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Brain : a Journal of Neurology|October 18, 2022
Randomized placebo-controlled crossover trial of memantine in children with epileptic encephalopathyKatharina Schiller, Saoussen Berrahmoune, Christelle Dassi, et al.
European Journal of Medical Genetics|June 13, 2017
Familial epilepsy with anterior polymicrogyria as a presentation of COL18A1 mutationsMark A Corbett, Samantha J Turner, Alison Gardner, et al.
Brain : a Journal of Neurology|April 6, 2021
Cation leak underlies neuronal excitability in an HCN1 developmental and epileptic encephalopathyLauren E Bleakley, Chaseley E McKenzie, Ming S Soh, et al.
Annals of Clinical and Translational Neurology|July 30, 2019
Second-hit DEPDC5 mutation is limited to dysmorphic neurons in cortical dysplasia type IIAWei Shern Lee, Sarah E M Stephenson, Katherine B Howell, et al.
Neurology|August 11, 2017
Not all SCN1A epileptic encephalopathies are Dravet syndrome: Early profound Thr226Met phenotypeLynette G Sadleir, Emily I Mountier, Deepak Gill, et al.
Neurology|October 3, 2022
Somatic Mosaic Pathogenic Variant Gradient Detected in Trace Brain Tissue From Stereo-EEG Depth ElectrodesZimeng Ye, Mark F Bennett, Andrew Neal, et al.
Epilepsia|March 4, 2010
Revised terminology and concepts for organization of seizures and epilepsies: report of the ILAE Commission on Classification and Terminology, 2005-2009Anne T Berg, Samuel F Berkovic, Martin J Brodie, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|October 11, 2024
Early mortality in STXBP1-related disordersFrancesca Furia, Charlene Son Rigby, Ingrid E Scheffer, et al.
Epilepsy Research|November 5, 2016
Is FGF13 a major contributor to genetic epilepsy with febrile seizures plus?Kristin A Rigbye, Peter M van Hasselt, Rosemary Burgess, et al.
Annals of Neurology|October 3, 2009
Early-onset absence epilepsy caused by mutations in the glucose transporter GLUT1Arvid Suls, Saul A Mullen, Yvonne G Weber, et al.
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