNeurological face of familial mediterranean feverKursat Bora Carmankbcarman@gmail.com
359YesNo6th Oct 2022Cerebral palsy 2- Management; current and future"Antigone Papavasiliou Greece"Kursat Bora Carmankbcarman@gmail.comHippotherapy in children with cerebral palsyKursat Bora Carmankbcarman@gmail.com
379YesNo4th Oct 2022Epilepsy: Semiology and ClinicalH CrossFatma Kusgozkusgozfatma@gmail.comIctal Nose Wiping in Frontal-Onset Absence Epilepsy; A case reportFatma Kusgozkusgozfatma@gmail.com
380YesNo5th Oct 2022Molecular geneticsT SultanFatma Kusgozkusgozfatma@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 Kusgozkusgozfatma@gmail.com
535YesNo4th Oct 2022Epilepsy: Treatment 2 – ASMsRamachandran NairMehmet Fatih ButunM_FBUTUN@YAHOO.COM"Rufinamide Experience in Childhood Epilepsy from a Tertiary Center Turkey"Mehmet Fatih ButunM_FBUTUN@YAHOO.COM
267YesNo5th Oct 2022Genetics and epilepsy IW HakamiMagdalena Bliznakovamaggie.bliznakova@gmail.comHypocalcemic Seizure in a Girl with FOXG1-Gene–Related EncephalopathyZhivka ChuperkovaZhivka.Chuperkova@mu-varna.bg
695YesNo4th Oct 2022"Epilepsy: DEEs TSC RETT and Comorbidities"Y JiangManasa Thangellamanasa6548@gmail.comEVALUATION OF HEALTH RELATED QUALITY OF LIFE IN CHILDREN WITH EPILEPSY USING QUALITY OF LIFE IN CHILDHOOD EPILEPSY QUESTIONNAIRE (QOLCE - 55)Venkatesan Srinath Melpakkamshribkcorp@gmail.com
206YesNo6th Oct 2022Headache 1"Ken Mack US"Mehmet Can Yeşilmenmcanyesilmen@gmail.comA case of first pediatric pseudotumor cerebri syndrome secondary to superior sagittal sinus thrombosis associated with SARS-CoV-2Mehmet Can Yeşilmenmcanyesilmen@gmail.com
589YesNo4th Oct 2022Epilepsy: Status epilepticus and MiscellaneousT LoddenkemperAyse Yasemin Celikmdayasminc@gmail.com"The effect of antiepileptic drugs on ischemia modified albumin myeloperoxidase and catalase levels in children with idiopathic epilepsy"Ayse Yasemin Celikmdayasminc@gmail.com
594YesNo6th Oct 2022Metabolic 6 Defects of bioenergetic and intermediary metabIngrid Tein CanadaAyse Yasemin Celikmdayasminc@gmail.comA rare cause of episodic vomiting: Late-onset multiple acyl-CoA dehydrogenase deficiency as a treatable metabolic myopathyAyse Yasemin Celikmdayasminc@gmail.com
648YesNo4th Oct 2022"Epilepsy: Syndromes 2 – IESS Dravet HHE EMAS"E WirrellBalamurugan Nagarajanmeetkabi@gmail.comGENOTYPIC AND PHENOTYPIC SPECTRUM OF CHILDREN WITH GENETIC WEST SYNDROME FROM NORTHERN INDIAJitendra Kumar Sahujsh2003@gmail.com
427YesNo5th Oct 2022"CNS Malformations NGS"A NarayanMohammed Alqahtanimohammed.alqahtani@sickkids.caThe Yield of Genetic and Metabolic Testing in Epileptic SpasmsMohammed Alqahtanimohammed.alqahtani@sickkids.ca
585YesNo4th Oct 2022Epilepsy: InvestigationsP MadaanMehpare Sari Yanartasmparesari2@gmail.comAnswer to seizures: The pediatric Covid-19 infectionMehpare Sari Yanartasmparesari2@gmail.com
587YesNo4th Oct 2022Epilepsy: Treatment 2 – ASMsRamachandran NairMehpare Sari Yanartasmparesari2@gmail.com"Lacosamide Experience in Childhood Epilepsy from a Tertiary Center Turkey"Mehpare Sari Yanartasmparesari2@gmail.com
336YesNo6th Oct 2022Headache/Stroke 2"Mahendra MoharirCanada"Nesrin Şenbiln.senbil.1965@gmail.comClinical Evaluation Of The Vestibular Functions In Pediatric Patients With Migraine And Probable Vestibular Migraine Of ChildhoodNesrin Şenbiln.senbil.1965@gmail.com
180YesNo4th Oct 2022Epilepsy: Genetics 2N SpecchioNaznin Rubynazninruby73@gmail.comPrevalence Proportion and Clinical Spectrum of Genetic Epilepsy in Children of Bangladesh: A Hospital Based StudyNaznin Rubynazninruby73@gmail.com
285YesNo4th Oct 2022Epilepsy: Genetics 3L LagaeNefise Arıbaş Öznefisearibas@hotmail.comIntractable epilepsy with Rahman SyndromeNefise Arıbaş Öznefisearibas@hotmail.com
387YesNo5th Oct 2022Genetics and epilepsy IW HakamiNefise Arıbaş Öznefisearibas@hotmail.comTBC1D24 gene Mutations Presented with Familial Infantile Myoclonic EpilepsyNefise Arıbaş Öznefisearibas@hotmail.com
705YesNo4th Oct 2022"Epilepsy: DEEs TSC RETT and Comorbidities"Y JiangNihal Yıldıznihalyildiz661@gmail.com"Evaluation of seizure semiology genetic magnetic resonance imaging and electroencephalogram findings in children with Rett syndrome: A multicenter retrospective study"Nihal Yıldıznihalyildiz661@gmail.com
227YesNo5th Oct 2022Neurogenetics practiceT Lerman-SagieNouha Bouayed Abdelmoulanouha_abdelmoulabouayed@yahoo.frSensorineural impairment in maternally inherited diabetes mellitus and deafness (MIDD) disorderNouha Bouayed Abdelmoulanouha_abdelmoulabouayed@yahoo.fr
662YesNo6th Oct 2022Metabolic 6 Defects of bioenergetic and intermediary metabIngrid Tein CanadaNurşah Yeniay Sütnursah_ny@hotmail.comA rare metabolic disease causing infantile spasm: Argininosuccinate lyase deficiencyNurşah Yeniay Sütnursah_ny@hotmail.com
305YesNo4th Oct 2022Epilepsy: Outcomes and EpidemiologyE KijaObrey Urioobreyharold@rocketmail.com"DRUG RESISTANT EPILEPSY AND ASSOCIATED FACTORS AMONG CHILDREN WITH EPILEPSIES IN TANZANIA A CROSS SECTIONAL STUDY"Obrey Urioobreyharold@rocketmail.com
522YesNo4th Oct 2022Epilepsy: Outcomes and EpidemiologyE KijaMehmet Oguz Demirogluoguzdr66@gmail.comThe effect of anti-epileptic treatment selection on prognosis in traumatic brain injuryMehmet Oguz Demirogluoguzdr66@gmail.com
698YesNo5th Oct 2022Spasticity and ataxiaC CatsmanOlgay Bildikolgaybildik@hotmail.comRing Chromosome 18 Case With 18p DeletionOlgay Bildikolgaybildik@hotmail.com
707YesNo6th Oct 2022Metabolic 1 Clinical phenotypes"Brahim Tabarki KSA"Olgay Bildikolgaybildik@hotmail.comA Case Of Vanishing White Matter Disease With Atypical Neuroimaging PresentationOlgay Bildikolgaybildik@hotmail.com
389YesNo5th Oct 2022Genetics and epilepsy IW HakamiÖzgen Hürozgenozyazicioglu@yahoo.comA case of ‘Joubert Syndrome 31’ due to CEP120 homozygous mutationÖzgen Hürozgenozyazicioglu@yahoo.com
414YesNo5th Oct 2022Genetics and epilepsy IIRamachandran NairÖzgen Hürozgenozyazicioglu@yahoo.comA Case of GRIN1 Mutation Presenting with Autistic FeaturesÖzgen Hürozgenozyazicioglu@yahoo.com
422YesNo6th Oct 2022"Movement 1 Chorea dyskinesias tremor spasms & tx""Biju Hameed UK"Özgen Hürozgenozyazicioglu@yahoo.comAn autosomal dominant familial dyskinesia gene: ADCY5 mutationÖzgen Hürozgenozyazicioglu@yahoo.com
425YesNo5th Oct 2022Genetics and epilepsy IIRamachandran NairÖzgen Hürozgenozyazicioglu@yahoo.comA rare cause of progressive myoclonic epilepsy: KCTD7 mutationÖzgen Hürozgenozyazicioglu@yahoo.com
92YesNo4th Oct 2022Epilepsy: Treatment 1 – ASMsB Sanchez-GanPawan Kashyapepawankashyape@yahoo.co.ukA Case of Carbamazepine Responsive Neonatal Epilepsy Secondary to PACS2 Gene mutationPawan Kashyapepawankashyape@yahoo.co.uk
747YesNo6th Oct 2022Metabolic 6 Defects of bioenergetic and intermediary metabIngrid Tein CanadaPinar Edempinaredem@gmail.comPhenotypic diversity of GLUT1 deficiency: A case report.Pinar Edempinaredem@gmail.com
600YesNo4th Oct 2022"Epilepsy: Neuroimaging Surgery and Basic Science"C AkmanPrashant Jauharipjauhari0@gmail.comReal-time cortical excitability in children with DRE and ESES and its correlation with treatment response: A TMS based comparative studyPrashant Jauharipjauhari0@gmail.com
773YesNo5th Oct 2022General neurogenetics IAR ZamaniRadu Perjocradu-stefan.perjoc@rez.umfcd.roWolf-Hirschhorn syndrome and Dup15q – review of the literature and case report.Radu Perjocradu-stefan.perjoc@rez.umfcd.ro
293YesNo4th Oct 2022Epilepsy: Semiology and ClinicalH CrossRamesh Konankirameshkonanki@gmail.comElectro-clinical spectrum of Absence epilepsy: A case series from IndiaRamesh Konankirameshkonanki@gmail.com
439YesNo6th Oct 2022Metabolic 3 Mitochondrial disorders II: Etiologies and mechanismsSaskia Wortmann NetherlandsRamesh Konankirameshkonanki@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 Konankirameshkonanki@gmail.com
58YesNo6th Oct 2022Cerebral palsy 2- Management; current and future"Antigone Papavasiliou Greece"Razia Sultanarazia4m@yahoo.comAssociation of Functional Ability with Nutritional status among Children with Cerebral PalsyRazia Sultanarazia4m@yahoo.com
683YesNo4th Oct 2022Epilepsy: Semiology and ClinicalH CrossRichard Idroridro1@gmail.comPathogenesis of nodding syndrome; Preliminary findingsRichard Idroridro1@gmail.com
746YesNo6th Oct 2022Cerebral palsy 2- Management; current and future"Antigone Papavasiliou Greece"Ruchika Jharuchicls@yahoo.comTo determine the prevalence of comorbidities among children with cerebral palsy (CP) and risk-factors predictive of different comorbidities.Ruchika Jharuchicls@yahoo.com
598YesNo4th Oct 2022"Epilepsy: DEEs TSC RETT and Comorbidities"Y JiangZara Hamills1706726@sms.ed.ac.ukHealth Economic Analysis of Psychology Adding Value Epilepsy Screening (PAVES) - a Screening and Intervention Programme for the Epilepsy ClinicZara Hamills1706726@sms.ed.ac.uk
225YesNo6th Oct 2022Neuroradiology 2"Kshitij Mankand UK"Sandra Patricia Toellesandra.toelle@kispi.uzh.chCongenital tonic pupil - what's behind?Sandra Patricia Toellesandra.toelle@kispi.uzh.ch
57YesNo6th Oct 2022"Cerebral palsy 1- Evaluation: clinic neurophysiologic""Catherine Arnaud France"Sanjida Ahmedsanjida.lipi@yahoo.comRelationship Between the Level of Gross Motor Function and Magnetic Resonance Imaging Findings in Children with Cerebral Palsy in a Tertiary Care HospitalSanjida Ahmedsanjida.lipi@yahoo.com
426YesNo6th Oct 2022"Movement 1 Chorea dyskinesias tremor spasms & tx""Biju Hameed UK"Sara Sopenasara.sopena@gstt.nhs.ukA novel psychological therapy approach for children with PNKDSara Sopenasara.sopena@gstt.nhs.uk
697YesNo4th Oct 2022"Epilepsy: Syndromes 2 – IESS Dravet HHE EMAS"E WirrellIngrid Schefferscheffer@unimelb.edu.auCan vaccine-proximate seizures in Dravet syndrome be prevented?Ingrid Schefferscheffer@unimelb.edu.au
586YesNo6th Oct 2022Metabolic 1 Clinical phenotypes"Brahim Tabarki KSA"Jan-christoph Schoene-bakeschoene-bake.christoph@mh-hannover.deMPS-like disease presumably caused by VPS16-associated impairment of intracellular traffickingJan-christoph Schoene-bakeschoene-bake.christoph@mh-hannover.de
449YesNo6th Oct 2022Headache/Stroke 2"Mahendra MoharirCanada"Secil Doga Tuncsecildogatunc@gmail.comTHE COURSE OF PEDIATRIC HEADACHES DURING COVID-19 PANDEMICHamit Ozyurekhozyurekibu@hotmail.com
601YesNo6th Oct 2022Headache/Stroke 3"Mubeen Rafay Canada"Semra Saygisemra_saygi@yahoo.comThe Prevalence of Adenoid Hypertrophy in Brain MRI Examination in Children with Headache in the Pediatric Neurology Outpatient ClinicSemra Saygisemra_saygi@yahoo.com
318YesNo6th Oct 2022Metabolic 2 Mitochondrial disorders I : clinical phenotypes and tx"Rita Horvath UK"Seren Aydinserenaydin5228@gmail.comThree Different Phenotypic Presentations of Leigh SyndromeSeren Aydinserenaydin5228@gmail.com
381YesNo4th Oct 2022Epilepsy: Treatment 2 – ASMsRamachandran NairSergiusz Jozwiaksergiusz.jozwiak@gmail.com"VIRAP - new randomized double-blind preventive study (vigabatrin vs sirolimus) on prevention of epilepsy in TSC"Sergiusz Jozwiaksergiusz.jozwiak@gmail.com
52YesNo4th Oct 2022Epilepsy: Treatment 1 – ASMsB Sanchez-GanEsra Özpınarseydabesen2000@gmail.comSirolimus in Tuberous Sclerosis Complex prior to epilepsy: evidence from a registry-based real-world studyLi-ping Zouzouliping21@sina.com
450YesNo4th Oct 2022"Epilepsy: DEEs TSC RETT and Comorbidities"Y JiangSharmila Manivannansharmila.manivannan@nhs.netQuality Improvement Project to ameliorate the provision of mental health support to our children with epilepsySharmila Manivannansharmila.manivannan@nhs.net
508YesNo6th Oct 2022Metabolic 4 Therapeutic approachesSamantha Marin CanadaYashu Sharmashrma.yashu@gmail.comImpact of COVID-19 on the care of children with neurometabolic disordersArushi Sainidoc.arushi@gmail.com
434YesNoSonali Singhsonali2017doc@gmail.comParoxysmal sympathetic hyperactivity in Pediatric Tuberculous meningitis: A New associationPrashant Jauharipjauhari0@gmail.com
696YesNo5th Oct 2022Molecular geneticsT SultanDidem Soydemirsoydemirdidem8@gmail.comEXPANDING PHENOTYPIC DIVERSITY OF PRUNE1 RELATED DISORDERS: AN EXPERIENCE OF FOUR CASES IN A TERTIARY CENTERDidem Soydemirsoydemirdidem8@gmail.com
347YesNo6th Oct 2022"Movement 1 Chorea dyskinesias tremor spasms & tx""Biju Hameed UK"Sukanya Vrushabhendrasukanyavi2005@gmail.comCaffeine significantly reduces frequency of Paroxysmal Dyskinesia in a child with an ADCY5 MutationSukanya Vrushabhendrasukanyavi2005@gmail.com
730YesNo6th Oct 2022"Metabolic 5 Neurodegenerative diseases (NBIAs metabolic causes of stroke CDG NCLs NKH"Suvasini Sharma IndiaEsra Ülgen Temelulgenesra@yahoo.comAn Infant With Movement Disorder And Infantile Spasm: Attenuated NKHEsra Ülgen Temelulgenesra@yahoo.com
741YesNo4th Oct 2022Epilepsy: Genetics 1S PerryEsra Ülgen Temelulgenesra@yahoo.comSTXBP1 as a Novel Gene for Sleep-Related Hypermotor Epilepsy: A Video-EEG Documented Case ReportEsra Ülgen Temelulgenesra@yahoo.com
547YesNo6th Oct 2022CNS Infections 1 Covid-related"Charles Newton Kenya"Varghese Abrahamvarghese.abraham@moscmc.edu.inA Comparative Study On The Risk Of Seizure In Children During The Delta And The Omicron variants of SARS-COV-2 InfectionVarghese Abrahamvarghese.abraham@moscmc.edu.in
