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Epilepsia|March 30, 2023
Familial adult myoclonus epilepsy: Clinical findings, disease course, and comorbiditiesBeatriz G Giraldez, José M Serratosa, Salvatore Striano, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|July 24, 2012
Clinical features of Sturge-Weber syndrome without facial nevus: five novel casesLaura Siri, Lucio Giordano, Patrizia Accorsi, et al.
Human Mutation|February 5, 2009
LGI1 mutations in autosomal dominant and sporadic lateral temporal epilepsyCarlo Nobile, Roberto Michelucci, Simonetta Andreazza, et al.
The Neurodiagnostic Journal|June 17, 2017
Early-Onset Shapiro Syndrome Variant Treated with Pizotifen: A Case ReportLaura Denegri, Giulia Prato, Maria Margherita Mancardi, et al.
Advances in Medical Education and Practice|September 10, 2025
Enhancing Pediatric Residency Training Through Peer-Education Based Gamified SimulationMarco Scaglione, Andrea Calandrino, Laura Puzone, et al.
Frontiers in Genetics|April 15, 2022
The Pathophysiological Link Between Reelin and Autism: Overview and New InsightsMarcello Scala, Eleonora A Grasso, Giuseppe Di Cara, et al.
Expert Review of Neurotherapeutics|February 25, 2022
Neurology's vital role in preventing unnecessary and potentially harmful pediatric studiesKlaus Rose, Earl B Ettienne, Jane M Grant-Kels, et al.
CNS Drugs|February 11, 2020
Adjunctive Cannabidiol in Patients with Dravet Syndrome: A Systematic Review and Meta-Analysis of Efficacy and SafetySimona Lattanzi, Francesco Brigo, Eugen Trinka, et al.
Epilepsia|March 24, 2011
Natural history and long-term evolution in families with autosomal dominant cortical tremor, myoclonus, and epilepsyAntonietta Coppola, Lia Santulli, Luigi Del Gaudio, et al.
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