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European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|May 13, 2014
Paternal germline mosaicism of a SCN2A mutation results in Ohtahara syndrome in half siblingsAyelet Zerem, Dorit Lev, Lubov Blumkin, et al.Epilepsia Open|August 24, 2024
Baseline characteristics and predictors for early implantation of vagus nerve stimulation therapy in people with drug-resistant epilepsy: Observations from an international prospective outcomes registry (CORE-VNS)Patrick Kwan, Massimiliano Boffini, Firas Fahoum, et al.Scientific Reports|October 20, 2015
De novo KCNB1 mutations in infantile epilepsy inhibit repetitive neuronal firingHirotomo Saitsu, Tenpei Akita, Jun Tohyama, et al.Annals of Neurology|October 22, 2005
Genotype-phenotype analysis of human frontoparietal polymicrogyria syndromesXianhua Piao, Bernard S Chang, Adria Bodell, et al.Journal of Autoimmunity|June 21, 2020
Dual-Targeted Autoimmune Sword in Fatal Epilepsy: Patient's glutamate receptor AMPA GluR3B peptide autoimmune antibodies bind, induce Reactive Oxygen Species (ROS) in, and kill both human neural cells and T cellsMia Levite, Daniel Zelig, Alon Friedman, et al.Annals of Neurology|January 3, 2013
Glucose transporter 1 deficiency in the idiopathic generalized epilepsiesTodor Arsov, Saul A Mullen, Sue Rogers, et al.European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|February 10, 2018
A de novo GABRA2 missense mutation in severe early-onset epileptic encephalopathy with a choreiform movement disorderNaama Orenstein, Hadassa Goldberg-Stern, Rachel Straussberg, et al.Neurology|October 19, 2012
PRRT2 phenotypic spectrum includes sporadic and fever-related infantile seizuresIngrid E Scheffer, Bronwyn E Grinton, Sarah E Heron, et al.Epilepsia|June 4, 2014
Early onset epileptic encephalopathy caused by de novo SCN8A mutationsChihiro Ohba, Mitsuhiro Kato, Satoru Takahashi, et al.Neurology|August 27, 2017
Genetic epilepsy with febrile seizures plus: Refining the spectrumYue-Hua Zhang, Rosemary Burgess, Jodie P Malone, et al.Pageof 9