Showing results (121-130 of 729) with videos related to
Sort By:
Pageof 73
European Journal of Medical Genetics|October 27, 2019
EXOME REPORT: Novel mutation in ATP6V1B2 segregating with autosomal dominant epilepsy, intellectual disability and mild gingival and nail abnormalitiesMarie Shaw, Anna Winczewska-Wiktor, Magdalena Badura-Stronka, et al.Epilepsia|June 23, 2011
A retrospective population-based study on seizures related to childhood vaccinationSarah von Spiczak, Ingo Helbig, Ursula Drechsel-Baeuerle, et al.Annual Review of Genomics and Human Genetics|April 28, 2020
The Genetics of EpilepsyPiero Perucca, Melanie Bahlo, Samuel F BerkovicEpilepsia|August 22, 2012
Sodium channels and the neurobiology of epilepsyMegan Oliva, Samuel F Berkovic, Steven PetrouEpilepsia|January 28, 2023
History of familial adult myoclonus epilepsy/benign adult familial myoclonic epilepsy around the worldSamuel F Berkovic, Pasquale Striano, Shoji TsujiEpilepsia|January 16, 2010
The Epilepsy Genetic Association Database (epiGAD): analysis of 165 genetic association studies, 1996-2008Nigel C K Tan, Samuel F BerkovicArchives of Neurology|May 11, 2011
Glucose transporter 1 deficiency as a treatable cause of myoclonic astatic epilepsySaul A Mullen, Carla Marini, Arvid Suls, et al.Epilepsy Research|November 28, 2012
Do mutations in SCN1B cause Dravet syndrome?Young Ok Kim, Leanne Dibbens, Carla Marini, et al.The Medical Journal of Australia|March 16, 2018
The management of epilepsy in children and adultsPiero Perucca, Ingrid E Scheffer, Michelle KileyEpilepsia|April 17, 2013
SCN1A testing for epilepsy: application in clinical practiceShinichi Hirose, Ingrid E Scheffer, Carla Marini, et al.Pageof 73