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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.Plos One|February 27, 2025
Study protocol: Exploratory trial of Forza™, an osmotin-based nutraceutical as adjuvant for the treatment of progressive multiple sclerosisViola Costa, Kenda Aluan, Irene Schiavetti, et al.Plos One|March 31, 2012
Hyccin, the molecule mutated in the leukodystrophy hypomyelination and congenital cataract (HCC), is a neuronal proteinElisabetta Gazzerro, Simona Baldassari, Caterina Giacomini, 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.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.Neurobiology of Disease|January 25, 2020
Distal motor neuropathy associated with novel EMILIN1 mutationMichele Iacomino, Roberto Doliana, Maria Marchese, et al.Journal of the Peripheral Nervous System : JPNS|June 5, 2026
A Quantitative Assessment of Upper Limb Motor Function Across Disease Stages in Hereditary Transthyretin AmyloidosisMehrnaz Hamedani, Valeria Prada, Sara Massucco, et al.Journal of Neurology, Neurosurgery, and Psychiatry|November 2, 2023
Use, tolerability, benefits and side effects of orthotic devices in Charcot-Marie-Tooth diseaseAlessandro Bertini, Fiore Manganelli, Gian Maria Fabrizi, et al.Neuropathology and Applied Neurobiology|July 29, 2022
The SPTLC1 p.S331 mutation bridges sensory neuropathy and motor neuron disease and has implications for treatmentChiara Fiorillo, Giovanna Capodivento, Alessandro Geroldi, et al.Pageof 4