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Annals of Clinical and Translational Neurology|May 18, 2021
Loss-of-function variants in Kv 11.1 cardiac channels as a biomarker for SUDEPMing S Soh, Richard D Bagnall, Mark F Bennett, et al.Brain : a Journal of Neurology|October 6, 2006
Temporal lobe epilepsy and GEFS+ phenotypes associated with SCN1B mutationsIngrid E Scheffer, Louise A Harkin, Bronwyn E Grinton, et al.Annals of Neurology|May 21, 2013
Mutations in TNK2 in severe autosomal recessive infantile onset epilepsyYuki Hitomi, Erin L Heinzen, Simona Donatello, et al.Epilepsy & Behavior : E&B|May 18, 2025
Toxoplasma gondii seropositivity as a risk factor for epilepsy: A discordant monozygotic twin studyYew Li Dang, Kate Esnault, Marcel J Leroi, et al.Expert Review of Neurotherapeutics|June 17, 2014
Concepts and controversies of juvenile myoclonic epilepsy: still an enigmatic epilepsyMatthias J Koepp, Rhys H Thomas, Britta Wandschneider, et al.Neurology|August 8, 2012
Evidence for genetic factors in vasovagal syncope: a twin-family studyKarl Martin Klein, San San Xu, Kate Lawrence, et al.Archives of Neurology|June 10, 2009
Automatisms in absence seizures in children with idiopathic generalized epilepsyLynette G Sadleir, Ingrid E Scheffer, Sherry Smith, 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.Human Molecular Genetics|May 22, 2025
Improving genetic diagnostic yield in familial and sporadic cerebral cavernous malformations: detection of copy number and deep Intronic variantsNeblina Sikta, Samuel Gooley, Timothy E Green, 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.Pageof 74