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Journal of Clinical Neurophysiology : Official Publication of the American Electroencephalographic Society|November 19, 2002
Transcranial magnetic stimulation and epilepsyRichard A L Macdonell, Josie M Curatolo, Samuel F BerkovicEpileptic Disorders : International Epilepsy Journal with Videotape|April 13, 2004
Sandifer syndrome misdiagnosed as refractory partial seizures in an adultSriudomkajorn Somjit, Yong Lee, Samuel F Berkovic, et al.Plos Computational Biology|October 15, 2021
State transitions through inhibitory interneurons in a cortical network modelAlexander Bryson, Samuel F Berkovic, Steven Petrou, et al.Epilepsia|October 29, 2004
Genetic association studies in epilepsy: "the truth is out there"Nigel C K Tan, John C Mulley, Samuel F BerkovicEpilepsy Research|October 1, 2015
Evaluation of multiple putative risk alleles within the 15q13.3 region for genetic generalized epilepsyJohn A Damiano, Saul A Mullen, Michael S Hildebrand, et al.Neurology. Genetics|January 31, 2022
Evidence for a Dual-Pathway, 2-Hit Genetic Model for Focal Cortical Dysplasia and EpilepsyMark F Bennett, Michael S Hildebrand, Sayaka Kayumi, et al.Neurology|August 10, 2014
Genetics of epilepsy: The testimony of twins in the molecular eraLata Vadlamudi, Roger L Milne, Kate Lawrence, et al.Molecular Pharmacology|May 6, 2008
Human nocturnal frontal lobe epilepsy: pharmocogenomic profiles of pathogenic nicotinic acetylcholine receptor beta-subunit mutations outside the ion channel poreJean-Charles Hoda, Wenli Gu, Marc Friedli, et al.EMBO Reports|March 27, 2014
A variant of KCC2 from patients with febrile seizures impairs neuronal Cl- extrusion and dendritic spine formationMartin Puskarjov, Patricia Seja, Sarah E Heron, et al.Brain & Development|July 27, 2002
Infantile spasms, dystonia, and other X-linked phenotypes caused by mutations in Aristaless related homeobox gene, ARXPetter Strømme, Marie E Mangelsdorf, Ingrid E Scheffer, et al.Pageof 74