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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.
CNS Drugs|March 23, 2021
Highly Purified Cannabidiol for Epilepsy Treatment: A Systematic Review of Epileptic Conditions Beyond Dravet Syndrome and Lennox-Gastaut SyndromeSimona Lattanzi, Eugen Trinka, Pasquale Striano, 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.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|January 16, 2025
Trauma, coping, and adjustment when parenting a child with Dravet syndromeAnthony Mercier, Liam Dorris, Andreas Brunklaus, et al.
Epilepsia Open|December 9, 2021
Guidance on Dravet syndrome from infant to adult care: Road map for treatment planning in EuropeElena Cardenal-Muñoz, Stéphane Auvin, Vicente Villanueva, et al.
Brain Communications|January 17, 2024
Long-term predictors of developmental outcome and disease burden in SCN1A-positive Dravet syndromeTony Feng, Phoebe Makiello, Benjamin Dunwoody, 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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