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117. Cost Reduction for Families and Healthcare System with the Implementation of a Paediatric Comprehensive Epilepsy Clinic
|
Michelle Kregel |
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119. Infantile epileptic spasms syndrome in Chinese cohort Southern China: the clinical practice based on the 2017 and 2022
|
Wen-Xiong Chen |
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120. The evolving spectrum of LAMA2 related congenital muscular dystrophy (MCD1)
|
Rahul Sinha |
|
122. Assessment of perceived mental health and quality of life in mothers of children with autism spectrum disorder (ASD)
|
Rahul Sinha |
|
124. TBCK related encephalopathy
|
Kun-Long Hung |
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126. Acute Neurological complications and risk factors for encephalitis in COVID-19 children: a retrospective cohort study
|
Ling Li |
|
128. What is the right choice? Is the answer the sodium channel blockers?
|
Mehpare Sarı Yanartaş |
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131. Clinical and Electrophysiological features of isolated tonic seizures
|
Amarachukwu Okafor |
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133. Paraneoplastic neurological syndromes in childhood: a single institution 8-year case series
|
Zhou |
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151. Recurrent Torticollis- A rare Adphrl mutation
|
Huseyin Per |
|
154. Mitochondrial aminoacyl-tRNA synthetases deficiency: report of seven cases with genotypic and phenotypic expansion
|
Thitiporn Fangsaad |
|
155. Epileptic seizures and Brugada syndrome in Tunisian patients
|
nouha bouayed |
|
156. Neurologic conditions in congenital lymphangiomas
|
nouha bouayed |
|
157. The Investigation of Mandarin Tone Perception and Production in Taiwanese Children with Tourette syndrome
|
Jung-Chieh Du |
|
167. Expert voices on non-specialist paediatric EEG training
|
Veena Kander |
|
167. Expert voices on non-specialist paediatric EEG training
|
Veena Kander |
|
168. Rafiq syndrome: old variant in MAN1B1 gene and some new phenotypic features
|
Nezir ÖZGÜN |
|
171. Guillain-Barré syndrome and acute transverse myelitis in a young child - a rare overlap syndrome
|
Jena Chung |
|
176. Congenital Brain Malformations in Neonates with Congenital Heart Disease
|
Vanna Kazazian |
|
177. A Rare Disease masquerading as Periodic Paralysis in a young child: A Case Report
|
Aakanksha Anand |
|
178. Acute Neurological Complications in Pediatric Patients Undergoing ECMO at a Tertiary Level Hospital in Buenos Aires
|
EUGENIA ANELISA JARA |
|
179. Clinical profile of Pediatric MOG antibody associated disease at a tertiary center in Dubai, UAE: A case series
|
anjaly nair |
|
183. An event-related potential study of P300 in preschool children with attention deficit hyperactivity disorder
|
Tao Mengjiao |
|
184. To study the characteristics of cognitive function in children with ADHD with normal and abnormal results of integrated
|
Li Ziqi |
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185. Neuronal migration disorder in 205 patients: A decade of a single centre experience
|
Abdul Hamid Al Hinai |
|
187. Sample for the Home Office
|
ilknur Erol' |
|
192. A Case Associated with Abdominal Asicets Accumulation in Congenital Disorder of Glycosylation Type Ia
|
Ayşe Aksoy |
|
193. Epilepsia Partialis Continua: a unique presentation of Anti-NMDAR encephalitis
|
Aditi Gupta |
|
195. Is there an increased risk of brain tumors during Sotos syndrome?
|
nouha bouayed |
|
196. Autonomic function assessed by blood-pressure-variability is a noble biomarker during hyperglycemia in late adolescents
|
Kiran Prakash. |
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198. Fever-induced paroxysmal weakness and encephalopathy (FIPWE): Report of a new family.
|
Krupa Torne |
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199. Fever-induced paroxysmal weakness and encephalopathy (FIPWE): Report of a new family. (2)
|
Meriem Ben Hafsa |
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201. Seizure Timing, Body Position and EEG Evaluation in Pediatric Patients with Refractory Epilepsy
|
Pinar Ozbudak |
|
203. Causes of microcephaly in children attending in a Disability Research Center
|
M A Wahed |
|
205. Childhood acute flaccid myelitis, including the first cases of enterovirus D68 myelitis in Singapore and South East Asia
|
Jillian Pakiam |
|
209. The Association of Node Assortativity and Internalizing Symptoms in Drug Resistant Epilepsy Case with Ketogenic diet
