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Epilepsia|May 20, 2014
Dravet syndrome--from epileptic encephalopathy to channelopathyAndreas Brunklaus, Sameer M ZuberiBrain : a Journal of Neurology|January 17, 2022
Gene variant effects across sodium channelopathies predict function and guide precision therapyAndreas Brunklaus, Tony Feng, Tobias Brünger, et al.Epilepsy Research|August 15, 2006
Developmental outcome in benign myoclonic epilepsy in infancy and reflex myoclonic epilepsy in infancy: a literature review and six new casesSameer M Zuberi, Mary E O'ReganEpilepsy & Behavior Reports|November 16, 2020
Infantile spasms: Etiology, lead time and treatment response in a resource limited settingPriyanka Surana, Joseph D Symonds, Prabhar Srivastava, et al.Epilepsia|June 15, 2011
Comorbidities and predictors of health-related quality of life in Dravet syndromeAndreas Brunklaus, Liam Dorris, Sameer M ZuberiEpileptic Disorders : International Epilepsy Journal with Videotape|March 3, 2005
Symptoms of narcolepsy in children misinterpreted as epilepsyStewart Macleod, Colin Ferrie, Sameer M ZuberiEpilepsia|January 7, 2020
Phenotypic spectrum and genetics of SCN2A-related disorders, treatment options, and outcomes in epilepsy and beyondMarkus Wolff, Andreas Brunklaus, Sameer M ZuberiHuman Mutation|November 30, 2019
SCN1A variants from bench to bedside-improved clinical prediction from functional characterizationAndreas Brunklaus, Stephanie Schorge, Alexander D Smith, et al.Epilepsia|August 22, 2015
Epileptic activity is a surrogate for an underlying etiology and stopping the activity has a limited impact on developmental outcomeChristian M Korff, Andreas Brunklaus, Sameer M ZuberiSeizure|December 17, 2018
The clinical utility of ambulatory EEG in childhoodRebeka Nagyova, Gillian Horsburgh, Angela Robertson, et al.Pageof 12