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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 MinassianPediatric Neurology Briefs|March 3, 2016
Todd Paralysis in Rolandic EpilepsyPasquale Striano, Maria Stella VariEpilepsia|August 1, 2013
Loss-of-function KCNH2 mutation in a family with long QT syndrome, epilepsy, and sudden deathSara Partemi, Sandrine Cestèle, Marianna Pezzella, et al.Nature Clinical Practice. Neurology|February 8, 2008
Typical progression of myoclonic epilepsy of the Lafora type: a case reportPasquale Striano, Federico Zara, Julie Turnbull, et al.Epilepsy Research|May 27, 2008
Hyperhomocysteinemia and retinal vascular changes in patients with epilepsyVincenzo Belcastro, Pasquale Striano, Daniela Caccamo, et al.Epilepsy & Behavior : E&B|February 1, 2016
Psychiatric comorbidities in patients from seven families with autosomal dominant cortical tremor, myoclonus, and epilepsyAntonietta Coppola, Carmela Caccavale, Lia Santulli, et al.Epilepsia|March 2, 2013
Different electroclinical picture of generalized epilepsy in two families with 15q13.3 microdeletionAntonietta Coppola, Irene Bagnasco, Monica Traverso, et al.Expert Opinion on Pharmacotherapy|August 27, 2019
A reappraisal of atypical absence seizures in children and adults: therapeutic implicationsFrancesco Brigo, Pasquale Striano, Vicenzo BelcastroCells|June 28, 2023
Familial Adult Myoclonus Epilepsy: A Non-Coding Repeat Expansion Disorder of Cerebellar-Thalamic-Cortical LoopClaudia Cuccurullo, Pasquale Striano, Antonietta CoppolaNeurology. Clinical Practice|November 16, 2022
Paroxysmal Nonepileptic Events in Children: A Video Gallery and a Guide for Differential DiagnosisIlaria Lagorio, Lorenzo Brunelli, Pasquale StrianoPageof 70