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ICNC 2014
Hits: 19958

POSTER SESSIONS
Abstracts selected for presentation will be available online by April 15, 2014
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 identified 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

Details
ICNC 2014
Hits: 17684

POSTER SESSION GROUP I
Abstracts selected for presentation will be available online by April 15, 2014
MONDAY 05 MAY – TUESDAY 06 MAY 2014 0800-1730
1.1 CEREBRAL PALSY , NEURODISABILITY & NEUROREHABILITATION
P1 Association of socioeconomic status of parents with cerebral palsy in children Mizanur Rahman, Bangladesh
P2 Adapting the Sniffin' Sticks smell identification test for the pediatric population Laís Bastos, Brazil
P3 Psychiatric disorder associated with Cerebral Palsy Alessandra Freitas Russo, Brazil
P4 Perspectives of Educators Regarding Physical Therapy Work in an Inclusive Context Môyra Patresi, Brazil
P5 Evaluation nutritional and gastrointestinal disorders in healthy and cerebral palsy patients Danielle Rodrigues, Brazil
P9 In vitro fertilization and cerebral palsy; the Pető Institute experience Anna Kelemen, Hungary
P10 Multi-level botulinum injections in lower limbs for patients with cerebral palsy: long term experience from a developing country Monica Juneja, India
P11 Impact of Educational intervention using communication strategies on Knowledge and Attitudes of first year health professional students towards cerebral palsy. Sujata Kanhere, India
P13 Analysis of Clinical Profile, Etiological factors and Co-morbidities of Hemiplegic Cerebral Palsy in North Indian children Arushi Saini, India
P14 Effectiveness of periodization loaded sit-to-stand strengthening exercise on walking ability and energy expenditure in spastic diplegic cerebral palsy Dian Sari, Indonesia
P15 Effect of affective visual stimuli in a virtual meal-making environment on children with cerebral palsy Sharon Kirshner, Israel
P16 A case of Korean infant with clinically diagnosed Cerebro-Oculo-Facio-Skeletal Syndrome Jun Hwa Lee, Korea. Repub
P17 Cerebral Palsy in a Mother Child Children's Hospital in Lima, Peru Maria Rivas Lozán, Peru
P18 Caracterãsticas de la atenciã“n de salud de niã‘os con parãlisis cerebral evaluados en la unidad de neurologãa pediãtrica del hospital nacional cayetano heredia durante el periodo 2011-2012 Judith Vila, Peru
P19 The biomechanical methods of the gait evaluation in children with cerebral palsy. Ilona Kopyta, Poland
P20 My Special Case: A Rare Storm In Pediatrics Mahmoud Abeidah, Qatar
P21 Diagnostic value of Brain stem auditory evoked potentials in children Gemunu Hewawitharana, Sri Lanka
P23 Concerns and felt needs of parents of disabled children living in urban slums Samata Singhi, USA
P215 Quality of life in children with Duchenne muscular dystrophy Tereza Cristina Faria, Brazil
P216 Quality of life in children from a public school Tereza Cristina Faria, Brazil
P217 Cardiovascular risks and level of physical activity in children in from a public school Tereza Cristina Faria, Brazil
P218 Respiratory muscle training in patients with duchenne muscular dystrophy: clinical trial with one group Tereza Cristina Faria, Brazil
P219-1 Effects of musical literacy acquisition on children with hemiplegic cerebral palsy: is it possible to improve the cognition? Isac Bruck, Brazil
P219-2 Long term follow-up of hemiplegic cerebral palsy treated with botulinum toxin type A: foreseeing better participation in life situations Isac Bruck, Brazil
P219-3 Long term follow-up of hemiplegic cerebral palsy treated with botulinum toxin type A: social interferences Isac Bruck, Brazil
P219-4 Long term follow-up of hemiplegic cerebral palsy treated with botulinum toxin type A: cognitive impact in outcome rehabilitation Isac Bruck, Brazil
