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058.Association of functional ability with nutritional status among children with cerebral palsy
Razia Sultana
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059.Improvement of hand hygiene practices among the healthcare workers in a neonatal intensive care unit
Abdullahel Amaan
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064.Seroprevalence of anti- n-methyl-d-aspartate receptor antibodies in children with seizures of unknown cause
Nebal Waill Saadi
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065.Neuromyelitis optica spectrum disorder in a sample of children: experience of children welfare teaching hospital- baghdad
Hayder Kadhim Jabbar
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067.Polymicrogyria and epilepsy with continuous spike-wave during sleep in pediatric patients
Sviatlana Kulikova
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068.Establishment of high-risk infant follow up clinic for implementation of early diagnosis of cerebral palsy guidelines
Khaled Ashour
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070.Effect of oxidative stress and glutathione on telomere length in a population of egyptian autistic children
Nagwa Meguid
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076.Diagnosis challenges of child abnormal movement in limited settings countries- the case of a little girl abandoned on the way to care
Dramane Coulibaly
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077.Health-related quality of life of children \with cerebral palsy at a tertiary hospital in nigeria
Naja'atu Hamza
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078.Thinning of the corpus callosum prominent in the splenium and colpocephaly: the AP-4 deficiency syndrome
Aydan Değerliyurt
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Presenters/Ilknur Erol
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080.A case of cav3 caveolinopathy / channelopathy with familial absence epilepsy and distal myoneuronopathy extending the clinical spectrum
Elif Perihan Öncel
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081.The first turkish case with early-juvenile-onset recessive distal titinopathy and the first case with prominent neurogenic involvement
Elif Perihan Öncel
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082.Second turkish case with micu1 mutation-related myopathy and extrapyramidal findings
Elif Perihan Öncel
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084.The first case of spastic ataxia type 4 associated with heterozygous mutations in mtpap gene
Şeyda Beşen
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085.An unusual cause of torticollis in childhood
Indrasish Ray Chaudhuri
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088.Online mother and baby yoga for preterm-born infants and their mothers in the time of covid-19 pandemic
Dilara Bozgan
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090.Predisposing factors to childhood epilepsy at the federal medical centre Umuahia- Nigeria
Amarachukwu Okafor
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092.A case of carbamazepine responsive neonatal epilepsy secondary to pacs2 gene mutation
Pawan Kashyape
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093.Solving a puzzle: an infant with developmental delay- epileptic spasms- and petechiae
Ayşe Yasemin Çelik
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095.Muscle cramps may be a clue for GFPT1 gene related congenital myasthenic syndrome
Özlem Yayıcı Köken
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101.Arthrogryposis multiplex congenita and scn1a mutations: another reported case and treatment guidance
Alyssa Robison
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102.Paraneoplastic guillain-barre syndrome: a case report and call for modified diagnostic criteria
Alyssa Robison
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103.Prevalence and outcomes of autoimmune encephalitis in a tertiary hospital in baguio city- philippines
Jaidi Sagay
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117. Cost Reduction for Families and Healthcare System with the Implementation of a Paediatric Comprehensive Epilepsy Clinic (2)
Michelle Kregel
Presenter/Arzu Ekici
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120.Flames (flair hyperintense lesions in anti-myelin oligodendrocyte glycoprotein-associated encephalitis with seizures)- a case report.
Ángeles Schteinschnaider
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121.Posterior reversible encephalopathy syndrome in pediatrics
Ángeles Schteinschnaider
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123.Overcoming adversities to promote early brain development in children - a study from rural india
Nandita Chattopadhyay
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125.Neurocutaneous melanosis: clinical and imaging characteristics in 7 patients
Angeles Schteinschnaider
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129.Do hyponatremia and anemia in simple febrile convulsions affect reccurence in the first 24 hours?
