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Epileptic Disorders : International Epilepsy Journal with Videotape|August 24, 2023
ILAE Genetics Literacy series: Progressive myoclonus epilepsiesJillian M Cameron, Colin A Ellis, Samuel F Berkovic, et al.Epilepsia|October 21, 2022
Extended follow-up after anterior temporal lobectomy demonstrates seizure recurrence 20+ years postsurgeryAnne M McIntosh, Alex W Wynd, Samuel F BerkovicCurrent Opinion in Genetics & Development|May 19, 2026
Somatic mosaicism in hypothalamic hamartomaTimothy E Green, Samuel F Berkovic, Michael S HildebrandEpilepsy 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.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.Neurology|October 19, 2012
PRRT2 phenotypic spectrum includes sporadic and fever-related infantile seizuresIngrid E Scheffer, Bronwyn E Grinton, Sarah E Heron, 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.Human Molecular Genetics|April 30, 2004
GABRD encoding a protein for extra- or peri-synaptic GABAA receptors is a susceptibility locus for generalized epilepsiesLeanne M Dibbens, Hua-Jun Feng, Michaella C Richards, et al.Pageof 73