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Angiology|February 21, 2003
The LONFLIT4-Concorde--Sigvaris Traveno Stockings in Long Flights (EcoTraS) Study: a randomized trialMaria Rosaria Cesarone, Gianni Belcaro, Andrew N Nicolaides, et al.Plos Pathogens|January 26, 2019
LANA oligomeric architecture is essential for KSHV nuclear body formation and viral genome maintenance during latencyAlessandra De Leo, Zhong Deng, Olga Vladimirova, et al.JAMA Neurology|May 2, 2022
Efficacy and Safety of Fenfluramine for the Treatment of Seizures Associated With Lennox-Gastaut Syndrome: A Randomized Clinical TrialKelly G Knupp, Ingrid E Scheffer, Berten Ceulemans, et al.Epilepsia|May 3, 2022
International League Against Epilepsy classification and definition of epilepsy syndromes with onset in childhood: Position paper by the ILAE Task Force on Nosology and DefinitionsNicola Specchio, Elaine C Wirrell, Ingrid E Scheffer, et al.Journal of Medical Genetics|September 16, 2009
Epilepsy and mental retardation limited to females with PCDH19 mutations can present de novo or in single generation familiesKim Hynes, Patrick Tarpey, Leanne M Dibbens, et al.Epilepsia|August 27, 2004
Familial partial epilepsy with variable foci: clinical features and linkage to chromosome 22q12Samuel F Berkovic, Jose M Serratosa, Hilary A Phillips, et al.Epilepsia|July 31, 2013
Role of the sodium channel SCN9A in genetic epilepsy with febrile seizures plus and Dravet syndromeJohn C Mulley, Bree Hodgson, Jacinta M McMahon, et al.Human Mutation|October 25, 2017
Gain-of-function HCN2 variants in genetic epilepsyMelody Li, Snezana Maljevic, A Marie Phillips, et al.Neurology|April 25, 2020
Keeping people with epilepsy safe during the COVID-19 pandemicJacqueline A French, Martin J Brodie, Roberto Caraballo, et al.Brain : a Journal of Neurology|April 3, 2023
Widespread genomic influences on phenotype in Dravet syndrome, a 'monogenic' conditionHelena Martins Custodio, Lisa M Clayton, Ravishankara Bellampalli, et al.Pageof 67