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| POSTER SESSIONS Abstracts selected for presentation will be available online by April 15, 2014 |
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| GROUP II WEDNESDAY 07 MAY – THURSDAY 08 MAY 2014 | ||
| 2.1 HEADACHE | ||
| P225 | Intracranial hypertensiã“n in infancy: idiopathic intracranial hypertension or sencundary pseudotumor cerebri syndrome | Micaela Pauni, Argentina |
| P226 | Acute headache at the emergency department of a pediatric hospital | Carolina Vilte, Argentina |
| P227 | A possible relation of methylenetetrahydrofolate reductase (MTHFR) gene polymorphisms 677T/1298C to migraine in boys and girls. | Anneli Kolk, Estonia |
| P228 | Chronic and Recurrent Vertigo and Dizziness in Children and Adolescents | Thyra Langhagen, Germany |
| P229 | Prevalence of Headache among Adolescents in Northern Israel | Jacob Genizi, Israel |
| P230 | Child Headache Outpatient Clinic | Akira Nishimura, Japan |
| P231 | Effectiveness of occipital nerve block for occipital neuralgia in pediatric patients | Sun Jun Kim, Korea. Repub |
| P232 | Significance of Head-up Tilt Test in the Intractable Pediatric Migraine with Dizziness | Kon-hee Lee, Korea. Repub |
| P233 | Efficacy and safety of flunarizine in treatment of pediatric headaches | Young-il Rho, Korea. Repub |
| P234 | Pediatric migraine: use of ICHD II. criteria and treatment efficacy | Zvonka Rener-primec, Slovenia |
| P235 | Prevalence of Headache among school children in a district in the dry zone in Sri Lanka | Jithangi Wanigasinghe, Sri Lanka |
| P236 | The evaluation of prophylactic treatment of the children with migraine by using pedmidas score | Yasemin Topcu, Turkey |
| P237 | Topiramate for migraine headaches in a pediatric population | Conrado Medici, Uruguay |
| P238 | Headaches Associated With Bilateral Choroid Plexus Xanthogranulomas - Are they always benign? Case Report and Literature Review | Ilya Bragin, USA |
| P451 | Opthalmoplegic migraine: Is it a recurrent 3rd cranial nerve neuropathy? | Mariana González Suarez, Argentina |
| 2.2 METABOLIC DISORDERS | ||
| P239 | Novel PEX3 mutations identiï¬ed as the cause of a peroxisomal biogenesis disorder with moderate clinical phenotype | Clarisa Maxit, Argentina |
| P240 | Management of patients with adrenoleukodystrophy | Gabriela Reyes Valenzuela, Argentina |
| P241 | Biopterin disorder causing hiperphenylalaninemia: two different cases | Cristina Alencar, Brazil |
| P242 | Tay-sachs disease b1 variant: case report | Cristina Alencar, Brazil |
| P243 | Mucopolysaccharidosis type IV A: Evidence of Primary and Secondary Central Nervous System Involvement | Felippe Borlot, Brazil |
| P244 | Remote Spinal Cord Injury in Mucopolysaccharidosis type IVA after Cervical Decompression | Felippe Borlot, Brazil |
| P245 | New insights in mucopolysaccharidosis type vi: neurological perspective | Felippe Borlot, Brazil |
| P246 | Clinical and radiologic features in 12 patients with juvenile and adult GM1 Gangliosidosis. | João Kannebley, Brazil |
| P247 | Differential diagnosis of the chronic encephalopathies: the importance of following the psychomotor development marks | Tania Saad, Brazil |
| P248 | Tetrahydrobiopterin (BH4) Deficiency: A Case Report | Ana Carolina Cyrino, Brazil |
| P249 | Insights into therapeutic mechanism of L-arginine therapy on cerebrovascular reactivity and cerebral blood flow in MELAS syndrome | Lance Rodan, Canada |