|
Yi-fen Chen |
|
210. Prematurity and Postnatal Neurological Sequelae – a review update
|
M A Wahed |
|
215. The Child with Hemiparesis – Don’t Forget the Spine!
|
Dipak Ram |
|
218. Navigating Atypical Hirayama Disease: Insights from a case presentation
|
Vishal Mehta |
|
221. Autism Spectrum Disorder and Intellectual Disability in a population of central Mexico.
|
Gessen Salmerón Gómez |
|
222. Oculomotor speed and control as markers of cognitive ability in Malawian adolescent population
|
Karoliina Videman |
|
225. Therapeutic Effects of Extracorporeal Shock Wave Therapy on Patients with Spastic Cerebral Palsy and Rett Syndrome
|
Ting-Yu Su |
|
227. Recent trend of SSPE in children: A reemergence and younger age of presentation: A study from Bangladesh.
|
Shaheen |
|
228. Seizure remission rates and adverse drug reaction profile in Nigerian children with West Syndrome treated with high dose
|
Joy Ibeh |
|
229. Infantile Subdural Hemorrhage and Cortical Vein Thrombosis
|
Joseph Scheller |
|
233. Management Implications of Multifactorial Pathophysiology of Ischemic Stroke in Pediatric Lemierre’s Syndrome
|
Maegan Newell |
|
234. A comparative study of VEP between childhood epilepsy with occipital paroxysms and symptomatic occipital epilepsy
|
Azmi habeeb |
|
238. Skull Infarction in Patients with Sickle Cell Disease
|
Danna Garcia |
|
239. Decreased motor cortex responsiveness during stopping in children with ADHD
|
Gilbert, Donald |
|
241. An Inpatient Period Prevalence Study of Acute Stroke among Children Living with Sickle Cell Disease at UTHCH
|
Derby Tembo |
|
243. HyperCKemia: An early sign of childhood-onset neutral lipid storage disease with myopathy
|
Xiaona Fu |
|
244. Post-traumatic tetra paresis with trivial mechanism of injury myelitis vs embolic spinal cord infarction in a pre-school
|
krupa torne |
|
245. : An unusual case presentation of graft versus host myositis secondary to bone marrow transplant in a toddler
|
krupa torne |
|
247. High diagnostic yield of non-contrast brain MRI with SWI in non-sedated children with Sturge-Weber syndrome
|
Csaba Juhasz |
|
248. White matter alterations in narcolepsy children with cataplexy
|
Zimeng Ma |
|
255. Tuberous Sclerosis Complex: A retrospective clinical review with a focus on epilepsy
|
Britta McLaren |
|
256. Response to Vigabatrin versus ACTH in Infantile Epileptic Spasms Syndrome at 6 Weeks: A randomized prospective study con
|
Prem Chand |
|
257. INFLUENCE OF ASSITED REPRODUCTIVE MEDICINE IN THE 2 YEAR OLD NEURODEVELOPMENTAL OUTCOME OF A COORT OF PREMATURE BABIES
|
Francisco Carratalá-Marco |
|
259. Paraneoplastic Cochleovestibulopathy in Adolescence: Illustrative Case, Large Series, and Clues Toward Earlier Diagnosis
|
Scott Eggers |
|
260. Parental decision making in fetal callosal abnormalities
|
Cacha Peeters-Scholte |
|
261. Onchocerciasis associated epilepsy (OAE) in children immigrated to the United States.
|
Samuel Dzodzomenyo |
|
263. Pura Syndrome: A Rare Case of Neonatal Hypotonia with a Novel Multi-Gene Deletion at 5q31.2q31.3 Diagnosed with rWES.
|
Samuel Dzodzomenyo |
|
264. A rare cause of refractory epilepsy and microcephaly: Asparagine Synthetase Deficiency
|
SERKAN KIRIK |
|
265. Diagnostic Utility Of Electroencephalogram In Developmental And Epileptic Encephalopathies
|
Smilu Mohanlal |
|
267. Hyperekplexia secondary to novel SLC6A5 homozygous deletion masquerading as neonatal seizures.
|
Samuel Dzodzomenyo |
|
268. Ischemic stroke in two patients with Duchenne muscular dystrophy and different risk factors
|
Manuel Pühringer |
|
270. Long-term Outcome of patients with Neonatal Hypoglycaemic Brain Injury: A Retrospective Study
|
Saheli Roy |
|
271. Pediatric Mitochondrial Disease: Clinical and Radiological profile, Experience from A Tertiary Care Hospital
|
Shaheen Akhter |
|
277. Intubation in Patients Presenting with Seizures to a Pediatric Emergency Department in a Safety Net Hospital
|
Danna Garcia |
|
278. An analysis of brain iron dynamics using quantitative susceptibility mapping in children with febrile seizures.
|
Gen Furukawa |
|
279. ‘Eyes that look and the eyes that see’- Common neurological manifestations with uncommon inherited metabolic disorders.
|
Abinaya Seenivasan |
|
280. First Systemic Myasthenic crisis after "BNT162b2 vaccine" previous healthy girl
|
SERKAN KIRIK |
|
282. Higher Economic Burden of Spinal Muscular Atrophy (SMA) Compared to Other Chronic Diseases
|
Stacey Tay |
|
283. Thiamine deficiency presenting as paraplegia in a child.
|
Arayamparambil Anilkumar |
|
285. The Involvement of Autoimmune System in Pediatric Intractable Epilepsy
|
Prastiya Indra Gunawan |
|
288. Case Reports of Teenage Onset Prolonged Debilitating Dysautonomia and Small Fiber Neuropathy: Pitfalls and Challenges
|
Audrey Lee |
|
290. Mapping first-choice hormonal therapy for infantile epileptic spasms syndrome in South Asia: A network meta analysis
|
Parth Lal |
|
292. Whether stem cell therapy is effective and safe compared to standard care in muscular dystrophies? A systematic review
