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Epileptic Disorders : International Epilepsy Journal with Videotape|September 2, 2016
SCARB2/LIMP2 deficiency in action myoclonus-renal failure syndromeLeanne Dibbens, Michael Schwake, Paul Saftig, et al.
Brain & Development|February 11, 2009
Dravet syndrome or genetic (generalized) epilepsy with febrile seizures plus?Ingrid E Scheffer, Yue-Hua Zhang, Floor E Jansen, et al.
Epilepsia|May 25, 2007
Is photosensitive epilepsy less common in males due to variation in X chromosome photopigment genes?Isabella Taylor, Bree Hodgson, Ingrid E Scheffer, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|February 3, 2006
Delta subunit susceptibility variants E177A and R220H associated with complex epilepsy alter channel gating and surface expression of alpha4beta2delta GABAA receptorsHua-Jun Feng, Jing-Qiong Kang, Luyan Song, et al.
Metabolites|May 26, 2023
Chromosomal Instability Causes Sensitivity to Polyamines and One-Carbon MetabolismAnowarul Islam, Zeeshan Shaukat, David L Newman, et al.
Developmental Medicine and Child Neurology|December 17, 2013
Atypical multifocal Dravet syndrome lacks generalized seizures and may show later cognitive declineYoung Ok Kim, Susannah Bellows, Jacinta M McMahon, et al.
Epilepsia|March 19, 2009
Does a SCN1A gene mutation confer earlier age of onset of febrile seizures in GEFS+?Angelique E J Sijben, Pasiri Sithinamsuwan, Ashalata Radhakrishnan, et al.
Epilepsy Research|November 28, 2012
Do mutations in SCN1B cause Dravet syndrome?Young Ok Kim, Leanne Dibbens, Carla Marini, et al.
Epilepsy Research|October 1, 2015
Evaluation of multiple putative risk alleles within the 15q13.3 region for genetic generalized epilepsyJohn A Damiano, Saul A Mullen, Michael S Hildebrand, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 20, 2007
Reduced cortical inhibition in a mouse model of familial childhood absence epilepsyHeneu O Tan, Christopher A Reid, Frank N Single, et al.
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