| P250 | Rapid clinical and neuroradiological reversal of stroke-like episodes in MELAS syndrome following high dose L-arginine | Ishita Siddiq, Canada |
| P251 | Quantitative Measurement of Cerebral Oxygen Extraction Fraction Using MRI in Patients with MELAS in Different Phases | Jiangxi Xiao, China |
| P252 | Clinical, biochemical and Genetic Spectrum of Mitochondrial disorders in Egyptian Children: A Study of 15 cases | Laila Selim, Egypt |
| P253 | Role of Plasma Aminoacids and Urinary Organic Acids in Diagnosis of Mitochondrial Diseases in Children | Hoda Tomoum, Egypt |
| P254 | First case of GLUT1 deficiency syndrome in a 2-year-old Estonian girl: a case presentation | Tiina Talvik, Estonia |
| P255 | Chondrodysplasia Punctata or Conradi-Hünnermann Syndrome. The first Guatemalan case | Christian D. López, Guatemala |
| P256 | Lysinuric proteinuria- First genetically proven case from from India | Vivek Jain, India |
| P257 | Manganese transporter defect in a child: A rare case report | Mahesh Kamate, India |
| P258 | Profile of iem cases (small molecule type) in a tertiary care referral centre from india | Lokesh Lingappa, India |
| P259 | Mutation spectrum of Glutaryl-CoA Dehydrogenase Deficiency in South Indian population with Glutaric Aciduria Type I | Lokesh Lingappa, India |
| P260 | Chronic peripheral neuropathy progressing to encephalopathy as a result of lead intoxication | Harshuti Shah, India |
| P261 | Multiple carboxylase deficiency presenting as acute encephalopathy | Harshuti Shah, India |
| P262 | An experience of childhood neurometabolic diseases registry in Iran,2010-2012 | Alireza Tavasoli, Iran |
| P263 | A case of Leigh syndrome caused by 3-methylglutaconic aciduria | Yoko Nishimura, Japan |
| P264 | X-linked adrenoleukodystrophy in childhood | Kim Young, Korea. Repub |
| P265 | Biotin Responsive Basal Ganglia Disease : Unusual presentation with spinal cord involvement | Fahad Bashiri, Saudi Arabia |
| P266 | Epilepsy as a form of presentation of hyperprolinemia type i: a purpose of two cases | Inmaculada Carreras Sáez, Spain |
| P267 | Life expectancy of Leigh syndrome in infants and children | Ching-shiang Chi, Taiwan |
| P268 | Characterization of behavioral and seizure related manifestations of guanidinoacetate-methyltransferase deficiency. | Gulcin Akinci, Turkey |
| P269 | Infantile Neuronal Ceroid Lipofucsinosis a case report | Cihan Meral, Turkey |
| P270 | Hallervorden-Spatz case report “Case Report” | Cihan Meral, Turkey |
| P271 | An Infrequent Neuroradiological Finding in Menkes Disease | Mohamed Babiker, United Kingdom |
| P272 | Leukoencephalopathy is a common finding in childhood onset Mitochondrial Disease? | Evangeline Wassmer, United Kingdom |
| P273 | Effect Of Miglustat On Neurological Outcome In Early Infantile Niemann Pick C | Evangeline Wassmer, United Kingdom |
| P274 | Association of dermal Melanocytosis with GM1-Gangliosidosis Type 1 | Conrado Medici, Uruguay |
| P275 | Newborn screening for X-linked adrenoleukodystrophy: a pilot study | Silvia Tortorelli, USA |
| 2.3 MOVEMENT DISORDERS | ||
| P276 | Status dystonicus in children. case reports | Monica Ferrea, Argentina |
| P277 | Hypomyelination with atrophy of the basal ganglia and cerebellum - case report | Ana Carolina Cyrino, Brazil |
| P278 | Paroxysmal Dyskinesias in childhood | Karla Henriquez Guaita, Chile |