781YesNo6th Oct 2022"Movement 2 Dystonia Parkinsons tremor and epidemiology""Jon Mink US"Wang-tso Leewangtsolee@ntu.edu.tw"An open-label single-dose study to evaluate the efficacy of probiotics PS128 in pediatric subjects with AADC deficiency"Wang-tso Leewangtsolee@ntu.edu.tw
782YesNo6th Oct 2022"Movement 3 Ataxias opsoclonus myoclonus and covid 19 impact""Russell Dale Australia"Wang-tso Leewangtsolee@ntu.edu.tw"Knockout of AGTPBP1 a gene for cerebellar ataxia lead to neuronal death and increased dopaminergic release"Wang-tso Leewangtsolee@ntu.edu.tw
471YesNo6th Oct 2022"Cerebral palsy 1- Evaluation: clinic neurophysiologic""Catherine Arnaud France"Yilmaz Satireryilmaz.satirer@gmail.comEVALUATION OF MOTOR AND SENSORY FUNCTIONS AND PSYCHOLOGICAL PROPERTIES IN CHILDREN WITH HEMIPARETIC CEREBRAL PALSY BETWEEN THE AGES OF 6 AND 16 YEARSYilmaz Satireryilmaz.satirer@gmail.com
358YesNo5th Oct 2022Neurogenetics practiceT Lerman-SagieZahra Rezaeizahra.rezaii84@gmail.comInfantile Neuroaxonal Dystrophy; A Rare Or Underdiagnosed Disease?Zahra Rezaeizahra.rezaii84@gmail.com
485YesNo6th Oct 2022Neuroradiology 2"Kshitij Mankand UK"Zahra Rezaeizahra.rezaii84@gmail.comA Common Neurologic Symptom Leads To A More Serious Oncologic Diagnosis!Zahra Rezaeizahra.rezaii84@gmail.com
211YesNo5th Oct 2022Neurogenetics practiceT Lerman-SagieAdelina GlangherNot AvailableClinical and genetic profiles of grey matter heterotopia – report of 28 patientsMagdalena Budisteanumagda_efrim@yahoo.com
356YesNo4th Oct 2022"Epilepsy: Syndromes 1 – Self-limited EE/DEE-SWAS"C JoshiTBCNot AvailableClinical and electroencephalographic characteristics of childhood epilepsy with centrotemporal spikes for antiseizure medications: monotherapy versus dualtherapy in a multicenter cohort studyBeril Dilberberiltem@gmail.com
419YesNo5th Oct 2022Genetics and epilepsy IIRamachandran NairTBCNot AvailableA case of ‘Smith Magenis Syndrome’ with self-injurious behaviors and dysmorphic facialÖzgen Hürozgenozyazicioglu@yahoo.com
452YesNo6th Oct 2022"Metabolic 5 Neurodegenerative diseases (NBIAs metabolic causes of stroke CDG NCLs NKH"Suvasini Sharma IndiaTBCNot AvailableMRI pattern recognition of neuroceroid lipofuschinosis in childrenMahesh Kamatedrmaheshkamate@gmail.com
728YesNo6th Oct 2022Neuroradiology 2"Kshitij Mankand UK"TBCNot AvailablePosterior reversible encephalopathy syndrome (PRES) without radiological correlate : Is it possible?Sachendra Badalbadalsachendra@yahoo.com
362NoNo4th Oct 2022"Epilepsy: Syndromes 1 – Self-limited EE/DEE-SWAS"C JoshiAakanksha Anandaakanksha.ucms@gmail.comContinuous spikes and waves during sleep (CSWS): A Descriptive Clinical-epidemiological Profile from IndiaAakanksha Anandaakanksha.ucms@gmail.com
364NoNo5th Oct 2022General neurogenetics IIA R TavasoliAakanksha Anandaakanksha.ucms@gmail.comSTURGE WEBER SYNDROME WITH PHAKOMATOSIS PIGMENTOVASCULARIS: A CASE REPORTAakanksha Anandaakanksha.ucms@gmail.com
59NoNo4th Oct 2022Neonatal 2: Neonatal neurology – otherLakshmiAbdullahel Amaanabdullahelamaan@gmail.comImprovement of Hand Hygiene Practices among the Healthcare Workers in a Neonatal Intensive Care UnitAbdullahel Amaanabdullahelamaan@gmail.com
323NoNo6th Oct 2022Metabolic 2 Mitochondrial disorders I : clinical phenotypes and tx"Rita Horvath UK"Abir Zioudiabir.zioudi@gmail.comMitochondrial disorders: a descriptive study of a Tunisian pediatric seriesAbir Zioudiabir.zioudi@gmail.com
175NoNo4th Oct 2022ASD/NDD/ADHD 1 ASD genetic / biomarkers /Chahnez TrikiAdelina Glangheradelina.glangher@gmail.com"Epileptiform discharges and epilepsy in non-syndromic ASD patients. Pre peri post-natal risk factors for epilepsy."Adelina Glangheradelina.glangher@gmail.com
411NoNo6th Oct 2022"Movement 3 Ataxias opsoclonus myoclonus and covid 19 impact""Russell Dale Australia"Adnan Denizadnandeniz85@hotmail.comCOVID-19 vaccine induced opsoclonus-myoclonus-ataxia syndromeAdnan Denizadnandeniz85@hotmail.com
413NoNo5th Oct 2022Neuromuscular 1H LochmüllerAdnan Denizadnandeniz85@hotmail.comParaneoplastic polyneuropathy associated with inflammatory myofibroblastic tumor in a pediatric patientAdnan Denizadnandeniz85@hotmail.com
429NoNo4th Oct 2022ASD/NDD/ADHD 2 ASD assessments / management / Rett syndrome / high risk infantsAntigone PapavasiliouAnnie Brandes-aitkenaitkenannie@gmail.com"A Comprehensive Personalized Medically Based Care Model Improves Adaptive Behavior Outcomes in Autism vs Standard of Care"Annie Brandes-aitkenaitkenannie@gmail.com
671NoNo6th Oct 2022Neuroradiology 3"Ajay Taranath Australia"Asli Kübra Ataseverakubrat@gmail.comA case with an epidermoid cyst in the cerebellopontine angle presenting with hemifacial spasmAsli Kübra Ataseverakubrat@gmail.com
383NoNo5th Oct 2022Genetics and epilepsy IW HakamiAli Modawebali.modaweb@ajch.aeEarly recurrent encephalopathy and subsequent hemiplegic migraine and intellectual disability caused by a de novo mutation in ATP2A2 geneAhmed Abd Alwahab NugudAhmed.Nugud@ajch.ae
101NoNo4th Oct 2022Epilepsy: Genetics 1S PerryAlyssa Robisonalyssarobison1@gmail.comArthrogryposis multiplex congenita and SCN1A mutations: Another reported case and treatment guidanceAlyssa Robisonalyssarobison1@gmail.com
102NoNo5th Oct 2022"Neuropathy GBS and CMS"C BönnemannAlyssa Robisonalyssarobison1@gmail.comParaneoplastic Guillain-Barre Syndrome: A case report and call for modified diagnostic criteriaAlyssa Robisonalyssarobison1@gmail.com
526NoNo5th Oct 2022General IIM SönmezAmal KentabAmkentab@hotmail.comVici syndrome: Experience at tertiary care centerAmal KentabAmkentab@hotmail.com
532NoNo5th Oct 2022"CNS Malformations NGS"A NarayanAmal KentabAmkentab@hotmail.comClinical Characteristics and Aetiology of Corpus Callosum Abnormalities: A single Centre Experience in Saudi Arabia.Amal KentabAmkentab@hotmail.com
120NoNo5th Oct 2022Neuroimmunology 2 Antibody mediated disorders / monophasic demyel disorderBanu AnlarÁngeles Schteinschnaiderangeles@fleni.org.ar"FLAMES (FLAIR Hyperintense Lesions in Anti-Myelin Oligodendrocyte Glycoprotein-associated Encephalitis with Seizures) a case report."Ángeles Schteinschnaiderangeles@fleni.org.ar
121NoNo6th Oct 2022Neuroradiology 1"Manohar Schroff Canada"Ángeles Schteinschnaiderangeles@fleni.org.arPOSTERIOR REVERSIBLE ENCEPHALOPATHY SYNDROME IN PEDIATRICSÁngeles Schteinschnaiderangeles@fleni.org.ar
125NoNo6th Oct 2022"Tuberous sclerosis Radiology"K AydınAngeles Schteinschnaiderangeles@fleni.org.arNEUROCUTANEOUS MELANOSIS: CLINICAL AND IMAGING CHARACTERISTICS IN 7 PATIENTSAngeles Schteinschnaiderangeles@fleni.org.ar
126NoNo5th Oct 2022Peripheral nerveD SelcenAngeles Schteinschnaiderangeles@fleni.org.arHIRAYAMA DISEASE: ABOUT TWO CASESAngeles Schteinschnaiderangeles@fleni.org.ar
473NoNo6th Oct 2022Headache/Stroke 3"Mubeen Rafay Canada"Ángeles Schteinschnaiderangeles@fleni.org.ar"Pediatric Bow Hunter Syndrome a case report."Ángeles Schteinschnaiderangeles@fleni.org.ar
653NoNo5th Oct 2022TreatmentF MuntoniNatalija Angelkovaangelkovan@gmail.comThree years follow up of 6-minute walk test and North Star Ambulatory Assessment in 30 ambulant DMD boys since the beginning of steroid treatmentNatalija Angelkovaangelkovan@gmail.com
479NoNo4th Oct 2022Epilepsy: Outcomes and EpidemiologyE KijaAngela Schulzanschulz@uke.deSeizures in children with CLN2 disease receiving cerliponase alfa for >5 yearsSara Dosenovicsara.dosenovic@bmrn.com
443NoNo5th Oct 2022"Neuropathy GBS and CMS"C BönnemannAyşe Nur Coşkunanurcoskun@gmail.com"Charcot-Marie-Tooth Disease So Which Type?"Ayşe Nur Coşkunanurcoskun@gmail.com
448NoNo5th Oct 2022General IIM SönmezArijit Chattopadhyayarijitchatto@hotmail.comIdentification of a novel variant of the CDKl5 gene associated with atypical Rett SyndromeArijit Chattopadhyayarijitchatto@hotmail.com
204NoNo4th Oct 2022"Epilepsy: Syndromes 2 – IESS Dravet HHE EMAS"E WirrellAristides Hadjinicolaouaris.hadjinicolaou@gmail.comChallenges of determination in date of onset of infantile spasms: A tertiary health center’s experienceAristides Hadjinicolaouaris.hadjinicolaou@gmail.com
412NoNo6th Oct 2022Neuroradiology 3"Ajay Taranath Australia"Aristides Hadjinicolaouaris.hadjinicolaou@gmail.comVariation in neuroimaging and outcomes in patients with SWS type IIIAristides Hadjinicolaouaris.hadjinicolaou@gmail.com
396NoNo5th Oct 2022Neuroimmunology 2 Antibody mediated disorders / monophasic demyel disorderBanu AnlarArzu Yilmazarzuotken@yahoo.comHuman Herpes Virüs-7 Enfeksiyonu Sonrası Gelişen Subakut Sklerozan Panensefalit OlgusuArzu Yilmazarzuotken@yahoo.com
97NoNo5th Oct 2022Neurogenetics practiceT Lerman-SagieAshna Kumarashnakumar99@gmail.comDancing eyes and lazy gut in an infant with developmental delayAshna Kumarashnakumar99@gmail.com
155NoNo4th Oct 2022"Epilepsy: Syndromes 1 – Self-limited EE/DEE-SWAS"C JoshiAshna Kumarashnakumar99@gmail.comSelf-Limited Epilepsy with Autonomic Seizures (SeLEAS): A Case seriesAshna Kumarashnakumar99@gmail.com
167NoNo5th Oct 2022Genetics and epilepsy IW HakamiAhmet Yaramisayaramis@gmail.comCOL4A1-related autosomal recessive encephalopathy in 2 Turkish childrenAhmet Yaramisayaramis@gmail.com
280NoNo5th Oct 2022"İon channel myopathy and metabolic"R HorvathAhmet Yaramışayaramis@gmail.comCompliance with riboflavin treatment in a patient with late-diagnosed Brovn-Vialetto-Van Laere syndromeAhmet Yaramışayaramis@gmail.com
281NoNo5th Oct 2022"İon channel myopathy and metabolic"R HorvathAhmet Yaramışayaramis@gmail.comRiboflavin treatment in 3 cases with ETFDH gene mutationAhmet Yaramışayaramis@gmail.com
521NoNo4th Oct 2022Epilepsy: Genetics 3L LagaeAyşe Yasemin Çelikayasminc@hotmail.comA Rare Cause of Epilepsy In A Child: Mosaic Ring Chromosome 21Ayşe Yasemin Çelikayasminc@hotmail.com
737NoNo6th Oct 2022Headache/Stroke 3"Mubeen Rafay Canada"Aysen Gokaysenngok@gmail.comA rare dual pathology: Idiopathic intracranial hypertension presenting with isolated unilateral facial nerve palsyAysen Gokaysenngok@gmail.com
732NoNo6th Oct 2022Neuroradiology 3"Ajay Taranath Australia"Sachendra Badalbadalsachendra@yahoo.comMirror movements in children: Case seriesSachendra Badalbadalsachendra@yahoo.com
753NoNo6th Oct 2022Metabolic 1 Clinical phenotypes"Brahim Tabarki KSA"Sachendra Badalbadalsachendra@yahoo.com"Congenital Icthyosis and neurological manifestations Sjogren Larsson and beyond: A study of seven children."Sachendra Badalbadalsachendra@yahoo.com
229NoNo4th Oct 2022Neonatal 2: Neonatal neurology – otherLakshmiBülent Karabkuskudar@gmail.comIs Screening of Congenital CMV Infection in Saliva by RT-PCR Feasible?Bülent Karabkuskudar@gmail.com
416NoNo5th Oct 2022Peripheral nerveD SelcenBurcin Nazli Karacabeybnazlikaracabey@hotmail.comSHEAR WAVE ELASTOGRAPHY IN PATIENTS WITH SPINAL MUSCULAR ATROPHY TYPE 2-3Burcin Nazli Karacabeybnazlikaracabey@hotmail.com
690NoNo6th Oct 2022"Cerebral palsy 1- Evaluation: clinic neurophysiologic""Catherine Arnaud France"Burce Emine Dortkardeslerburceyasar@gmail.com"Assessment of Nutritional Status Resuscitation Modalities of Malnutrition and Enteral Feeding Products for Children with Neurological Disorders"Burce Emine Dortkardeslerburceyasar@gmail.com
606NoNo5th Oct 2022"CNS Malformations NGS"A NarayanCemile Busra Olculubusra.olculu@ege.edu.trA Dynamic Genetic Testing Approachment for Neurological Disorders in The Pediatric Neurogenetic Case-Management CouncilsCemile Busra Olculubusra.olculu@ege.edu.tr
183NoNo5th Oct 2022Neuroimmunology 1 Demyelinating / MS relatedRussell DaleÇağatay Günaycagataygunaymd@gmail.comOptic Neuritis in CD59 Deficiency: An Extremely Rare PresentationÇağatay Günaycagataygunaymd@gmail.com
369NoNo5th Oct 2022Spasticity and ataxiaC CatsmanChahnez Charfi Trikichahnezct@gmail.comALPHA-FŒTOPROTEINE PROGNOSIS VALUE IN PATIENTS MONITORING WITH ATAXIA-TELANGIECTASIASalma Zouari Malloulimallouli.salma26@gmail.com
626NoNo6th Oct 2022CNS Infections 1 Covid-related"Charles Newton Kenya"Chahnez Charfi Trikichahnezct@gmail.comPost-COVID-19 related neurological features in a pediatric populationSalma Zouari Malloulimallouli.salma26@gmail.com
123NoNo4th Oct 2022ASD/NDD/ADHD 3 NDD / IDCharuta JoshiNandita Chattopadhyaychattnan@gmail.comOVERCOMING ADVERSITIES TO PROMOTE EARLY BRAIN DEVELOPMENT IN CHILDREN - A STUDY FROM RURAL INDIANandita Chattopadhyaychattnan@gmail.com
146NoNo5th Oct 2022General neurogenetics IAR ZamaniMiaomiao Chengchengmiaomiao57@126.comGenetics and clinical phenotypes of epilepsy associated with Dup15q syndromeYuehua Zhangzhangyhdr@126.com
191NoNo4th Oct 2022Epilepsy: Treatment 1 – ASMsB Sanchez-GanSi-jia Chuchu_sj@163.comEfficacy and tolerability of adjunctive perampanel in pediatric patients (aged 4–12 years) with inadequately controlled focal-onset seizuresSi-jia Chuchu_sj@163.com
128NoNo5th Oct 2022Neuromuscular 1H LochmüllerÇiğdem Genç Selcigdemsel@yahoo.comContinuous Glucose Monitoring in Obese/Overweight Children and Adolescents with Neurological Manifestations: A Single Reference Center ExperienceÇiğdem Genç Selcigdemsel@yahoo.com
162NoNo5th Oct 2022TreatmentF MuntoniChristian Wernercwerner@ptcbio.comUpdated demographics and safety data from patients with nonsense mutation Duchenne muscular dystrophy receiving ataluren in the STRIDE RegistryChristian Wernercwerner@ptcbio.com
165NoNo5th Oct 2022TreatmentF MuntoniChristian Wernercwerner@ptcbio.comAge at loss of ambulation in STRIDE Registry and CINRG Natural History Study patients with DMD: a matched cohort analysisChristian Wernercwerner@ptcbio.com