|
Parth Lal |
|
293. Drug resistance to commonly used AEDs in children in the Kazakh population.
|
Inkar Orazbayeva |
|
294. Mimics diseases among patients with CP in Kazakhstan
|
Inkar Orazbayeva |
|
296. Febrile Seizures in Children with COVID-19 According to COVİD-19 Variant Periods
|
Nihal Olgac Dundar |
|
297. New-Onset Focal Seizures in Children: Aetiology, Comorbidities and Outcomes
|
Shekeeb Mohammad |
|
304. Utilization of Intravenous Immunoglobulin in the Neurology Department of A Middle Eastern Tertiary Pediatric Hospital
|
Sarah Gharaibeh |
|
305. EEG PHENOTIPE IN ASD PATIENTS WITH AND WITHOUT CLINICAL EVIDENCE OF EPILEPTIC SINDROMES.
|
Francisco Carratalá-Marco |
|
309. Myalgic encephalomyelitis presenting as orthostatic intolerance in an adolescent.
|
Samuel Dzodzomenyo |
|
310. THE TREATMENT BY SMALL DOSE OF SUSTAINED RELEASE VALPROIC ACID FOR AUDITORY HYPERSENSITIVITY IN ASD
|
Shigeru HANAOKA |
|
313. ScRNA-seq- with the combined use of RNA-Scope to reveal functional populations and heterogeneity of hOPCs
|
Dou Ye |
|
314. Is there a spectrum within Lennox Gastaut Syndrome?
|
Adaobi Bisi-Onyemaechi |
|
318. Childhood Epilepsy Management in Indonesia: Challenge and Current Condition
|
Sunny Mariana |
|
326. Generate the peptide-specific AQP4 monoclonal antibody to compete with human NMOSD NMO-IgG in vitro - A Pilot study
|
Shyi-Jou Chen |
|
329. Long Term Outcome Following Revascularization Surgery in Children with Moyamoya Syndrome.
|
Smilu Mohanlal |
|
331. Real-world Insights on the Use of Cannabidiol (CBD) in Adults With LGS, DS, or TSC: A Physician Survey
|
Pasquale Striano |
|
332. Real-world Insights on the Use of Cannabidiol (CBD) in Children Aged
|
Rima Nabbout |
|
333. To study the impact of the COVID-19 pandemic on the clinical profile and treatment outcomes of pediatric GBS.
|
Rishitha Pravallika |
|
335. Disease modifying therapies in Spinal Muscular Atrophy – A Single Centre Experience
|
Saheli Roy |
|
337. An exploratory study of cognitive functions characteristics of children with different subtypes of ADHD based on IVA
|
Yang Jian |
|
339. Seizure reduction in pediatric drug resistant epilepsy (child epileptologist versus non-epileptologists child neurologis
|
Jara Eugenia |
|
340. Attenuated Form of Glycine Encephalopathy: An Unusual Cause of Intermittent Ataxia and Hyperactivity
|
Areeba Wasim |
|
341. Missing or a Mystery? -a retrospective study on Febrile infection-related epilepsy syndrome (FIRES)
|
Abinaya Seenivasan |
|
346. Rapidly Progressive Subacute Sclerosing Panencephalitis
|
Nihal Olgaç Dündar |
|
351. Exploring Neurodevelopmental Outcomes: A Prospective Study on Intraventricular Hemorrhage (IVH) among Ugandan infants
|
Noella Okalany |
|
352. Epileptic Seizures in Acute Leukemia in Children: A Clinical Analysis
|
Shaanvar Shamansurov |
|
354. profile of infants with neonatal-onset epilepsy (genetic and metabolic causes): single center study
|
Elsayed Ali |
|
355. The Expanding Phenotypic Spectrum of ATP1A3 Gene Mutations – A Case Series.
|
Ali Elsir |
|
356. Structural focal epilepsy or idiopathic generalised epilepsy?
|
Ceren Günbey |
|
357. A rare case of autosomal recessive spastic paraplegia with learning difficulties, optic atrophy and neuropathy (SPG55)