| P279 | Primary myoclonus-dystonia Often underdiagnosed entity: Report of four affected families | Puneet Jain, India |
| P280 | Movement Disorder in Three Filipino Adolescents with Anti NMDA Receptor Encephalitis: A case series | Philomine Daphne Obligar, Philippines |
| P281 | Chorea as a Manifestation of CNS Vasculitis in a 6-Year-Old Boy with Systemic Lupus Erythematosus | Jocelyn Montalvo-ortiz, Puerto Rico |
| P282 | Botulinum toxin- A in pediatric stiff hips | Tamer Rizk, Saudi Arabia |
| P284 | Efficacy of finasteride in the treatment of adults with refractory Tourette disorders. | Huei-shyong Wang, Taiwan |
| P285 | A Gilles de la Tourette (TS) case fully recovered by Topiramat | Nezir Özgün, Turkey |
| P286 | Redefining the clinical phenotype of psychomotor disabilities with X-Linked MCT8 Disease: Implications for improved therapies. | Rebecca Lehman, USA |
| P287 | Treatment of Tremor in Cerebral Palsy with Deep Brain Stimulation | Aimee Morris, USA |
| 2.4 MUSCLE & NERVE | ||
| P288 | Stiff person: pediatric case report | Pablo Jorrat, Argentina |
| P289 | Chronic Inflammatory Demyelinating Polyneuropathy Secondary (CIDP) to Inflammatory Bowel Disease (IBD) and Associated to Vitamin B12 Deficiency | Fernanda Goes, Brazil |
| P290 | Atypical clinical and histological presentations in patients with mutations on the RYR1 gene | Cristiane Martins, Brazil |
| P291 | CMTPedS.br: Brazilian version of the Charcot-Marie-Tooth Pediatric scale | Anita Saporta, Brazil |
| P292 | Polysomnographic abnormalities in children with Duchenne muscular dystrophy | Susana Lara, Chile |
| P293 | The Investigation of Genetics, Serum Biochemistry and Pathology in Duchenne Muscular Dystrophy | Jianxiang Liao, China |
| P294 | Clinical of different phenotypes with spinal muscular atrophy in children | Ping Yuan, China |
| P295 | A child with anti-GQ1b syndrome presenting with complete ophthalmoplegia and unilateral facial palsy. | Puneet Jain, India |
| P296 | Limb Girdle Myasthenia: An uncommon, treatable cause of proximal muscle weakness in children | Ramesh Konanki, India |
| P297 | Cognitive assessment in children with duchenne muscular dystrophy | Karthik Muthusamy, India |
| P298 | Unusual neuroimaging findings in two families with giant axonal neuropathy | Suvasini Sharma, India |
| P299 | Psychosocial intervention programme for families of patients with Duchenne Muscular Dystrophy | Priya Thomas, India |
| P300 | Array-cgh technology in the discovery of x-chromosome copy number variants in male patients with mental retardation syndromes | Arif Anwar, Malaysia |
| P301 | Síndrome Somatomorfo posterior a la vacunación contra la Hepatitis B notificado como ESAVI y su impacto en la vacunación contra la Hepatitis B en Ica, Perú | Ines Caro Kahn, Peru |
| P302 | Poliomielitis Aguda Pos Vacunal en el Perú Reporte de cinco casos y análisis del impacto social y sanitario entre los años 2009 y 2011 | Ines Caro Kahn, Peru |
| P303 | Does Acute Motor Axonal Neuropathy hurt? | Mireya Bolo-diaz, Puerto Rico |
| P305 | Triplication of PMP22 gene region associated with Charcot-Marie-Tooth disease-1A | Manjeet Raina, United Kingdom |
| P306 | Infantile Axonal Neuropathy -a case series | Nikil Sudarsan, United Kingdom |
| P307 | Prepubertal Myasthenia Gravis-Is infection a trigger or the cause? | Sandya Tirupathi, United Kingdom |
| 2.5 NEONATAL & FETAL NEUROLOGY | ||
| P308 | New antiepileptic drugs in newborns | Cecilia Vázquez, Argentina |
