Showing results (81-90 of 210) with videos related to

Sort By:
Pageof 21
Epileptic Disorders : International Epilepsy Journal with Videotape|June 27, 2026
NMDAR-antibody encephalitis: Seizure semiology and EEG findingsMaria Emilia C Andraus, Bernard Liem, Sidra Aurangzeb, et al.
American Journal of Human Genetics|April 17, 2007
Nova2 interacts with a cis-acting polymorphism to influence the proportions of drug-responsive splice variants of SCN1AErin L Heinzen, Woohyun Yoon, Sarah K Tate, et al.
European Journal of Medical Genetics|May 26, 2022
Defining causal variants in rare epilepsies: an essential team effort between biomedical scientists, geneticists and epileptologistsAmy McTague, Andreas Brunklaus, Giulia Barcia, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|March 22, 2015
Homozygous mutations in the SCN1A gene associated with genetic epilepsy with febrile seizures plus and Dravet syndrome in 2 familiesAndreas Brunklaus, Rachael Ellis, Helen Stewart, et al.
Hippocampus|August 3, 2018
Binding deficits in visual short-term memory in patients with temporal lobe lobectomyNahid Zokaei, Matthew M Nour, Annie Sillence, et al.
Nature Reviews. Neurology|May 10, 2022
Why won't it stop? The dynamics of benzodiazepine resistance in status epilepticusRichard J Burman, Richard E Rosch, Jo M Wilmshurst, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|December 18, 2021
Vaccination and childhood epilepsiesDana Craiu, Zvonka Rener Primec, Lieven Lagae, et al.
Epilepsia Open|August 5, 2022
Impact of the COVID-19 pandemic on people with epilepsy: findings from the US arm of the COV-E studyPatricia Dugan, Elizabeth Carroll, Jennifer Thorpe, et al.
Epilepsia|June 7, 2018
Heart rate variability in epilepsy: A potential biomarker of sudden unexpected death in epilepsy riskKenneth A Myers, Luis E Bello-Espinosa, Joseph D Symonds, et al.
Pageof 21