|
Manish Prasad |
|
358. Child Neurology Residency in Brazil: Current Scenario
|
Ana Carolina Coan |
|
359. Odyssey of few year
|
Prasad Manish |
|
360. Georges Gilles de la Tourette. The man and his times
|
Asit Tripathy |
|
361. Celebrities with Headaches- Through Philately
|
Asit Tripathy |
|
362. Pediatric Neuroscience on Stamps
|
Asit Tripathy |
|
364. Assessment of Functional Connectivity Patterns in Children with Epilepsy with Myoclonic-Atonic Seizures
|
Charuta |
|
366. Quality of life in Uruguayan children with cerebral palsy assessed by CPQoL questionnaire.
|
Alfredo Cerisola |
|
368. Mitochondrial Complex 1 Deficiency Nuclear Type 4 in a Toddler: A Case Report of NDUFV1 Gene Mutation
|
Mehmet Canpolat |
|
371. Incidence of Hypoxic Ischemic Encephalopathy (HIE) in neonates admitted to the Aga Khan Medical Center – Gilgit (AKMC-G)
|
Salman Hashim |
|
373. Evolution of resting state functional connectivity following interventions in children with Autism spectrum disorders
|
Soumya Sundaram |
|
375. Presentation of the Second Case in the World of “Cortıcal Myoclonıc Tremor with Epilepsy, Familial 7”
|
Mehmet CANPOLAT |
|
376. The Importance of Examination in Febrile Convulsions: Hypotonic Infant Case with Coenzyme Q10 Deficiency
|
Mehmet CANPOLAT |
|
378. Abnormal post-stress anxiety response related to locus coeruleus dysfunction in Prader-Willi syndrome mice
|
Shi Bing Wong |
|
379. Peripheral hypotonia and areflexia in infants and young children- not always SMA
|
J Rohitha |
|
383. Interaction of immune response in Niemann pick disease type C1 of children
|
Ling Li |
|
386. A Rare Case Diagnosed with Developmental and Epileptic Encephalopathy
|
Hakan Gümüş |
|
387. Mitochondrial Diseases In Pediatric Neurology Practice: A Single Center Experience
|
ilknur Erol' |
|
388. Clinical, imaging, and Genetic Spectrum of Polymicrogyria in Indian Children-Single Centre experience
|
Ramesh Konanki |
|
396. Acute Necrotizing Encephalopathy of Childhood: Insights from a Tertiary Care Center in Pakistan
|
Prem Chand |
|
397. Anti-seizure Medication Adherence among Adolescents with Epilepsy in a Tertiary Hospital in the Philippines
|
Sally Andrea Gaspi |
|
398. Moyamoya Disease Presenting as Hemichorea in a Filipino Adolescent: A Case Report
|
Sally Andrea Gaspi |
|
399. Tertiary centre experience in management of pre-pubertal children presenting with asymptomatic papilloedema
|
Sharmila Manivannan |
|
401. An Uncommon Intellectual Disability Attributed to METTL-23 Mutation Accompanied by Mitral Valve Prolapse
|
Hüseyin Per |
|
405. A Unique Case of Subclinical Becker Muscular Dystrophy Due to a Single Exon 48 Deletion in the Dystrophin Gene
|
Mehmet Canpolat |
|
406. Learning disability and ADHD in children with nocturnal versus diurnal seizures - An analytical study
|
Dona Teresa Thomas |
|
407. A child with prolonged fever, chronic raised ICP and vision loss: No its not CNS TB
|
Ashna Kumar |
|
408. Atonic Head Drops: A New Seizure Mimic
|
Ashna Kumar |
|
412. Serial Endovascular Embolization as a Novel Treatment for Refractory Epilepsy in Hemispheric Overgrowth: A Case Series
|
Catherine Brown |
|
413. Effect of Long-term ACTH therapy on refractory infantile epileptic spasms syndrome
|
Naoko Ishihara |
|
415. Deep Brain Stimulation of bilateral Globus Pallidus internus in a 5 year-old boy with SGCE-related myoclonus dystonia
|
Xiaojuan Tian |
|
417. Comparative Analysis of Validated Measures of Cognitive, Behavioral, and Motor Impairments in a Pediatric Population of
|
Donald Gilbert |
|
419. Phenotypical Variability Of GNAO1 Gene Mutations
|
Angeles Schteinschnaider |
|
420. Evaluating the impact of an educational intervention on knowledge and perception of autism spectrum disorder in Uganda
|
Pamela Tiiti |
|
421. An early diagnosed cerebral small vessel disease in a 12-year-old girl
|
Xiaojuan Tian |
|
424. Clinical characteristics and gene analysis of SYNGAP1-related epilepsy in children
|
Xiaojuan Tian |
|
426. ICF Matrix For Early Monitoring Of Adverse Events In The Neonatal Period
|
Gina Rencken |
|
429. Electro-clinical spectrum of epilepsy as per ILAE 2022 diagnostic system in children up to 2 years of age
|
Ganesh Kumar |
|
430. Neuro-ophtalmological manifestations in neurometabolic diseases: The eye is a window to the brain
|
Meriem Ben Hafsa |
|
431. Etiology, early and late term neurological prognosis in cases with meningoencephalitis/encephalitis
|
Gokce Cirdi |
|
432. Healthcare Utilization and Neonatal Stroke Outcomes: A Neighborhood-based Study
|
Akshat Pai |
|
434. Electro-clinical spectrum of children having epilepsy secondary to perinatal asphyxia as per ILAE 2022 diagnostic system
|
Praveen Barala |
|
438. Mitochondrial complex I deficiency: clinical manifestation, neuroimaging and genetic profiling in pediatric patients
|
Arushi Gahlot Saini |
|
439. Response To Treatment With Tocilizumab In Fires, Experience Of Two Cases
|
ROCIO ALAMO |
|
440. Aspects from the quadruple burden of disease in South Africa and newborn neurobehaviour
|
Gina Rencken |
|
441. Single-center Single-reader Prolonged Pediatric Routine EEGs and Long-term Outcome
|
Joyce Wu |
|
442. GENETIC ATAXIAS: TEN YEARS EXPERIENCE
|
Angeles Schteinschnaide |
|
445. SUBCORTICAL BAND HETEROTOPIA: CLINICAL AND IMAGENOLOGICAL CHARACTERISTICS.
|
ROCIO ALAMO |
|
446. Six-Month Responses of Patients with Refractory Epilepsy Treated with Low Glycemic Index Therapy
|
Nihal Olgac Dundar |
|
448. Early use of Tocilizumab is associated with favorable outcome in FIRES: A Case Report
|
Sukanya Vrushabhendra |
|
451. Clinical and Genetic Spectrum of Omani children with EAST/SeSAME Syndrome caused by KCNJ10 Mutation
|
Areeba Wasim |
|
452. Guillian Barre Syndrome associated with COVID : A new twist
|
Aditi Gupta |
|
453. MPV17 and the mitochondrial genetic landscape in South Africa-finding the way forward
|
Gillian Riordan |
|
455. Neurologic and Psychiatric Symptoms of Long COVID in a Pediatric Neurology Clinic
|
Molly Wilson-Murphy |
|
456. Subacute Sclerosing Panencephalitis in Children: A Reemerging Disease
|
Meriem Ben Hafsa |
|
457. Acquired epilepsy after neonatal encephalopathy is associated with alterations in pathway-specific circulating cytokines
|
Adam Numis |
|
458. Intersection of social disparity, brain injury and neurodevelopmental outcomes in children with congenital heart disease
