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Pediatric Neurology Briefs|March 3, 2016
Todd Paralysis in Rolandic EpilepsyPasquale Striano, Maria Stella VariPharmacological Research|April 16, 2016
Management of genetic epilepsies: From empirical treatment to precision medicinePasquale Striano, Maria Stella Vari, Chiara Mazzocchetti, et al.Birth Defects Research|May 3, 2017
A novel Xp22.13 microdeletion in Nance-Horan syndromeAndrea Accogli, Monica Traverso, Francesca Madia, et al.Seizure|March 24, 2018
De novo 12q22.q23.3 duplication associated with temporal lobe epilepsyMaria Stella Vari, Monica Traverso, Tommaso Bellini, et al.Seizure|June 21, 2017
De novo 12q22.q23.3 duplication associated with temporal lobe epilepsyMaria Stella Vari, Monica Traverso, Tommaso Bellini, et al.European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|June 10, 2019
Abnormal circadian rhythm in patients with GRIN1-related developmental epileptic encephalopathyMarcello Scala, Elisabetta Amadori, Lucia Fusco, et al.Expert Opinion on Pharmacotherapy|September 20, 2022
Current and promising therapeutic options for Dravet syndromeAntonella Riva, Gianluca D'Onofrio, Elisabetta Amadori, et al.European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|January 24, 2018
A novel homozygous MFN2 mutation associated with severe and atypical CMT2 phenotypeGiulia Iapadre, Giovanni Morana, Maria Stella Vari, et al.Journal of Pediatric Genetics|September 10, 2021
Complex Neurological Phenotype Associated with a De Novo <i>DHDDS</i> Mutation in a Boy with Intellectual Disability, Refractory Epilepsy, and Movement DisorderGianluca Piccolo, Elisabetta Amadori, Maria Stella Vari, et al.Children (Basel, Switzerland)|May 27, 2026
Studying Familial Bainbridge-Ropers Syndrome Due to a Novel <i>ASXL3</i> Germline Variant and Expanding the Clinical SpectrumDaiana Mariano, Valentina Petrone, Francesca Madia, et al.Pageof 4