P219-5 Long term follow-up of hemiplegic cerebral palsy treated with botulinum toxin type A: best functional responders Isac Bruck, Brazil
P219-6 Long term follow-up of hemiplegic cerebral palsy treated with botulinum toxin type A: factors of participation in life situations Isac Bruck, Brazil
P219-7 Long term follow-up of hemiplegic cerebral palsy treated with botulinum toxin type A: epilepsy impact Isac Bruck, Brazil
P219-8 Long term follow-up of hemiplegic cerebral palsy treated with botulinum toxin type A: neuroimage influence Isac Bruck, Brazil
P220 How to effectively evaluate the outcome of neurocognitive rehabilitation in children with neurological disorders? Anneli Kolk, Estonia
P221 Comparison of the Denver and TIMP tests in infants with cytomegalovirus infection Dorota Dunin-wasowicz, Poland
P222 General movements quality in preterm infants-correlation with intraventricular hemorrhage Dorota Dunin-wasowicz, Poland
P223 Intrathecal Baclofen Pump: KSA Experience Tamer Rizk, Saudi Arabia
P224 Childhood Cavernomas. A 12-year experience Mónica Troncoso, Chile
P449 A Prospective analytical study on clinical and neuroradiological profile of term and preterm children with spastic diplegia. Prashant Jauhari, India
1.2 CNS INFECTIONS
P24 Paradoxical reaction in the central nervous system after tuberculosis treatment in an immunocompetent child. Analia Pastrana, Argentina
P25 Forma infanto-juvenil da Mielopatia associada ao HTLV-1/ paraparesia espástica tropical (HAM / TSP): Seguimento clínico em uma coorte de 10 ano Janeusa Chagas, Brazil
P26 Dengue with neurological complications of difficult diagnosis in pediatric patient- a case report Francisco Nobre, Brazil
P27 Neurological manifestations in childhood Baggio-Yoshinari Syndrome (Lyme Disease-like Syndrome in Brazil) Virginia Aparecida Virginia, Brazil
P28 Meningitis in childrens, in Quetzaltenango, Guatemala. Factor of Prognosis. Henry Galvez, Guatemala
P29 Tuberculosis (TB) of the Central Nervous System in Children: Clinical and MR Imaging Findings Paramdeep Singh, India
P30 Epidemiological features of purulent bacterial meningitis among children of Almaty. Galiya Kuttykuzhanova, Kazakhstan
P31 A case of infective endocarditis presented with bacterial meningitis Seong Joon Kim, Korea. Repub
P32 Paediatric Bacterial Meningitis in Southern Nigeria. Angela Frank-Briggs, Nigeria
P33 Menigoencefalitis tuberculosa en niños Johnny Montiel Blanco, Peru
P34 Neurologic Outcomes among Filipino Children Diagnosed with Central Nervous System Infection Martha Bolanos, Philippines
P35 Tumoral Cerebral Neuroschistosomiasis in a Filipino Child: A Case Report Alpha Mallillin, Philippines
P36 Pediatric central nervous system (cns) aspergillosis: a case report Alpha Mallillin, Philippines
P37 Opportunities of emergency chemoprophylaxis of tick-borne encephalitis in children Natalia Skripchenko, Russia
P38 Cervical Spinal Cord Compression in a Child with Cervicofacial Actinomycosis Po-cheng Hung, Taiwan
P455 Multiple cerebral abscesses following salmonella meningitis in a neonate Maciel Barrantes, Peru
1.3 DEVELOPMENT, COGNITION & PSYCHIATRY
P39 Adaptive Behavior and Developmental Level in Preschool Children Referred for Possible Autism Spectrum Disorder Paulina Carullo, Argentina
P40 Blindness and Autism Spectrum Disorders (ASDs) Rubin Jure, Argentina
P41 Atention Deficit Hyperactivity Disorder and Videogames: Which games do they play when they play? Esteban Vaucheret, Argentina
P42 Assessment of working memory and its relationship to the general intellectual performance in patients with Tuberous Sclerosis assessed by the Wechsler Intelligence Scale Sergio Antoniuk, Brazil
P43 Effects of stimulant medications for Attention Deficit/ Hyperactivity Disorder: study of 452 Brazilian patients Sergio Antoniuk, Brazil
P44 Cognitive Functions and Emotional Aspects in Children with Attention Deficit and Hyperactivity Disorder Iuri Capelatto, Brazil
