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Epilepsia Open|January 17, 2023
Risk of sudden unexpected death in epilepsy (SUDEP) with lamotrigine and other sodium channel-modulating antiseizure medicationsRussell Nightscales, Sarah Barnard, Juliana Laze, et al.
Epilepsy Research|October 8, 2021
Dravet syndrome: A quick transition guide for the adult neurologistDanielle M Andrade, Anne T Berg, Veronica Hood, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 27, 2024
Constitutive opening of the Kv7.2 pore activation gate causes KCNQ2-developmental encephalopathyMario Nappi, Giulio Alberini, Alessandro Berselli, et al.
Epilepsia|April 17, 2015
Early and effective treatment of KCNQ2 encephalopathyTiziana Pisano, Adam L Numis, Sinéad B Heavin, et al.
Neurology|December 14, 2018
SYNGAP1 encephalopathy: A distinctive generalized developmental and epileptic encephalopathyDanique R M Vlaskamp, Benjamin J Shaw, Rosemary Burgess, et al.
Epilepsia Open|January 14, 2025
PAK3 pathogenic variant associated with sleep-related hypermotor epilepsy in a family with parental mosaicismAntonio Gambardella, Yu-Chi Liu, Mark F Bennett, et al.
Neurology|January 24, 2016
Multiplex families with epilepsy: Success of clinical and molecular genetic characterizationZaid Afawi, Karen L Oliver, Sara Kivity, et al.
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