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Expert Review of Neurotherapeutics|June 15, 2007
Genetics of epilepsiesDanielle M Andrade, Berge A MinassianExpert Opinion on Pharmacotherapy|June 17, 2009
Treatment options for epileptic myoclonus and epilepsy syndromes associated with myoclonusDanielle M Andrade, Clement Hamani, Berge A MinassianEpilepsy Research|August 26, 2006
Protein therapy for Unverricht-Lundborg disease using cystatin B transduction by TAT-PTD. Is it that simple?Danielle M Andrade, Stephen W Scherer, Berge A MinassianEpilepsia|July 12, 2012
Dravet syndrome: seizure control and gait in adults with different SCN1A mutationsJennifer J Rilstone, Fernando M Coelho, Berge A Minassian, et al.Neurology. Genetics|April 12, 2016
Two definite cases of sudden unexpected death in epilepsy in a family with a DEPDC5 mutationFábio A Nascimento, Felippe Borlot, Patrick Cossette, et al.Pediatric Neurology|August 14, 2012
Mutation of the CLN6 gene in teenage-onset progressive myoclonus epilepsyDanielle M Andrade, Tara Paton, Julie Turnbull, et al.Epileptic Disorders : International Epilepsy Journal with Videotape|September 16, 2016
Post-modern therapeutic approaches for progressive myoclonus epilepsyBerge A MinassianPediatric Neurology|February 4, 2014
Genetic testing in infantile spasms identifies a chromosome 13q deletion and retinoblastomaKevin Jones, Berge A MinassianEpilepsia Open|June 9, 2018
Extraneurological sparing in long-lived typical Lafora diseaseDanielle Goldsmith, Berge A MinassianPageof 25