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The 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.
Epilepsy Currents|November 18, 2024
The Multidisciplinary Team in the Treatment of Patients With EpilepsyJohn Stern, Susan Stanton, Laura Howe-Martin, et al.
Frontiers in Neurology|October 5, 2020
Are Variants Causing Cardiac Arrhythmia Risk Factors in Sudden Unexpected Death in Epilepsy?Lauren E Bleakley, Ming S Soh, Richard D Bagnall, et al.
Neurology|September 25, 2023
Movement Disorders in Patients With Genetic Developmental and Epileptic EncephalopathiesSterre van der Veen, Gabrielle T W Tse, Alessandro Ferretti, et al.
Epilepsy Research|June 20, 2015
Myoclonic occipital photosensitive epilepsy with dystonia (MOPED): A familial epilepsy syndromeLynette G Sadleir, Sarah Paterson, Katherine R Smith, et al.
Developmental Medicine and Child Neurology|April 28, 2015
Favourable response to ketogenic dietary therapies: undiagnosed glucose 1 transporter deficiency syndrome is only one factorNatasha E Schoeler, Judith Helen Cross, Suzanne Drury, 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.
Neurology|August 15, 2002
X-linked myoclonic epilepsy with spasticity and intellectual disability: mutation in the homeobox gene ARXIngrid E Scheffer, R H Wallace, F L Phillips, 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.
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