169NoNo5th Oct 2022TreatmentF MuntoniChristian Wernercwerner@ptcbio.comPulmonary function in Duchenne muscular dystrophy patients from the STRIDE Registry and CINRG Natural History Study: a matched cohort analysisChristian Wernercwerner@ptcbio.com
525NoNoXiaolu Chencxlnj@qq.comThe first case of Streptococcus intermedius brain abscess with hemophagocyic histiocytosisXiaolu Chencxlnj@qq.com
545NoNo6th Oct 2022Neuroradiology 2"Kshitij Mankand UK"Xiaolu Chencxlnj@qq.comClinical characteristics of 50 cases of cerebral cystic necrosis in childrenXiaolu Chencxlnj@qq.com
260NoNo5th Oct 2022"Neuropathy GBS and CMS"C BönnemannDarshan Dasdarshan.das@rajagirihospital.comIsolated unilateral Palatal Palsy- a postinfectious inflammatory mononeuritis of the pharyngeal branch of the vagal nerveDarshan Dasdarshan.das@rajagirihospital.com
202NoNo5th Oct 2022General neurogenetics IAR ZamaniXianru Jiaodc1981021@163.comPhenotype of heterozygous variants of dehydrodolichol diphosphate synthaseXianru Jiaodc1981021@163.com
399NoNo4th Oct 2022Epilepsy: Genetics 2N SpecchioXianru Jiaodc1981021@163.com"A rare presentation characterized by epileptic spasms in ALDH7A1 pyridox(am)ine-5’-phosphate oxidase (PNPO) and PLPBP deficiency"Xianru Jiaodc1981021@163.com
400NoNo4th Oct 2022"Epilepsy: Syndromes 2 – IESS Dravet HHE EMAS"E WirrellXianru Jiaodc1981021@163.comThe clinical features and long-term follow-up of vitamin B6-responsive infantile spasms in a Chinese cohortXianru Jiaodc1981021@163.com
212NoNo6th Oct 2022Metabolic 4 Therapeutic approachesSamantha Marin CanadaDefne Alikılıçdefnekocaoglu@hotmail.com"Pyrimidine Metabolism Disorders as Rare Cause of Psycho-motor Retardation Dysmorphism and Epilepsy"Defne Alikılıçdefnekocaoglu@hotmail.com
213NoNo5th Oct 2022"İon channel myopathy and metabolic"R HorvathDefne Alikılıçdefnekocaoglu@hotmail.comClinical Features Beyond Myopathy: Three Calpainopathy Patients with CAPN3 MutationDefne Alikılıçdefnekocaoglu@hotmail.com
538NoNo4th Oct 2022Neonatal 2: Neonatal neurology – otherLakshmiDemet Terekdemet.terek@yahoo.comInvestigation of Risk Factors in Neural Tube Defects in NewbornsDemet Terekdemet.terek@yahoo.com
588NoNo4th Oct 2022ASD/NDD/ADHD 2 ASD assessments / management / Rett syndrome / high risk infantsAntigone PapavasiliouDemet Terekdemet.terek@yahoo.comOur cases with hypoxic ischemic encephalopathy in which we applied hypothermiaDemet Terekdemet.terek@yahoo.com
185NoNo6th Oct 2022CNS Infections 1 Covid-related"Charles Newton Kenya"Ari̇fe Derda Yücel Şenderdayucel@hotmail.comA pediatric case of reversible splenial lesion syndrome associated with SARS-CoV-2: Case reportAri̇fe Derda Yücel Şenderdayucel@hotmail.com
193NoNo5th Oct 2022SMAN ChrestianAri̇fe Derda Yücel Şenderdayucel@hotmail.comCLİNİCAL CHARACTERİSTİCS OF CASES WİTH SPİNAL MUSCULAR ATROPHYAri̇fe Derda Yücel Şenderdayucel@hotmail.com
584NoNo6th Oct 2022Neuroradiology 1"Manohar Schroff Canada"Dhanalakshmi AngappanDhanalakshmivj@gmail.comAnte-natal and post-natal factors affecting the rate of growth of corpus callosum in preterm infants: a retrospective studyDhanalakshmi AngappanDhanalakshmivj@gmail.com
224NoNo4th Oct 2022ASD/NDD/ADHD 3 NDD / IDCharuta JoshiDhanya Lakshmi Narayanandhanya.lakshmi@manipal.eduPhenotypic and genotypic expansion of TRAPPC12-related disorderDhanya Lakshmi Narayanandhanya.lakshmi@manipal.edu
438NoNo5th Oct 2022"İon channel myopathy and metabolic"R HorvathDidem Ardiclididem.aydogdu@gmail.com"A rare cause of hypotonia arthrogryposis and early-onset scoliosis: Autosomal recessive PIEZO2-associated neuromuscular disease"Didem Ardiclididem.aydogdu@gmail.com
760NoNo5th Oct 2022Peripheral nerveD SelcenDidem Ardiclididem.aydogdu@gmail.comCardiac impairment in Duchenne Muscular Dystrophy: A single-center retrospective experienceDidem Ardiclididem.aydogdu@gmail.com
701NoNo5th Oct 2022Neuroimmunology 3 Autoimmune encephalitis plusSilvia TenenbaumDilara Ece Toprakdilaraecetoprak@yahoo.comAcute disseminated encephalomyelitis (ADEM) in children: a multicenter retrospective studySeda Kanmazseda.kanmaz@ege.edu.tr
704NoNo5th Oct 2022Neuroimmunology 3 Autoimmune encephalitis plusSilvia TenenbaumDilara Ece Toprakdilaraecetoprak@yahoo.comAnti-Hu associated encephalitis as the initial presentation of neuroblastomaDilara Ece Toprakdilaraecetoprak@yahoo.com
51NoNo5th Oct 2022Neuromuscular 1H LochmüllerDilek Cavusogludilekcavusoglu83@gmail.comSubcutaneous immunoglobulin in anti-HMGCR myopathy with children for long-term maintenanceDilek Cavusogludilekcavusoglu83@gmail.com
297NoNo5th Oct 2022Neurogenetics practiceT Lerman-SagieDilek Cavusogludilekcavusoglu83@gmail.com"Evaluation of clinical laboratory and imaging findings of patients with the diagnosis of Pontocerebellar Hypoplasia: A multicenter national study"Dilek Cavusogludilekcavusoglu83@gmail.com
514NoNo5th Oct 2022General neurogenetics IAR ZamaniDilek Cebecidilekcebeci@yahoo.com"Lafora disease: Case report of a 13 years old patient with cognitive decline ataxia and seizures"Dilek Cebecidilekcebeci@yahoo.com
476NoNo4th Oct 2022Neonatal 2: Neonatal neurology – otherLakshmiDipak Ramdipak.ram@mft.nhs.ukNeonatal Spinal Cord Injury: Not To be MissedDipak Ramdipak.ram@mft.nhs.uk
501NoNo5th Oct 2022"CNS Malformations NGS"A NarayanArushi Sainidoc.arushi@gmail.comExploring the genetic basis of Leukodystrophies through an in-house targeted panel approach in resource-poor settingsArushi Sainidoc.arushi@gmail.com
266NoNo5th Oct 2022Neuroimmunology 2 Antibody mediated disorders / monophasic demyel disorderBanu AnlarGülen Gül Mertdr_gulen@hotmail.comEvaluation of Prognostic Factors in Pediatric Transverse Myelitis: A Multicenter Cohort StudySevim Şahinsevimsahin1@yahoo.com
114NoNo5th Oct 2022"CNS Malformations NGS"A NarayanMaha Zakidr_mahazaki@yahoo.comThe landscape of Lissencephaly among Egyptian PatientsMaha Zakidr_mahazaki@yahoo.com
103NoNo5th Oct 2022Neuroimmunology 3 Autoimmune encephalitis plusSilvia TenenbaumAyten Güleçdr.aytengulec@gmail.com"PREVALENCE AND OUTCOMES OF AUTOIMMUNE ENCEPHALITIS IN A TERTIARY HOSPITAL IN BAGUIO CITY PHILIPPINES"Jaidi Sagayjdee2308@gmail.com
762NoNo4th Oct 2022Epilepsy: Genetics 3L LagaeAyten Güleçdr.aytengulec@gmail.com"National Based Retrospective Study on the Evaluation of Clinical Laboratory and Imaging Research of Tuberous Sclerosis Cases"Hüseyin Perhuseyinper@yahoo.com
325NoNo4th Oct 2022ASD/NDD/ADHD 1 ASD genetic / biomarkers /Chahnez TrikiBilgihan Bikmazerdr.bilgihan@hotmail.comAssociation Between Sleep Problems and Perinatal Factors and Maternal Psychopathology in Toddlers at Risk for AutismBilgihan Bikmazerdr.bilgihan@hotmail.com
725NoNo4th Oct 2022ASD/NDD/ADHD 4 ADHD and Behav / syndromes / LDPratibha SinghiBilgihan Bikmazerdr.bilgihan@hotmail.comNeurocognitive Functions and Behavior Outcome of Preschool-Age Children with a History of Febrile ConvulsionsBilgihan Bikmazerdr.bilgihan@hotmail.com
129NoNo4th Oct 2022Epilepsy: InvestigationsP MadaanElif Yildirimdr.elif.ksglyldrm@gmail.comDo Hyponatremia and Anemia in Simple Febrile Convulsions Affect Reccurence in The First 24 Hours?Huseyin Tanhtan@atauni.edu.tr
133NoNoElif Yildirimdr.elif.ksglyldrm@gmail.comChronic meningitis mimicking idiopathic intracranial hypertension: a surprising diagnosisElif Yildirimdr.elif.ksglyldrm@gmail.com
135NoNo4th Oct 2022Epilepsy: Genetics 1S PerryElif Yildirimdr.elif.ksglyldrm@gmail.comNew two findings in idiopathic generalized epilepsy-15 (EIG-15); happy demeanor and gait disturbance: a case reportElif Yildirimdr.elif.ksglyldrm@gmail.com
709NoNo6th Oct 2022"Movement 3 Ataxias opsoclonus myoclonus and covid 19 impact""Russell Dale Australia"Esra Ozpinardr.esraozpinar@gmail.comA rare neurodegenerative disorder mimicking autoimmune encephalitis induced by COVID-19: CONDSIASEsra Ozpinardr.esraozpinar@gmail.com
713NoNo6th Oct 2022Metabolic 2 Mitochondrial disorders I : clinical phenotypes and tx"Rita Horvath UK"Esra Ozpi̇nardr.esraozpinar@gmail.comA case with mutation of Vps13D: Leigh syndrome or spinocerebellar ataxia?Esra Ozpi̇nardr.esraozpinar@gmail.com
736NoNo6th Oct 2022Neuroradiology 1"Manohar Schroff Canada"Esra Özpınardr.esraozpinar@gmail.comBrain computed tomography still plays a critical role in the diagnosis of Aicardi-Goutières syndromeKürşad Aydınkursadaydin@hotmail.com
199NoNo4th Oct 2022Neonatal 1: Neonatal seizures and EEGHannah GlassVrushabh Gavalidr.vrushabhgavali@gmail.comAn Observational Study to Assess Inter-observer agreement for neonatal EEG InterpretationVrushabh Gavalidr.vrushabhgavali@gmail.com
433NoNo4th Oct 2022Neonatal 2: Neonatal neurology – otherLakshmiVrushabh Gavalidr.vrushabhgavali@gmail.comA prospective observational study to determine difference in motor developmental outcomes & effect of early intervention in Full Term vs. Late Preterm neonates using INFANIB.Vrushabh Gavalidr.vrushabhgavali@gmail.com
76NoNo6th Oct 2022"Movement 1 Chorea dyskinesias tremor spasms & tx""Biju Hameed UK"Dramane Coulibalydramanecoul@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 Coulibalydramanecoul@yahoo.fr
597NoNo6th Oct 2022"Tuberous sclerosis Radiology"K AydınAmi Shahdrami.rajesh.shah@gmail.comUnravelling the diagnostic dilemma – A case series of radiologically diagnosed pontocerebellar hypoplasia.Ami Shahdrami.rajesh.shah@gmail.com
136NoNo6th Oct 2022Metabolic 1 Clinical phenotypes"Brahim Tabarki KSA"Arzu Ekicidrarzuekici@gmail.comTemporary Consciousness Disturbance in Van der Knaap disease after Minor Head TraumaArzu Ekicidrarzuekici@gmail.com
710NoNo4th Oct 2022ASD/NDD/ADHD 2 ASD assessments / management / Rett syndrome / high risk infantsAntigone PapavasiliouAyfer Arduc Akcaydrayfer@gmail.comThe Determinants of Quality of Life in Rett Syndrome: A Cross-sectional StudyAyfer Arduc Akcaydrayfer@gmail.com
652NoNo4th Oct 2022ASD/NDD/ADHD 2 ASD assessments / management / Rett syndrome / high risk infantsAntigone PapavasiliouAyşe Kaçar Bayramdraysebayram@gmail.comAutonomic Nervous System Function Changes during Arousals in Children with Primary Nocturnal EnuresisAyşe Kaçar Bayramdraysebayram@gmail.com
478NoNo5th Oct 2022Neuroimmunology 1 Demyelinating / MS relatedRussell DaleSeyfeddine Baouiadrbaouiaseyf@gmail.comDevic's neuromyelitis optica (NMO) or a pediatric onset multiple sclerosis (MS)? A case reportSeyfeddine Baouiadrbaouiaseyf@gmail.com
480NoNo6th Oct 2022Metabolic 2 Mitochondrial disorders I : clinical phenotypes and tx"Rita Horvath UK"Seyfeddine Baouiadrbaouiaseyf@gmail.com"A case of mitochondrial neuro-gastrointestinal encephalopathy or MNGIE syndrome why not?"Seyfeddine Baouiadrbaouiaseyf@gmail.com
335NoNo5th Oct 2022Neurogenetics practiceT Lerman-SagieCanan Üstündrcananustun@hotmail.comAn Aicardi-Goutieres Syndrome 2 CaseCanan Üstündrcananustun@hotmail.com
255NoNo5th Oct 2022Neuroimmunology 1 Demyelinating / MS relatedRussell DaleDeniz Yukseldrdeniz_yuksel@yahoo.com.trClinical efficacy and safety of intrathecal methotrexate in the treatment of Balo’s concentric sclerosis: a case reportDeniz Yukseldrdeniz_yuksel@yahoo.com.tr
360NoNo5th Oct 2022Muscular dystrophyY NevoDerya Guderdrderyaguderkurt@gmail.comLİMBE GİRDLE MUSCULAR DYSTROPHY WİTH A MUTATİON İN THE CAVEOLİN-3 (CAV-3) GENEDerya Guderdrderyaguderkurt@gmail.com
363NoNo5th Oct 2022General neurogenetics IAR ZamaniDerya Guderdrderyaguderkurt@gmail.comA RARE CAUSE OF AUTISM AND EPILEPSY COMBINATION: GRM7 GENE MUTATIONDerya Guderdrderyaguderkurt@gmail.com
71NoNo5th Oct 2022Neuromuscular 1H LochmüllerGokce Eserdrgokceeser@gmail.comCLINICAL SPECTRUM OF THE LIMB-GIRDLE MUSCULAR DYSTROPHY TYPE 2E (LGMD2E)Gokce Eserdrgokceeser@gmail.com
72NoNo6th Oct 2022Metabolic 2 Mitochondrial disorders I : clinical phenotypes and tx"Rita Horvath UK"Gokce Eserdrgokceeser@gmail.comTHE MIRACLE OF NUCLEOSIDE TREATMENT IN THYMIDINE KINASE 2 DEFICIENCYGokce Eserdrgokceeser@gmail.com
641NoNo4th Oct 2022Epilepsy: Status epilepticus and MiscellaneousT LoddenkemperHarshkumar Pateldrharsh9@gmail.comNovel treatment approach to NORSE (new onset refractory status epilepticus) in children: Skipping the pharmacological comaHarshkumar Pateldrharsh9@gmail.com
624NoNoIbrahim Onceldribrahimoncel@gmail.comGlobal burden of measles: A registry of neurological complicationsIbrahim Onceldribrahimoncel@gmail.com
315NoNo4th Oct 2022"Epilepsy: DEEs TSC RETT and Comorbidities"Y Jiangİpek Dokurel Cetindripekdokurel@gmail.comThe Impact of Epilepsy on Sleep Characteristics in Epileptic Adolescents and their Caregiversİpek Dokurel Cetindripekdokurel@gmail.com
486NoNo4th Oct 2022Neonatal 1: Neonatal seizures and EEGHannah Glassİpek Dokurel Cetindripekdokurel@gmail.com"Clinical electrophysiological and neuroimaging predictors for antiseizure medication in infants with neonatal clinical seizures"İpek Dokurel Cetindripekdokurel@gmail.com
564NoNo4th Oct 2022Neonatal 2: Neonatal neurology – otherLakshmiLokesh Sainidrlokeshsaini@gmail.comGeneral Movement Assessment for predicting the neurodevelopmental outcomes in cohort of infants exposed to severe hyperbilirubinemia and hypoxic ischaemic encephalopathy respectively in the neonatal periodLokesh Sainidrlokeshsaini@gmail.com
733NoNo6th Oct 2022Neuroradiology 3"Ajay Taranath Australia"Marya Hameeddrmash84@gmail.comKEEP AN AYE ON LUMPY BUMPY HEAD: A CASE SERIES HIGHLIGHTING SPECTRUM OF PRESENTATION IN CRANIOSYNOSTOSISMarya Hameeddrmash84@gmail.com
