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

Abstract

View all access options for this article.

Siegler

Barsi

Neuwirth

. Hippocampal sclerosis in severe myoclonic epilepsy in infancy: a retrospective MRI study. Epilepsia. 2005;46:704–708.

Striano

Mancardi

Biancheri

. Brain MRI findings in severe myoclonic epilepsy in infancy and genotype-phenotype correlations. Epilepsia. 2007;48:1092–1096.

Korff

Laux

Kelley

Goldstein

Koh

Nordli

Jr . Dravet syndrome (severe myoclonic epilepsy in infancy): a retrospective study of 16 patients. J Child Neurol. 2007;22:185–194.

Hesdorffer

Shinnar

Lewis

. Design and phenomenology of the FEBSTAT study. Epilepsia. 2012;53:1471–1480.