DOI: 10.1055/s-00029030

Journal of Pediatric Neurology

Issue 03 · Volume 14 · September 2016 DOI: 10.1055/s-006-32356

Original Article

095
Ogwumike, Omoyemi Olubunmi; Agboke, Monsurat Afolake; Adeniyi, Ade Fatai: Association between Physical Activity Level and Health-Related Quality of Life of Children With and Without Epilepsy
102
Yetkin, İlhan; Shermatova, Kabil; Abuhandan, Mahmut; Demir, Mahmut; Aksoy, Nurten: Evaluation of Serum S-100B Protein Levels in Patients with Simple Febrile Convulsions

Case Report

105
Ruth, Natasha M.; Amrhein, Timothy; Passo, Murray; Gilkeson, Gary: Childhood-onset Systemic Lupus Erythematosus Complicated by Posterior Reversible Encephalopathy Syndrome in The Context of Kidney Dialysis and Plasma Exchange in Pediatric Lupus
110
Ganesh, Ramaswamy; Janakiraman, Lalitha; Viswanathan, Venkataraman: Eosinophilic Meningitis in an Infant
112
Iodice, Alessandro; Ferrari, Simona; Pinelli, Lorenzo; Molinaro, Anna; Spagnoli, Carlotta; Vezzoli, Cesare; Palestra, Filippo; Giordano, Lucio: A Case of Alpers–Huttenlocher Syndrome Due to a New POLG1 Mutation with Rapid Onset of Partial Status Epilepticus: Serial Neuroradiological and Neurophysiological Evaluation
119
McLaren, John; Conus, Sean; Craig, Alexa: Reversal of Cerebral Atrophy in a 4-Year-Old African Immigrant with Infantile-Onset Cerebral Folate Deficiency
122
Inaloo, Soroor; Khorshidi, Soorena; Jalli, Reza; Haghbin, Saeedeh: Seckel Syndrome and Vasculopathy: A Case Report
126
Silwal, Arpana; Morris, Alistair; Warren, Daniel; Vadlamani, Gayatri; Alston, Charlotte L.; Taylor, Robert W.: Cystic Leukoencephalopathy due to NDUFV1 mutation—A Report of the Phenotype and Its Rare Co-occurrence with Primary Hyperoxaluria

Letter to the Editor

133
Gras, Domitille; Hainque, Elodie; Fabre-Teste, Jennifer; Apartis, Emmanuelle; Roze, Emmanuel: Tremor-Like Myoclonus Associated with Klinefelter Syndrome in a Child