689NoNo6th Oct 2022Metabolic 4 Therapeutic approachesSamantha Marin CanadaMert Altıntaşdrmertcanaltintas@gmail.comA case of asparagine synthetase deficiency successfully treated with ketogenic dietMiraç Yıldırımmiracyildirim81@hotmail.com
107NoNo6th Oct 2022"Tuberous sclerosis Radiology"K AydınMaureen Njorogedrmuthoninjoroge@gmail.comNEUROIMAGING CHARACTERISTICS OF TUBEROUS SCLEROSIS COMPLEX IN PAEDIATRIC PATIENTS AT A TERTIARY HEALTH FACILITY IN KENYA: A CASE SERIESMaureen Njorogedrmuthoninjoroge@gmail.com
302NoNo4th Oct 2022ASD/NDD/ADHD 4 ADHD and Behav / syndromes / LDPratibha SinghiMaureen Njorogedrmuthoninjoroge@gmail.comBROAD SPECTRUM MICRONUTRIENT SUPPLEMENTATION IN THE MANAGEMENT OF ADHD: A CLINICAL TRIAL AND SYSTEMATIC REVIEWMaureen Njorogedrmuthoninjoroge@gmail.com
242NoNo4th Oct 2022ASD/NDD/ADHD 4 ADHD and Behav / syndromes / LDPratibha SinghiÖmer Karacadromerkaraca@gmail.comPURA Syndrome: A Specific PhenotypeÖmer Karacadromerkaraca@gmail.com
243NoNo6th Oct 2022"Movement 1 Chorea dyskinesias tremor spasms & tx""Biju Hameed UK"Ömer Karacadromerkaraca@gmail.comEfficacy of zinc treatment in 2 cases with Arg209Cys mutation in GNAO1 geneÖmer Karacadromerkaraca@gmail.com
751NoNo5th Oct 2022Neuroimmunology 1 Demyelinating / MS relatedRussell DaleÖzben Akıncı Göktaşdrozben@gmail.comTwo Pediatric Cases of Initial Manifestation of Multiple Sclerosis After Immunization with the Pfizer-BioNTech COVID 19 VaccineÖzben Akıncı Göktaşdrozben@gmail.com
78NoNo6th Oct 2022"Tuberous sclerosis Radiology"K AydınÖzlem Yayıcı Kökendrozlemkoken@gmail.comThinning of the corpus callosum prominent in the splenium and colpocephaly: the AP-4 deficiency syndromeÖzlem Yayıcı Kökendrozlemkoken@gmail.com
95NoNo5th Oct 2022Neuromuscular 1H LochmüllerÖzlem Yayıcı Kökendrozlemkoken@gmail.comMuscle cramps may be a clue for GFPT1 gene related congenital myasthenic syndromeÖzlem Yayıcı Kökendrozlemkoken@gmail.com
88NoNo6th Oct 2022Education"Jorge Vidaurre US"Pınar Özkan Kartdrpinar_ozkan@yahoo.comOnline Mother and Baby Yoga for Preterm-Born Infants and Their Mothers in the Time of COVID-19 PandemicDilara Bozgandilarabozgan@gmail.com
650NoNo4th Oct 2022Epilepsy: Status epilepticus and MiscellaneousT LoddenkemperPınar Özkan Kartdrpinar_ozkan@yahoo.comIncreased Post-Seizure ACTH Peak May Have a Role in the Benign Characteristics of Febrile SeizuresSevim Şahinsevimsahin1@yahoo.com
132NoNo4th Oct 2022Epilepsy: InvestigationsP MadaanRahul Sinhadrrahul_2000@yahoo.comThe Diagnostic Utility of the Video EEG at a Tertiary Care Center of North India: A Retrospective StudyRahul Sinhadrrahul_2000@yahoo.com
691NoNoRenu Suthardrrenusuthar@gmail.comSerious neurological complication associated with COVID 19 and MISC: Do we need to be more vigilant?Renu Suthardrrenusuthar@gmail.com
592NoNo5th Oct 2022Genetics and epilepsy IIRamachandran NairSakir Gencdrsakirgenc@yahoo.comA Cause of Severe Hypotonia in Infancy: Allan-Herndon-Dudley SyndromeSakir Gencdrsakirgenc@yahoo.com
613NoNo4th Oct 2022Neonatal 1: Neonatal seizures and EEGHannah GlassSeda Kanmazdrsedakanmaz@gmail.comA new scoring model for outcomes in neonates with seizures: ENEOSS (Ege Neonatal Seizure Scoring Model)Seda Kanmazdrsedakanmaz@gmail.com
620NoNo4th Oct 2022Neonatal 2: Neonatal neurology – otherLakshmiSeda Kanmazdrsedakanmaz@gmail.comA multimodal prognostic evaluation of preterm and term infants with neonatal encephalopathy in a prospective follow-up studySeda Kanmazdrsedakanmaz@gmail.com
757NoNo5th Oct 2022Peripheral nerveD SelcenSelcan Öztürkdrselcanozturk@gmail.comEvaluation Of Pediatric Cases With Gullian Barre Syndrome: A National Multicenter StudyMehmet Canpolatdrmehmetcanpolat@gmail.com
474NoNo6th Oct 2022Headache/Stroke 3"Mubeen Rafay Canada"Sevcan İpekdrsevcanipek@gmail.comThe Case of a 15-year-old Adolescent with Cerebral and Pulmonary Fat Embolism Syndrome without Dermatologic InvolvementSevcan İpekdrsevcanipek@gmail.com
301NoNo5th Oct 2022SMAN ChrestianSmilu Mohanlaldrsmilu@gmail.comSetting up of a standard of care for children with spinal muscular atrophy at a tertiary care center in North Kerala: South IndiaSmilu Mohanlaldrsmilu@gmail.com
489NoNoSuhani Shahdrsuhaniashah@gmail.com"Efficacy safety and tolerability of Gabapentin as monotherapy for dystonic cerebral palsy"Suhani Shahdrsuhaniashah@gmail.com
493NoNo6th Oct 2022Cerebral palsy 2- Management; current and future"Antigone Papavasiliou Greece"Suhani Shahdrsuhaniashah@gmail.comGabapentin: Efficacy and tolerability as adjuvant therapy for dystonic cerebral palsySuhani Shahdrsuhaniashah@gmail.com
565NoNo6th Oct 2022"Movement 2 Dystonia Parkinsons tremor and epidemiology""Jon Mink US"Suhani Shahdrsuhaniashah@gmail.comSpectrum of genetically determined movement disorder in Indian CohortSuhani Shahdrsuhaniashah@gmail.com
410NoNo4th Oct 2022Epilepsy: Status epilepticus and MiscellaneousT LoddenkemperSevim Türaydrsvm@yahoo.comCan the gut microbiota be a guide in the diagnosis and treatment of childhood epilepsy?Sevim Türaydrsvm@yahoo.com
627NoNo4th Oct 2022Epilepsy: Treatment 3 – ASM/ Dietary TreatmentsJ SahuEdibe Pembegul Yildizedibepembegul@hotmail.comManagement of Valproat Monotherapy in Adolescent Girls with Epilepsy; Evaluation of Predictive Factors of Seizure RecurrensEdibe Pembegul Yildizedibepembegul@hotmail.com
643NoNo4th Oct 2022ASD/NDD/ADHD 1 ASD genetic / biomarkers /Chahnez TrikiElif Didinmez Taşkırdıedidinmez@hotmail.comNeurological Evaluation and Electroencephalographic Findings in Children with Autism DiagnosisElif Didinmez Taşkırdıedidinmez@hotmail.com
546NoNo5th Oct 2022SMAN ChrestianEli̇f Acar Arslanelifacararslan@gmail.comSpinal Muscular Atrophy with Two SMN2 Copies and Preserved Deep Tendon Reflexes: An Extremely Rare CaseEli̇f Acar Arslanelifacararslan@gmail.com
561NoNo5th Oct 2022SMAN ChrestianEli̇f Acar Arslanelifacararslan@gmail.comThe effect of Nusinersen and starting age on the improvement of motor performance in Spinal Muscular Atrophy (SMA): Preliminary resultsEli̇f Acar Arslanelifacararslan@gmail.com
571NoNo5th Oct 2022TreatmentF MuntoniEli̇f Acar Arslanelifacararslan@gmail.comInterobserver Reliability of the Turkish Translation of Timed Tests in Duchenne Muscular DystrophyEli̇f Acar Arslanelifacararslan@gmail.com
577NoNo6th Oct 2022Headache/Stroke 3"Mubeen Rafay Canada"Eli̇f Acar Arslanelifacararslan@gmail.comA Child with Cerebral Venous Thrombosis Secondary to COVID 19 Infection Successfully Treated with ThrombectomyEli̇f Acar Arslanelifacararslan@gmail.com
651NoNo4th Oct 2022Epilepsy: Semiology and ClinicalH CrossElif Karatoprakelifyuksel2001@yahoo.comEvaluation of Childhood Epilepsies with Frontal ParoxysmElif Karatoprakelifyuksel2001@yahoo.com
160NoNo4th Oct 2022"Epilepsy: Syndromes 1 – Self-limited EE/DEE-SWAS"C JoshiEmily Innesemily.innes@health.nsw.gov.auNeurodevelopmental outcomes and clinical utility of genetic testing in a cohort of Australian families with self-limited (familial) epilepsy (neonatal/infantile onset)Emily Innesemily.innes@health.nsw.gov.au
91NoNo6th Oct 2022Education"Jorge Vidaurre US"Emine Tekinemine.tekin@giresun.edu.trOnline paediatric EEG handbook: a survey on its usefulnessVeena Kanderveena.kander@uct.ac.za
512NoNo4th Oct 2022ASD/NDD/ADHD 3 NDD / IDCharuta JoshiEnise Avci Durmusalioglueniseavci.ea@gmail.comA Novel Candidate Gene For Neurodevelopmental Disorders: JKAMPEnise Avci Durmusalioglueniseavci.ea@gmail.com
141NoNo6th Oct 2022"Movement 2 Dystonia Parkinsons tremor and epidemiology""Jon Mink US"Esra Serdarogluesra.serdaroglu@gmail.comAn Investigation of the relationship between dystonia severity and functional independence and quality of life in children with dystonia: A Preliminary StudyKamile Uzun Akkayakuzun87@hotmail.com
134NoNo6th Oct 2022"Cerebral palsy 1- Evaluation: clinic neurophysiologic""Catherine Arnaud France"Esra Serdarogluesras@gazi.edu.trClinical characteristic of oropharyngeal dysphagia and swallowing safety in children with dystonia: a preliminary reportMuserrefe Nur Kelesmuserrefkeles19@gmail.com
569NoNo4th Oct 2022ASD/NDD/ADHD 3 NDD / IDCharuta JoshiElena Sukarova-angelovskaesukarova@doctor.comApplication of advanced molecular technologies in revealing the etiology of intellectual disability – clarification or more questionsElena Sukarova-angelovskaesukarova@doctor.com
556NoNo6th Oct 2022"Movement 2 Dystonia Parkinsons tremor and epidemiology""Jon Mink US"Eugenia Rozaeugenia.roza@umfcd.roNovel mutation variant in GCH1 gene - a new cause for infantile-onset severe dystonic encephalopathy?Eugenia Rozaeugenia.roza@umfcd.ro
590NoNo5th Oct 2022"İon channel myopathy and metabolic"R HorvathFatema Al Amranifatemaamrani@gmail.comMLIP-associated myopathy; report of a patient and review of the literatureFatema Al Amranifatemaamrani@gmail.com
780NoNo4th Oct 2022ASD/NDD/ADHD 3 NDD / IDCharuta JoshiFrancisco Carratalá-marcofcarratalamarco@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-marcofcarratalamarco@gmail.com
491NoNo5th Oct 2022Spasticity and ataxiaC CatsmanFaruk Incecikfincecik@yahoo.comHereditary spastic paraplegia type 26 with a novel mutation in B4GALNT1 gene and literature review of the clinical featuresFaruk Incecikfincecik@yahoo.com
492NoNo5th Oct 2022Spasticity and ataxiaC CatsmanFaruk Incecikfincecik@yahoo.comHomozygous mutation in CWF19L1 with recessive ataxia syndrome in a Turkish childFaruk Incecikfincecik@yahoo.com
288NoNo5th Oct 2022Neuromuscular 1H LochmüllerGamze Sarıkaya Uzangamzeuzan36@gmail.comPediatric Onset Chronic Inflammatory Demyelinating Polyneuropathy: A Multicenter Study from TürkiyeGamze Sarıkaya Uzangamzeuzan36@gmail.com
574NoNo6th Oct 2022"Movement 3 Ataxias opsoclonus myoclonus and covid 19 impact""Russell Dale Australia"Gautam Kamilagautamkamila7@gmail.comCLINICO-EPIDEMIOLOGICAL PROFILE OF CHILDREN WITH OPSOCLONUS MYOCLONUS ATAXIA SYNDROME: A DECADE’S EXPERIENCE FROM A TERTIARY CARE CENTRE IN NORTH INDIASheffali Gulatisheffaligulati1@gmail.com
633NoNo5th Oct 2022Neuroimmunology 3 Autoimmune encephalitis plusSilvia TenenbaumGautam Kamilagautamkamila7@gmail.comAnti-NMDA receptor encephalitis in children – tale of ten years at a tertiary care centerSheffali Gulatisheffaligulati1@gmail.com
456NoNo4th Oct 2022Epilepsy: Genetics 1S PerryHande Gazeteci Tekingazetecihande@yahoo.com.tr"Very rare novel DHDDS mutation of infant with severe mental-motor retardation resistant epilepsy movement disorder"Hande Gazeteci Tekingazetecihande@yahoo.com.tr
279NoNo5th Oct 2022Muscular dystrophyY NevoGokcen Oz Tuncergokcenoz@hotmail.comA Multicenter Retrospective Study in Turkish Children with Myotonic Dystrophy Type 1Gokcen Oz Tuncergokcenoz@hotmail.com
282NoNo5th Oct 2022"İon channel myopathy and metabolic"R HorvathGokcen Oz Tuncergokcenoz@hotmail.comClinical And Genetic Spectrum of Myotonia Congenita in Turkish ChildrenGokcen Oz Tuncergokcenoz@hotmail.com
482NoNo4th Oct 2022ASD/NDD/ADHD 3 NDD / IDCharuta JoshiHideyo Gomagoma@kyokyo-u.ac.jpDevelopmental trends and changes in children: Comparing assessment data of Japanese children from 1983 and 2020Hideyo Gomagoma@kyokyo-u.ac.jp
417NoNo4th Oct 2022Epilepsy: Genetics 1S PerryHyo Jeong Kimgreatelena@naver.comMissense variants in RHOBTB2 in a patient with developmental and epileptic encephalopathy and paroxysmal movement disorderHyo Jeong Kimgreatelena@naver.com
611NoNo5th Oct 2022Neuroimmunology 2 Antibody mediated disorders / monophasic demyel disorderBanu AnlarGülcan Akyüzgulcan.akyuz@hotmail.comA VERY YOUNG GİRL LİMBİC ENCEPHALİTİS WİTH LGI1 ANTİBODİESGülcan Akyüzgulcan.akyuz@hotmail.com
306NoNoPembe Gültutangultutanp@gmail.comAcute Cerebellit: Is it always benign?Pembe Gültutangultutanp@gmail.com
572NoNo4th Oct 2022Epilepsy: Status epilepticus and MiscellaneousT LoddenkemperPembe Gültutangultutanp@gmail.comPosterior Ocular Structure Parameters by Optical Coherence Tomography Angiography in Pediatric Epilepsy patientsPembe Gültutangultutanp@gmail.com
435NoNo5th Oct 2022General neurogenetics IIA R TavasoliGunce Basarirguncebasarir@gmail.comPhenotypic diversity of 15q11.2 copy number variants: a case series and review of the literatureNihal Olgac Dundarnodundar@gmail.com
144NoNo4th Oct 2022Epilepsy: Treatment 1 – ASMsB Sanchez-GanTimothy B Saurergw2022encoresubmissions@heliosmedcomms.comEfficacy and Safety of Cannabidiol Dose Adjustment in Patients with Lennox-Gastaut Syndrome in a Phase 3 Trial and Open-label ExtensionTimothy B Saurergw2022encoresubmissions@heliosmedcomms.com
541NoNo4th Oct 2022ASD/NDD/ADHD 1 ASD genetic / biomarkers /Chahnez TrikiWen-xiong Chengzchcwx@126.com"Parental age socioeconomic status and parity related with the clinical phenotypes in children with autism spectrum disorder"Wen-xiong Chengzchcwx@126.com
772NoNo5th Oct 2022Neuroimmunology 3 Autoimmune encephalitis plusSilvia TenenbaumHale Atalay Celikhale.atalay@gmail.comAnti-NMDA receptor encephalitis after Human Bocavirus infectionHale Atalay Celikhale.atalay@gmail.com
776NoNo5th Oct 2022"İon channel myopathy and metabolic"R HorvathHale Atalay Celi̇khale.atalay@gmail.comClinical Spectrum of Voltage-gated Sodium Channelopaties; One-center ExperienceHale Atalay Celi̇khale.atalay@gmail.com