P45 PANDAS Diagnosis in the Ultimate Context of Pediatric Neurology Carolina Carvalho, Brazil
P46 Application of youth self-report for ages 11-18 for assessment of mental disorders among teenagers from school Marcos Cristovam, Brazil
P47 Early-onset schizophrenia associated with Cerebral Palsy and Autism Spectrum Disorder: a case report Alessandra Freitas Russo, Brazil
P48 Twin-twin transfusion syndrome: follow up of infants treated with laser surgery Marilisa Guerreiro, Brazil
P49 Myelomeningocele : psychiatric symptoms and neuropsychological profile Melanie Mendoza, Brazil
P50 Influence of congenital hypothyroidism on psychomotor performance in infants Michelle Ouro, Brazil
P51 Intuitive physics in high functioning autists Cristina Pozzi, Brazil
P52 Autism Spectrum Disorders in a Brazilian Developmental Disorders Project Cristina Pozzi, Brazil
P53 Delivery and breastfeeding in autism. Alexandra Prufer De Q. C. Araujo, Brazil
P54 School phobia secundary to bullying by gigante nevus congenital – amazonas’ case report Joao Tussolini, Brazil
P55 Repetitive transcranial magnetic stimulation of dorsolateral prefrontal cortex in adolescent depression: Clinical and neurochemical effects. Adam Kirton, Canada
P56 Is Autism a Curable Disease: The Successful OSHA Program From Alex Hussein Abdeldayem, Egypt
P57 Study of auditory processing in children with autistic disorder Hesham Kozou, Egypt
P58 Prevalence of sleep abnormalities in autistic children - a cross sectional study Rachna Dubey, India
P59 Prevalence of Pervasive Developmental Disorders (PDDs) in siblings of children with PDDs: A cross sectional study from a developing country. Ankur Jindal, India
P60 Adaptation of the Vineland Adaptive Behavior Scale and its use in 3-9 year old Indian Children Rashmi Kumar, India
P61 Diagnostic accuracy of 'Indian Scale of Assessment of Autism (ISAA)' in 2 “ 9 year old Indian children with Autism Spectrum Disorder Sharmila Mukherjee, India
P62 Evaluation of adaptive profiles of Indian children aged 2 – 9 years with Autism Spectrum Disorder Sharmila Mukherjee, India
P63 Therapy of low dose levodopa in developmental disorders in Japan – a preliminary questionnaire survey Kyoko Hoshino, Japan
P64 Attention-Deficit Hyperactivity disorder in girls Mariko Maezawa, Japan
P65 Perinatal thyroid hormone deficiency and ultrasonic vocalization in neonatal and juvenile rats Hiromi Wada, Japan
P66 Epileptiform discharges in children with attention deficit/hyperactivity disorder Sajun Chung, Korea Repub.
P67 Psycho-emotional and psychosomatic disorders in mothers of children with Autism Spectrum Disorders Marco Casartelli, Paraguay
P68 Stereotypies as a marker of autism severity Cláudia Melo, Portugal
P69 New diagnostic method of Developmental dyspraxia in children Julia Sadovskaya, Russia
P70 Developmental features in children with dysphasia. Nikolay Zavadenko, Russia
P71 Endothelial Antibody Levels in the Sera of Children with Autistic Spectrum Disorders Shahid Bashir, Saudi Arabia
P72 The Influence of Fish Oil on Neurological Development and Function Mohammed Jan, Saudi Arabia
P73 Early white matter effects of alcohol exposure on the infant brain Kirsty Donald, South Africa
P74 The role of epilepsy in autistic regression Jana Domínguez-Carral, Spain
P75 Hyperactivity and impulsivity in children with pure, untreated allergic rhinitis Ming-tao Yang, Taiwan
P76 Autism spectrum disorder in Sotos syndrome: Two cases Nouha Bouayed, Tunisia
P77 Sleeping beauty syndrome!! A case report of Kleine-Levine syndrome Mehtab Iqbal, United Kingdom
P78 Learning difficulty in risk children Is it possible to prevent? Maria Delucchi Bottaro, Uruguay
P79 Functional neurological disorder in the pediatric emergency room: characteristics, outcome and diagnostic accuracy Claudio de Gusmão, USA