|
Thiviya Selvanathan |
|
459. Pediatric stroke in a new-onset type 1 diabetes mellitus with and without DKA: Case series.
|
Amal Y. Kentab |
|
460. Isolated mitochondrial complex IV (cytochrome c oxidase) deficiency mimicking ADEM
|
Amal Y. Kentab |
|
462. A Rare Case of HNRNPU-Related Neurodevelopmental Disorder
|
Miraç Yıldırım |
|
463. Strategies for assisting children with developmental challenges including autism in coping with persistent trauma
|
Lidia Gabis |
|
465. Neuroimaging in Cerebral Palsy: A Reliable Biomarker For Predicting Motor And Cognitive Severity
|
Meriem Ben Hafsa |
|
467. Sleep-related hypermotor epilepsy related to CHRNA4 successfully treated with nicotine and literature review
|
Ana Carolina Coan |
|
468. Associations between Total Body Parasite Burden and Malarial Retinopathy in Children with Cerebral Malaria
|
Douglas Postels |
|
469. Opsoclonus Myoclonus Syndrome: a Brazilian perspective
|
Ming Lim |
|
475. Chronic headache revealing chronic infantile neurological cutaneous and articular syndrome
|
Cyrine Karray |
|
476. Multi-dimensions of sleep health among in-school adolescents in rural and urban areas in Southwestern Nigeria
|
Oluwatosin Olorunmoteni |
|
481. A case of methotrexate intoxication presenting with stroke-like episodes
|
Gulsen Ersoz |
|
482. Infantile Epileptic Spasms: Impact of a Community-driven Awareness Campaign in the North West Region of Cameroon
|
Mundih Njohjam |
|
484. Evaluation of joint attention and perception of 3D motion and depth through virtual and augmented reality methods
|
Sheffali Gulati |
|
490. EEG analysis during sleep onset in autism spectrum disorder
|
Eiji Nakagawa |
|
495. Exercise Habits and Health-Related Quality of Life in Adolescents with Epilepsy
|
Chi Fan |
|
497. Evaluation of Patients Diagnosed with Optic Neuritis in Childhood: Single Center Experience
|
Olcay Ünver |
|
499. Children with Acute-onset Ptosis and Quadriparesis – Don’t forget to rule out Snake Bite
|
Juhi Gupta |
|
500. Evaluation of role of theta burst transcranial magnetic stimulation in autism: a randomized controlled trial
|
Sheffali Gulati |
|
505. ARV1 Gene: A Novel Cause of Autosomal Recessive Cerebellar Ataxia with Elevated Alpha-Fetoprotein
|
Thanuja Basavanagowda |
|
506. Acute Necrotizing Encephalopathy of Childhood and Central Nervous System Haemophagocytic lymphohistiocytosis: Two faces
|
Thanuja Basavanagowda |
|
507. Neuroimaging in hypoglycaemia beyond the neonatal age-group
|
Thanuja Basavanagowda |
|
508. Clinico-aetiological profile of hereditary spastic paraplegia in children attending a tertiary care hospital in India
|
Thanuja Basavanagowda |
|
512. Clinical profile and long term fine motor outcome in pediatric patients of GBS
|
Ashna Kumar |
|
515. Effect of Health Education on Knowledge and Attitude of Parents Towards Epilepsy in Egyptian Children
|
Maha Zakariya Mohammed |
|
516. Anti-NMDAR encephalitis combined with MOG antibody in a child with good prognosis: case report.
|
Leidi Vilchez Fernandez |
|
517. Electroclinical Characteristics of Patients with Childhood Absence Epilepsy for Seizures Outcome
|
Seda Kanmaz |
|
521. Late onset dystonia- a rare presentation of GM1 gangliosidosis
|
Payal Shah |
|
522. The value of clinical factors for genetic testing utility in infantile developmental and epileptic encephalopathies
|
Sada Kanmaz |
|
524. Heart Rate Variability as Early Prediction for Children with COVID-19 Associated Encephalopathy/Encephalitis
|
Jainn-Jim Lin |
|
525. Compassionate use with cannabidiol for Dravet Syndrome and tuberous sclerosis complex in Taiwan: a multicenter study
|
Kuang-Lin Lin |
|
527. A Case of Recurrent Autoimmune Encephalitis Due to Homozygous TNFAIP3 Mutation
|
Ibrahim Oncel |
|
531. Rising epidemiology of autism ? : real life observations from a french first line regional dispensary
|
Christian Zix |
|
532. Clinical Spectrum and genetic variations of Rett syndrome experienced from the child neurodevelopmental centre of a tert
