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Nature Genetics|March 13, 2002
Mutations in the human ortholog of Aristaless cause X-linked mental retardation and epilepsyPetter Strømme, Marie E Mangelsdorf, Marie A Shaw, et al.
Ebiomedicine|May 31, 2022
Common risk variants for epilepsy are enriched in families previously targeted for rare monogenic variant discoveryKaren L Oliver, Colin A Ellis, Ingrid E Scheffer, et al.
Epilepsia|March 10, 2017
Instruction manual for the ILAE 2017 operational classification of seizure typesRobert S Fisher, J Helen Cross, Carol D'Souza, et al.
Epilepsia|February 8, 2014
Is focal cortical dysplasia sporadic? Family evidence for genetic susceptibilityRichard J Leventer, Floor E Jansen, Simone A Mandelstam, et al.
Annals of Neurology|July 21, 2021
Postictal Psychosis in Epilepsy: A Clinicogenetic StudyVera Braatz, Helena Martins Custodio, Costin Leu, et al.
Epilepsia|July 4, 2026
Prolonged fenfluramine use in open-label studies of Dravet or Lennox-Gastaut syndromes: Long-term safety, tolerability, patient global functioning, and considerations for interpreting effectivenessAntonio Gil-Nagel, Kelly G Knupp, Boudewijn Gunning, et al.
Neurology. Genetics|April 12, 2016
Epileptic spasms are a feature of DEPDC5 mTORopathyGemma L Carvill, Douglas E Crompton, Brigid M Regan, et al.
Scientific Reports|December 10, 2015
Loss of synaptic Zn2+ transporter function increases risk of febrile seizuresMichael S Hildebrand, A Marie Phillips, Saul A Mullen, et al.
Epilepsia|May 3, 2022
ILAE classification and definition of epilepsy syndromes with onset in neonates and infants: Position statement by the ILAE Task Force on Nosology and DefinitionsSameer M Zuberi, Elaine Wirrell, Elissa Yozawitz, et al.
Epilepsia|April 16, 2014
ILAE official report: a practical clinical definition of epilepsyRobert S Fisher, Carlos Acevedo, Alexis Arzimanoglou, et al.
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