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Epilepsia|March 4, 2025
Dravet syndrome: From neurodevelopmental to neurodegenerative disease?Arunan Selvarajah, Andrea Sabo, Carolina Gorodetsky, et al.Epilepsia|November 18, 2025
Cognitive stagnation and executive function deficits in young children with SCN1A+ Dravet syndrome: Detailed characterization of onset, progression, and impact in the ENVISION natural history studyJoseph Sullivan, M Scott Perry, Ingrid E Scheffer, et al.Epilepsia|December 4, 2023
Severe communication delays are independent of seizure burden and persist despite contemporary treatments in SCN1A+ Dravet syndrome: Insights from the ENVISION natural history studyM Scott Perry, Ingrid E Scheffer, Joseph Sullivan, et al.Epilepsia|November 15, 2021
Surgical evaluation in children <3 years of age with drug-resistant epilepsy: Patient characteristics, diagnostic utilization, and potential for treatment delaysMichael Scott Perry, Sabrina Shandley, Max Perelman, et al.Seizure|January 8, 2024
Epilepsy surgery in children with genetic etiologies: A prospective evaluation of current practices and outcomesJason Coryell, Rani Singh, Adam P Ostendorf, et al.Pediatric Neurology|June 19, 2024
Pediatric Palliative Epilepsy Surgery: A Report From the Pediatric Epilepsy Research Consortium (PERC) Surgery DatabaseMary Jeno, M Bridget Zimmerman, Sabrina Shandley, et al.Epilepsia|December 8, 2023
A multi-center comparison of surgical techniques for corpus Callosotomy in pediatric drug-resistant epilepsyDaniel Hansen, Sabrina Shandley, Joffre Olaya, et al.Medrxiv : the Preprint Server for Health Sciences|March 13, 2026
Gene Portals: A Framework for Integrating Clinical, Functional, and Structural Evidence into Rare Disease Variant ClassificationTobias Brünger, Ilona Krey, Suyeon Kim, et al.Pageof 10