Elif Yildirim
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132.The diagnostic utility of the video eeg at a tertiary care center of north india: a retrospective study
Rahul Sinha
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133.Chronic meningitis mimicking idiopathic intracranial hypertension: a surprising diagnosis
Elif Yildirim
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135.New two findings in idiopathic generalized epilepsy-15 (eig-15); happy demeanor and gait disturbance: a case report
Elif Yildirim
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136.Temporary Consciousness Disturbance in Van der Knaap disease after Minor Head Trauma (2)
Arzu Ekici
Presenter/Arzu Ekici
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140.A novel founder mutation in the sgcb gene causes severe form of limb girdle muscular dystrophy (lgmd) 2e in sathwara community
Siddharth Shah
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142.Early infantile epileptic encephalopathy (ohtahara syndrome): a case report with stxbp1 mutation
Senem Ayça
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144.Efficacy and safety of cannabidiol dose adjustment in patients with lennox-gastaut syndrome in a phase 3 trial and open-label extension
Timothy B Saurer
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Hits: 25
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Hits: 9
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Hits: 13
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156.Acute necrotizing encephalopathy (ane) is a feature of dengue virus encephalitis
Terrence Thomas
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157.Linear scleroderma as one of the manifestations of collagenosis
Sarafroz Fayzullaeva
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161.The efficacy of everolimus ontsc associated drug resistant epilepsy
Mohammad Barzegar
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162.Updated demographics and safety data from patients with nonsense mutation duchenne muscular dystrophy receiving ataluren in the stride registry
Christian Werner
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163.Comparison of timed function test results in nmdmd patients receiving ataluren: stride registry vs phase 3 clinical trial
Panayiota Trifillis
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164.Comparing the change in 6-minute walk distance in nmdmd patients receiving ataluren: stride registry compared with phase 3 clinical trial
Panayiota Trifillis
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165.Age at loss of ambulation in stride registry and cinrg natural history study patients with dmd: a matched cohort analysis
Christian Werner
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169.Pulmonary function in duchenne muscular dystrophy patients from the stride registry and cinrg natural history study: a matched cohort analysis
Christian Werner
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170.Comparison of north star ambulatory assessment score change in nmdmd patients receiving ataluren: stride registry vs phase 3 clinical trial
Panayiota Trifillis
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172.A mobile domiciliary phlebotomy service to support patients with rare disease and screening study recruitment in the uk
Jo-anna Allen
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175.Epileptiform discharges and epilepsy in non-syndromic asd patients. Pre- peri- post-natal risk factors for epilepsy.
Adelina Glangher
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177.Primary headache with onset in childhood and adolescence: natural history and prognostic factors in a portuguese population
Juliana Da Silva Cardoso
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181.Recurrent painful ophthalmoplegic neuropathy: report of the two new pediatric cases
Çağatay Günay
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Hits: 14
182.The fate of spikes in self-limited epilepsy with centrotemporal spikes: are clinical and baseline eeg features effective?
Çağatay Günay
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184.Covid-19 vaccine hesitancy among neuromuscular disorder children and adolescents
Michael Kwan Leung Yu
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185.A pediatric case of reversible splenial lesion syndrome associated with sars-cov-2: case report
Ari̇fe Derda Yücel Şen
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186.New ways of treatment for childhood autism: are we moving in the right direction?
Taras Voloshyn
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193.Clinical characetristics of cases with muscular atrophy
Ari̇fe Derda Yücel Şen
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Hits: 15
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199.An observational study to assess inter-observer agreement for neonatal eeg interpretation
Vrushabh Gavali
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200.Posterior fossa malformations in tasp1-related disorder (suleiman-el-hattab syndrome)
Jehan Suleiman
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201.Assessing risk for relapse among children with infantile spasms using the based score
Guang Yang
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Hits: 6
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Category: ePosters
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Hits: 9
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Category: ePosters
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204.Challenges of determination in date of onset of infantile spasms: a tertiary health center‚äôs experience
Aristides Hadjinicolaou
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Hits: 9
206.A case of first pediatric pseudotumor cerebri syndrome secondary to superior sagittal sinus thrombosis associated with sars-cov-2
Mehmet Can Yeşilmen
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Hits: 13
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209.Levetiracetam monotherapy for the treatment of febrile and febrile induced seizures
Gamze Sarıkaya Uzan
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Hits: 18
211.Clinical and genetic profiles of grey matter heterotopia- a report of 28 patients
Adelina Glangher
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Hits: 20
212.Pyrimidine metabolism disorders as rare cause of psycho-motor retardation- dysmorphism and epilepsy
Defne Alikılıç
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Hits: 16
213.Clinical features beyond myopathy: three calpainopathy patients with capn3 mutation
Defne Alikılıç
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214.Analysis of clinical features and genetic variants among patients with slc6a1 mutations
Yunjian Zhang
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Category: ePosters
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224.Phenotypic and genotypic expansion of trappc12-related disorder
Dhanya Lakshmi Narayanan
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Hits: 9
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Hits: 19
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Category: ePosters
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Hits: 20
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Category: ePosters
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239.A pediatric case with primary familial brain calcification due to a homozygous variant on the jam2 gene
Leman Tekin Orgun
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Hits: 12
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Category: ePosters
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Hits: 17
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Category: ePosters
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Hits: 15
246.Two siblings with combined oxidative phosphorylation defect 11 with a novel mutation in the rmnd1 gene
Leman Tekin Orgun
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Category: ePosters
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Hits: 13
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Category: ePosters
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Hits: 11
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Category: ePosters
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Hits: 7
249.Onasemnogene abeparvovec for spinal muscular atrophy: experience from one center in the united arab emirates
