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Seizure|September 3, 2019
The best evidence for progressive myoclonic epilepsy: A pathway to precision therapyAlessandro Orsini, Angelo Valetto, Veronica Bertini, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 9, 2005
Suppression of myoclonus in SCA2 by piracetamAnna De Rosa, Pasquale Striano, Fabrizio Barbieri, et al.
Italian Journal of Pediatrics|July 19, 2022
Impact and management of drooling in children with neurological disorders: an Italian Delphi consensusAntonella Riva, Elisabetta Amadori, Maria Stella Vari, et al.
Epilepsia Open|June 17, 2024
Epilepsy in rural South Africa: Patient experiences and healthcare challengesLufuno Makhado, Angelina Maphula, Richard Teke Ngomba, et al.
Journal of Pediatric Genetics|September 10, 2021
Complex Neurological Phenotype Associated with a De Novo DHDDS Mutation in a Boy with Intellectual Disability, Refractory Epilepsy, and Movement DisorderGianluca Piccolo, Elisabetta Amadori, Maria Stella Vari, et al.
Brain : a Journal of Neurology|December 20, 2019
Homozygous STXBP1 variant causes encephalopathy and gain-of-function in synaptic transmissionHanna C A Lammertse, Annemiek A van Berkel, Michele Iacomino, et al.
Expert Opinion on Pharmacotherapy|November 21, 2025
Optimizing pharmacological management of the febrile childMarco Bianchi, Mattia Costa, Fabio Cardinale, et al.
Journal of Child Neurology|March 4, 2026
Managing Fever and Vaccination Risks in Dravet Syndrome: From Pathophysiology to Clinical PracticeAlessandro Ferretti, Marco Bianchi, Mattia Costa, et al.
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