77NoNo6th Oct 2022Cerebral palsy 2- Management; current and future"Antigone Papavasiliou Greece"Naja'atu Hamzahamzanajaatu@gmail.comHEALTH-RELATED QUALITY OF LIFE OF CHILDREN \WITH CEREBRAL PALSY AT A TERTIARY HOSPITAL IN NIGERIANaja'atu Hamzahamzanajaatu@gmail.com
119NoNo4th Oct 2022Epilepsy: Treatment 1 – ASMsB Sanchez-GanNaja'atu Hamzahamzanajaatu@gmail.comPyridoxine in Management of Super-Refractory Status Epilepticus: A Case ReportNaja'atu Hamzahamzanajaatu@gmail.com
250NoNo6th Oct 2022"Cerebral palsy 1- Evaluation: clinic neurophysiologic""Catherine Arnaud France"Hanan Azouzhananazouz@hotmail.comClinical and electophysiological evaluation of autonomic dysfunction in children with spastic cerebral palsyHanan Azouzhananazouz@hotmail.com
472NoNo6th Oct 2022Headache/Stroke 2"Mahendra MoharirCanada"Hanan Azouzhananazouz@hotmail.comCLINICAL PROFILE OF HEADACHE AMONG CHILDREN ATTENDING EMERGENCY DEPARTMENT AT ALEXANDRIA UNIVERSITY CHILDREN'S HOSPITALHanan Azouzhananazouz@hotmail.com
171NoNo5th Oct 2022Molecular geneticsT SultanHandan Kavahandankava@gmail.comEvaluation of the etiology of epilepsy and/or developmental delay in children with next generation sequencing: A single center experienceHandan Kavahandankava@gmail.com
458NoNo5th Oct 2022General neurogenetics IAR ZamaniHande Dilberhandecozeli@hotmail.comPROGRESSIVE MYOCLONIC EPILEPSY RELATED TO SEMA6B GENE MUTATIONHande Dilberhandecozeli@hotmail.com
616NoNo5th Oct 2022Molecular geneticsT SultanJiyoon Hanhanji024@naver.com"Bi-allelic POLR3A null variants cause autosomal recessive leukodystrophy hypomyelinating 7"Jiyoon Hanhanji024@naver.com
351NoNo6th Oct 2022Neuroradiology 2"Kshitij Mankand UK"Hans Hartmannhartmann.hans@mh-hannover.deCerebral microstructural changes in children suffering from hemolytic uremic syndromeHans Hartmannhartmann.hans@mh-hannover.de
386NoNo6th Oct 2022Headache/Stroke 3"Mubeen Rafay Canada"Hans Hartmannhartmann.hans@mh-hannover.deAnterior spinal artery syndrome due to fibrocartilaginous embolism – case report and treatment optionsHans Hartmannhartmann.hans@mh-hannover.de
407NoNo4th Oct 2022"Epilepsy: Syndromes 2 – IESS Dravet HHE EMAS"E WirrellHasan Tekgulhasan.tekgul@ege.edu.trElectro-clinic features and outcome in children with “pure” epilepsy with myoclonic atonic seizures (EMAS)Hasan Tekgulhasan.tekgul@ege.edu.tr
621NoNo4th Oct 2022Neonatal 1: Neonatal seizures and EEGHannah GlassHasan Tekgulhasan.tekgul@ege.edu.trThe clinical value of amplitude-integrated EEG for neonatal seizures: comparison of short-term (6-12 hours) and long-term (24-48 hours) monitoringHasan Tekgulhasan.tekgul@ege.edu.tr
734NoNo4th Oct 2022Neonatal 1: Neonatal seizures and EEGHannah GlassHasan Tekgulhasan.tekgul@ege.edu.trThe adaptability of health care professionals to the new neonatal seizure classification : ILAE-2020Seda Kanmazseda.kanmaz@ege.edu.tr
65NoNo5th Oct 2022Neuroimmunology 1 Demyelinating / MS relatedRussell DaleHayder Kadhim Jabbarhayderkadhim84@gmail.com"Neuromyelitis Optica Spectrum Disorder in a sample of children: Experience of Children Welfare Teaching Hospital Baghdad"Nebal Waill Saadinebalpedneu2013@gmail.com
562NoNo4th Oct 2022Epilepsy: Genetics 1S PerryHazem Eltoukhyhazemeltoukhy98@gmail.comSPTAN1 related epileptic encephalopathy- a case studyHazem Eltoukhyhazemeltoukhy98@gmail.com
331NoNo6th Oct 2022"Tuberous sclerosis Radiology"K AydınHepsen Mine Serinhepsenmine@yahoo.comClinical and molecular spectrum of tuberous sclerosis complex in a regional cohort: an efficacy and outcome study with antiseizure medication plus mTOR inhibitor therapyHepsen Mine Serinhepsenmine@yahoo.com
518NoNo5th Oct 2022SMAN ChrestianHoi Ning Hayley Iphnhayleyip@gmail.comThe impact of Nusinersen treatment on scoliosis progression in patients with Spinal Muscular AtrophyHoi Ning Hayley Iphnhayleyip@gmail.com
498NoNo4th Oct 2022Epilepsy: Treatment 2 – ASMsRamachandran NairHamit Özyürekhozyurekibu@hotmail.comTopiramate alters the erythrocyte osmotic fragility and whole blood viscosityAyşe Meltem Sevgilimsevgili@gazi.edu.tr
138NoNo5th Oct 2022Neuroimmunology 2 Antibody mediated disorders / monophasic demyel disorderBanu AnlarHuseyin Tanhtan@atauni.edu.trMyelin oligodendrocyte glycoprotein antibody-associated disorder due to COVID 19 infection: a child case reportHuseyin Tanhtan@atauni.edu.tr
322NoNo5th Oct 2022Neuromuscular 1H LochmüllerHuseyin Tanhtan@atauni.edu.trGuillain–Barre Syndrome due to COVID 19 in a child with acute lymphoblastic leukemia: a case reportHuseyin Tanhtan@atauni.edu.tr
275NoNo4th Oct 2022ASD/NDD/ADHD 3 NDD / IDCharuta JoshiHülya Maraş Gençhulyamaras@gmail.comClinical characteristics of children with neurodevelopmental delay and pathogenic copy number variations who underwent microarray analysisHülya Maraş Gençhulyamaras@gmail.com
460NoNo4th Oct 2022ASD/NDD/ADHD 4 ADHD and Behav / syndromes / LDPratibha SinghiHussein Abdeldayemhusseindayem@hotmail.comStudy of computerized cognitive training technique for treatment of children with attention deficit hyperactivity disorder. A new treatment modality experience.Hussein Abdeldayemhusseindayem@hotmail.com
79NoNo4th Oct 2022Epilepsy: Genetics 1S Perryİlknur Erolilknur_erol@yahoo.comCHEDDA syndrome associated with epileptic encephalopathy and hand stereotypiesİlknur Erolilknur_erol@yahoo.com
83NoNo5th Oct 2022General neurogenetics IIA R Tavasoliİlknıur Erolilknur_erol@yahoo.comA novel mutation in the RUNX2 gene; a rare cause of enlarged fontanelİlknıur Erolilknur_erol@yahoo.com
236NoNo5th Oct 2022General neurogenetics IIA R Tavasoliİlknur Erolilknur_erol@yahoo.comFirst case of Bohring-Opitz syndrome inherited from the fatherİlknur Erolilknur_erol@yahoo.com
237NoNo4th Oct 2022Epilepsy: Genetics 1S Perryİlknur Erolilknur_erol@yahoo.comFOXG1 gene related epileptic diskinetic encephalopathyYasemin Özkaledryaseminozkale@gmail.com
238NoNo6th Oct 2022Metabolic 1 Clinical phenotypes"Brahim Tabarki KSA"İlknur Erolilknur_erol@yahoo.comIntermediate severe Salla Disease in differential diagnosis of hypomyelinating leukodystrophy: the second and third case from Turkeyİlknur Erolilknur_erol@yahoo.com
405NoNo5th Oct 2022"İon channel myopathy and metabolic"R Horvathİlknur Erolilknur_erol@yahoo.comKetogenic diet for 134 cases of SCN1A related drug-resistant epilepsyJianxiang Liaoliaojianxiang@vip.sina.com
326NoNo4th Oct 2022Neonatal 1: Neonatal seizures and EEGHannah GlassIlknur Cankurtilknurcankurt@gmail.com"Neonatal Amplitude Integrated EEG (aEEG): Contribution to Clinical Etiologic and Prognosis"Ilknur Cankurtilknurcankurt@gmail.com
327NoNo4th Oct 2022"Epilepsy: Neuroimaging Surgery and Basic Science"C Akmanİlknur Cankurtilknurcankurt@gmail.comPRE-SURGERY PHASE 1 EVALUATION RESULTS AND CONTRIBUTION TO SURGERY IN PEDIATRIC PATIENTS WITH DRUG-RESISTANT EPILEPSYİlknur Cankurtilknurcankurt@gmail.com
366NoNo4th Oct 2022Epilepsy: Treatment 2 – ASMsRamachandran NairIlknur Cankurtilknurcankurt@gmail.comCOMPARISON OF CORTİCOSTEROİDS VERSUS CLOBAZAM TREATMENT OF EPİLEPTİC ENCEPHALOPATHY WİTH ELECTRİCAL STATUS EPİLEPTİCUS FOR ELECTROCLINICAL REMISSIONIlknur Cankurtilknurcankurt@gmail.com
75NoNo6th Oct 2022Education"Jorge Vidaurre US"Zeinab Koneinakone82@yahoo.frThe challenges of training in Child Neurology in West Africa countriesZeinab Koneinakone82@yahoo.fr
85NoNo6th Oct 2022Cerebral palsy 2- Management; current and future"Antigone Papavasiliou Greece"Indrasish Ray Chaudhuriindrasishraychaudhuri162@gmail.comAn unusual cause of torticollis in childhoodIndrasish Ray Chaudhuriindrasishraychaudhuri162@gmail.com
56NoNo4th Oct 2022ASD/NDD/ADHD 1 ASD genetic / biomarkers /Chahnez TrikiIngrid Teiningtein@sympatico.caIdentification of candidate genetic susceptibility variants in the carnitine (Cn) transporter and carnitine biosynthesis gene families in Autism Spectrum Disorder: A novel precision medicine targetIngrid Teiningtein@sympatico.ca
317NoNo6th Oct 2022Neuroradiology 1"Manohar Schroff Canada"Dasaratha Ramaiah Jinkajdashrath86@gmail.comClinico-Etiological Spectrum of Children with Bilateral Basal ganglia lesions: An Observational Study from A Tertiary Care CentreLokesh Lingappasiriloki@gmail.com
622NoNo5th Oct 2022Molecular geneticsT SultanJee Min Kimjee.raphaela.kim@gmail.comComplete Penetrance but Different Phenotypes in a Korean Family with Maternal Interstitial Duplication at 15q11.2-q13.1: A Case ReportJee Min Kimjee.raphaela.kim@gmail.com
551NoNo6th Oct 2022Neuroradiology 3"Ajay Taranath Australia"Jessica Ringshawjess.ringshaw@uct.ac.zaEffects of maternal and early-life anaemia on child brain development: a South African birth cohort studyJessica Ringshawjess.ringshaw@uct.ac.za
261NoNo4th Oct 2022"Epilepsy: Syndromes 2 – IESS Dravet HHE EMAS"E WirrellPeifang Jiangjiangpeifang@zju.edu.cnTreatments and Seizure Outcome of 327 Patients with Infantile Spasms: A Retrospective AnalysisPeifang Jiangjiangpeifang@zju.edu.cn
603NoNo4th Oct 2022Epilepsy: InvestigationsP MadaanJithangi Wanigasinghejithangi@gmail.comMaturation of the auditory evoke potentials with age: data from a pilot studyJithangi Wanigasinghejithangi@gmail.com
420NoNo4th Oct 2022Epilepsy: Genetics 3L LagaeLinjie JiangJJJLJ2020@163.comFeatures of a male with MACF1 mutation suffered from West syndrome：a case report and literature reviewLinjie JiangJJJLJ2020@163.com
200NoNo5th Oct 2022"CNS Malformations NGS"A NarayanJehan Suleimanjsuleiman10@gmail.comPosterior fossa malformations in TASP1-related disorder (Suleiman-El-Hattab Syndrome)Jehan Suleimanjsuleiman10@gmail.com
177NoNo6th Oct 2022Headache 1"Ken Mack US"Juliana Da Silva Cardosojulianapsilvacardoso@gmail.comPrimary headache with onset in childhood and adolescence: natural history and prognostic factors in a Portuguese populationJuliana Da Silva Cardosojulianapsilvacardoso@gmail.com
436NoNo4th Oct 2022ASD/NDD/ADHD 3 NDD / IDCharuta JoshiKarthika Ajit Valaparambilkarthikaajitv@gmail.comCLINICAL UTILITY OF NEXT GENERATION SEQUENCING IN NEURODEVELOPMENTAL DISORDERS —EXPERIENCE FROM A TERTIARY CARE CENTREKarthika Ajit Valaparambilkarthikaajitv@gmail.com
629NoNo4th Oct 2022Epilepsy: Outcomes and EpidemiologyE KijaBrahmini Korraikbrahmini49@gmail.comPredicting seizure recurrence risk in pediatric epilepsy patients who are seizure free and stopped Anti-Epileptic DrugsBrahmini Korraikbrahmini49@gmail.com
68NoNo6th Oct 2022"Cerebral palsy 1- Evaluation: clinic neurophysiologic""Catherine Arnaud France"Khaled Ashourkhaled3shour77@gmail.comEstablishment of High-Risk Infant Follow up Clinic for Implementation of Early Diagnosis of Cerebral Palsy GuidelinesKhaled Ashourkhaled3shour77@gmail.com
758NoNo4th Oct 2022Epilepsy: InvestigationsP MadaanKun-long Hungklhung@ms10.hinet.netNEXT GENERATION WHOLE EXOME SEQUENCING IN THE GENETIC DIAGNOSIS OF DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHYKun-long Hungklhung@ms10.hinet.net
481NoNo5th Oct 2022Neuroimmunology 2 Antibody mediated disorders / monophasic demyel disorderBanu AnlarKonika Bansalkonikabansal2@gmail.comClinico-radiological spectrum of MOG antibody associated disorder (MOGAD) in Pediatric population.Konika Bansalkonikabansal2@gmail.com
370NoNo5th Oct 2022SMAN ChrestianKatarzyna Kotulskakotulska.jozwiak@gmail.com"Safety tolerability and efficacy of widely available nusinersen program in children with Spinal Muscular Atrophy."Katarzyna Kotulskakotulska.jozwiak@gmail.com
502NoNo6th Oct 2022"Metabolic 5 Neurodegenerative diseases (NBIAs metabolic causes of stroke CDG NCLs NKH"Suvasini Sharma IndiaRoshan KoulKoulroshan@gmail.comEEG and ONSD in management of hepatic encephalopathy: additional role of EEG in prognosisRoshan KoulKoulroshan@gmail.com
769NoNo6th Oct 2022"Tuberous sclerosis Radiology"K AydınIchraf Kraouakraoua_ichraf@yahoo.frClinical and genetic study of leukodystrophies in Tunisian cohortThouraya Ben Younesbythouraya@yahoo.fr
477NoNo6th Oct 2022Education"Jorge Vidaurre US"Tina KrysiakKrysiakT@childrensdayton.orgTitle: Measuring Transition Readiness in Adolescents with Epilepsy: Opportunities and ChallengesTina KrysiakKrysiakT@childrensdayton.org
499NoNo4th Oct 2022Neonatal 1: Neonatal seizures and EEGHannah GlassFatma Kusgozkusgozfatma@gmail.comLevetiracetam as mono-and polytherapy in the treatment of neonatal-onset seizuresPinar Gencpinarpinargencpinar@gmail.com
530NoNo6th Oct 2022CNS Infections 1 Covid-related"Charles Newton Kenya"Young Jun Kokyjmillenium@naver.comChanges in the patient number of viral infections and febrile seizure before and after the COVID-19 pandemicSoo Ahn Chaekidbrain@cau.ac.kr
239NoNo5th Oct 2022"CNS Malformations NGS"A NarayanLeman Tekin Orgunlemantekin15@yahoo.comA pediatric case with primary familial brain calcification due to a homozygous variant on the JAM2 geneİlknur Erolilknur_erol@yahoo.com
246NoNo6th Oct 2022Metabolic 2 Mitochondrial disorders I : clinical phenotypes and tx"Rita Horvath UK"Leman Tekin Orgunlemantekin15@yahoo.comTwo siblings with combined oxidative phosphorylation defect 11 with a novel mutation in the RMND1 geneİlknur Erolilknur_erol@yahoo.com
766NoNo4th Oct 2022Epilepsy: Genetics 1S PerryLeman Tekin Orgunlemantekin15@yahoo.comPyridoxine Dependent Epilepsy with ALDH7A1 Mutation: Clinical Spectrum and Outcome in A Multicenter Study Cohort From TurkeyLeman Tekin Orgunlemantekin15@yahoo.com
