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Neurotherapeutics : the Journal of the American Society for Experimental Neurotherapeutics|January 26, 2020
From Genetic Testing to Precision Medicine in EpilepsyPasquale Striano, Berge A MinassianEpileptic Disorders : International Epilepsy Journal with Videotape|September 14, 2016
The history of progressive myoclonus epilepsiesPierre Genton, Pasquale Striano, Berge A MinassianEpileptic Disorders : International Epilepsy Journal with Videotape|October 6, 2016
Lafora diseaseJulie Turnbull, Erica Tiberia, Pasquale Striano, et al.Epileptic Disorders : International Epilepsy Journal with Videotape|September 16, 2016
Post-modern therapeutic approaches for progressive myoclonus epilepsyBerge A MinassianSeizure|September 3, 2019
The best evidence for progressive myoclonic epilepsy: A pathway to precision therapyAlessandro Orsini, Angelo Valetto, Veronica Bertini, et al.Pediatric Neurology|February 4, 2014
Genetic testing in infantile spasms identifies a chromosome 13q deletion and retinoblastomaKevin Jones, Berge A MinassianEpilepsia Open|June 9, 2018
Extraneurological sparing in long-lived typical Lafora diseaseDanielle Goldsmith, Berge A MinassianEpilepsy & Behavior : E&B|July 27, 2016
Efficacy and tolerability of perampanel in ten patients with Lafora diseaseDanielle Goldsmith, Berge A MinassianBrain Pathology (Zurich, Switzerland)|September 12, 2009
22-year-old girl with status epilepticus and progressive neurological symptomsPasquale Striano, Cameron A Ackerley, Mariarosaria Cervasio, et al.Pageof 83