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Epilepsia|July 23, 2011
Investigation of the 15q13.3 CNV as a genetic modifier for familial epilepsies with variable phenotypesJohn C Mulley, Ingrid E Scheffer, Tarishi Desai, 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.
Epilepsy Research|July 12, 2019
Somatic mutation: The hidden genetics of brain malformations and focal epilepsiesZimeng Ye, Lara McQuillan, Annapurna Poduri, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|February 7, 2025
Fulfilling the needs of caregivers in delivering health services to children with developmental and epileptic encephalopathiesLauren Kelada, Stephanie Best, Kristine Pierce, et al.
Epilepsy Currents|July 7, 2025
Epilepsy Care in the Real World of Multiple Medical ConsiderationsJohn Stern, Shilpa Klocke, Sara Eyal, et al.
Epilepsia|December 24, 2011
Long-term follow-up of febrile infection-related epilepsy syndromeKatherine B Howell, Kamornwan Katanyuwong, Mark T Mackay, et al.
Epilepsia Open|May 25, 2021
Seizures in Sotos syndrome: Phenotyping in 49 patientsOlivier Fortin, Christian Vincelette, Afsheen Q Khan, et al.
Translational Psychiatry|January 27, 2024
Multiomic analysis implicates nuclear hormone receptor signalling in clustering epilepsyRebekah de Nys, Clare L van Eyk, Tarin Ritchie, et al.
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