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Developmental Medicine and Child Neurology|December 17, 2013
Atypical multifocal Dravet syndrome lacks generalized seizures and may show later cognitive declineYoung Ok Kim, Susannah Bellows, Jacinta M McMahon, et al.Epilepsia|January 7, 2012
Clinical genetic studies in benign childhood epilepsy with centrotemporal spikesDanya F Vears, Meng-Han Tsai, Lynette G Sadleir, et al.Annals of Neurology|August 19, 2007
Extended spectrum of idiopathic generalized epilepsies associated with CACNA1H functional variantsSarah E Heron, Houman Khosravani, Diego Varela, et al.Neurology|December 3, 2017
Precision therapy for epilepsy due to KCNT1 mutations: A randomized trial of oral quinidineSaul A Mullen, Patrick W Carney, Annie Roten, et al.Epilepsia|May 16, 2008
Severe autosomal dominant nocturnal frontal lobe epilepsy associated with psychiatric disorders and intellectual disabilityChristopher P Derry, Sarah E Heron, Fiona Phillips, et al.Developmental Medicine and Child Neurology|June 7, 2016
Evaluation of non-coding variation in GLUT1 deficiencyYu-Chi Liu, Jia Wei Audrey Lee, Susannah T Bellows, et al.European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|January 14, 2020
Deciphering the concepts behind "Epileptic encephalopathy" and "Developmental and epileptic encephalopathy"Ingrid E Scheffer, Jianxiang LiaoEpilepsia|January 7, 2020
SCN1A-related phenotypes: Epilepsy and beyondIngrid E Scheffer, Rima NabboutEpilepsia|September 12, 2014
Transition to adult life in the monogenic epilepsiesIngrid E Scheffer, Charlotte DravetEpilepsy Currents|September 29, 2020
Genetic Contributions to Acquired EpilepsiesPiero Perucca, Ingrid E SchefferPageof 73