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First published 2009-02

Ictal Vomiting as an Initial Symptom of Severe Myoclonic Epilepsy in Infancy: A Case Report

Naomi Hino-Fukuyo, Kazuhiro Haginoya, Noriko Togashi [...]

Journal of Child Neurology

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First published 2010-10

Four Novel SCN1A Mutations in Turkish Patients With Severe Myoclonic Epilepsy of Infancy (SMEI)

Zulfikar Arlier, Yasar Bayri, Luis E. Kolb [...]

Journal of Child Neurology

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First published 2004-07

Severe Myoclonic Epilepsy in Infancy: Toward an Optimal Treatment

Berten Ceulemans, Marc Boel, Lieve Claes [...]

Journal of Child Neurology

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First published 2007-02

Dravet Syndrome (Severe Myoclonic Epilepsy in Infancy): A Retrospective Study of 16 Patients

Christian Korff, Linda Laux, Kent Kelley [...]

Journal of Child Neurology

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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 2009-8

Severe Epilepsy Syndromes of Early Childhood: The Link Between Genetics and Pathophysiology With a Focus on SCN1A Mutations

Carl E. Stafstrom

Journal of Child Neurology

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First published 2010-11

Genotype-Phenotype Correlations in a Group of 15 SCN1A-Mutated Italian Patients with GEFS+ Spectrum (Seizures plus,Classical and Borderline Severe Myoclonic Epilepsy of Infancy)

Francesco Nicita, Alberto Spalice, Laura Papetti [...]

Journal of Child Neurology

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Research article

First published 2013-8

The Ketogenic Diet in Dravet Syndrome

Linda Laux, Robyn Blackford

Journal of Child Neurology

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First published 2011-6

Leber’s Hereditary Optic Neuropathy Mutations Associated With Infantile-Onset Myoclonic Epilepsy

Richard E. Frye

Journal of Child Neurology

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Research article

First published 2017-4

Vagus Nerve Stimulation in Intractable Epilepsy Associated With SCN1A Gene Abnormalities

Stephen P. Fulton, Kate Van Poppel, Amy L. McGregor [...]

Journal of Child Neurology

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