| P309 | The neurological development of newborns at high risk through outpatient services by multidisciplinary team | Alexandre Serafim, Brazil |
| P310 | Congenital amyoplasia: report of 7 cases | Andres Barrios, Chile |
| P311 | Effect of severe perinatal asphyxia on pituitary and thyroid functions in neonates | Reetika Saini, India |
| P312 | EEG and MRI comparison as a predicting factor for neurodevelopmental outcome in hypoxic ischemic encephalopathy infant treated with hypothermia | Alberto Spalice, Italy |
| P313 | Hypomelanosis of ito associated with multiple brain malformations | Bosanka Jocic-jakubi, Kuwait |
| P314 | Seguimiento neurológico de recién nacidos pretérmino en una unidad del imss | Dianey Flores, Mexico |
| P315 | Neurologic manifestations of infant chronic lead poisoning. report of 9 cases | Ines Caro Kahn, Peru |
| P317 | An Unusual Cause of Brachial Plexus Palsy in Neonatal Period: Retropharyngeal Abscess | Pinar Gencpinar, Turkey |
| P318 | Fetal MR neuroimaging - what is the outcome? | Prakash Satodia, United Kingdom |
| P319 | Neonatal seizures and metabolic disorders in a tertiary NICU | Prakash Satodia, United Kingdom |
| P320 | EEG Monitoring in preterm neonates using a new portable EEG device "microEEG" | Geetha Chari, USA |
| 2.6 NEUROCRITICAL CARE, NEUROTRAUMA, NEUROPROTECTION | ||
| P321 | Alterações autonômicas em empiema pleural septado: relato de dois casos pediátricos | Iara Bittencourt, Brazil |
| P322 | Vestibular Dysfunction Following Paediatric Traumatic Brain Injury - exploration of a novel diagnostic tool | Karen Barlow, Canada |
| P323 | The feasibility of performing computerized cognitive testing after mild TBI in a paediatric Emergency Department | Aneesh Khetani, Canada |
| P324 | Protective effect of Niuhuang Qingxin Powders on experimental seizure in developing rats | Xiaolu Chen, China |
| P325 | Protective effect of Niuhuang Qingxin Powders on hyperthermia induced seizure in developing rats | Xiaolu Chen, China |
| P326 | Predictors of outcome in non-traumatic coma in a pediatric cohort from South India: Results of a multivariate analysis. | Vykuntaraju Gowda, India |
| P328 | The Tympanic Membrane Displacement Analyser for Monitoring Intracranial Pressure in Childhood Acute Coma | Samson Gwer, Kenya |
| P329 | Neuroprotective effect of mild hypoxia in organotypic hippocampal slice cultures of rat | Soo Ahn Chae, Korea. Repub |
| P330 | Protective effects of novel antiepileptic drug lacosamide in experimentally induced transient cerebral ischemia | Sung Koo Kim, Korea. Repub |
| P331 | Cclinical features of encephalopathy in children with burns | Olga Lvova, Russia |
| P332 | Zonisamide Attenuates Hyperoxia-Induced Apoptosis In The Developing Rat Brain | Yasemin Topcu, Turkey |
| P333 | A novel method of experimental traumatic brain injury in rodents: validation study | Biju Hameed, UK |
| P334 | Spironolactone, but not mifepristone, enhances upregulation of Brain Derived Neurotrophic Factor (BDNF) and neurotrophic Trk B receptor (Trk B) gene expression in a rat model of Traumatic Brain Injury (TBI) | Biju Hameed, UK |
| P335 | Fatal Outcome Following First Infliximab Infusion in a Child with Inflammatory Bowel Disease | Fiona Baumer, USA |
| 2.7 NEUROENDOCRINOLOGY & NEUROGENETICS | ||
| P337 | ROHHAD: Rapid onset obesity and the idiopathic hypothalamic syndrome in children | Jon Soo Kim, Malaysia |
