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Neurology|October 19, 2012
PRRT2 phenotypic spectrum includes sporadic and fever-related infantile seizuresIngrid E Scheffer, Bronwyn E Grinton, Sarah E Heron, et al.
Epilepsy Research|August 8, 2007
Absence of mutations in the LGI1 receptor ADAM22 gene in autosomal dominant lateral temporal epilepsyElodie Chabrol, Isabelle Gourfinkel-An, Ingrid E Scheffer, et al.
Epilepsy Research|November 23, 2015
Variants in KCNJ11 and BAD do not predict response to ketogenic dietary therapies for epilepsyNatasha E Schoeler, Costin Leu, Jon White, et al.
Lancet (London, England)|September 24, 2002
Sodium-channel defects in benign familial neonatal-infantile seizuresSarah E Heron, Kathryn M Crossland, Eva Andermann, et al.
Epilepsia|March 15, 2006
Analyzing the etiology of benign rolandic epilepsy: a multicenter twin collaborationLata Vadlamudi, Marianne J Kjeldsen, Linda A Corey, et al.
Epilepsia Open|August 3, 2026
Changes in effectiveness and safety in patients with Lennox-Gastaut syndrome transitioning from the fenfluramine randomized controlled trial to open-label extension studyRima Nabbout, Orrin Devinsky, Lieven Lagae, et al.
Brain & Development|May 29, 2004
Etiological heterogeneity of familial periventricular heterotopia and hydrocephalusVolney L Sheen, Lina Basel-Vanagaite, Jean R Goodman, et al.
Annals of Neurology|November 23, 2019
SCN1A Variants in vaccine-related febrile seizures: A prospective studyJohn A Damiano, Lucy Deng, Wenhui Li, et al.
Epilepsy Research|March 6, 2012
Febrile infection-related epilepsy syndrome is not caused by SCN1A mutationsDaniel Carranza Rojo, A Simon Harvey, Xenia Iona, et al.
Neurology. Genetics|April 29, 2021
Phenotypic Spectrum of Seizure Disorders in MBD5-Associated Neurodevelopmental DisorderKenneth A Myers, Carla Marini, Gemma L Carvill, et al.
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