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Neurology|February 13, 2015
CHD2 myoclonic encephalopathy is frequently associated with self-induced seizuresRhys H Thomas, Lin Mei Zhang, Gemma L Carvill, et al.Brain : a Journal of Neurology|September 25, 2010
Familial mesial temporal lobe epilepsy: a benign epilepsy syndrome showing complex inheritanceDouglas E Crompton, Ingrid E Scheffer, Isabella Taylor, et al.The Lancet. Neurology|September 9, 2019
Epilepsy genetics: clinical impacts and biological insightsColin A Ellis, Slavé Petrovski, Samuel F BerkovicProgress in Neurobiology|October 28, 2008
Mechanisms of human inherited epilepsiesChristopher A Reid, Samuel F Berkovic, Steven PetrouEpileptic Disorders : International Epilepsy Journal with Videotape|December 10, 2021
ILAE Genetic Literacy Series: familial focal epilepsy syndromesSamuel Gooley, Douglas E Crompton, Samuel F BerkovicAnnals of Neurology|May 4, 2010
Augmented currents of an HCN2 variant in patients with febrile seizure syndromesLeanne M Dibbens, Christopher A Reid, Bree Hodgson, et al.American Journal of Human Genetics|December 19, 2001
Truncation of the GABA(A)-receptor gamma2 subunit in a family with generalized epilepsy with febrile seizures plusLouise A Harkin, David N Bowser, Leanne M Dibbens, 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.Epilepsia|March 13, 2020
Inherited RORB pathogenic variants: Overlap of photosensitive genetic generalized and occipital lobe epilepsyLynette G Sadleir, Guillem de Valles-Ibáñez, Chontelle King, et al.Neurotherapeutics : the Journal of the American Society for Experimental Neurotherapeutics|October 28, 2021
Natural History Studies and Clinical Trial Readiness for Genetic Developmental and Epileptic EncephalopathiesElizabeth E Palmer, Katherine Howell, Ingrid E SchefferPageof 73