P80 Unexpected Subclinical Spikes: Clinical and Neuropsychological Correlations Mark Mintz, USA
P81 Ctalopram treatment of young children with autism spectrum disorder (asd): correlation with maternal history of depression Andrew Zimmerman, USA
1.4 EDUCATION & TRAINING
P82 Reporting of Systematic Reviews and/or Meta-Analyses in Eight Child Neurology Journals- a Quantitative Bibliometric Analysis of Research Publications Senthil Kumar, India
P83 Promoting Pediatric Neurology care in Cape Verde a Portuguese Project Rita Silva, Portugal
1.5 EPILEPSY
P84 Infantile spasms: Ictal video-EEG classification based on the Delphi West Group proposal Marina Aberastury, Argentina
P85 Complex Febrile Seizures: Neuroimaging and electroencephalogram utility in emergency Marina Aberastury, Argentina
P86 Multimodal intraoperative monitoring in spinal surgery: retrospective multicentric analysis and recomendations based in 1890 cases. Guillermo Agosta, Argentina
P87 Epilepsy phenotype in patients with double cortex: an Argentine series Betiana Comas, Argentina
P88 Morbidity in epilepsy surgery using grids or depth electrodes or combined implantations Betiana Comas, Argentina
P89 Surgical treatment of status epilepticus Betiana Comas, Argentina
P90 Reflex epilepsy in childhood Monica Ferrea, Argentina
P91 EEG monitoring in critically ill children: Indications, findings and impact on clinical management. Micaela Pauni, Argentina
P92 Epilepsia partialis continua: presenting symptom of alpers disease Angeles Schteinschnaider, Argentina
P93 Treatment with modified Atkins diet type in nine patients with drug-resistant epilepsy Marisol Toma, Argentina
P94 Ketogenic Diet National Consensus. Ketogenic diet Argentinian Group Maria Vaccarezza, Argentina
P95 Effectiveness and safety of ketogenic diet in a population of drug resistant epilepsy Maria Vaccarezza, Argentina
P96 Epilepsy due to protocadherin 19 gene mutation: report of the first argentinean case. Cecilia Vázquez, Argentina
P97 The SCN1A gene, early epilepsies, and genotype/phenotype correlation Hector Waisburg, Argentina
P98 Transcranial Direct Current Stimulation tDCS in Refractory Focal Epilepsy: Case Report Lakshmi Nagarajan, Australia
P99 Lacosmide as adjunctive therapy in Children with Refractory Focal Epilepsy Lakshmi Nagarajan, Australia
P100 New Onset Seizure Clinic for Children: Need and Importance Lakshmi Nagarajan, Australia
P101 Epilepsy risk factors in children Leanid Shalkevich, Belarus
P102 Early epileptic encephalopathy with suppression-burst revealing RFT1-CDG syndrome: report of two new cases. Alec Aeby, Belgium
P103 Vagus nerve stimulation in children with drug-resistant epilepsy: two case reports. Luciane Baratelli, Brazil
P104 Surgical treatment for seizure control in children and adolescents with brain tumor Marília Bernardino, Brazil
P105 Hemispheric surgery for epilepsy in children: outcome regarding seizures and language Joceli Da Silva, Brazil
P106 Prevalence of febrile seizure - a population-based study Juliane Dalbem, Brazil
P107 Epilepsy surgery in the first 3 years of life: clinical outcome and risk-benefits Marcela De Almeida, Brazil
P108 Predictors of recurrence of a first unprovoked seizure in children. A prospective study. Dirce Fujiwara, Brazil
P109 Hot executive functionm in children with epilepsy Luciane Lunardi, Brazil
P110 Infantile Spasms: a serious neurological disorder following whole-cell pertussis vaccine Conceicao Pereira, Brazil
P111 Epilepsy surgery in posterior cortex: short and long-term outcomes Nilton Santos, Brazil
P112 Evaluation of the Quality of Life of Parents and Carers of Children and Adolescents with Refractory Epilepsy in comparison with Parents and Caregivers of Children with Down Syndrome Ingrid Zavaleta, Brazil
P113 Down Syndrome: Clinical and EEG Correlates during Development Ahmed Bamaga, Canada
