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Neurology|June 11, 2013
Etiology of hippocampal sclerosis: evidence for a predisposing familial morphologic anomalyMeng-Han Tsai, Heath R Pardoe, Yuliya Perchyonok, et al.Epilepsy Research|March 26, 2013
Genetics of febrile seizure subtypes and syndromes: a twin studyJazmin Eckhaus, Kate M Lawrence, Ingo Helbig, et al.Annals of Neurology|July 6, 2004
Is benign rolandic epilepsy genetically determined?Lata Vadlamudi, A Simon Harvey, Mary M Connellan, et al.Epilepsia|August 27, 2016
Hippocampal malrotation is an anatomic variant and has no clinical significance in MRI-negative temporal lobe epilepsyMeng-Han Tsai, David N Vaughan, Yuliya Perchyonok, et al.Journal of Medical Genetics|March 8, 2013
Recent advances in the molecular genetics of epilepsyMichael S Hildebrand, Hans-Henrik M Dahl, John Anthony Damiano, et al.Epilepsy Research|April 19, 2017
Evaluation of GLUT1 variation in non-acquired focal epilepsyAlexander Peeraer, John A Damiano, Susannah T Bellows, et al.Epilepsia|October 30, 2009
Neonatal seizures and long QT syndrome: a cardiocerebral channelopathy?Sarah E Heron, Marta Hernandez, Caitlin Edwards, et al.Epilepsia|April 10, 2013
Mutations in PRRT2 are not a common cause of infantile epileptic encephalopathiesSarah E Heron, Yeh Sze Ong, Simone C Yendle, et al.Epilepsia|January 9, 2013
Clinical genetic study of the epilepsy-aphasia spectrumMeng-Han Tsai, Danya F Vears, Samantha J Turner, et al.Epilepsy Research|May 4, 2012
Rare protein sequence variation in SV2A gene does not affect response to levetiracetamLeanne M Dibbens, Bree L Hodgson, Katherine L Helbig, et al.Pageof 73