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Journal of the Peripheral Nervous System : JPNS|October 13, 2015
Innovative quantitative testing of hand function in Charcot-Marie-Tooth neuropathyMaria A Alberti, Laura Mori, Luca Francini, et al.Life (Basel, Switzerland)|April 28, 2023
Comparing the Impact of COVID-19 on Vaccinated and Unvaccinated Patients Affected by Myasthenia GravisElena Scarsi, Sara Massucco, Pilar M Ferraro, et al.Frontiers in Genetics|December 20, 2024
Case report: A single novel calpain 3 gene variant associated with mild myopathySara Massucco, Paola Fossa, Chiara Fiorillo, et al.Pediatric Neurology|March 1, 2024
Early Onset Inherited Peripheral Neuropathies: The Experience of a Specialized Referral Center for Genetic Diagnosis AchievementAlessandro Geroldi, Clarissa Ponti, Alessia Mammi, et al.European Journal of Neurology|March 15, 2022
Real-life experience with inotersen in hereditary transthyretin amyloidosis with late-onset phenotype: Data from an early-access program in ItalyMarco Luigetti, Giovanni Antonini, Andrea Di Paolantonio, et al.European Journal of Human Genetics : EJHG|January 4, 2024
DAG1 haploinsufficiency is associated with sporadic and familial isolated or pauci-symptomatic hyperCKemiaMonica Traverso, Serena Baratto, Michele Iacomino, et al.Muscle & Nerve|October 23, 2021
An integrated approach to the evaluation of patients with asymptomatic or minimally symptomatic hyperCKemiaChiara Gemelli, Monica Traverso, Lucia Trevisan, et al.Brain Sciences|October 29, 2020
hATTR Pathology: Nerve Biopsy Results from Italian Referral CentersMarco Luigetti, Marina Romozzi, Giulia Bisogni, et al.Journal of Neurology|August 5, 2020
Nerve ultrasound in hereditary transthyretin amyloidosis: red flags and possible progression biomarkersAlessandro Salvalaggio, Daniele Coraci, Mario Cacciavillani, et al.Life (Basel, Switzerland)|March 25, 2022
Genetic Workup for Charcot-Marie-Tooth Neuropathy: A Retrospective Single-Site Experience Covering 15 YearsChiara Gemelli, Alessandro Geroldi, Sara Massucco, et al.Pageof 10