Showing results (61-70 of 729) with videos related to
Sort By:
Pageof 73
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|June 19, 2012
Diagnosis and long-term course of Dravet syndromeIngrid E SchefferEpilepsy Currents|August 13, 2011
Genetic testing in epilepsy: what should you be doing?Ingrid E SchefferThe New England Journal of Medicine|October 1, 2010
Timing of de novo mutagenesis--a twin study of sodium-channel mutationsLata Vadlamudi, Leanne M Dibbens, Kate M Lawrence, et al.Brain : a Journal of Neurology|October 16, 2012
In vivo loss of slow potassium channel activity in individuals with benign familial neonatal epilepsy in remissionSusan E Tomlinson, Hugh Bostock, Bronwyn Grinton, et al.Proceedings of the National Academy of Sciences of the United States of America|May 31, 2018
Dynamic action potential clamp predicts functional separation in mild familial and severe de novo forms of SCN2A epilepsyGéza Berecki, Katherine B Howell, Yadeesha H Deerasooriya, et al.Journal of Medical Genetics|July 11, 2009
De novo SCN1A mutations in Dravet syndrome and related epileptic encephalopathies are largely of paternal originSarah E Heron, Ingrid E Scheffer, Xenia Iona, et al.American Journal of Human Genetics|August 21, 2024
Inflation of polygenic risk scores caused by sample overlap and relatedness: Examples of a major risk of biasColin A Ellis, Karen L Oliver, Rebekah V Harris, et al.Epilepsia|February 4, 2014
Glucose metabolism transporters and epilepsy: only GLUT1 has an established roleMichael S Hildebrand, John A Damiano, Saul A Mullen, et al.Pageof 73