|
Naznin Ruby |
|
534. Exploring the connection between Autism and Epilepsy
|
Sheffali Gulati |
|
536. Myotonia congenita, a case series of possible founder mutation
|
Lina Altaf |
|
537. Grange syndrome, Moyamoya mimicker
|
Lina Altaf |
|
541. Clinical and molecular aspects of DYSF mutations in dysferlinopathy: A single centre experience
|
Gunce Basarir |
|
542. Serum Orexin-A Levels in Childhood Generalized Epilepsies
|
Gunce Basarir |
|
544. A case of mitochondrial neurogastrointestinal encephalopathy or MNGIE syndrome, why not?
|
Seyfeddine Baouia |
|
548. Knowledge and attitude among doctors, nurses and other allied health workers on childhood neurodevelopmental disorders
|
Snikitha Tummala |
|
550. Outcome of epilepsy comorbid with attention-deficit/hyperactivity disorder or autism spectrum disorder
|
Kento Ohta |
|
551. Predictors of response to hormonal therapy in children with treatment naïve West syndrome: An observational study
|
Sheffali Gulati |
|
555. Correlation of parental knowledge with ketogenic diet compliance in West syndrome through diary counts & ketone records
|
Sheffali Gulati |
|
561. Girl with Duchenne muscular dystrophy due to copy number gain of exons 3 to 12 in dystrophin gene and DiGeorge Syndrome
|
Dana Craiu |
|
562. Broadening the clinical spectrum: Molecular mechanisms and clinical phenotypes of paediatric ANO3-dystonia
|
Juan Dario Ortigoza Escobar |
|
564. Management and Treatment choices in Pediatric Rasmussen’s Encephalitis: a single center case series.
|
Dana Craiu |
|
565. Epilepsy in Mali, State of art
|
Zeinab Kone |
|
573. The Severity of Hyperlactatemia as a Guide of Targeted Temperature Management (TTM) for Pediatric Asphyxial OHCA
|
Chen Ying Ching |
|
583. Case report: Two siblings with UNC80 deficiency
|
Elga Honey |
|
584. Effect of Thalidomide in immune mediated paradoxical reaction in childhood CNS tuberculosis
|
Prashant Jauhari |
|
585. Impact of COVID-19 on health utilisation and services in paediatric neurosciences
|
Ming Lim |
|
587. A case of SLC6A1 gene mutation with isolated, early-onset absence seizures and learning disability
|
Gokce Cirdi |
|
588. EEG Service for children with seizure and epilepsy in a tertiary hospital in the Eastern Cape of South Africa
|
Isabel Michaelis |
|
592. The role of selected serum cytokines in the pathogenesis of simple and complex febrile seizures
|
Damindri Herath |
|
596. Canavan disease: Atypical Disease Presentation
|
Noopur Navandar |
|
598. Vagus Nerve Stimulation as a Potential Intervention for cognitive and motor development in Rett patients
|
Yangyang Wang |
|
600. Two Siblings with Myopathy and choreoathetosis and a Novel Variant of ATP8A2
|
Sukanya Vrushabhendra |
|
603. Epileptic encephalopathy of genetic origin clinical-electro-radiological correlations in a Tunisian pediatric population
|
Cyrine Karray |
|
604. Evaluation of Clinical Features and Quality of Life in Children Diagnosed with Myotonic Dystrophy Type 1
|
Hatice Bektas Ontas |
|
605. Clobazam in Adjunctive Therapy in Children with Infantile Spasm
|
Esra Ozpinar |
|
606. Neuroimaging in focus: engaging with mothers around child brain development
|
Kirsty Donald |
|
608. Anti-Seizure Medications Costs in the United States: A Decade in Review
|
Pradeep Javarayee |
|
609. The ratio of Niemann-Pick A/B disease to cases of Gaucher disease varies by country
|
Marie Dantl |
|
611. Clinical profile and Outcome of Opsoclonus Myoclonus Ataxia Syndrome
|
Veena Surendran |
|
614. Unveiling the hidden masks of neuro tuberculosis - think out of the box!!
|
Sindhu Pappula |
|
617. A Case of an Anoctamine 5 (ANO5) Muscle Disorder Presenting with an Asymptomatic HyperCKemia Phenotype
|
Mirac Yildirim |
|
618. SURF1 Mutations in Leigh Syndrome: A Deep Dive into Two Cases
|
Olcay Ünver |
|
623. Association of molecular and environmental markers in childhood neurodevelopmental disorders: a cross-sectional study