P114 Epilepsy Transition: challenges of caring for adults with childhood-onset seizures Felippe Borlot, Canada
P115 Absence status epilepticus in children as their first presentation of absence epilepsy: a report of 4 cases. Helene Dubreuil, Canada
P116 Infra-slow EEG activity and sleep spindle expression - potential window into thalamic function in infantile spasms Alice Ho, Canada
P117 Alternating Hemiplegia extends beyond Childhood to Adulthood Paul Hwang, Canada
P118 Clinical spectrum and handling in 13 children with electric sleep status Maria Lopez, Chile
P119 Electroencephalographic characterization of patients with pervasive disorder development Claudia Lopez, Chile
P120 West syndrome in child with down syndrome: description of a number of cases Carla Rojas, Chile
P121 Seizures not related to hypoglycemia in type 1 diabetic patients (DM1) Verónica Isabel Sáez Galaz, Chile
P122 Epilepsy associated to inborn errors of metabolism, study and evolution of 68 patients Scarlet Witting, Chile
P123 Dravet syndrome: description of 4 patients with genetic confirmation Scarlet Witting, Chile
P124 Febrile seizure recurrence reduced by intermittent oral levetiracetam Lin-yan Hu, China
P125 Application of hydrogen proton magnetic resonance spectrum in infant spasm Du Kaixian, China
P126 Array-CGH detection of chromosomal abnormalitiesin cryptogenic patients with infantile spasms Xiu-yu Shi, China
P127 The change of Wnt3a and Wnt5a mRNA in the process of epileptogenesis in the Kainate-induced epilepsy model Xiangping Xu, China
P128 Clinical diagnosis, treatment, and ALDH7A1 mutations in pyridoxine-dependent epilepsy in three Chinese infants Yang Zhixian, China
P129 Can Genes Predict Response to Hormonal Treatment in Infantile Spasms Li-ping Zou, China
P130 Quality of life in children with West Syndrome in Santiago de Cuba Paediatric Hospital Gelsy Naranjo Pelayo, Cuba
P131 Serum vitamin d and some bone markers levels in Epilepsy Marian Girgis, Egypt
P133 The use of chromosomal microarray in common clinical practice of newly diagnosed epilepsy of children in Estonia. Tiina Talvik, Estonia
P134 Does vigabatrin treatment for infantile spasms cause visual field defects ? An international multicenter study Raili Riikonen, Finland
P136 Using a self-regulation frame of reference for the prediction of quality of life in adolescents with epilepsy Antigone Papavasiliou, Greece
P137 Clinical profile of children with late onset spasms - A report of 24 cases Satinder Aneja, India
P138 Attention Deficit Hyperactivity Disorder in children with epilepsy Rachna Dubey, India
P139 Long term outcome of children with West syndrome: A retrospective case record analysis Sheffali Gulati, India
P140 Efficacy and safety of oral Triclofos as sedative for children undergoing sleep EEG "An observational study"  Puneet Jain, India
P141 Serum trace element levels in children receiving antiepileptic drug therapy: a cross-sectional study Ashish Kakkar, India
P142 Hyperhomocysteinemia: Essential evil in children on Anti Epileptics? Praveen Kishore, India
P143 The effect of depression on cognitive performance in children with refractory mesial temporal sclerosis (mts) Gopukumar Kumarpillai, India
P144 Comparative study of Febrile seizures Vs Generalised epilepsy with febrile seizure plus syndrome Lokesh Lingappa, India
P145 Clinico-etiological Profile of Infants with first seizure: An Observational Study from a Developing Country Devendra Mishra, India
P146 Ketogenic diet can be improved with a high polyunsaturated fatty acid content Janak Nathan, India
P147 Significant Male Prevalence in Children with West syndrome in India Kiran Prakash, India
P148 Long-term outcome of medically-treated drug-resistant epilepsy in children Vrajesh Udani, India
