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Neurology. Genetics|July 20, 2019
Human GABRG2 generalized epilepsy: Increased somatosensory and striatothalamic connectivityMangor Pedersen, Magdalena Kowalczyk, Amir Omidvarnia, et al.
JAMA Network Open|September 3, 2021
Safety and Tolerability of Transdermal Cannabidiol Gel in Children With Developmental and Epileptic Encephalopathies: A Nonrandomized Controlled TrialIngrid E Scheffer, Joe Hulihan, John Messenheimer, et al.
Epilepsia|January 27, 2010
Genetic testing in the epilepsies--report of the ILAE Genetics CommissionRuth Ottman, Shinichi Hirose, Satish Jain, et al.
Epilepsia|October 30, 2009
Neonatal seizures and long QT syndrome: a cardiocerebral channelopathy?Sarah E Heron, Marta Hernandez, Caitlin Edwards, et al.
Epilepsia|March 5, 2019
Schizophrenia is a later-onset feature of PCDH19 Girls Clustering EpilepsyDanique R M Vlaskamp, Anne S Bassett, Joseph E Sullivan, et al.
Scientific Reports|October 14, 2016
Early neuroimaging markers of FOXP2 intragenic deletionFrédérique J Liégeois, Michael S Hildebrand, Alexandra Bonthrone, et al.
Pediatrics|March 24, 2017
Fatal Cerebral Edema With Status Epilepticus in Children With Dravet Syndrome: Report of 5 CasesKenneth A Myers, Jacinta M McMahon, Simone A Mandelstam, et al.
Epilepsia|January 19, 2017
Frequency of CNKSR2 mutation in the X-linked epilepsy-aphasia spectrumJohn A Damiano, Rosemary Burgess, Sara Kivity, et al.
The New England Journal of Medicine|May 25, 2017
Trial of Cannabidiol for Drug-Resistant Seizures in the Dravet SyndromeOrrin Devinsky, J Helen Cross, Linda Laux, et al.
Epilepsia|April 10, 2013
Mutations in PRRT2 are not a common cause of infantile epileptic encephalopathiesSarah E Heron, Yeh Sze Ong, Simone C Yendle, et al.
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