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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.Neurology|August 30, 2019
Efficacy and tolerability of adjunctive lacosamide in pediatric patients with focal seizuresViktor Farkas, Barbara Steinborn, J Robert Flamini, et al.Epilepsia|January 7, 2012
Clinical genetic studies in benign childhood epilepsy with centrotemporal spikesDanya F Vears, Meng-Han Tsai, Lynette G Sadleir, et al.Frontiers in Neurology|April 1, 2022
Impaired Color Recognition in HCN1 Epilepsy: A Single Case ReportChaseley E Mckenzie, Chen-Jui Ho, Ian C Forster, et al.Journal of Clinical Neurophysiology : Official Publication of the American Electroencephalographic Society|August 3, 2016
American Clinical Neurophysiology Society Guideline 6: Minimum Technical Standards for EEG Recording in Suspected Cerebral DeathMark M Stecker, Dragos Sabau, Lucy Sullivan, et al.Epileptic Disorders : International Epilepsy Journal with Videotape|July 21, 2010
Detection of microchromosomal aberrations in refractory epilepsy: a pilot studyJacinta M McMahon, Ingrid E Scheffer, Jillian K Nicholl, et al.European Journal of Human Genetics : EJHG|May 16, 2025
Understanding speech and language in KIF1A-associated neurological disorderLottie D Morison, Adam P Vogel, John Christodoulou, et al.NAR Genomics and Bioinformatics|April 7, 2025
Identifying individuals with rare disease variants by inferring shared ancestral haplotypes from SNP array dataErandee Robertson, Bronwyn E Grinton, Karen L Oliver, et al.The Lancet. Neurology|May 23, 2006
De-novo mutations of the sodium channel gene SCN1A in alleged vaccine encephalopathy: a retrospective studySamuel F Berkovic, Louise Harkin, Jacinta M McMahon, et al.Pageof 57