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Epilepsia|May 1, 2022
International consensus on diagnosis and management of Dravet syndromeElaine C Wirrell, Veronica Hood, Kelly G Knupp, et al.
Nature Communications|July 21, 2022
Heterogeneous nuclear ribonucleoprotein U (HNRNPU) safeguards the developing mouse cortexTamar Sapir, Aditya Kshirsagar, Anna Gorelik, et al.
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.
American Journal of Medical Genetics. Part A|December 29, 2015
A mutation in COL4A2 causes autosomal dominant porencephaly with cataractsThuong T Ha, Lynette G Sadleir, Simone A Mandelstam, et al.
Epilepsia|February 8, 2012
Efficacy of the ketogenic diet: which epilepsies respond?Sasipa Thammongkol, Danya F Vears, Jillian Bicknell-Royle, 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.
Neurology. Genetics|July 20, 2019
Human GABRG2 generalized epilepsy: Increased somatosensory and striatothalamic connectivityMangor Pedersen, Magdalena Kowalczyk, Amir Omidvarnia, et al.
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