Showing results (1621-1630 of 3,401) with videos related to

Sort By:
Pageof 341
Neuromuscular Disorders : NMD|December 19, 2025
Identification of novel potentially causative RYR1 variants in individuals with malignant hyperthermia susceptibilityDaniela Rossi, Carlotta Pranzo, Sara Roccabianca, et al.
Neuromuscular Disorders : NMD|December 10, 2025
Aseptic pyomyositis in Behçet's disease: a case report and narrative review of muscle involvement phenotypesEleonora Torchia, Werner Stenzel, Raphael Raspe, et al.
Neuromuscular Disorders : NMD|December 10, 2025
Safety and efficacy of dichlorphenamide in patients with periodic paralysis: A systematic review and meta-analysisSamna Haider, Ahmed Daud Siddiqui, Muhammad Asad, et al.
Neuromuscular Disorders : NMD|February 11, 2025
MRC Centre for Neuromuscular Diseases Biobank London: its role in the advancement of rare and neuromuscular diseases researchPierpaolo Ala, Silvia Torelli, Aisha Ahmed, et al.
Neuromuscular Disorders : NMD|January 26, 2025
The influence of genotype on the natural history of types 1 - 3 spinal muscular atrophyC Simone Sutherland, Sophie Schneider, Valerie Aponte Ribero, et al.
Neuromuscular Disorders : NMD|February 20, 2025
Strength and functional correlates of reachable workspace in facioscapulohumeral muscular dystrophyLeo H Wang, Maya N Hatch, Michael P McDermott, et al.
Neuromuscular Disorders : NMD|March 22, 2025
Assessing disease progression in spinal muscular atrophy, current gaps, and opportunities: a narrative reviewR Muni-Lofra, G Coratti, T Duong, et al.
Neuromuscular Disorders : NMD|January 11, 2025
Holter electrocardiography findings in Fukuyama congenital muscular dystrophyRyo Sugiyama, Eri Takeshita, Yuko Shimizu-Motohashi, et al.
Neuromuscular Disorders : NMD|February 28, 2025
Obstetric and gynaecological features in females carrying variants in the skeletal muscle ryanodine receptor type 1 (RYR1) gene: a questionnaire studyArti M Mistry, Georgia Saldanha, Luuk R van den Bersselaar, et al.
Neuromuscular Disorders : NMD|November 7, 2024
Mitochondrial disorders are associated with morphological neuromuscular junction defectsLola E R Lessard, Emmanuelle Girard, Nathalie Streichenberger, et al.
Pageof 341