| P338 | Clinical and radiological findings in malformations of cortical development: clues for genetic testing | Paulina Carullo, Argentina |
| P339 | Hotfoot mutant in human characterized by cerebellar ataxia and early-onset retinal dystrophy caused by homozygous GRID2 deletion | Nicolas Deconinck, Belgium |
| P340 | Treatment of facial myotonia with botulinum toxin type A (BTX-A) in the Schwartz-Jampel syndrome (SJS): report of two cases | Igor Bandeira, Brazil |
| P341 | The cromossome 14q terminal deletion syndrome: case report with emphasis on neurological aspects | Clay Brites, Brazil |
| P342 | Brown-Vialetto-van Laere syndrome: a case report | Aline Lemos, Brazil |
| P343 | GM2 synthase deficiency: a New Inborn Error of Metabolism presenting as Hereditary Spastic Paraplegia with Infantile Onset | Charles Lourenco, Brazil |
| P344 | Lisdexanfetamine as a treatment option for narcholepsia | Heloisa Viscaino Pereira, Brazil |
| P345 | Protein C deficiency in children and adolescents with sickle cell anemia post-stroke | João Jg, Brazil |
| P346 | Infantile pompe's disease: a case report | Juliana Peixoto, Brazil |
| P347 | Torsion dystonia (DYT 1) caused by mutation in TOR 1A presenting with Myoclonic dystonia | André Luiz Santos Pessoa, Brazil |
| P348 | A case of GLUT1 deficiency syndrome with developmental delay and absence of seizures and movement disorder | André Luiz Santos Pessoa, Brazil |
| P349 | Mutation screening of FOXP2 gene in autism and Asperger syndrome | Michele Pozzato, Brazil |
| P350 | Pontocerebellar hypoplasia in the differential diagnosis of floppy infant syndrome | Tania Saad, Brazil |
| P351 | Case Report: Joubert Syndrome | Giuliana Salmazo, Brazil |
| P352 | Use of cyclodextrin in two Brazilian girls with Niemann-Pick disease type C | Camilo Santos, Brazil |
| P353 | Rett syndrome: clinical phenotypes associated to mutations in mecp2 gene | Mónica Troncoso, Chile |
| P354 | Defects in the synthesis of proteolipid protein, different forms of presentation for defects in the same gene. | Mónica Troncoso, Chile |
| P355 | Vanishing white matter disease (vwm): clinical features, genetic study and evolution in 10 chilean patients. | Mónica Troncoso, Chile |
| P356 | The Relationship between Academic Performance and Academic-related Boredom: the 5-HTTLPR Gene Polymorphism as a Moderator | Yangyang Liu, China |
| P357 | Next generation massively parallel sequencing of targeted exomes to identify genetic mutations in Chinese unknown cause early-onset epileptic encephalopathies | Jing Peng, China |
| P358 | ATP1A3 gene de novo mutation causing Alternating Hemiplegia of Childhood in an Ecuadorian girl. | Bolivar Quito-betancourt, Ecuador |
| P359 | Rett Syndrome,Genotype-Phenotype correlations | Lobna Mansour, Egypt |
| P360 | Novel mitochondrial mutation in an Indian family causing autosomal recessive neurodegenerative disorder | Sheffali Gulati, India |
| P361 | TOSCA - TuberOus SClerosis registry to increAse disease awareness | Paolo Curatolo, Italy |
| P362 | Aicardi syndrome in a genotypic male. Case report | Bakhytkul Myrzaliyeva, Kazakhstan |
| P363 | Neuropsychiatric Manifestations in Children with 22q11.2 microdeletion syndrome : Single Center Study | Eunhee Kim, Korea. Repub |
| P364 | Tuberous Sclerosis Complex in Paraguay. Report of 8 cases. | Laura Arredondo, Paraguay |
| P365 | Novel GLRB Gene Mutation in a Saudi Baby with Hyperekplexia | Tamer Rizk, Saudi Arabia |