404NoNo4th Oct 2022Epilepsy: Genetics 2N SpecchioXiao LiLexiecqmu@hotmail.comFocal cortical dysplasia type II related to a new pathogenic gene-RAB6BYuwu Jiangjiangyw@263.net
533NoNo5th Oct 2022Peripheral nerveD SelcenXiaomei Zhulisymei@126.comNusinersen safety and effects in children with spinal muscular atrophy: a single center experienceWenhui Liwenhuili@fudan.edu.cn
409NoNo5th Oct 2022Muscular dystrophyY NevoYi-dan Liuliuyidan322@163.comUniparental disomy unmasks a homozygous mutation of POMGNT1 in a case of muscle-eye-brain diseaseYi-dan Liuliuyidan322@163.com
147NoNo6th Oct 2022Metabolic 2 Mitochondrial disorders I : clinical phenotypes and tx"Rita Horvath UK"Asburce Olgacmabolgac@yahoo.comA case of mitochondrial depletion syndrome type 13 due to a FBXL4 variantAsburce Olgacmabolgac@yahoo.com
440NoNo4th Oct 2022"Epilepsy: DEEs TSC RETT and Comorbidities"Y JiangMadhavi Shelkemadhavishelke@yahoo.comGenetic spectrum of Developmental and Epileptic EncephalopathiesMadhavi Shelkemadhavishelke@yahoo.com
89NoNo6th Oct 2022Neuroradiology 1"Manohar Schroff Canada"Kanij Fatemamailmonami@gmail.comPediatric Moya Moya Disease: Clinical and Radio-Angiographic characteristics- A study from a Tertiary care center in BangladeshKanij Fatemamailmonami@gmail.com
98NoNo5th Oct 2022Genetics and epilepsy IW HakamiKanij Fatemamailmonami@gmail.comGene Panel Testing in children with Early Onset Epileptic Encephalopathies : A study in a Tertiary car center in BangladeshKanij Fatemamailmonami@gmail.com
464NoNo5th Oct 2022Neuroimmunology 2 Antibody mediated disorders / monophasic demyel disorderBanu AnlarMaria Shumilinamaria_shumilina@yahoo.comGAD antibody-spectrum disorders: case reportMaria Shumilinamaria_shumilina@yahoo.com
558NoNo6th Oct 2022Headache 1"Ken Mack US"Maria Vumaria.vu@sickkids.ca"Vascular Endothelial Dysfunction Cognition and Stroke in Early Life Study (VECSELS)"Maria Vumaria.vu@sickkids.ca
634NoNo5th Oct 2022"Neuropathy GBS and CMS"C BönnemannSibğatullah Ali Orakmaviihsan@gmail.comTwo Cases With Typical GBS And Rare GBS Variant Associated With Covid-19Sibğatullah Ali Orakmaviihsan@gmail.com
311NoNo5th Oct 2022General IIM SönmezWahedmawahed.rangpur@gmail.comPrematurity and Postnatal Neurological SequelaeWahedmawahed.rangpur@gmail.com
312NoNo6th Oct 2022"Cerebral palsy 1- Evaluation: clinic neurophysiologic""Catherine Arnaud France"Wahed Wahedmawahed.rangpur@gmail.comWasting Syndrome is a predictor of early death in Spastic Cerebral PalsyWahed Wahedmawahed.rangpur@gmail.com
62NoNo5th Oct 2022Neuromuscular 1H LochmüllerDuygu Yılmazmd.duyguyilmaz@gmail.comCongenital myotonic dystrophy: a retrospective study of a single centerHaluk Topalogluhtopalog@hacettepe.edu.tr
93NoNo6th Oct 2022Metabolic 3 Mitochondrial disorders II: Etiologies and mechanismsSaskia Wortmann NetherlandsAyse Yasemin Celikmdayasminc@gmail.com"Solving a puzzle: An infant with developmental delay epileptic spasms and petechiae"Ayse Yasemin Celikmdayasminc@gmail.com
70NoNo4th Oct 2022ASD/NDD/ADHD 1 ASD genetic / biomarkers /Chahnez TrikiNagwa Meguidmeguidna@yahoo.comEffect of oxidative stress and Glutathione on telomere length in a population of Egyptian autistic childrenNagwa Meguidmeguidna@yahoo.com
693NoNo6th Oct 2022Cerebral palsy 2- Management; current and future"Antigone Papavasiliou Greece"Mehmet Akif Kılıçmehmetakifkilic1@istanbul.edu.trRelationship between MRI patterns and refractory epilepsy in children with cerebral palsy: Cross-sectional study from a tertiary centerMehmet Akif Kılıçmehmetakifkilic1@istanbul.edu.tr
715NoNo6th Oct 2022Metabolic 3 Mitochondrial disorders II: Etiologies and mechanismsSaskia Wortmann NetherlandsMehmet Palazmehmetpalaz_md@hotmail.comVentricular septation on MRI could be diagnostic clue for PDH: Two case reportsMehmet Palazmehmetpalaz_md@hotmail.com
719NoNo6th Oct 2022Metabolic 3 Mitochondrial disorders II: Etiologies and mechanismsSaskia Wortmann NetherlandsMehmet Palazmehmetpalaz_md@hotmail.comCan leukodystrophy be reversible? a LTBL case reportMehmet Palazmehmetpalaz_md@hotmail.com
500NoNo5th Oct 2022Peripheral nerveD SelcenBiljana Mitrevskamitrevskabiljana@hotmail.comFunccional testing and rehabilitation of spinal muscular atrophy patientsBiljana Mitrevskamitrevskabiljana@hotmail.com
462NoNo4th Oct 2022ASD/NDD/ADHD 3 NDD / IDCharuta JoshiF. Müjgan Sonmezmjgsonmez@yahoo.comTRAPPC9-related intellectual disability: report of two new casesEyyüp Üçtepeeyupsvs@hotmail.com
161NoNo4th Oct 2022Epilepsy: Treatment 1 – ASMsB Sanchez-GanMohammad Barzegarmm_barzegar@yahoo.comThe efficacy of Everolimus onTSC associated drug resistant epilepsyMohammad Barzegarmm_barzegar@yahoo.com
638NoNo6th Oct 2022Education"Jorge Vidaurre US"Michael E. Msallmmsall@peds.bsd.uchicago.eduChildren’s Medical Home in China (CHMC) – Promoting Early Development of Chinese ChildrenMichael E. Msallmmsall@peds.bsd.uchicago.edu
272NoNo5th Oct 2022Spasticity and ataxiaC CatsmanMuhammad Mahajnahmohamedm@hymc.gov.ilThe neuronal ceroid lipofuscinoses type 8 (CLN8) gene mutations: A new compound heterozygous case and the protein's bioinformatic analysesMuhammad Mahajnahmohamedm@hymc.gov.il
539NoNo6th Oct 2022Headache/Stroke 2"Mahendra MoharirCanada"Moran Hausman-kedemmoranhk@gmail.comSleep-related difficulties and decreased sleep quality among adolescents with idiopathic intracranial hypertensionMoran Hausman-kedemmoranhk@gmail.com
754NoNo4th Oct 2022Epilepsy: Status epilepticus and MiscellaneousT LoddenkemperMüge Ayanoğlumugeayanoglu_05@hotmail.comAssessment of the knowledge level of physicians regarding the management of acute seizures in children and adolescentsMüge Ayanoğlumugeayanoglu_05@hotmail.com
307NoNo5th Oct 2022Muscular dystrophyY NevoBakhytkul Myrzaliyevamyrzaliyeva@gmail.com"Diagnostics clinical and genetic characteristics of Duchenne muscular dystrophy in Kazakhstan"Bakhytkul Myrzaliyevamyrzaliyeva@gmail.com
771NoNo4th Oct 2022ASD/NDD/ADHD 2 ASD assessments / management / Rett syndrome / high risk infantsAntigone PapavasiliouNaama Yosha-orpaznaamaorpaz@gmail.comA Protocol for Evaluation and Treatment of Children with Autistic/Psychotic RegressionNaama Yosha-orpaznaamaorpaz@gmail.com
537NoNo6th Oct 2022Cerebral palsy 2- Management; current and future"Antigone Papavasiliou Greece"Zhao-qing Linnaeun.tw@gmail.com"Erythropoietin for Hypoxic-Ischemic Encephalopathy: A Follow up Study in New Taipei City Taiwan"Zhao-qing Linnaeun.tw@gmail.com
617NoNo4th Oct 2022Epilepsy: Semiology and ClinicalH CrossEiji Nakagawanakagawa@ncnp.go.jpEvaluation of periodic slow head nodding seizureEiji Nakagawanakagawa@ncnp.go.jp
270NoNo6th Oct 2022"Cerebral palsy 1- Evaluation: clinic neurophysiologic""Catherine Arnaud France"Nargiz Aliyevanargis.asadova@gmail.comGeneral Movements Assessment in Term Newborns with Moderate HyperbilirubinemiaNargiz Aliyevanargis.asadova@gmail.com
470NoNo6th Oct 2022Neuroradiology 2"Kshitij Mankand UK"Natalia BroninaNata-dim@mail.ruPosterior reversible encephalopathy syndrome in children with malignancesNatalia BroninaNata-dim@mail.ru
348NoNo4th Oct 2022Epilepsy: Genetics 2N SpecchioNuriye Ayca Gulnaycagul@gmail.comCase report: Potassium sodium-activated channel subfamily T member 1 gene mutation related epilepsy.Nuriye Ayca Gulnaycagul@gmail.com
310NoNo5th Oct 2022Muscular dystrophyY NevoNidheesh ChencheriNCChencheri@ajch.aeClinical Experience of gene replacement therapy in children with Spinal Muscular Atrophy: A single center retrospective study of 25 childrenNidheesh ChencheriNCChencheri@ajch.ae
64NoNo4th Oct 2022Epilepsy: InvestigationsP MadaanNebal Waill Saadinebalpedneu2013@gmail.comSeroprevalence of Anti- N-methyl-D-aspartate receptor antibodies in children with seizures of unknown causeNebal Waill Saadinebalpedneu2013@gmail.com
289NoNo5th Oct 2022Neuroimmunology 2 Antibody mediated disorders / monophasic demyel disorderBanu AnlarNefise Arıbaş Öznefisearibas@hotmail.comA Rare Complication of COVID-19 in a Pediatric Patient; Acute Transverse MyelitisNefise Arıbaş Öznefisearibas@hotmail.com
578NoNo5th Oct 2022Genetics and epilepsy IIRamachandran NairNeil Atkinsonneil.atkinson@nhs.netClinical and genetic features of acute deterioration with resulting neurological regression in children with Dravet SyndromeNeil Atkinsonneil.atkinson@nhs.net
415NoNoNezir Özgünnezirozgun@hotmail.com12-Year Surveillance Results of Acute Flask Paralysis Cases in Southeast Turkey and the Effect of Refugee Movements on Surveillance ResultsNezir Özgünnezirozgun@hotmail.com
596NoNo6th Oct 2022"Metabolic 5 Neurodegenerative diseases (NBIAs metabolic causes of stroke CDG NCLs NKH"Suvasini Sharma IndiaNicolas Abreunicolas.abreu@nyulangone.orgClarifying missense variants of uncertain significance in CLN6 Batten disease through the use of skin biopsy – a case reportNicolas Abreunicolas.abreu@nyulangone.org
188NoNo5th Oct 2022Neuroimmunology 1 Demyelinating / MS relatedRussell DaleNihal Yıldıznihalyildiz661@gmail.comEvaluation of the Risk Factors for Developing Demyelinating Disease after Optic Neuritis in Children: A Single Center ExperienceSevim Şahinsevimsahin1@yahoo.com
354NoNo6th Oct 2022"Tuberous sclerosis Radiology"K AydınNihal Yıldıznihalyildiz661@gmail.comKetogenic Diet Therapy for Drug-resistant Epilepsy and Cognitive Impairment in Children with Tuberous Sclerosis ComplexJianxiang Liaoliaojianxiang@vip.sina.com
687NoNo5th Oct 2022Neuroimmunology 1 Demyelinating / MS relatedRussell DaleNihal Yıldıznihalyildiz661@gmail.comEffects of Oleuropein on Systemic Lipopolysaccharide-Induced Neuroinflammation in RatsSevim Şahinsevimsahin1@yahoo.com
563NoNo5th Oct 2022Neuroimmunology 1 Demyelinating / MS relatedRussell DaleNisreen Badernisreen_bader2006@hotmail.comSuccessful management of Pediatric-onset Multiple sclerosis with OcrelizumabNisreen Badernisreen_bader2006@hotmail.com
226NoNo5th Oct 2022"İon channel myopathy and metabolic"R HorvathNouha Bouayed Abdelmoulanouha_abdelmoulabouayed@yahoo.frMyotonia congenita associated to multiple sclerosis in a Tunisian familyNouha Bouayed Abdelmoulanouha_abdelmoulabouayed@yahoo.fr
228NoNo5th Oct 2022"Neuropathy GBS and CMS"C BönnemannNouha Bouayed Abdelmoulanouha_abdelmoulabouayed@yahoo.frPreconceptional diagnosis for giant axonal neuropathy before wedding engagement decisionNouha Bouayed Abdelmoulanouha_abdelmoulabouayed@yahoo.fr
664NoNo5th Oct 2022Neuromuscular 1H LochmüllerNurşah Yeniay Sütnursah_ny@hotmail.comA rare manifestation of pediatric CIDP: hypoglossal nerve involvementNurşah Yeniay Sütnursah_ny@hotmail.com
90NoNo4th Oct 2022Epilepsy: Outcomes and EpidemiologyE KijaAmarachukwu Okaforokaforamara2@gmail.comPredisposing factors to childhood Epilepsy at the Federal Medical Centre Umuahia NigeriaAmarachukwu Okaforokaforamara2@gmail.com
722NoNoOlgay Bildikolgaybildik@hotmail.comThe Rare Central Nervous System Findings in Pediatric SARS-COV-2 PatientsOlgay Bildikolgaybildik@hotmail.com
352NoNo5th Oct 2022Neuroimmunology 3 Autoimmune encephalitis plusSilvia TenenbaumLiu Liuosier0615xw@zju.edu.cnPaediatric anti-gamma aminobutyric acid-B receptor encephalitis with benign prognosisFeng Gaoepilepsy@zju.edu.cn
428NoNo5th Oct 2022Genetics and epilepsy IIRamachandran NairLiu Liuosier0615xw@zju.edu.cnClinical and genetic characteristics of PCDH19-related epilepsy syndromes：differences between East-Asians and European-AmericansFeng Gaoepilepsy@zju.edu.cn
424NoNo5th Oct 2022Muscular dystrophyY NevoÖzgen Hürozgenozyazicioglu@yahoo.com"A rare phenotype of congenital muscular dystrophy: 'Muscular dystrophy-dystroglycanopathy type B1'"Özgen Hürozgenozyazicioglu@yahoo.com
513NoNo6th Oct 2022"Movement 3 Ataxias opsoclonus myoclonus and covid 19 impact""Russell Dale Australia"Özge Tanıdır Artanozgetanidir@hotmail.comAtaxia oculomotor apraxia type 4 due to a pathogenic variant in PNKP geneÖzge Tanıdır Artanozgetanidir@hotmail.com
557NoNo4th Oct 2022"Epilepsy: Syndromes 1 – Self-limited EE/DEE-SWAS"C JoshiÖzge Tanıdır Artanozgetanidir@hotmail.comHeart Rate Variability in Childhood Benign Rolandic EpilepsyÖzge Tanıdır Artanozgetanidir@hotmail.com
221NoNo5th Oct 2022Neuroimmunology 3 Autoimmune encephalitis plusSilvia TenenbaumMerve Öztürkozturk_merve@hotmail.comEfficacy of Rituximab Treatment in Rasmussen’s EncephalitisMerve Öztürkozturk_merve@hotmail.com
222NoNo4th Oct 2022Epilepsy: Status epilepticus and MiscellaneousT LoddenkemperMerve Öztürkozturk_merve@hotmail.comLeuprolide Acetate Induced Non-convulsive Status Epilepticus: Case ReportMerve Öztürkozturk_merve@hotmail.com
80NoNo5th Oct 2022General IJ VajsarElif Perihan Öncelperi_elif@hotmail.comA case of CAV3 caveolinopathy / channelopathy with familial absence epilepsy and distal myoneuronopathy extending the clinical spectrumElif Perihan Öncelperi_elif@hotmail.com
81NoNo5th Oct 2022General IJ VajsarElif Perihan Öncelperi_elif@hotmail.comThe first Turkish case with early-juvenile-onset recessive distal titinopathy and the first case with prominent neurogenic involvementElif Perihan Öncelperi_elif@hotmail.com
82NoNo5th Oct 2022General IJ VajsarElif Perihan Öncelperi_elif@hotmail.comFirst Turkish case with MICU1 mutation-related myopathy and extrapyramidal findingsElif Perihan Öncelperi_elif@hotmail.com