Vivek Mundada
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Category: ePosters
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Hits: 7
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Category: ePosters
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Hits: 6
258.Epileptic encephalopathy secondary to homozygous tbc1 domain-containing kinase (tbck) mutation in four patients of puerto rican descent
Johanna De Luca-ramirez
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Category: ePosters
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Hits: 7
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Category: ePosters
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Hits: 7
261.Treatments and seizure outcome of 327 patients with infantile spasms: a retrospective analysis
Peifang Jiang
- Details
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Category: ePosters
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Hits: 5
271.Congenital myasthenia syndrome: correlation between clinical features and genetics from north india
Renu Suthar
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Category: ePosters
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Hits: 7
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Category: ePosters
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Hits: 20
291.A novel combined heterozygous mutation in the pla2g6 gene associated with early-onset parkinson‚äôs disease
Elif Perihan Öncel
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Category: ePosters
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Hits: 16
292.A Rare Cause of Developmental Epileptic Encephalopathy: D-Bifunctional Protein Deficiency with a Novel Pathogenic Variant
Cemile Busra Olculu
Presenter/Cemile Busra Olculu
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Category: ePosters
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Hits: 10
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Category: ePosters
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Hits: 7
301.Setting up of a standard of care for children with spinal muscular atrophy at a tertiary care center in north kerala: south india
Smilu Mohanlal
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Category: ePosters
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Hits: 5
302.Broad spectrum micronutrient supplementation in the management of adhd: a clinical trial and systematic review
Maureen Njoroge
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Category: ePosters
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Hits: 24
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Category: ePosters
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Hits: 13
304.Stroke secondary to thoracic outlet syndrome- treated successfully with thrombolytics and thrombectomy in a teenager: a case report
Dhanalakshmi Angappan
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Category: ePosters
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Hits: 7
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Category: ePosters
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Hits: 12
307.Diagnostics- clinical and genetic characteristics of duchenne muscular dystrophy in kazakhstan
Bakhytkul Myrzaliyeva
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Category: ePosters
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Hits: 6
308.Comparison of 3d printing techniques with patient-specific models for epilepsy surgery
Bilal Berke Ayvaz
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Category: ePosters
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Hits: 14
310.Clinical experience of gene replacement therapy in children with spinal muscular atrophy: a single center retrospective study of 25 children
Nidheesh Chencheri
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Category: ePosters
-
Hits: 15
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Category: ePosters
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Hits: 6
315.The impact of epilepsy on sleep characteristics in epileptic adolescents and their caregivers
İpek Dokurel Cetin
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Category: ePosters
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Hits: 13
316.Is there a relation between hippocampal measurements and childhood idiopathic generalized epilepsy?
Hilal Altas
- Details
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Category: ePosters
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Hits: 17
317.Clinico-etiological spectrum of children with bilateral basal ganglia lesions: an observational study from a tertiary care centre
Dasaratha Ramaiah Jinka
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Category: ePosters
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Hits: 15
- Details
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Category: ePosters
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Hits: 11
320.Ketamine: an effective and safe treatment for patients with melas and refractory status epilepticus
Jorge Vidaurre
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Category: ePosters
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Hits: 14
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Category: ePosters
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Hits: 15
322.Guillain‚äìbarre syndrome due to covid 19 in a child with acute lymphoblastic leukemia: a case report
Huseyin Tan
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Category: ePosters
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Hits: 17
696.Expanding phenotypic diversity of prune1 related disorders: an experience of four cases in a tertiary center
Didem Soydemir
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Category: ePosters
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Hits: 19
701.Acute disseminated encephalomyelitis (ADEM) in children: a multicenter retrospective study
Dilara Ece Toprak
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Category: ePosters
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Hits: 17
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Category: ePosters
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Hits: 18
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Category: ePosters
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Hits: 16
706.Clinical features of kcnq2 mutation in a romanian family
Florinela Gisela Rotaru
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Category: ePosters
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Hits: 12
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Category: ePosters
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Hits: 11
709.A rare neurodegenerative disorder mimicking autoimmune encephalitis induced by covid-19: condsias
Esra Özpınar
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Category: ePosters
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Hits: 13
711.Chylous blood in an infant with febrile encephalopathy: clues to metabolic etiology (very long chain acyl coa dehydrogenase deficiency)
Sachendra Badal
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Category: ePosters
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Hits: 12
- Details
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Category: ePosters
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Hits: 12
714.Home-eeg long term monitoring versus in house long term eeg monitoring
Yael Michaeli Yossef
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Category: ePosters
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Hits: 7
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Category: ePosters
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Hits: 11
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Category: ePosters
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Hits: 13
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Category: ePosters
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Hits: 11
- Details
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Category: ePosters
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Hits: 10
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Category: ePosters
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Hits: 15
721.Paroxysmal sympathetic hyperactivity in a child with high grade glioma post resection surgery.