| P366 | Pellagra-like Syndrome Proves to be a Variant of Xeroderma Pigmentosum-Cockayne Syndrome and Niacin Confers Clinical Benefit | Mustafa Salih, Saudi Arabia |
| P367 | Plexiform neurofibromas in South African children with Neurofibromatosis 1 | Veruschka Ramanjam, South Africa |
| P368 | Prevalence of LIS1 and related genes mutations in a population sample of 109 patients with structural CNS abnormalities. | Francisco Carratalá-Marco, Spain |
| P369 | Congenital fibrosis of extra ocular muscles (CFEOM) resulting from mutations in tubulin 3 (TUBB3) can mimic Moebius syndrome | Kosmapatabendige Dalpatadu, United Kingdom |
| P370 | Pontocerebellar Hypoplasia | Min Ong, United Kingdom |
| P371 | A Novel Variant in GABRB2 Associated with Intellectual Disability and Epilepsy | Ali Fatemi, USA |
| P372 | Adult Onset Tay-Sachs and Sandhoff Diseases Present with Non-specific Motor and Psychiatric Symptoms | Claire Teigen, USA |
| 2.8 NEUROIMMUNOLOGY | ||
| P373 | Anti-gq1b igg antibody syndrome: miller fisher syndrome and bickerstaff's brainstem encephalitis superposition | Pablo Jorrat, Argentina |
| P374 | Therapeutic plasma exchange in children with immune-mediated encephalopathy and a partial response to immunomodulatory treatment. | Analia Pastrana, Argentina |
| P375 | The aetiology, outcome and MRI of acute childhood encephalitis in a retrospective Australian cohort; emerging antibody-mediated encephalitides | Sekhar Pillai, Australia |
| P376 | Hemorrhagic Acute Diffuse Encephalomyelitis associated with Bordetella pertussis | Marcela Gonçalves, Brazil |
| P377 | Mesenteric ischemia following immunoglobin infusion for treatment of anti-NMDA receptor encephalitis | Bárbara Hackbart, Brazil |
| P378 | Case report: subacute sclerosing panencephalitis | Patricia Mariano Da Costa, Brazil |
| P379 | Optic neuritis in juvenile idiopathic arthritis patient | Fernanda Monti, Brazil |
| P380 | Neuromyelitis optica in children - a severe disease. | Fernanda Morgado, Brazil |
| P381 | Recurrent acute disseminated encephalomyelitis (adem): a case report | Avessandra Costa Avê, Brazil |
| P382 | Striving for the best treatment for Pediatric Acute demyelinating syndromes: results from cohort analysis | Tania Saad, Brazil |
| P383 | Extensive unihemispheric white matter lesion as atypical presentation of X-linked adrenoleukodystrophy | Ellen Siqueira, Brazil |
| P384 | Association between acute disseminated encephalomyelitis and Guillain-Barré syndrome in a child | Rafaela Viana, Brazil |
| P385 | Anti-NMDA receptor encephalitis. First case with confirmed circulating antibodies in Ecuador | Bolivar Quito-betancourt, Ecuador |
| P386 | A pediatric cohort of recurrent central nervous system demyelination; experience of a tertiary centre from north India | Sheffali Gulati, India |
| P387 | Variable manifestations of Anti-NMDA receptor encephalitis in children: Case series from tertiary care centre in India | Lokesh Lingappa, India |
| P388 | Clinical profile and outcome of children with opsoclonus myoclonus ataxia syndrome (oma) | Karthik Muthusamy, India |
| P389 | Does increased intracranial pressure contribute to the clinical symptomatology of acute disseminated encephalomyelitis (ADEM)? | Rotem Orbach, Israel |
| P391 | The clinical natural course after a first episode of central nerve systems demyelination in children | Cha Gon Lee, Korea. Repub |
| P392 | Screening autoimmune synaptic antibodies in pediatric patients suspecting autoimmune encephalitis | Byungchan Lim, Korea. Repub |
