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Annals of Neurology|October 3, 2009
Early-onset absence epilepsy caused by mutations in the glucose transporter GLUT1Arvid Suls, Saul A Mullen, Yvonne G Weber, et al.
Epilepsy Research|November 5, 2016
Is FGF13 a major contributor to genetic epilepsy with febrile seizures plus?Kristin A Rigbye, Peter M van Hasselt, Rosemary Burgess, et al.
Plos Genetics|November 30, 2017
A case-control collapsing analysis identifies epilepsy genes implicated in trio sequencing studies focused on de novo mutationsXiaolin Zhu, Raghavendra Padmanabhan, Brett Copeland, et al.
Communications Biology|May 31, 2022
Functional correlates of clinical phenotype and severity in recurrent SCN2A variantsGéza Berecki, Katherine B Howell, Jacqueline Heighway, et al.
The Lancet. Neurology|June 22, 2007
Early seizures: causal events or predisposition to adult epilepsy?Olivier Dulac, Rima Nabbout, Perrine Plouin, et al.
Brain & Development|February 11, 2009
Dravet syndrome or genetic (generalized) epilepsy with febrile seizures plus?Ingrid E Scheffer, Yue-Hua Zhang, Floor E Jansen, et al.
American Journal of Speech-Language Pathology|May 29, 2026
Viewpoint: Decline in Speech and Language Skills May Signal Childhood DementiaLottie D Morison, Kris Elvidge, Ingrid E Scheffer, et al.
Annals of Neurology|December 26, 2015
Exome-based analysis of cardiac arrhythmia, respiratory control, and epilepsy genes in sudden unexpected death in epilepsyRichard D Bagnall, Douglas E Crompton, Slavé Petrovski, et al.
Annals of Neurology|March 4, 2014
Mutations in mammalian target of rapamycin regulator DEPDC5 cause focal epilepsy with brain malformationsIngrid E Scheffer, Sarah E Heron, Brigid M Regan, et al.
Neurology|April 17, 2013
Autosomal dominant vasovagal syncope: clinical features and linkage to chromosome 15q26Karl Martin Klein, Catherine J Bromhead, Katherine R Smith, et al.
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