Sachendra Badal
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Category: ePosters
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Hits: 21
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Category: ePosters
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Hits: 14
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Category: ePosters
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Hits: 11
725.Neurocognitive functions and behavior outcome of preschool-age children with a history of febrile convulsions
Bilgihan Bikmazer
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Category: ePosters
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Hits: 13
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Category: ePosters
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Hits: 6
727.Efficiency of rufinamide as add-on treatment of drug resistant generalized and focal epilepsies: one center
Yasemin Topcu
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Category: ePosters
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Hits: 14
728.Posterior reversible encephalopathy syndrome (pres) without radiological correlate : is it possible?
Apoorva Saxena
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Category: ePosters
-
Hits: 13
729.Co-morbid psychiatric disorders in patients with arachnoid cyst: a case series
Yeliz Engindereli
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Hits: 12
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Category: ePosters
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Hits: 12
733.Keep an aye on lumpy bumpy head: a case series highlighting spectrum of presentation in craniosynostosis
Marya Hameed
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Category: ePosters
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Hits: 6
734.The adaptability of health care professionals to the new neonatal seizure classification : ilae-2020
Hasan Tekgul
- Details
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Category: ePosters
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Hits: 12
735.Evaluation of efficacy and tolerability of lacosamide in children with drug-resistant epilepsy: a multicenter cohort study
Pınar Özkan Kart
- Details
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Category: ePosters
-
Hits: 23
736.Brain computed tomography still plays a critical role in the diagnosis of aicardi-goutières syndrome
Esra Özpınar
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Category: ePosters
-
Hits: 13
- Details
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Category: ePosters
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Hits: 9
740.A case of acute ophthalmoplegia presenting after multisystem inflammatory syndrome in children (mis-c)
Yavuz Sayar
- Details
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Category: ePosters
-
Hits: 15
741.Stxbp1 as a novel gene for sleep-related hypermotor epilepsy: a video-eeg documented case report
Esra Ülgen Temel
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Category: ePosters
-
Hits: 19
- Details
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Category: ePosters
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Hits: 13
744.The role of genetic factors in electroclinic and therapeutic effectiveness in children with dravet syndrome: a multi-center cohort study
Pınar Özkan Kart
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Category: ePosters
-
Hits: 11
- Details
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Category: ePosters
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Hits: 10
- Details
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Category: ePosters
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Hits: 10
751.Two pediatric cases of initial manifestation of multiple sclerosis after immunization with the pfizer-biontech covid 19 vaccine
Özben Akıncı Göktaş
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Category: ePosters
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Hits: 14
- Details
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Category: ePosters
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Hits: 6
753.Congenital icthyosis and neurological manifestations- sjogren larsson and beyond: a study of seven children.
Sachendra Badal
- Details
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Category: ePosters
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Hits: 11
754.Assessment of the knowledge level of physicians regarding the management of acute seizures in children and adolescents
Müge Ayanoğlu
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Category: ePosters
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Hits: 13
- Details
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Category: ePosters
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Hits: 13
757.Evaluation of pediatric cases with gullian barre syndrome: a national multicenter study
Selcan Öztürk
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Category: ePosters
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Hits: 14
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Category: ePosters
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Hits: 12
760.Cardiac impairment in duchenne muscular dystrophy: a single-center retrospective experience
Didem Ardicli
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Category: ePosters
-
Hits: 12
- Details
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Category: ePosters
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Hits: 21
- Details
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Category: ePosters
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Hits: 20
766.Pyridoxine dependent epilepsy with aldh7a1 mutation: clinical spectrum and outcome in a multicenter study cohort from turkey
Leman Tekin Orgun
- Details
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Category: ePosters
-
Hits: 16
767.Two cases with pontine tegmental cap dysplasia: a rare hindbrain anomaly which may be misdiagnosed as moebius sequence
Hülya Maraş Genç
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Category: ePosters
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