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journal of pediatric neurology
سال:2016 - دوره:14 - شماره:3
A Case of Alpers-Huttenlocher Syndrome Due to a New POLG1 Mutation with Rapid Onset of Partial Status Epilepticus: Serial Neuroradiological and Neurophysiological Evaluation
- صفحه:112-118
Association between Physical Activity Level and Health-Related Quality of Life of Children with and Without Epilepsy
- صفحه:95-101
Childhood-onset Systemic Lupus Erythematosus Complicated by Posterior Reversible Encephalopathy Syndrome in the Context of Kidney Dialysis and Plasma Exchange in Pediatric Lupus
- صفحه:105-109
Cystic Leukoencephalopathy due to NDUFV1 mutation-A Report of the Phenotype and Its Rare Co-occurrence with Primary Hyperoxaluria
- صفحه:126-132
Eosinophilic Meningitis in an Infant
- صفحه:110-111
Evaluation of Serum S-100B Protein Levels in Patients with Simple Febrile Convulsions
- صفحه:102-104
Reversal of Cerebral Atrophy in a 4-Year-Old African Immigrant with Infantile-Onset Cerebral Folate Deficiency
- صفحه:119-121
Seckel Syndrome and Vasculopathy: A Case Report
- صفحه:122-125
Tremor-Like Myoclonus Associated with Klinefelter Syndrome in a Child
- صفحه:133-134
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