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First published 2011-4

Ohtahara Syndrome With Biotinidase Deficiency

Pratibha Singhi, Munni Ray

Journal of Child Neurology

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First published 2007-5

Persistence of Suppression-Bursts in a Patient With Ohtahara Syndrome

Russell P. Saneto, Marcio Sotero de Menezes

Journal of Child Neurology

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Research article

First published 2015-3

Early Modified Functional Hemispherectomy in a Young Infant with Ohtahara Syndrome and Hemimegalencephaly

Antoine Nachanakian, Ghassan Hmaimess, Antonios El-Helou [...]

Journal of Child Neurology

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Research article

First published 2013-12

Epilepsy Surgery for Early Infantile Epileptic Encephalopathy (Ohtahara Syndrome)

Saleem I. Malik, Carlos A. Galliani, Angel W. Hernandez [...]

Journal of Child Neurology

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Research article

First published 2016-3

Diagnostic Approach to Genetic Causes of Early-Onset Epileptic Encephalopathy

Semra Gürsoy, Derya Erçal

Journal of Child Neurology

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Research article

First published 2014-2

A Novel Mutation in STXBP1 Gene in a Child With Epileptic Encephalopathy and an Atypical Electroclinical Pattern

Romina Romaniello, Claudio Zucca, Erika Tenderini [...]

Journal of Child Neurology

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First published 2014-9

Genotype & Phenotype of Ohtahara Syndrome–What's SCN2A Got to Do with It? a Clinician's Read

Jeffrey Buchhalter

Epilepsy Currents

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First published 2016-9

Heterozygous STXBP1 Mutations Associated with Ohtahara Syndrome: Two Littles Make a Lot

Vanesa Nieto-Estévez, Jenny Hsieh

Epilepsy Currents

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Research article

First published 2009-8

Clinical Evaluation and Diagnosis of Severe Epilepsy Syndromes of Early Childhood

Mary L. Zupanc

Journal of Child Neurology

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Research article

First published 2015-8

Pyridox(am)ine-5-Phosphate Oxidase Deficiency Treatable Cause of Neonatal Epileptic Encephalopathy With Burst Suppression

Andrea Guerin, Aly S. Aziz, Carly Mutch [...]

Journal of Child Neurology

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