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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 SchefferEpilepsia|January 14, 2017
De novo SCN1A pathogenic variants in the GEFS+ spectrum: Not always a familial syndromeKenneth A Myers, Rosemary Burgess, Zaid Afawi, et al.Plos One|January 21, 2018
KANSL1 variation is not a major contributing factor in self-limited focal epilepsy syndromes of childhoodKenneth A Myers, Amelia McGlade, Bernd A Neubauer, et al.American Journal of Medical Genetics. Part A|November 22, 2017
Mosaic uniparental disomy results in GM1 gangliosidosis with normal enzyme assayKenneth A Myers, Mark F Bennett, Chung W Chow, et al.Epilepsia|December 22, 2017
ADGRV1 is implicated in myoclonic epilepsyKenneth A Myers, Steven Nasioulas, Amber Boys, et al.Epilepsia|April 26, 2017
The epileptology of Koolen-de Vries syndrome: Electro-clinico-radiologic findings in 31 patientsKenneth A Myers, Simone A Mandelstam, Georgia Ramantani, et al.Pediatrics|March 24, 2017
Fatal Cerebral Edema With Status Epilepticus in Children With Dravet Syndrome: Report of 5 CasesKenneth A Myers, Jacinta M McMahon, Simone A Mandelstam, et al.Pageof 66