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Nutrients|July 15, 2026
Beyond Ketosis: Dietary Therapies and the Microbiota-Gut-Brain Axis in EpilepsyValentina Biagioli, Mariarosaria Matera, Ilaria Imola, et al.
Italian Journal of Pediatrics|June 13, 2021
Symptomatic eating epilepsy: two novel pediatric patients and review of literatureFabiana Vercellino, Laura Siri, Giacomo Brisca, et al.
Neurotherapeutics : the Journal of the American Society for Experimental Neurotherapeutics|March 23, 2024
Pharmacodynamic rationale for the choice of antiseizure medications in the paediatric populationGianluca D'Onofrio, Roberta Roberti, Antonella Riva, et al.
Neuromuscular Disorders : NMD|December 5, 2006
Inherited neuromyotonia: a clinical and genetic study of a familyAntonio Falace, Pasquale Striano, Fiore Manganelli, et al.
Expert Review of Neurotherapeutics|June 12, 2014
Usefulness of video-EEG in the paediatric emergency departmentRaffaele Falsaperla, Pasquale Striano, Pasquale Parisi, et al.
Frontiers in Neurology|March 18, 2022
Sleep Disorders in Rett Syndrome and Rett-Related Disorders: A Narrative ReviewGiorgia Tascini, Giovanni Battista Dell'Isola, Elisabetta Mencaroni, et al.
Brain Communications|March 2, 2022
Abnormal sensorimotor cortex and thalamo-cortical networks in familial adult myoclonic epilepsy type 2: pathophysiology and diagnostic implicationsRaffaele Dubbioso, Pasquale Striano, Leo Tomasevic, et al.
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.
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