|
Sheffali Gulati |
|
624. Focal Cortical Dysplasias Secondary To Depdc5 With Good Response To Ketogenic Therapy
|
Rocio Elizabeth Alamo |
|
625. Cerebral vs ‘CNS’ malaria: Does classification matter long-term?
|
Shaida Nishat |
|
628. An Extremely Rare Cause of Thalamic Tremor: MOGAD
|
Mirac Yildirim |
|
630. Acute Fulminant Cerebellitis Managed by Posterior Fossa Decompression Surgery with Favourable Neurologic Outcome
|
Gokce Cirdi |
|
633. Glut-1 deficiency with Leukoencephalopathy on MRI in a 2 months old
|
Yoshua Collins-Sawaragi |
|
636. Clinical and brain imaging correlates in Romanian cohort of children diagnosed with cerebral palsy
|
Oana Cernomazu |
|
637. Strategy for Diagnosis of Neuronal Ceroid Lipofuscinoses
|
Petra Oliva |
|
638. Immunological aspects in children with neurological manifestations of SARS-CoV-2 infection
|
Elena Capestru |
|
643. Multiple Mitochondrial Dysfunctions Syndrome-5 caused by Iron Sulphur Cluster Assembly 1 (ISCA 1) – a case report.
|
Ashwin Sardesai |
|
644. TBC1D24 gene related disorders: A unique cause of myoclonus and developmental encephalopathy
|
Ashwin Sardesai |
|
645. Early Nusinersen treatment and newborn screening in spinal muscular atrophy: a comparatıve study
|
İsmail Hakkı Akbeyaz |
|
646. Efficacy of Risdiplam in severe Spinal Muscular Atrophy type 2 patients: Acase series
|
Maureen Njoroge |
|
650. Premature rupture of membranes: A silent cause of Cerebral Palsy
|
Mahesh Kamate |
|
651. A case series of HHV -6 encephalitis with clinic-radiological profile in children at a tertiary care centre.
|
Dona Teresa Thomas |
|
652. Neurocutaneous Syndrome of Infantile B12 Deficiency: A Case Series from India
|
Juhi Gupta |
|
663. Safety and Efficacy of Adjunctive Fenfluramine in an Open-Label Extension Study of Children (Under 6 Years Old) With Dra
|
Nicola Specchio |
|
665. Radiographic Findings as Indicators of Neurodevelopmental Outcomes in Abusive Head Trauma
|
Maegan Newell |
|
667. Safety and Effectiveness of Adjunctive Fenfluramine in an Open-Label Extension Study of Patients With Dravet Syndrome
|
Lieven Lagae |
|
668. Intra-familial variability in patients with dominant RYR1 variations: analysis of 10 families
|
Xingzhi Chang |
|
670. Gelastic Seizures Beyond Hypothalamic Hamartomas - Prevalence And Outcome
|
Manisha Karamala Yalapalli |
|
675. Feeding Challenges in children with Cerebral Palsy in Dar Es Salaam, Tanzania
|
Edward Kija |
|
676. Magnitude of underweight among children with Cerebral Palsy in Dar Es Salaam, Tanzania: Using Cerebral Palsy Specific Gr
|
Victoria Ndembo |
|
678. Communication Challenges in children with Cerebral Palsy in Dar Es Salaam, Tanzania
|
Victoria Ndembo |
|
680. Acute malnutrition among children with epilepsy attending Mulago National Referral Hospital.
|
Juliana Kayaga |
|
687. Mental Retardation As A Main Indicator Of Patologic Genetic Variants In Exome Studies. Stratified Analysis In A Reference
|
Francisco Carratalá-Marco |
|
690. Epilepsy Care in Kenya: Gaps and Opportunities from Targeted Survey of Health Workers
|
Yael Shiloh-Malawsky |
|
691. Expression of genetic peripheral neuropathies in Southern African children
|
Gwendoline Kandawasvika |
|
692. An Atypical Presentation of Acute Disseminated Encephalomyelitis: Prolonged Fever
|
Mirac Yildirim |
|
693. Guillain-Barré Syndrome with Anti-GT1a Ganglioside Antibody: A Case Report
|
Mirac Yildirim |
|
695. Challenges in the diagnosis and management of children with spinal muscular atrophy in Ghana: a five-year retrospective
|
Charles K. Hammond |
|
700. The evaluation of the clinical usefulness of the preexisting diagnostic criteria for hemorrhagic shock encephalopathy.
|
Tsuyoshi Aihara |
|
701. Salient cases demonstrating benefit of consideration of simultaneous ECG recording together with routine interictal EEG
|
Kutluhan Yilmaz |
|
702. The recurrent PACS1 variant disrupting trans-Golgi-membrane trafficking: A recognizable phenotype
|
Tuğçe Aksu Uzunhan |
|
703. can we predict the occurrence of hypsarrhythm in term newborn with HIE ?: a prospective observational study
|
Harshkumar Patel |
|
706. Screening for autonomic disorders in ataxia-telangiectasia using the modified COMPASS-31: preliminary results
|
William Whitehouse |
|
708. Treatment and outcomes of epileptic spasms at the Komfo Anokye Teaching Hospital, Kumasi, Ghana - a 5-year retrospective
|
Perpetua Kanzie |
|
709. Prevalence, associated risk factors and management of Cerebral Palsy at a tertiary paediatric neurology clinic in Ghana
|
Efua Nuamah Yankah |
|
710. Clinical Characteristics of Juvenile Myasthenia Gravis in Patients Reporting to a Tertiary Health Care Facility in Ghana
