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Epilepsia|August 3, 2005
Reflex seizures in patients with malformations of cortical development and refractory epilepsyAndré Palmini, Peter Halasz, Ingrid E Scheffer, et al.
Annals of Neurology|August 19, 2007
Extended spectrum of idiopathic generalized epilepsies associated with CACNA1H functional variantsSarah E Heron, Houman Khosravani, Diego Varela, et al.
Neurology|December 3, 2017
Precision therapy for epilepsy due to KCNT1 mutations: A randomized trial of oral quinidineSaul A Mullen, Patrick W Carney, Annie Roten, et al.
Epilepsia Open|March 29, 2018
Classification of the epilepsies: New concepts for discussion and debate-Special report of the ILAE Classification Task Force of the Commission for Classification and TerminologyIngrid E Scheffer, Jacqueline French, Edouard Hirsch, et al.
Epilepsia|May 16, 2008
Severe autosomal dominant nocturnal frontal lobe epilepsy associated with psychiatric disorders and intellectual disabilityChristopher P Derry, Sarah E Heron, Fiona Phillips, et al.
Epilepsy Research|November 12, 2013
Seizure semiology in autosomal dominant epilepsy with auditory features, due to novel LGI1 mutationsLynette G Sadleir, Dahbia Agher, Elodie Chabrol, 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.
Neurology. Genetics|May 8, 2024
Perisylvian and Hippocampal Anomalies in Individuals With Pathogenic GRIN2A VariantsDaisy G Y Thompson-Lake, Frederique J Liegeois, Ruth O Braden, et al.
Developmental Medicine and Child Neurology|June 7, 2016
Evaluation of non-coding variation in GLUT1 deficiencyYu-Chi Liu, Jia Wei Audrey Lee, Susannah T Bellows, et al.
Epilepsia|October 20, 2020
Fenfluramine HCl (Fintepla® ) provides long-term clinically meaningful reduction in seizure frequency: Analysis of an ongoing open-label extension studyJoseph Sullivan, Ingrid E Scheffer, Lieven Lagae, et al.
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