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Research article

First published 2012-7

Mesial Temporal Sclerosis in a Cohort of Children With SCN1A Gene Mutation

Katherine Van Poppel, Zoltan Patay, Donna Roberts [...]

Journal of Child Neurology

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Other

First published 2010-12

Benign Convulsions With Mild Gastroenteritis: Is It Associated With Sodium Channel Gene SCN1A Mutation?

Wen-Chin Weng, Shinichi Hirose, Wang-Tso Lee

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

Free access

Research article

First published 2017-11

A novel SCN1A mutation identified in a Chinese family with familial hemiplegic migraine: A case report

Yang Zhang, Ning Chen, Muke Zhou [...]

Cephalalgia

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Research article

First published 2022-4

Extending the Phenotype Related to SCN1A Gene: Arthrogryposis,Movement Disorders,and Malformations of Cortical Development

Ana Victoria Marco-Hernández, Alfonso Caro-Llopis, Pilar Rubio Sánchez [...]

Journal of Child Neurology

Free access

Research article

First published 2009-3

First Mutation in the Voltage-Gated Na v 1.1 Subunit Gene SCN1A with Co-Occurring Familial Hemiplegic Migraine and Epilepsy

M-J Castro, AH Stam, C Lemos [...]

Cephalalgia

Open access

Research article

First published 2022-06

Cell-Selective Adeno-Associated Virus-Mediated SCN1A Gene Regulation Therapy Rescues Mortality and Seizure Phenotypes in a Dravet Syndrome Mouse Model and Is Well Tolerated in Nonhuman Primates

Annie Tanenhaus, Timothy Stowe, Andrew Young [...]

Human Gene Therapy

Open access

Research article

First published 2025-1

Exploring the association between familial hemiplegic migraine genes ( CACNA1A,ATP1A2 and SCN1A ) with migraine and epilepsy: A UK Biobank exome-wide association study

Christian Staehr, Mette Nyegaard, Flemming W. Bach [...]

Cephalalgia

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Research article

First published 2018-11

Evolution of Brain Glucose Metabolic Abnormalities in Children With Epilepsy and SCN1A Gene Variants

Ananyaa Kumar, Csaba Juhász, Aimee Luat [...]

Journal of Child Neurology

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Letter

First published 2013-4

Authors’ Response to Correspondence on “Mesial Temporal Sclerosis in a Cohort of Children With SCN1A Gene Mutation”

Katherine Van Poppel, Zoltan Patay, Donna Roberts [...]

Journal of Child Neurology

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