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Epilepsia|January 6, 2011
A duplication in 1q21.3 in a family with early onset and childhood absence epilepsyHiltrud Muhle, Ines Steinich, Sarah von Spiczak, 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.Annals of Neurology|November 26, 2013
GRIN2B mutations in West syndrome and intellectual disability with focal epilepsyJohannes R Lemke, Rik Hendrickx, Kirsten Geider, et al.Elife|January 25, 2022
Preexisting memory CD4 T cells in naïve individuals confer robust immunity upon hepatitis B vaccinationGeorge Elias, Pieter Meysman, Esther Bartholomeus, et al.Scientific Reports|December 10, 2015
Loss of synaptic Zn2+ transporter function increases risk of febrile seizuresMichael S Hildebrand, A Marie Phillips, Saul A Mullen, et al.Brain : a Journal of Neurology|July 21, 2016
Loss of SYNJ1 dual phosphatase activity leads to early onset refractory seizures and progressive neurological declineKatia Hardies, Yiying Cai, Claude Jardel, et al.Human Mutation|July 26, 2006
Microdeletions involving the SCN1A gene may be common in SCN1A-mutation-negative SMEI patientsArvid Suls, Kristl G Claeys, Dirk Goossens, et al.The Journal of Infectious Diseases|January 9, 2024
Unraveling the Immune Signature of Herpes Zoster: Insights Into the Pathophysiology and Human Leukocyte Antigen Risk ProfileRomi Vandoren, Marlies Boeren, Jolien Schippers, et al.Annals of Neurology|January 26, 2012
KCNQ2 encephalopathy: emerging phenotype of a neonatal epileptic encephalopathySarah Weckhuysen, Simone Mandelstam, Arvid Suls, et al.Epilepsia|February 16, 2013
Reduction of seizure frequency after epilepsy surgery in a patient with STXBP1 encephalopathy and clinical description of six novel mutation carriersSarah Weckhuysen, Philip Holmgren, Rik Hendrickx, et al.Pageof 7