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Annals of Neurology|February 3, 2018
Mutations in MICAL-1cause autosomal-dominant lateral temporal epilepsyEmanuela Dazzo, Kati Rehberg, Roberto Michelucci, et al.
Seizure|June 24, 2014
Panayiotopoulos syndrome with convulsive status epilepticus at the onset: a long-term studyAlberto Verrotti, Marianna Sebastiani, Lucio Giordano, et al.
Frontiers in Neurology|August 1, 2022
Case Report: Effect of Targeted Therapy With Carbamazepine in KCNQ2 Neonatal EpilepsyRobertino Dilena, Eleonora Mauri, Alessio Di Fonzo, et al.
Drugs|September 11, 2023
Pharmacotherapy for Dravet Syndrome: A Systematic Review and Network Meta-Analysis of Randomized Controlled TrialsSimona Lattanzi, Eugen Trinka, Emilio Russo, et al.
Epilepsia Open|March 29, 2018
Classification of the epilepsies: New concepts for discussion and debate-Special report of the ILAE Classification Task Force of the Commission for Classification and TerminologyIngrid E Scheffer, Jacqueline French, Edouard Hirsch, et al.
Epilepsy & Behavior Reports|November 16, 2020
Infantile spasms: Etiology, lead time and treatment response in a resource limited settingPriyanka Surana, Joseph D Symonds, Prabhar Srivastava, et al.
JAMA Network Open|April 16, 2024
Treatments and Outcomes Among Patients with Sydenham Chorea: A Meta-AnalysisMichael Eyre, Terrence Thomas, Emanuela Ferrarin, et al.
Epilepsia Open|July 8, 2022
An examination of the efficacy and safety of fenfluramine in adults, children, and adolescents with Dravet syndrome in a real-world practice setting: A report from the Fenfluramine European Early Access ProgramRenzo Guerrini, Nicola Specchio, Ángel Aledo-Serrano, et al.
Epilepsia|December 20, 2014
A novel KCNQ3 mutation in familial epilepsy with focal seizures and intellectual disabilityFrancesco Miceli, Pasquale Striano, Maria Virginia Soldovieri, et al.
Frontiers in Pharmacology|October 29, 2020
Cannabidiol Treatment for Refractory Epilepsies in PediatricsUmberto Raucci, Nicola Pietrafusa, Maria Chiara Paolino, et al.
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