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Epilepsia|June 26, 2003
Hypothalamic hamartoma and seizures: a treatable epileptic encephalopathySamuel F Berkovic, Alexis Arzimanoglou, Ruben Kuzniecky, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|January 2, 2021
Self-limited focal epilepsy and childhood apraxia of speech with WAC pathogenic variantsAbdulla Alawadhi, Angela T Morgan, Bettina E Mucha, et al.
The Lancet. Neurology|November 25, 2015
The genetic landscape of the epileptic encephalopathies of infancy and childhoodAmy McTague, Katherine B Howell, J Helen Cross, 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.
Developmental Medicine and Child Neurology|February 24, 2018
Stiripentol efficacy and safety in Dravet syndrome: a 12-year observational studyKenneth A Myers, Paul Lightfoot, Shekhar G Patil, et al.
Developmental Medicine and Child Neurology|January 26, 2019
Speech and language in bilateral perisylvian polymicrogyria: a systematic reviewRuth O Braden, Richard J Leventer, Anna Jansen, et al.
Epilepsia|July 31, 2013
Role of the sodium channel SCN9A in genetic epilepsy with febrile seizures plus and Dravet syndromeJohn C Mulley, Bree Hodgson, Jacinta M McMahon, et al.
Human Mutation|October 25, 2017
Gain-of-function HCN2 variants in genetic epilepsyMelody Li, Snezana Maljevic, A Marie Phillips, 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.
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