| P393 | Posterior Reversible Leukoencephalopathy Syndrome. Report of two cases. | Zulma Valenzuela, Paraguay |
| P394 | Non-paraneoplastic limbic encephalitis- clinical course in 10-years-old boy | Ilona Kopyta, Poland |
| P395 | Spinal cord involvement in children and adolescents with multiple sclerosis | Katarzyna Kotulska, Poland |
| P396 | The clinical and predictive factors for relapse after an initial event of acute disseminated encephalomyelitis in children. | Marie Hidalgo, Puerto Rico |
| P397 | Acute Necrotizing Encephalopathy of Childhood in a Non-Asian 4-Year-Old Child after Varicella Immunization | Leyda Sanchez-ortiz, Puerto Rico |
| P398 | Autoimmune Anti-N-methyl-D-Aspartate Receptor(antiNMDAR) encephalitis: 2 case reports from Saudi Arabia | Fahad Bashiri, Saudi Arabia |
| P399 | Neuropsychological Outcomes of Anti-NMDA Receptor Encephalitis in Children: A Case Series | Cristelle Chow, Singapore |
| P400 | Anti-N-methyl-D-aspartate Receptor Encephalitis in Taiwan | Kuang-lin Lin, Taiwan |
| P401 | Hashimoto encephalopathy presenting as seizure and acute psychiatric findings | Ayse Aksoy, Turkey |
| P402 | Longitudinally extensive transverse myelitis in a-17-month old girl patient with recurrent hypotonia attacks treated with intravenous immunoglobulin | Pinar Gencpinar, Turkey |
| P403 | Hemiconvulsion-Hemiplegia-Epilepsy (HHE) syndrome presenting with no apparent hemiconvulsion: A case report. | Rahul Singh, United Kingdom |
| P404 | Electrophysiological features of childhood autoimmune encephalitis | Rahul Singh, United Kingdom |
| P405 | Anti-MOG antibodies in Paediatric Demyelinating Disease | Sandya Tirupathi, United Kingdom |
| P406 | Kinsbourne Syndrome. Should we modify our therapeutic behavior? | Virginia Pedemonte, Uruguay |
| P407 | Kleine-Levin syndrome with rapid cycling - case report and review of the literature | Claudio de Gusmão, USA |
| P408 | Evaluation of neuroinflammation in pediatric multiple sclerosis patients | Mitchel Williams, USA |
| 2.9 NEUROONCOLOGY , NEURORADIOLOGY & NEUROPHTHALMOLOGY | ||
| P409 | The Posterior Fossa Syndrome predicts a poor long term functional outcome | Coriene Catsman-berrevoets, Netherlands |
| P411 | The utility of a semi-quantitative scoring of orbital imaging following the first episode of optic neuritis: A pilot study. | Rahul Singh, United Kingdom |
| P412 | Neurofibromatosis Type 1 (NF1) in children and Unidentified Bright Objects (UBOs) on Magnetic Resonance imaging (MRI). | Rita Ilari, Argentina |
| P413 | Inherited manganism: typical clinical and neuroimaging features | Marcela Avelino, Brazil |
| P414 | An unusual cause of blindness: bilateral geniculate lesion. | Renata Silva, Brazil |
| P415 | Clinical spectrum and neuroimaging in children with malformations of cortical development | Lobna Mansour, Egypt |
| P417 | The spectrum of leukodystrophies in children: experience at a tertiary care centre from north India | Puneet Jain, India |
| P418 | Phelan-McDermid syndrome associated with polymicrogyria | Alberto Spalice, Italy |
| P419 | The use of susceptibility-weighted imaging for epileptic focus localization in acute stage pediatric encephalopathy: A case report | Hiroki Iwasaki, Japan |
| P420 | Arterial spin labeling perfusion MRI analysis in a patient with brain swelling following acute subdural hemorrhage | Akiko Tamasaki, Japan |
