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Neurology|October 29, 2025
Integrative Deep Learning of Genomic and Clinical Data for Predicting Treatment Response in Newly Diagnosed EpilepsyWei Feng, Duong Nhu, Alison Anderson, et al.Proceedings of the National Academy of Sciences of the United States of America|November 5, 2002
Altered kinetics and benzodiazepine sensitivity of a GABAA receptor subunit mutation [gamma 2(R43Q)] found in human epilepsyDavid N Bowser, David A Wagner, Cynthia Czajkowski, et al.Neuron|February 26, 2020
Pathogenic Variants in CEP85L Cause Sporadic and Familial Posterior Predominant LissencephalyMeng-Han Tsai, Alison M Muir, Won-Jing Wang, et al.Brain : a Journal of Neurology|January 13, 2022
Genome-wide association study of febrile seizures implicates fever response and neuronal excitability genesLine Skotte, João Fadista, Jonas Bybjerg-Grauholm, et al.Epilepsy & Behavior : E&B|August 8, 2020
Enlarged hippocampal fissure in psychosis of epilepsyJames Allebone, Richard A Kanaan, Jerome J Maller, et al.American Journal of Human Genetics|April 2, 2021
Progressive myoclonus epilepsies-Residual unsolved cases have marked genetic heterogeneity including dolichol-dependent protein glycosylation pathway genesCarolina Courage, Karen L Oliver, Eon Joo Park, et al.Epilepsy Research|November 23, 2015
Variants in KCNJ11 and BAD do not predict response to ketogenic dietary therapies for epilepsyNatasha E Schoeler, Costin Leu, Jon White, et al.Epilepsia Open|August 3, 2026
Changes in effectiveness and safety in patients with Lennox-Gastaut syndrome transitioning from the fenfluramine randomized controlled trial to open-label extension studyRima Nabbout, Orrin Devinsky, Lieven Lagae, et al.Brain & Development|May 29, 2004
Etiological heterogeneity of familial periventricular heterotopia and hydrocephalusVolney L Sheen, Lina Basel-Vanagaite, Jean R Goodman, et al.Neurology. Genetics|April 29, 2021
Phenotypic Spectrum of Seizure Disorders in MBD5-Associated Neurodevelopmental DisorderKenneth A Myers, Carla Marini, Gemma L Carvill, et al.Pageof 74