P149 Safety, feasibility and effectiveness of oral zonisamide monotherapy in comparison with intramuscular adrenocorticotropic hormone in infants with west syndrome Jitendra Sahu, India
P150 A study on unique association of polymicrogyria, sleep-related electrical status-epilepticus and intractable drop-attacks Jitendra Sahu, India
P151 Use of the modified Atkins diet in Lennox Gastaut syndrome Suvasini Sharma, India
P152 Feasibility of a Parenting Training Programme in Pediatric Epilepsy Priya Thomas, India
P153 SCN1A mutations in Indian patients with SCN1A-related epileptic disorders Vrajesh Udani, India
P154 Prevalence of haemostatic abnormalities in epileptic children on valproate monotherapy: a cross sectional study Sangeetha Yoganathan, India
P155 The effectiveness of intramuscular midazolam compared to rectal diazepam for anticonvulsant in children Prastiya Gunawan, Indonesia
P156 Vigabatrin Efficacy and Safety in Iranian Epileptic Children Mohammadkazem Bakhshandeh Bali, Iran
P157 Attention impairments in Benign Childhood Epilepsy with Centrotemporal spikes and Childhood Absence Epilepsy Paolo Curatolo, Italy
P158 Early EEG monitoring following prenatal diagnosis predicts epileptogenesis in tuberous sclerosis Romina Moavero, Italy
P159 Rufinamide as adjunctive drug in refractory epilepsy due to neuronal migration disorders Romina Moavero, Italy
P160 Early Predictors of Status Epilepticus-associated Mortality and Morbidity in Japanese Children Yoshihiro Maegaki, Japan
P161 Reflex periodic spasms are specific seizure type to 5p- syndrome Kentaro Shirai, Japan
P163 The Attention Deficit Hyperactivity Disorder in Children with Epilepsy Won-seop Kim, Korea Repub.
P164 A Case of Van der Knaap disease presenting seizure as the first symptom Youngchang Kim, Korea. Repub
P165 A Comparison Study on Simple and Complex Febrile Seizures in Korea Dong Wook Kim, Korea Repub.
P166 A retrospective analysis of patients with febrile convulsion(FC) followed by subsequent epilepsy on Jeju Island, South Korea Seunghyo Kim Kim, Korea. Repub
P167 Characteristics of Hypoxic ischemic encephalopathy with seizure in children Young Se Kwon, Korea Repub.
P168 Clinical and Genetic Characteristics of Febrile Infection-Related Epilepsy Syndrome Soonhak Kwon, Korea Repub.
P169 Relation to Cortical blood flow and electrographic activity in Childhood-onset Seizures: Correlation Between MRI-SWI and EEG Yun-jin Lee, Korea. Repub
P170 EEG study in Myanmar children with complex febrile seizures Aye Saan, Myanmar
P171 Epilepsy: Beliefs on causes and treatment modalities amongst caregivers in Southern Nigeria. Angela Frank-briggs, Nigeria
P172 Risk factors for intractable epilepsy in children Farida Iftikhar, Pakistan
P173 Clinical and Epidemiological Characteristics of Children with Refractory Epilepsy Treated at a Tertiary Hospital in Lima, Peru. Iván Espinoza, Peru
P174 Quality of life of filipino children with epilepsy aged 5-12 years old using pedsql tm 4.0 Philomine Daphne Obligar, Philippines
P175 Simultaneous ACTH and antiviral therapy in West syndrome Dorota Dunin-wasowicz, Poland
P176 Lack of efficacy of monotherapy in epilepsy of the 1st year of life- possible correlation with etiology? Dorota Dunin-wasowicz, Poland
P177 Eepistop - international, long-term, prospective study evaluating clinical and molecular biomarkers of epileptogenesis in a genetic model of epilepsy tuberous sclerosis complex Sergiusz Jozwiak, Poland
P178 Predictors of post-stroke seizures in Polish paediatric patients Ilona Kopyta, Poland
P179 Epilepsy in Tuberous Sclerosis Complex. Katarzyna Kotulska, Poland
P180 Epileptic encephalopathy with STXBP1 mutations - expanding the eletroclinical phenotype Cláudia Melo, Portugal
P181 Investigation of calcium content among children with epilepsy Viktoria Guzeva, Russia
P182 Parent's Knowledge and Attitudes toward Children with Epilepsy Mohammed Jan, Saudi Arabia