| P421 | Comparison of cranial magnetic resonance imaging findings and clinical features in patients with corpus callosum abnormalities | Erhan Bayram, Turkey |
| P423 | N-methyl D-aspartate receptor (NMDAR) antibodies associated with distinct clinico-radiological white matter syndromes: clinical evidence for an anti-NMDAR leukoencephalopathy? | Rahul Singh, UK |
| P422 | Generalised radiological abnormality associated with acute neurological presentations in sickle cell disease | Borna Guevel, United Kingdom |
| 2.10 STROKE AND NEUROVASCULAR DISORDERS | ||
| P424 | Spontaneous Recurrent Bilateral Vertebral Artery Dissection: Two different outcomes of the same event | Maria Buompadre, Argentina |
| P425 | Vascular malformations of the spinal cord: presentation of a case series | Gabriela Reyes Valenzuela, Argentina |
| P426 | Social competence in survivors of pediatric stroke. | Vicki Anderson, Australia |
| P427 | Clinical Presentation of Moyamoya Disease and its association with Neuroimaging among Bangladeshi Children. | Narayan Saha, Bangladesh |
| P428 | Fibrocartilaginous embolism as a cause of spinal cord infarction A case report. | Leticia Miranda, Brazil |
| P429 | Posterior reversible encephalopathy syndrome: retrospective analysis of a pediatric intensive care unity | Patricia Takahashi, Brazil |
| P430 | STURGE-WEBER: A retrospective study of 28 pacients | Joao Tussolini, Brazil |
| P431 | Study of Stroke in Childhood and Adolescence | Ingrid Zavaleta, Brazil |
| P432 | Resting-state functional magnetic resonance imaging of motor networks in perinatal stroke | Jennifer Saunders, Canada |
| P433 | Familial moyamoya in 3 siblings with confirmed c.14576G>A variant mutation in RNF213 gene of South Asian (Bangladeshi) descent | Ivanna Yau, Canada |
| P434 | Pediatric arterial ischemic stroke in a serie of 63 patients: Clinical profile, risk factors and severity | Maria Hidalgo, Chile |
| P435 | Risk Factors for Perinatal Arterial Ischaemic Stroke: a Case-control Study | Mónica Troncoso, Chile |
| P436 | Evolution and prognosis in pediatric arterial ischemic stroke in a serie of 64 patients | Mónica Troncoso, Chile |
| P437 | Are methylenetetrahydrofolate reductase polymorphisms A1298C and C677T genetic risk factors for pediatric stroke and is there difference between boys and girls? | Anneli Kolk, Estonia |
| P438 | Epilepsy after presumed perinatal stroke | Rael Laugesaar, Estonia |
| P439 | Neurological Involvement in Children with E. coli O104:H4-induced Haemolytic Uraemic Syndrome | Hans Hartmann, Germany |
| P440 | Ischemic stroke in childhood | Konstantin Pushkarev, Kazakhstan |
| P442 | Preventing Stroke in Sickle Cell Disease in Portugal | Rita Silva, Portugal |
| P443 | Transient cerebral arteriopathy in a child associated with cytomegalovirus infection | Tai-heng Chen, Taiwan |
| P444 | Epidemiology and Characteristics of Pediatric stroke in Taiwan: a Nationwide Population based study | Kuo-liang Chiang, Taiwan |
| P445 | Stroke Outcome Prognostication in the Critical Care Setting | Jean-Pierre Lin, United Kingdom |
| P446 | To report a unique case of bilateral middle cerebral artery infarction associated with sildenafil use in a child. | Manjeet Raina, United Kingdom |
| P447 | Rationale and design of an International Maternal Newborn Stroke Registry : | Mariana Ciobanu, USA |
| P448 | Leptomeningeal phosphorylated ERK expression and urine vascular biomarkers in Sturge-Weber syndrome | Anne Comi, USA |
