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American Journal of Human Genetics|April 14, 2015
Mutations in the GABA Transporter SLC6A1 Cause Epilepsy with Myoclonic-Atonic SeizuresGemma L Carvill, Jacinta M McMahon, Amy Schneider, et al.
Seizure|January 29, 2016
Effectiveness of antiepileptic therapy in patients with PCDH19 mutationsJan Lotte, Thomas Bast, Peter Borusiak, et al.
Epilepsy & Behavior : E&B|August 4, 2020
A European questionnaire survey on epilepsy monitoring units' current practice for postoperative psychogenic nonepileptic seizures' detectionSofia Markoula, Andreas Liampas, Guido Rubboli, et al.
Neurology|June 15, 2018
European trends in epilepsy surgeryMaxime O Baud, Thomas Perneger, Attila Rácz, et al.
Epilepsia|December 27, 2019
Trends in pediatric epilepsy surgery in Europe between 2008 and 2015: Country-, center-, and age-specific variationCarmen Barba, Judith Helen Cross, Kees Braun, et al.
American Journal of Human Genetics|November 12, 2013
De novo loss-of-function mutations in CHD2 cause a fever-sensitive myoclonic epileptic encephalopathy sharing features with Dravet syndromeArvid Suls, Johanna A Jaehn, Angela Kecskés, et al.
Epilepsia|June 11, 2026
Pediatric epilepsy surgery: Global survey of invasive explorationsGeorgia Ramantani, Martha Feucht, Dorottya Cserpan, et al.
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