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Journal of Neuromuscular Diseases|November 19, 2023
Findings from the Longitudinal CINRG Becker Natural History StudyPaula R Clemens, Heather Gordish-Dressman, Gabriela Niizawa, et al.Neurology|March 16, 2018
A multinational study on motor function in early-onset FSHDJean K Mah, Jia Feng, Marni B Jacobs, et al.Muscle & Nerve|June 22, 2020
The CINRG Becker Natural History Study: Baseline characteristicsPaula R Clemens, Gabriela Niizawa, Jia Feng, et al.Annals of Clinical and Translational Neurology|August 20, 2025
Long-Term Evaluation of Givinostat in Duchenne Muscular Dystrophy, and Natural History ComparisonsCraig M McDonald, Michela Guglieri, Dragana Vučinić, et al.Journal of Personalized Medicine|November 24, 2020
Multi-Omics Identifies Circulating miRNA and Protein Biomarkers for Facioscapulohumeral DystrophyChristopher R Heier, Aiping Zhang, Nhu Y Nguyen, et al.Journal of Neuromuscular Diseases|February 6, 2026
A randomized, double-blind, placebo-controlled study of losmapimod in patients with facioscapulohumeral muscular dystrophy: Results of the REACH studyNicol C Voermans, Jeffrey M Statland, Lawrence J Hayward, et al.Neurology|February 9, 2024
Efficacy and Safety of Vamorolone Over 48 Weeks in Boys With Duchenne Muscular Dystrophy: A Randomized Controlled TrialUtkarsh J Dang, Jesse M Damsker, Michela Guglieri, et al.Pageof 3