P183 Public Awareness and Attitudes towards Epilepsy Mohammed Jan, Saudi Arabia
P184 Primary School Teacher's knowledge and attitudes toward children with epilepsy Mohammed Jan, Saudi Arabia
P185 The role of melatonin in the effective attainment of Electroencephalograms in Children in a sub-Saharan African setting Roland Ibekwe, South Africa
P186 Doose Syndrome: review and evolution-related factors in 20 cases Teresa Escobar-delgado, Spain
P187 Atomoxetine treatment in patients with attention deficit hyperactivity disorder and epilepsy Veronica Puertas Martin, Spain
P189 Sustained short term spasm control with intramuscular ACTH or oral prednisolone: Randamised, single blind clinical trial – preliminary report Jithangi Wanigasinghe, Sri Lanka
P190 Prescription pattern of anti-epileptic medications for childhood epilepsy among paediatric neurologists Jithangi Wanigasinghe, Sri Lanka
P192 Status epilepticus in infants and children Hsiu-fen Lee, Taiwan
P193 Dispersion durations of P-wave and QT interval in children treated with ketogenic diet Onder Doksoz, Turkey
P194 Mediterranean Style Ketogenic diet: Efficacy and Safety Orkide Guzel, Turkey
P195 Three-year Follow-up on the Intavenous Immunoglobulin Therapy in Landau-Kleffner Syndrome Bulent Unay, Turkey
P196 The effect of ketogenic diet on thyroid function in children with refractory epilepsy Unsal Yilmaz, Turkey
P197 Nodding syndrome patients improve with symptomatic treatment Richard Idro, Uganda
P198 Visually induced epilepsies Imad Saadeldin, United Arab Emirates
P199 The spectrum of benign neonatal and infantile seizures Imad Saadeldin, United Arab Emirates
P200 Seizure and Developmental Outcome of Infantile (epileptic) Spasms Starting as FE in Early Infancy Siddharth Jain, United Kingdom
P201 Chronic Pancreatitis in child treated for refractory epilepsy with Zonisamide Venkateswaran Ramesh, United Kingdom
P202 Head-to-Head Comparison of Ketogenic Diet and Vagus Nerve Stimulation in Paediatric Population with Pharamacoresistant Epilepsies Nikil Sudarsan, United Kingdom
P203 Ketogenic Diet Efficacy in the Treatment of Intractable Epileptic Spasms Ahmed Abdelmoity, USA
P204 The simultaneous use of Ketogenic diet and Vagus Nerve Stimulator in patients with pharmacologically refractory epilepsy Ahmed Abdelmoity, USA
P205 Autoimmune Encephalitis with Anti-VGKC Antibodies Mimicking HSV Encephalitis in a Teenage Boy Huiyuan Jiang, USA
P206 Designing a Clinical Study of Clobazam for Dravet Syndrome Using Pharmacokinetic/Pharmacodynamic Modeling Deborah Lee, USA
P207 Quantification of connectivity strength between epileptogenic cortex and remote FDG PET abnormalities in children with ETL epilepsy Otto Muzik, USA
P208 Can Epilepsy Etiology Predict Response to Ketogenic Diet in Children? Katherine Nickels, USA
P209 An easy to use diagnostic tool for pediatric epilepsy in low-resource regions Archana Patel, USA
P210 Human Papillomavirus Infection Is Not Causally Related to FCD IIB Kevin Shapiro, USA
P211 Assessment of the Implementation of the Epilepsy Quality Measures in the Commission for Children with Special Health Care Needs (CCSHCN) Alejandra Stewart, USA
P212 Does Antiepileptic Drug (AED) Failure for Lack of Efficacy Affect Long-Term Prognosis in Children with Generalized Epilepsy? Elaine Wirrell, USA
P213 Stroke in childhood lead epilepsy. is it true? Ziyodakhon Saidazizova, Uzbekistan
P214 Some clinical features of Mesial Temporal Lobe Epilepsy in Children Shaanvar Shamansurov, Uzbekistan
P450 Mutational analysis of TSC1 and TSC2 in Korean patients with tuberous sclerosis complex: genotype and epilepsy Jin Sook Lee, Korea Repub.
P452 The Knock in mouse model of Alternating Hemiplegia of Childhood Ute Hochgeschwender, USA
P453 Infantile spasms and focal seizures: A previously unreported presentation of a WDR45 mutation Mohamad Mikati, USA

