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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

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Visa Requirements
You may need a visa to enter Türkiye if you arrive by plane. This can easily be checked via https://www.mfa.gov.tr/visa-information-for-foreigners.en.mfa. Please note that a visa needs to be obtained prior to arrival. You can either acquire your visa from a local Turkish embassy or consulate or alternatively obtain it easily via an online application form.

Delegates are able to request and official letter of invitation here at  https://icnapedia.org/icnc-registration/letter-of-invitation-icnc2022

Transport in Antalya
Major cities in Türkiye, including Istanbul and Antalya, have a good quality public transport system. Many taxis are available at the airport, or you can arrange your private hotel transfer via SOLO Events (Phone Number: +90 2122790020 / E-Mail: accommodation_icnc2022@soloevent.net)

The distance between Antalya Airport and Sueno Hotel is 30km. It takes approximately 40-45 minutes by taxi and minibus.

Electricity
Türkiye operates on 220 volts, 50 Hz and uses round European style plugs.

Weather in Antalya
The area around the city is known as the Turkish Riviera for a good reason. It experiences a typical Mediterranean climate throughout the year, with hot and dry summers and mild rainy winters. Antalya on average experiences around 300 sunny days every year. Expect a warm October in Antalya during the congress, but be prepared for occasional rain falls.

Credit Card Transactions
All major credit card providers (such as Mastercard, VISA and AmEx) are widely accepted. Please check additional fees before your transaction.

Covid-19 Situation in Turkey
As of June 1, 2022, almost all of the measures have been canceled. This means:

  • There is no requirement of vaccination certificate and/or PCR or antigen tests before entering Türkiye.
  • Wearing a mask on international flights to Türkiye is at the passenger’s discretion.
  • Mask requirements on international flights from Türkiye depend upon the regulations set by the destination country.

Please note that wearing a mask is only mandatory in hospitals. We encourage you to carry your masks with you in case you don’t feel comfortable. Many Turkish citizens are still wearing masks while in public. Please consult your airline’s website before your travel for any updates on Covid-19 measures. Should the Covid-19 situation change, the necessary precautions will be taken both in public areas as at the congress venue.

Safety in Antalya
Antalya, being the tourism capital of Türkiye and the region, is one of the safest travel destinations in the world. Many travelers comment on the friendliness and hospitality of the Turkish people. Türkiye is not only friendly, it is, in many ways, as safe as North America and Western Europe with one of the lowest police-recorded offences (criminal acts) rates in Europe.

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Invited speakers who are unable to travel and have requested to pre-record their talks

  • Adam Kirton (Plenary speaker; Alberta, Canada)
    Plenary Session: 08:00-08:45 Thursday 6 October
    Parallel Symposia: 10:00-12:00 Friday 7 October (Neuronal Plasticity)
  • Bernard Dan (Belgium) - Files received
  • Mubeen Rafay (Manitoba) - Files received
    Parallel Symposia: 10:00-12:00 Wed 5 October (Paediatric Stroke)
  • Samantha Marin - Files received
    Parallel Symposia: 10:00-12:00 Wed 5 October (Neurometabolic)
  • Tobias Loddenkemper (Boston) - Files Received
    Controversies: 17:30-18:30 Tue 4 October
  • Audrey Foster-Barber (San Francisco)
    07:00-08:00 Thu 6 Oct - Rise & Shine Seminar (Neuropalliative care)
  • Peter sidgwick
    07:00-08:00 Thu 6 Oct - Rise & Shine Seminar (Neuropalliative care)
  • Howard Goodkin
  • Parallel Symposia: 10:00-12:00 Fri 7 October (Status epilepticus)
  • Matthis Synofzik (Germany)
    Parallel Symposia: 10:00-12:00 Tue 4 October (Orphans without borders)
  • Timothy Yu (US)
    Parallel Symposia: 10:00-12:00 Tue 4 October (Orphans without borders)

 

Speakers who are not attending

Manju Kurian

Martino

Richard Edwards

Francesco Pisani
Parallel Symposia: 10:00-12:00 Thu 6 October (Epilepsy networks: seizures, surgery and neuronal plasticity)

Victoria Ruiz (Uruguay)



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Individuals requiring an official Letter of Invitation can request one here. The Letter of Invitation does not financially obligate the Congress organisers in any way. All expenses incurred in relation to the Congress are the sole responsibility of the attendee.

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  1. Ballot 2022
  2. Proceedings
  3. Events Calendar
  4. Sahar Hassanein

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