291NoNo6th Oct 2022"Movement 2 Dystonia Parkinsons tremor and epidemiology""Jon Mink US"Elif Perihan Öncelperi_elif@hotmail.comA novel combined heterozygous mutation in the PLA2G6 gene associated with early-onset Parkinson’s diseaseŞeyda Beşenseydabesen2000@gmail.com
353NoNo6th Oct 2022Metabolic 6 Defects of bioenergetic and intermediary metabIngrid Tein CanadaElif Perihan Öncelperi_elif@hotmail.comSLC2A1 mutations associated Glucose Transport Type 1 Deficiency Syndrome: A Single Center Case SeriesElif Perihan Öncelperi_elif@hotmail.com
583NoNo5th Oct 2022Genetics and epilepsy IIRamachandran NairElif Perihan Öncelperi_elif@hotmail.comFirst Turkish case with UNC80 deficiencyİlknur Erolilknur_erol@yahooo.com
759NoNo5th Oct 2022Genetics and epilepsy IIRamachandran NairElif Perihan Öncelperi_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 Öncelperi_elif@hotmail.com
752NoNo4th Oct 2022Epilepsy: Genetics 1S PerryEbru Arhanpetekarhan@yahoo.com.trWhole Exome Sequencing Results of 101 Epilepsy-Related PatientsEmriye Ferda Perçinferdaep@yahoo.com
86NoNo6th Oct 2022"Movement 3 Ataxias opsoclonus myoclonus and covid 19 impact""Russell Dale Australia"Pinar Yavuzpinaryavuz@hacettepe.edu.trNeurological and immunological phenotypes in Ataxia TelangiectasiaPinar Yavuzpinaryavuz@hacettepe.edu.tr
738NoNo4th Oct 2022Neonatal 2: Neonatal neurology – otherLakshmiPrajakta Ghatageprajaktaghatage38@gmail.comTo study the most efficacious drug combination for drug resistant NHBI cases.Prajakta Ghatageprajaktaghatage38@gmail.com
503NoNo6th Oct 2022"Metabolic 5 Neurodegenerative diseases (NBIAs metabolic causes of stroke CDG NCLs NKH"Suvasini Sharma IndiaPrashant Utageprashant.utage1@gmail.comCongenital disorder of glycosylation : clinical case study of patients harboring pathogenic mutations in phosphomannomutase 2 gene (PMM2-CDG)Umesh Umesh Bhammarkardr_umeshbh@yahoo.co.in
163NoNo5th Oct 2022TreatmentF MuntoniPanayiota Trifillisptrifillis@ptcbio.comComparison of timed function test results in nmDMD patients receiving ataluren: STRIDE Registry vs phase 3 clinical trialPanayiota Trifillisptrifillis@ptcbio.com
164NoNo5th Oct 2022TreatmentF MuntoniPanayiota Trifillisptrifillis@ptcbio.comComparing the change in 6-minute walk distance in nmDMD patients receiving ataluren: STRIDE Registry compared with phase 3 clinical trialPanayiota Trifillisptrifillis@ptcbio.com
170NoNo5th Oct 2022TreatmentF MuntoniPanayiota Trifillisptrifillis@ptcbio.comComparison of North Star Ambulatory Assessment score change in nmDMD patients receiving ataluren: STRIDE Registry vs phase 3 clinical trialPanayiota Trifillisptrifillis@ptcbio.com
300NoNo6th Oct 2022"Movement 1 Chorea dyskinesias tremor spasms & tx""Biju Hameed UK"Qiao Huqiaohu1989@163.comEarly-onset spontaneously relieved spasms of infancy in sleep: electroclinical characteristics and differential diagnosesShuang Liaoshuangliao20211123@163.com
418NoNo4th Oct 2022Neonatal 1: Neonatal seizures and EEGHannah GlassŞeyda Beşenrameshkonanki@gmail.comNeonatal-onset epilepsy: Clinico-etiological spectrum and developmental outcomesPrasanthi Aripiralamimu2010@gmail.com
444NoNo5th Oct 2022SMAN ChrestianRamesh Konankirameshkonanki@gmail.comSpinal muscular atrophy with lower extremity-predominant (SMA-LED)Ramesh Konankirameshkonanki@gmail.com
469NoNo6th Oct 2022Education"Jorge Vidaurre US"Ryan Sauerrasa238@uky.eduMaking it Home on Time: Improving Child Neurology Inpatient Discharge TimingRyan Sauerrasa238@uky.edu
283NoNo4th Oct 2022Neonatal 1: Neonatal seizures and EEGHannah GlassRecep Kamil Kilicrecepkamil09@hotmail.comNEONATAL EEG: IMPORTANCE AND UTILITY IN DIFFERANTIAL DIAGNOSIS and PROGNOSISRecep Kamil Kilicrecepkamil09@hotmail.com
373NoNo4th Oct 2022Neonatal 2: Neonatal neurology – otherLakshmiRecep Kamil Kilicrecepkamil09@hotmail.comTHE RELATİONSHİP BETWEEN FİRST TRİMESTER MATERNAL SERUM PAPP-A LEVEL AND POSTNATAL NEUROLOGİCAL DEVELOPMENT LEVELRecep Kamil Kilicrecepkamil09@hotmail.com
654NoNo5th Oct 2022"Neuropathy GBS and CMS"C BönnemannRecep Kamil Kilicrecepkamil09@hotmail.comPERONEAL NERVE PALSY DUE TO OSTEOCHONDROMA OF THE FİBULAR HEAD: A RARE CAUSE OF FOOT DROPRecep Kamil Kilicrecepkamil09@hotmail.com
655NoNoRecep Kamil Kilicrecepkamil09@hotmail.comCOVID-19 RELATED ADEM AND LONGITUDINAL EXTENSIVE TRANSVERSE MYELITIS WITH ACUTE ADENOVIRUS CO-INFECTION IN A NINE-YEAR-OLD CHILDRecep Kamil Kilicrecepkamil09@hotmail.com
116NoNo6th Oct 2022Neuroradiology 1"Manohar Schroff Canada"Robert Hendesonrobert.henderson2@health.wa.gov.auA Pictorial Review of Paediatric Histiocytic Disorders in the Head and NeckRobert Hendesonrobert.henderson2@health.wa.gov.au
536NoNo4th Oct 2022Epilepsy: Treatment 2 – ASMsRamachandran NairSait Aciksaitopen@yahoo.com"Clobazam Experience in Childhood Epilepsy from a Tertiary Center Turkey"Sait Aciksaitopen@yahoo.com
661NoNo5th Oct 2022General IIM SönmezSaleel Ramesh Chandratresaleel.chandratre@gmail.comERCC5 novel missense mutation causing developmental delay and spasticitySaleel Ramesh Chandratresaleel.chandratre@gmail.com
256NoNo6th Oct 2022Metabolic 4 Therapeutic approachesSamantha Marin CanadaSalih Akbaşsalihakbas89@gmail.comEfficacy and Safety of Cerliponase Alpha Therapy in Neuronal Ceroid Lipofuscinosis Type 2Salih Akbaşsalihakbas89@gmail.com
257NoNo4th Oct 2022Epilepsy: Semiology and ClinicalH CrossSalih Akbaşsalihakbas89@gmail.com"Childhood Frontal Lobe Epilepsies: Etiology Classification and EEG Findings"Salih Akbaşsalihakbas89@gmail.com
777NoNo5th Oct 2022Peripheral nerveD SelcenSalih Akbaşsalihakbas89@gmail.comPRIDOSTIGMIN TREATMENT IN X-LINKED MYOTBULAR MYOPATHYSalih Akbaşsalihakbas89@gmail.com
442NoNo4th Oct 2022Epilepsy: Semiology and ClinicalH CrossSanem Yilmazsanem.yilmaz@ege.edu.trIntractable epilepsy due to cerebellar ganglioneural hamartoma: Evidence for seizures originating from cerebellumSanem Yilmazsanem.yilmaz@ege.edu.tr
157NoNo5th Oct 2022General IIM SönmezSarafroz Fayzullaevasarafrozerkinova@gmail.comLinear scleroderma as one of the manifestations of collagenosisSarafroz Fayzullaevasarafrozerkinova@gmail.com
330NoNo6th Oct 2022Metabolic 6 Defects of bioenergetic and intermediary metabIngrid Tein CanadaEsra Sarigecilisarigeciliesra@gmail.comA RARE GLUT 1 DEFICIENCY SYNDROME PRESENTING WITH SPEECH DELAYEsra Sarigecilisarigeciliesra@gmail.com
657NoNo4th Oct 2022ASD/NDD/ADHD 4 ADHD and Behav / syndromes / LDPratibha SinghiSaurodip Maitysaurodipcmc@gmail.comSTUDY TO DETERMINE SENSORY PROCESSING DYSFUNCTION IN CHILDREN WITH ATTENTION DEFICIT HYPERACTIVITY DISORDERSaurodip Maitysaurodipcmc@gmail.com
295NoNo4th Oct 2022ASD/NDD/ADHD 2 ASD assessments / management / Rett syndrome / high risk infantsAntigone PapavasiliouSelin Akyüz Oktayselinakyuz93@gmail.com"Evaluation of Psychomotor Behavioral and Sensory Development in Hypoxic Ischemic Encephalopathy Patients"Selin Akyüz Oktayselinakyuz93@gmail.com
61NoNo5th Oct 2022Neuroimmunology 1 Demyelinating / MS relatedRussell DaleSemra Saygisemra_saygi@yahoo.comHigh-efficacy treatment for aggressive pediatric Multiple SclerosisMaria ShumilinaMARIA_SHUMILINA@YAHOO.COM
602NoNo6th Oct 2022CNS Infections 1 Covid-related"Charles Newton Kenya"Semra Saygisemra_saygi@yahoo.comCOVID-19-associated Retrobulbar Neuritis In A ChildSemra Saygisemra_saygi@yahoo.com
614NoNo4th Oct 2022Epilepsy: Semiology and ClinicalH CrossSemra Saygisemra_saygi@yahoo.comVermian dysplasia and lipoma in a child with headache and epileptic seizureSenay Demirdrsenaydemir@hotmail.com
615NoNo6th Oct 2022Neuroradiology 3"Ajay Taranath Australia"Semra Saygisemra_saygi@yahoo.comPosterior periventricular extensive diffusion restriction in a 17 years old boy after cardiopulmonary resuscitationSenay Demirdrsenaydemir@hotmail.com
639NoNo5th Oct 2022Neuroimmunology 1 Demyelinating / MS relatedRussell DaleSemra Saygisemra_saygi@yahoo.comOptic Neuritis And Pseudotumor Cerebri Co-Existence İn A Patient With A Recent COVID-19 InfectionSemra Saygisemra_saygi@yahoo.com
642NoNo6th Oct 2022Metabolic 1 Clinical phenotypes"Brahim Tabarki KSA"Semra Saygisemra_saygi@yahoo.comA Rare Case Of Mucopolysaccharidosis Type VI (Maroteaux–Lamy Syndrome)Semra Saygisemra_saygi@yahoo.com
645NoNo5th Oct 2022"Neuropathy GBS and CMS"C BönnemannSemra Saygisemra_saygi@yahoo.comFacial Nerve Venous Malformation Presenting As Bell's PalsySemra Saygisemra_saygi@yahoo.com
142NoNo4th Oct 2022Epilepsy: Genetics 2N SpecchioSenem Aycasenemkaleci85@gmail.comEarly infantile epileptic encephalopathy (Ohtahara Syndrome): A case report with STXBP1 mutationSenem Aycasenemkaleci85@gmail.com
178NoNo5th Oct 2022Spasticity and ataxiaC CatsmanSenem Ayçasenemkaleci85@gmail.com"A case of a ADPRHL2 Mutation; Neurodegeneration with Developmental Delay Ataxia and Axonal Neuropathy"Senem Ayçasenemkaleci85@gmail.com
640NoNo5th Oct 2022Muscular dystrophyY NevoSenem Ayçasenemkaleci85@gmail.comA case of Emery Dreifuss Muscular Dystrophy with SYNE1 and SYNE2 mutations and white matter involvementSenem Ayçasenemkaleci85@gmail.com
264NoNo6th Oct 2022"Movement 1 Chorea dyskinesias tremor spasms & tx""Biju Hameed UK"Seren Aydinserenaydin5228@gmail.comHereditary Spastic Paraparesis Type 55: A Case ReportSeren Aydinserenaydin5228@gmail.com
113NoNo4th Oct 2022Epilepsy: Semiology and ClinicalH CrossSevgi Yimenicioglusevgifahri@yahoo.comOpercular syndrome due to Herpes EncephalitisSevgi Yimenicioglusevgifahri@yahoo.com
84NoNo5th Oct 2022Spasticity and ataxiaC CatsmanŞeyda Beşenseydabesen2000@gmail.comThe first case of spastic ataxia type 4 associated with heterozygous mutations in MTPAP geneİlknur Erolilknur_erol@yahoo.com
240NoNo5th Oct 2022General neurogenetics IIA R TavasoliŞeyda Beşenseydabesen2000@gmail.comThe First Turkish case with HIVEP2-related intellectual disabilityİlknur Erolilknur_erol@yahoo.com
244NoNo5th Oct 2022General neurogenetics IIA R TavasoliŞeyda Beşenseydabesen2000@gmail.comIs pyridoxine effective in the treatment of hyperphosphatasia with mental retardation syndrome type 4: Single center experienceŞeyda Beşenseydabesen2000@gmail.com
245NoNo5th Oct 2022General neurogenetics IIA R TavasoliŞeyda Beşenseydabesen2000@gmail.comThe first siblings with TRAPPC6B mutationİlknur Erolilknur_erol@yahoo.com
247NoNo5th Oct 2022General neurogenetics IIA R TavasoliŞeyda Beşenseydabesen2000@gmail.comTwo Turkish siblings with intellectual disability associated with TUSC3 mutationİlknur Erolilknur_erol@yahoo.com
765NoNo5th Oct 2022Spasticity and ataxiaC CatsmanŞeyda Beşenseydabesen2000@gmail.comChildren with genetically confirmed Hereditary Spastic Paraplegia (HSP): A case series from Eastern Mediterranean Region of TurkeyŞeyda Beşenseydabesen2000@gmail.com
507NoNo4th Oct 2022ASD/NDD/ADHD 4 ADHD and Behav / syndromes / LDPratibha SinghiSheffali Gulatisheffaligulati@gmail.comSpectrum of co-morbidities and psychopathology in children with Attention-deficit hyperactivity disorder (ADHD): A retrospective studySheffali Gulatisheffaligulati@gmail.com
534NoNo4th Oct 2022ASD/NDD/ADHD 4 ADHD and Behav / syndromes / LDPratibha SinghiSheffali Gulatisheffaligulati@gmail.comThe spectrum of specific learning disability and associated co-morbidities in children at a tertiary care center: A retrospective study.Sheffali Gulatisheffaligulati@gmail.com
568NoNo4th Oct 2022ASD/NDD/ADHD 1 ASD genetic / biomarkers /Chahnez TrikiSheffali Gulatisheffaligulati@gmail.comThe Spectrum of Co-morbidities in children with ASD (Autism Spectrum Disorder): a retrospective studySheffali Gulatisheffaligulati@gmail.com
580NoNo4th Oct 2022ASD/NDD/ADHD 1 ASD genetic / biomarkers /Chahnez TrikiSheffali Gulatisheffaligulati@gmail.comBiomarkers in children with Autism: A case control StudySheffali Gulatisheffaligulati@gmail.com
529NoNoSheffali Gulatisheffaligulati1@gmail.comClinico-etiological profile of Acute Encephalitic syndrome from Northern IndiaSheffali Gulatisheffaligulati1@gmail.com
542NoNo4th Oct 2022Epilepsy: Treatment 3 – ASM/ Dietary TreatmentsJ SahuSheffali Gulatisheffaligulati1@gmail.comChildren with Tuberous Sclerosis Complex (TSC) on Ketogenic diet therapies: Outcome of a retrospective cohortSheffali Gulatisheffaligulati1@gmail.com
560NoNo4th Oct 2022Epilepsy: Treatment 3 – ASM/ Dietary TreatmentsJ SahuSheffali Gulatisheffaligulati1@gmail.comEfficacy of Ketogenic Diet therapies in Lennox Gastaut Syndrome: A Prospective Cohort StudySheffali Gulatisheffaligulati1@gmail.com
647NoNo5th Oct 2022Peripheral nerveD SelcenSheffali Gulatisheffaligulati1@gmail.comSpinal Muscular Atrophy - Emerging therapies: Experience from a tertiary care hospitalSheffali Gulatisheffaligulati1@gmail.com
756NoNo6th Oct 2022Headache/Stroke 3"Mubeen Rafay Canada"Shikha Jainshikha.5dec@gmail.commineralising angiopathy presenting as strokeShikha Jainshikha.5dec@gmail.com
764NoNo6th Oct 2022Neuroradiology 1"Manohar Schroff Canada"Shikha Jainshikha.5dec@gmail.comclinical and radiological profile of focal cortical dysplasia in childrenShikha Jainshikha.5dec@gmail.com
540NoNoShreya Gandhishreyagandhi317@gmail.comNeuro-tuberculosis in COVID: Our experienceShreya Gandhishreyagandhi317@gmail.com
504NoNo6th Oct 2022Neuroradiology 2"Kshitij Mankand UK"Shubham Kaudinyashubham.kaudinya@gmail.comNeurological manifestations of lympho-haematopoietic malignanciesShubham Kaudinyashubham.kaudinya@gmail.com