ICNC2014 Schedule Monday

Details

 Monday 5 May 2014 

02:00 PM - 02:15 PM

 

 

03:15 PM - 03:30 PM

 

 

04:30 PM - 04:45 PM

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04:00 PM - 04:15 PM

 

 

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Programme

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Details
ICNC 2014
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02 December 2013
2400 HRS GMT

Abstract submissions for the 13th International Child Neurology Congress (ICNC2014) is now CLOSED. Those who were in the middle of submitting the abstract while the deadline passed will still be able to complete the submission process.

Many thanks to all those who have submitted their abstracts to the conference. In keeping with the high standards of the congress, we have had an overwhelming response to the call for papers.

The submitted abstracts will now be assigned for blind peer review. Authors who originally submitted the abstracts will be able to keep track of their papers by logging on at http://icnapedia.org/icnc/index.php/icnc/2014  [Please note that this is different from your normal ICNApedia login]

We will endeavour to complete the peer review process and announce acceptances of abstracts for both oral and poster presentations  by early January 2014. All authors will be kept informed of the progress regularly.

The ICNC2014  Organising Committee and Scientific Program Committee would like to thank all of your for your cooperation and wishes everyone a very festive christmas and is looking forward to welcoming you all at the Iguazu Falls in May 2014

Please do not hesitate to contact us if you have any queries regarding your abstract submission at  support@icnapedia.org

Late breaking abstracts

Authors who have already submitted their abstracts are not prohibited from submitting late-breaking abstracts. However please note that late-breaking abstracts are not a second chance for those who missed the official abstract deadline. Only state-of-the-art researches with up-to-date results are considered as late-breaking abstracts. The selection of abstracts will be based on scientific quality and novelty of research either in basic or clinical science. All late breaking abstracts should be emailed to icnc@icnapedia.org

 

Details
ICNC 2014
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General Information

To find out whether you need a visa to visit Brazil, see the Embassy of Brazil website or check with your local Brazil Embassy/Consulate or other diplomatic representative before you travel. The rules change regularly, so you should check you have the most up to date information for your trip. The visa requirements for Brazil by country can also be viewed here

In general foreign citizens travelling to Brazil as tourists or as participants in conferences, seminars, must have a ‘Tourist Visa’.Applicants intending to travel accompanied by spouses and children should also apply for a tourist visa for them.

 When travelling to Brazil on tourism, citizens of the following countries are exempted from a tourist visa:

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Nationals of Kosovo and Taiwan: Visas are to be issued on a Brazilian “Laissez-Passer”, for a period not exceeding ninety days. Prior approval required.

Citizens from the following countries are subject to prior approval from the Brazilian Ministry of External Relations: Central African Republic, Nepal, Nigeria, North Korea and Senegal.

Holders of travel documents/Certificate of Identity (as opposed to an ordinary passport) issued by any country also require prior approval.

Further information can be found on the Brazilian Embassy / Consulate website in your country.

Letter of Invitation

Participants that require an official letter of invitation in order to obtain a visa, to raise travel funds or for administrative purposes should apply for this invitation by at least 8 weeks prior to the meeting at the very latest. It should be understood, however, that such an invitation is not a commitment on the part of the organisers to provide financial support. 

An invitation letter can only be issued which includes the period of the conference plus the Saturdays and Sundays directly before and after the conference, respectively.

Letters of invitation for those not registered by March 1, 2014 will be cancelled

We would like to point out that invitation letters are only sent to the address indicated by the applicant. The provided name and address must exactly match that on your passport. All letters will be emailed to you as a signed PDF document, for you to print as required. The ICNC2014 organizing committee will NOT send invitation letters to embassies, neither by fax/email nor by separate post. The applicants are responsible to take care of their own visa application and need to directly contact the respective embassy. Please consider that the invitation letter is a standard letter which will not be modified individually.

In order to request an invitation letter you need to complete the form available here. Please note that you are responsible for contacting the relevant Brazilian Embassy and for finding out what kind of visa you require. Please allow sufficient time for the  local Embassy to process your visa.

If you are travelling to one of the three countries (Brazil, Argentina, Paraguay) below then you
do not need a VISA if you are from any of the countries listed under each of them.
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(*) Reciprocity Tax to Argentina

  1. North American US$ 160 - Worth for more than one entry; valid for 10 years.
  2. Canadians US$ 75 – Valid for a single entry; valid for 90 days or US$ 150 - Valid for more than one entry; valid for 05 years
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Payments and information:
www.provinciapagos.com.ar/dnm 
https://virtual.provinciapagos.com.ar/ArgentineTaxes/Registro.aspx

 

  1. ICNC2014 registrants
  2. ICNC2014 Speakers
  3. ICNC2014- Who's attending
  4. Registration

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