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Pediatric Neurology|May 4, 2023
Awake Craniotomy Language Mapping in Children With Drug-Resistant Epilepsy due to Focal Cortical DysplasiaAriane St-Denis, Meredith Hooker, Katherine L'Abbée Lacas, et al.Cell Reports|June 15, 2017
Cytoplasmic Dynein Transports Axonal Microtubules in a Polarity-Sorting MannerAnand N Rao, Ankita Patil, Mark M Black, et al.Journal of Neurology|April 2, 2025
Investigating the safety and efficacy of deoxycytidine/deoxythymidine in mitochondrial DNA depletion disorders: phase 2 open-label trialSaoussen Berrahmoune, Christelle Dassi, Heather Pekeles, et al.Epilepsia Open|June 6, 2023
Sleep and respiratory abnormalities in adults with developmental and epileptic encephalopathies using polysomnography and video-EEG monitoringShobi Sivathamboo, Kenneth A Myers, Andreas Pattichis, et al.European Journal of Human Genetics : EJHG|March 16, 2017
Gonadal mosaicism of a novel IQSEC2 variant causing female limited intellectual disability and epilepsyLisa J Ewans, Michael Field, Ying Zhu, et al.Epilepsia Open|October 30, 2021
Infantile-onset myoclonic developmental and epileptic encephalopathy: A new RARS2 phenotypeGuillem de Valles-Ibáñez, Michael S Hildebrand, Melanie Bahlo, et al.Archives of Neurology|May 11, 2011
Glucose transporter 1 deficiency as a treatable cause of myoclonic astatic epilepsySaul A Mullen, Carla Marini, Arvid Suls, et al.The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|February 22, 2023
Retinal Dysfunction in a Mouse Model of HCN1 Genetic EpilepsyDa Zhao, Paulo Pinares-Garcia, Chaseley E McKenzie, et al.Neurology|November 2, 2022
Complications of Influenza A or B Virus Infection in Individuals With SCN1A-Positive Dravet SyndromeKatherine B Howell, Sophie Butcher, Amy L Schneider, et al.Epilepsy Research|November 28, 2012
Do mutations in SCN1B cause Dravet syndrome?Young Ok Kim, Leanne Dibbens, Carla Marini, et al.Pageof 67