509NoNo5th Oct 2022Neuroimmunology 2 Antibody mediated disorders / monophasic demyel disorderBanu AnlarShubham Kaudinyashubham.kaudinya@gmail.comRISING SURGE OF SUBACUTE SCLEROSING PANENCEPHALITIS IN PANDEMIC ERAShubham Kaudinyashubham.kaudinya@gmail.com
510NoNo5th Oct 2022Neuroimmunology 3 Autoimmune encephalitis plusSilvia TenenbaumShubham Kaudinyashubham.kaudinya@gmail.comCLINICAL PROFILE OF AUTOIMMUNE ENCEPHALITIS IN WESTERN INDIAShubham Kaudinyashubham.kaudinya@gmail.com
140NoNo5th Oct 2022Muscular dystrophyY NevoSiddharth Shahsidh909@hotmail.comA Novel Founder Mutation in the SGCB Gene Causes Severe Form of Limb Girdle Muscular Dystrophy (LGMD) 2E in Sathwara CommunitySiddharth Shahsidh909@hotmail.com
549NoNo6th Oct 2022"Cerebral palsy 1- Evaluation: clinic neurophysiologic""Catherine Arnaud France"Siddharth Shahsidh909@hotmail.comA Retrospective Case Series of Indian Children With Homozygous RNASEH2B Mutations Presenting As ‘Cerebral Palsy’ MimicSiddharth Shahsidh909@hotmail.com
528NoNo6th Oct 2022"Movement 3 Ataxias opsoclonus myoclonus and covid 19 impact""Russell Dale Australia"Sihem Ben Nsirsihambn@yahoo.frHereditary cerebellar ataxias: descriptive study of a hospital cohortSihem Ben Nsirsihambn@yahoo.fr
559NoNo6th Oct 2022Neuroradiology 1"Manohar Schroff Canada"Sindhura Psindhupappula84@gmail.comCLINICAL PROFILE OF CONGENITAL MALFORMATIONS OF NERVOUS SYSTEM - IS IT STILL AN ICEBERG???Sindhura Psindhupappula84@gmail.com
495NoNo4th Oct 2022Epilepsy: Treatment 2 – ASMsRamachandran NairLokesh Lingappasiriloki@gmail.comPermampenel in Refractory Epilepsy - Investigator initiated studyLokesh Lingappasiriloki@gmail.com
579NoNo4th Oct 2022ASD/NDD/ADHD 3 NDD / IDCharuta JoshiAleya Remtullasisaleya@gmail.comNeuroimaging for children with Neurodevelopmental Disorders (NDDs) in the African PopulationAleya Remtullasisaleya@gmail.com
432NoNo5th Oct 2022SMAN ChrestianSophelia Hoi-shan Chansophehs@hku.hkBone Health in Children with Spinal Muscular AtrophyJoanna Yuet-ling Tungtyl404@ha.org.hk
371NoNo5th Oct 2022Muscular dystrophyY NevoDidem Soydemirsoydemirdidem8@gmail.comGENETIC LANDSCAPE OF CONGENITAL MUSCULAR DYSTROPHIES(CMD) FROM CENTRAL AEGEAN PART OF TURKEYDidem Soydemirsoydemirdidem8@gmail.com
241NoNo5th Oct 2022General IJ VajsarSerkan Kiriksrknkrk@hotmail.comCLINICAL FEATURES OF PEDIATRIC ACUTE RHABDOMYOLYSISSerkan Kiriksrknkrk@hotmail.com
374NoNo5th Oct 2022Neurogenetics practiceT Lerman-SagieSergio Rosembergsrosem@uol.com.brProgressive encephalopathy due to SLC1A4 mutations in two non Ashkenazi Brazilian siblings.Sergio Rosembergsrosem@uol.com.br
377NoNo4th Oct 2022ASD/NDD/ADHD 2 ASD assessments / management / Rett syndrome / high risk infantsAntigone PapavasiliouSoumya Sundaramssdr.soumya@gmail.comBroad Autism Phenotype Questionnaire— Translation and Validation in a South Indian language followed by pilot studySoumya Sundaramssdr.soumya@gmail.com
394NoNo5th Oct 2022Neuroimmunology 2 Antibody mediated disorders / monophasic demyel disorderBanu AnlarSedef Terzioğlu Öztürkssedef_88@hotmail.comAcute transverse myelitis related to BNT162b2 vaccine in a teenage girlSedef Terzioğlu Öztürkssedef_88@hotmail.com
455NoNo6th Oct 2022Headache/Stroke 2"Mahendra MoharirCanada"Sedef Terzioğlu Öztürkssedef_88@hotmail.comAN ATYPİCAL CASE OF POST VARİCELLA STROKE İN A CHİLD ASSOCİATED WİTH HYPERHOMOCYSTEİNEMİA AND MTHFR A1298C MUTATİONSedef Terzioğlu Öztürkssedef_88@hotmail.com
497NoNo5th Oct 2022General neurogenetics IAR ZamaniSedef Terzioğlu Öztürkssedef_88@hotmail.com"DE NOVO MUTATION IN SETD1B IS ASSOCİATED WITH INTELLECTUAL DISABILITY EPILEPSY AND AUTISTIC BEHAVIOR"Sedef Terzioğlu Öztürkssedef_88@hotmail.com
573NoNo4th Oct 2022Epilepsy: Treatment 3 – ASM/ Dietary TreatmentsJ SahuSuvasini Sharmasuvasini.sharma@sickkids.caEffect of concurrent anti-seizure medications on the efficacy of the ketogenic diet in children with epilepsySuvasini Sharmasuvasini.sharma@sickkids.ca
67NoNo4th Oct 2022"Epilepsy: Syndromes 1 – Self-limited EE/DEE-SWAS"C JoshiSviatlana Kulikovasviatlana.kulikova@gmail.comPolymicrogyria and epilepsy with continuous spike-wave during sleep in pediatric patientsSviatlana Kulikovasviatlana.kulikova@gmail.com
393NoNo5th Oct 2022Genetics and epilepsy IW HakamiDandan Tantandandan18@163.comClinical and genetic study of rare cases with coexistence of dual genetic diagnosesHui Xiongxh_bjbj@163.com
137NoNo4th Oct 2022ASD/NDD/ADHD 2 ASD assessments / management / Rett syndrome / high risk infantsAntigone PapavasiliouTelma Dagmar Obergtelmaoberg@hotmail.comPerformance of Physiotherapy Through Early Stimulation in High Risk Babies. Experience Report on the Insertion of this Elective Internship Program for Physiotherapy StudentsRegina Turolla De Souzareginaturolla@yahoo.com.br
108NoNo4th Oct 2022ASD/NDD/ADHD 1 ASD genetic / biomarkers /Chahnez TrikiHiromi Wadaterrence_thomas@me.comAcoustic alterations of ultrasonic vocalization in the autism model mice (duplication of 15 q11-13) upon maternal isolationHiromi Wadawada@let.hokudai.ac.jp
156NoNo5th Oct 2022Neuroimmunology 3 Autoimmune encephalitis plusSilvia TenenbaumTerrence Thomasterrence_thomas@me.comAcute necrotizing encephalopathy (ANE) is a feature of dengue virus encephalitisTerrence Thomasterrence_thomas@me.com
100NoNo5th Oct 2022Genetics and epilepsy IW HakamiThomas Murraythomas.murray@nationwidechildrens.orgA case report of sequential seizure semiology as a sign of genetic etiologyThomas Murraythomas.murray@nationwidechildrens.org
152NoNo6th Oct 2022Metabolic 4 Therapeutic approachesSamantha Marin CanadaTuna Kocatkoca@ptcbio.comEladocagene Exuparvovec Gene Therapy Improves Motor Development in Patients With Aromatic L-Amino Acid Decarboxylase DeficiencyPanayiota Trifillisptrifillis@ptcbio.com
153NoNo6th Oct 2022Metabolic 4 Therapeutic approachesSamantha Marin CanadaTuna Kocatkoca@ptcbio.comEladocagene Exuparvovec Improves Body Weight and Reduces Respiratory Infections in Patients With Aromatic L-Amino Acid Decarboxylase DeficiencyPanayiota Trifillisptrifillis@ptcbio.com
154NoNo6th Oct 2022Metabolic 4 Therapeutic approachesSamantha Marin CanadaTuna Kocatkoca@ptcbio.comGene Therapy With Eladocagene Exuparvovec Improves Cognition and Language in Patients With Aromatic L-Amino Acid Decarboxylase DeficiencyPanayiota Trifillisptrifillis@ptcbio.com
609NoNo4th Oct 2022ASD/NDD/ADHD 1 ASD genetic / biomarkers /Chahnez TrikiTuğçe Aksu Uzunhantugceuzunhan@yahoo.comMacrocephaly/autism syndrome exhibits neuroradiological abnormalities including Arnold-Chiari syndrome type I: Clinico-radiological spectrum of a PTEN-opathyTuğçe Aksu Uzunhantugceuzunhan@yahoo.com
184NoNo5th Oct 2022TreatmentF MuntoniMichael Kwan Leung Yuu3005180@connect.hku.hkCOVID-19 Vaccine Hesitancy Among Neuromuscular Disorder Children and AdolescentsMichael Kwan Leung Yuu3005180@connect.hku.hk
262NoNo5th Oct 2022TreatmentF MuntoniMichael Kwan Leung Yuu3005180@connect.hku.hkImpact of COVID-19 pandemic on healthcare utilitsation and psychosocial well-being of children with neuromuscular disorderMichael Kwan Leung Yuu3005180@connect.hku.hk
459NoNo6th Oct 2022Cerebral palsy 2- Management; current and future"Antigone Papavasiliou Greece"Madina Taghiyevavagabova_medina@yahoo.comFeatures of epilepsy drug therapy in children with cerebral palsyMadina Taghiyevavagabova_medina@yahoo.com
249NoNo5th Oct 2022SMAN ChrestianVivek Mundadavbmundada@gmail.comOnasemnogene abeparvovec for Spinal Muscular Atrophy: Experience from one center in the United Arab EmiratesVivek Mundadavbmundada@gmail.com
159NoNo5th Oct 2022"CNS Malformations NGS"A NarayanVinodh Narayananvnarayanan@tgen.orgPrevention of Inherited Genetic Disease using WGS (whole genome sequencing)Vinodh Narayananvnarayanan@tgen.org
186NoNo4th Oct 2022ASD/NDD/ADHD 2 ASD assessments / management / Rett syndrome / high risk infantsAntigone PapavasiliouTaras Voloshynvoloshynt@yandex.ruNew ways of treatment for childhood autism: are we moving in the right direction?Taras Voloshynvoloshynt@yandex.ru
674NoNo5th Oct 2022General IIM SönmezWafa Bouchaalawafabouchaala85@gmail.comClinical evolution in patients with autosomal recessive limb-girdle muscular dystrophy (LGMDR5): A Tunisian cohortWafa Bouchaalawafabouchaala85@gmail.com
203NoNo5th Oct 2022Neurogenetics practiceT Lerman-SagieXiaofan Yangxiaofan.yang@sdu.edu.cnSocial deficits and cerebellar degeneration in Purkinje cell Scn8a knockout miceXiaofan Yangxiaofan.yang@sdu.edu.cn
195NoNo6th Oct 2022Neuroradiology 1"Manohar Schroff Canada"Xuemei Wuxmwu@jlu.edu.cnRisk factors and prognosis of spinal cord injury without radiological abnormality in children in ChinaXuemei Wuxmwu@jlu.edu.cn
714NoNo4th Oct 2022Epilepsy: InvestigationsP MadaanYael Michaeli Yossefyaelyos@gmail.comHome-EEG long term monitoring versus in house long term EEG monitoringYael Michaeli Yossefyaelyos@gmail.com
201NoNo4th Oct 2022"Epilepsy: Syndromes 2 – IESS Dravet HHE EMAS"E WirrellGuang Yangyangg301@sina.comAssessing risk for relapse among children with infantile spasms using the BASED scoreGuang Yangyangg301@sina.com
274NoNo4th Oct 2022ASD/NDD/ADHD 4 ADHD and Behav / syndromes / LDPratibha SinghiJian Yangyangjian1306@sina.comResponse Inhibition in Children with Different Subtypes/Presentations of Attention deficit hyperactivity disorder: a Near-infrared Spectroscopy StudyJian Yangyangjian1306@sina.com
329NoNo4th Oct 2022ASD/NDD/ADHD 4 ADHD and Behav / syndromes / LDPratibha SinghiJian Yangyangjian1306@sina.comExploration of serum B vitamin levels in children with ADHD and their correlation with clinical symptomsFan Zhangcmufanzhang@163.com
727NoNo4th Oct 2022Epilepsy: Treatment 3 – ASM/ Dietary TreatmentsJ SahuYasemin Topcuyasemintopcu35@gmail.comEfficiency of Rufinamide as add-on Treatment of Drug Resistant Generalized and Focal Epilepsies: One centerYasemin Topcuyasemintopcu35@gmail.com
608NoNo5th Oct 2022Neuromuscular 1H LochmüllerYavuz Ataşyavuzatas23@gmail.comThe Utility of Prognostic Models in Pediatric Guillain Barre Syndrome : A Regional Cohort Study-EGEYavuz Ataşyavuzatas23@gmail.com
729NoNo4th Oct 2022ASD/NDD/ADHD 4 ADHD and Behav / syndromes / LDPratibha SinghiYeliz Engindereliyeliz.engindereli@neu.edu.trCo-morbid psychiatric disorders in patients with arachnoid cyst: A case seriesBurçin Şanlıdağburcinsanlidag@yahoo.com
628NoNo4th Oct 2022Epilepsy: Genetics 3L LagaeYi̇ğithan Güzinyguzin@hotmail.comClinical Evaluation of Childhood Rare Genetic Epilepsies; Multicentric collaboration studyYi̇ğithan Güzinyguzin@hotmail.com
637NoNo4th Oct 2022Epilepsy: Treatment 3 – ASM/ Dietary TreatmentsJ SahuYiğithan Güzinyguzin@hotmail.comKidney Stone Formation İn Children Receiving Ketogenic Diet TherapyYiğithan Güzinyguzin@hotmail.com
286NoNo6th Oct 2022Headache/Stroke 2"Mahendra MoharirCanada"Ziyodakhon Abduyaminovaz.saidazizova@gmail.com«Risk factors of the stroke in early age children»Ziyodakhon Abduyaminovaz.saidazizova@gmail.com
328NoNo6th Oct 2022Metabolic 1 Clinical phenotypes"Brahim Tabarki KSA"Zahra Rezaeizahra.rezaii84@gmail.comCystic Leukoencephalopathy; a confusing neuroimaging feature!Zahra Rezaeizahra.rezaii84@gmail.com
197NoNo5th Oct 2022Molecular geneticsT SultanGang Zhangzhanggangnjmu@126.comIdentification of 1q21.1 Microduplication in a familyGang Zhangzhanggangnjmu@126.com
214NoNo5th Oct 2022General neurogenetics IAR ZamaniYunjian Zhangzhangyunjian2008@sina.comAnalysis of clinical features and genetic variants among patients with SLC6A1 mutationsYunjian Zhangzhangyunjian2008@sina.com
483NoNo5th Oct 2022General IJ VajsarZhuldyz Nukebayevazhuldyz_nm@mail.ruClinical case of acromicric dysplasia syndrome (ACMICD-syndrome)Zhuldyz Nukebayevazhuldyz_nm@mail.ru
53NoNo5th Oct 2022Molecular geneticsT SultanTBCzouliping21@hotmail.comSLC25A12 as a new candidate for febrile seizures: a case-control association studyLi-ping Zouzouliping21@hotmail.com
54NoNo6th Oct 2022"Tuberous sclerosis Radiology"K AydınTBCzouliping21@hotmail.comLong-term prognosis of neurological system in tuberous sclerosis complex with neonatal onset epilepsyLi-ping Zouzouliping21@hotmail.com
66NoNo6th Oct 2022Metabolic 6 Defects of bioenergetic and intermediary metabIngrid Tein CanadaTBCdr.iramjaved@gmail.comClinical profile and outcome of 6 patients with Biotinidase deficeince: An experience from a tertiary care hospital of PakistanDr.iram Javeddr.iramjaved@gmail.com
196NoNo4th Oct 2022"Epilepsy: Neuroimaging Surgery and Basic Science"C AkmanTBCxmwu@jlu.edu.cnDynamic changes of cytoskeleton in epileptic miceXuemei Wuxmwu@jlu.edu.cn
271NoNo5th Oct 2022"Neuropathy GBS and CMS"C BönnemannTBCdrrenusuthar@gmail.comCongenital Myasthenia Syndrome: Correlation between clinical features and genetics from North IndiaRenu Suthardrrenusuthar@gmail.com
333NoNo4th Oct 2022Epilepsy: Treatment 3 – ASM/ Dietary TreatmentsJ SahuTBCliaojianxiang@vip.sina.comThe ketogenic diet for Dravet syndrome: a multi-center retrospective studyJianxiang Liaoliaojianxiang@vip.sina.com
566NoNo5th Oct 2022Muscular dystrophyY NevoIchraf Kraouabythouraya@yahoo.frGamma-sarcoglycanopathy (LGMDR5): clinical and genetic study of a pediatric Tunisian cohortThouraya Ben Younesbythouraya@yahoo.fr
775NoNo5th Oct 2022"Neuropathy GBS and CMS"C BönnemannTBCrjnipek@hotmail.comFour Different Types of Cases with Charcot-Marie-Tooth Axonal InvolvementRojan İpekrjnipek@hotmail.com

Join Our Newsletter

Log in

X