|
Hannah-Sharon Mills |
|
711. Tertiary centre experience in investigating and diagnosing floppy babies
|
Sharmila Manivannan |
|
712. Subependymal giant cell astrocytoma (SEGA) in a neonate with multiple cardiac rhabdomyoma
|
April Jann Tutor-Malaza |
|
714. Cerebral Plasy Risk Factors At A District Hospital In Rural Malawi - Analysis of Interim Data
|
Thembi Katangwe |
|
716. Virginia Apgar: From Woman to Acronym
|
Bapi Tripata |
|
718. Quality of Life and Associated Factors among Pediatric Patients with Epilepsy in a Tertiary Hospital
|
Kimberly Dianne Mejia |
|
721. Nutritional Assessment in children with Cerebral palsy in Ibadan, Nigeria
|
Joy Ibeh |
|
722. Clinical Presentation and outcome of Children with Convulsive Status Epilepticus in Dar Es Salaam, Tanzania.
|
Aika Abia Shoo |
|
726. Comparison of Efficacy and Safety of Low- Versus High-Dose Oral Prednisolone in Infantile Spasm (IS)
|
Fawad Saleem |
|
728. Overt long QT syndrome in children presenting with seizure disoder
|
Faisal Zafar |
|
729. Role of Folinic Acid In Improving The Adaptive Skills And Language Impairment In Children With Autism Spectrum Disorder
|
Fawad Saleem |
|
730. Fetal neurological malformations where doppler solved the riddle: A series of three independent cases
|
Prashant Jauhari |
|
734. Frequency and clinical relevance of myositis-specific autoantibodies in children
|
Chahnez Charfi Triki |
|
735. Acute Treatment of Migraine in Pre-Adolescents: Real-World Analysis of Remote Electrical Neuromodulation (REN)
|
Badal Suthar |
|
738. Efficacy and safety of the ketogenic diet therapy in pakistani children with refractory epilepsy: a tertiary care hospit
|
faisal zafar |
|
739. Epilepsy following auto-immune encephalitis; a retrospective cohort study
|
Jithangi Wanigasinghe |
|
741. Retrospective analysis of influenza-associated encephalitis who presenting to a pediatric emergency department
|
Mei Hua Hu |
|
745. Cannabidiol treatment in intractable paediatric epilepsy – assessment using video-EEG
|
Stephen Malone |
|
746. A pilot study of precision medicine and personalised care of drug-resistant epilepsy in children in South Africa
|
Ian Olivier |
|
749. Sphingosine-1-phosphate lyase insufficiency syndrome presenting with oculomotor nerve paralysis
|
Esra Ozpınar |
|
750. Risperidone is highly effective in children with breath holding spells and reflex anoxic seizures: A proof-of-concept st
|
Sandhya A P |
|
751. The situation of care in Canavan Patients
|
Franziska Held |
|
754. Mild cases in Canavan disease
|
Janna Bredow |
|
755. Prevalence and factors associated with epilepsy among children with hydrocephalus at Cure Children's Hospital of Uganda
|
Agatha Namutosi |
|
757. Case report of anti-NMDA receptor encephalitis in a 12-year-old male: a challenging case from Tanzania.
|
Victoria Ndembo |
|
758. The Attention Deficit Hyperactivity Disorder (ADHD) phenotype in Preterm Graduates
|
Nerica Ramsundhar |
|
760. Unexpected seizure outcome in two cases of milder spectrum of SCN1A
|
Abinaya Seenivasan |
|
763. Evolving spectrum of COL4A1 related drug refractory epilepsy
|
Sonali Singh |
|
764. From prospective newborn screening for metachromatic leukodystrophy to gene therapy - the German experience
|
Annette Bley |
|
767. Prevalence of Active Epilepsy Among Children in northern Nigeria: Results from the BRIDGE project
|
Aminu Abdullahi |
|
768. COPE : CBITS Over Telehealth Promotes Empowerment- results of a pilot study in individuals with Autism
|
Deepa Menon |
|
769. RITUXIMAB AS A PROPHYLACTIC AGENT IN RECURRENT PEDIATRIC AUTOIMMUNE OPTIC NEURITIS – A RETROSPECTIVE ANALYSIS FROM A SI
|
Manish Prasad |
|
770. Pediatric bacterial meningitis in southern China: analysis of 838 cases
|
Wen-Xiong Chen |
|
771. NDUFV1 Mutation Related Mitochondrial Complex-1 Disorders- A Retrospective Case Series and Literature Review
|
Puneet Choudhary |
|
772. Paroxysmal non-epileptic disorders among children and adolescents in Ibadan, Nigeria
|
Joy Ibeh |
|
773. Expanding the Phenotype: Case Report of a Novel Alanyl-tRNA Synthetase 2 (AARS2) Homozygous Mutation in a 9-Year-Old
|
Anjaly Nair |
|
774. Utility of Next Generation Sequencing in Paediatric Neurological Disorders: experience from South Africa
|
Magriet van Niekerk |
|
775. Hereditary spastic paraplegia experience in a tertiary center in Taiwan
|
Wang-Tso Lee |
|
776. Childhood status epilepticus associated short-term mortality in Kano northern Nigeria
|
Umar Abba Sabo |
|
781. Risdiplam: the South African Experience - Challenges and Successes. A case series of 3 SMA patients.
|
Britta McLaren |
|
786. Hemorrhagic cerebellar pilocytic astrocytoma in a Filipino adolescent with sudden onset “worst headache of her life"
|
Patricia Orduna |
|
787. Genotype-Phenotype spectrum of Children with Epilepsy undergoing Whole Exome Sequencing
|
Jeevana Bollineni |
|
791. Sirolimus as alternative to surgery in TSC-associated bilateral SEGAs: An affordable option in resource-limited setting
|
Patricia Orduna |
|
795. Evaluation of Neurodevelopmental Status of Patients With Breath-Holding Spells(BHS) - Single Center Experience
|
Meltem Çobanoğulları Direk |
|
796. Application of The ILAE Recommendation for Maintenance of Anti-Seizure Medications Therapy in Neonates with HIE
|
Farhan Ali |
|
798. Balamuthia mandrillaris granulomatous amoebic encephalitis: a report of two cases
|
Kaajal Parbhoo |
|
800. Aicardi-Goutieres Syndrome: A single center cohort of thirty-eight genetically confirmed cases from Southern India
|
N BALAMURUGAN |
|
803. Subacute Cerebellar Ataxia in a Filipino Child: A Case of Overlap Syndrome of Anti-NMDAr encephalitis and MOGAD
|
Karina Terese Santos |