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Expert Review of Neurotherapeutics|August 15, 2017
Monitoring disease progression in spinocerebellar ataxias: implications for treatment and clinical researchLidia Sarro, Lorenzo Nanetti, Anna Castaldo, et al.Journal of Neurology|August 1, 2009
Rare association of motor neuron disease and spinocerebellar ataxia type 2 (SCA2): a new case and review of the literatureLorenzo Nanetti, Roberto Fancellu, Chiara Tomasello, et al.Neuropediatrics|November 7, 2023
A Novel Pathogenic Variant in the SCA25-Related Gene Expanding the Etiology of Early-Onset and Progressive Cerebellar Ataxia in ChildhoodGiulia Ferrera, Rossella Izzo, Daniele Ghezzi, et al.Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|September 2, 2022
Comorbidities in Friedreich ataxia: incidence and manifestations from early to advanced disease stagesMario Fichera, Anna Castaldo, Alessia Mongelli, et al.American Journal of Medical Genetics. Part A|November 28, 2020
Missing the pathological expansion in Huntington disease: de novo c.51C>G variant on the expanded allele causing intrafamilial allele dropoutStefania Magri, Lorenzo Nanetti, Alessia Mongelli, et al.Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|March 3, 2023
Italian cross-cultural adaptation of the patient-reported outcome measure of ataxiaAnna Castaldo, Mariangela Farinotti, Mario Fichera, et al.Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|July 12, 2021
Spastic paraplegia type 46: novel and recurrent GBA2 gene variants in a compound heterozygous Italian patient with spastic ataxia phenotypeMarta Gatti, Stefania Magri, Daniela Di Bella, et al.Journal of Huntington'S Disease|May 31, 2024
Oropharyngeal Dysphagia Phenotypes Across Huntington's Disease Stages: Endoscopic Findings and Tongue Pressure AnalysisNicole Pizzorni, Andrea Ciammola, Chiara Pirola, et al.American Journal of Medical Genetics. Part A|February 19, 2019
Homozygous variant in OTX2 and possible genetic modifiers identified in a patient with combined pituitary hormone deficiency, ocular involvement, myopathy, ataxia, and mitochondrial impairmentAlessia Catania, Andrea Legati, Lorenzo Peverelli, et al.Gait & Posture|May 29, 2017
Stance instability in preclinical SCA1 mutation carriers: A 4-year prospective posturography studyLorenzo Nanetti, Dario Alpini, Valentina Mattei, et al.Pageof 7