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Journal of Neuromuscular Diseases|February 20, 2025
A Parent Project Muscular Dystrophy-sponsored International Workshop Report on Endocrine and Bone Issues in Patients with Duchenne Muscular Dystrophy: An Ever-changing LandscapeLeanne M Ward, David R Weber, Sze Choong Wong, et al.Stroke|August 5, 2021
Clinical Performance Measures for Stroke Rehabilitation: Performance Measures From the American Heart Association/American Stroke AssociationJoel Stein, Douglas I Katz, Randie M Black Schaffer, et al.Journal of Neuromuscular Diseases|December 30, 2025
New SMA era: A broad-range tiered assessment of function for the evolving SMA phenotype (EVOLVE-SMA)Meghan Moore Burk, Thomas O Crawford, Kristen Johnson, et al.Journal of Neuromuscular Diseases|July 13, 2026
Navigating sexual health, fertility, and adult wellness in individuals with Duchenne muscular dystrophy: Current standards of care and future directionsNat Nasomyont, Amanda Appel, Susan Apkon, et al.JAMA Neurology|June 25, 2019
Efficacy of Home-Based Telerehabilitation vs In-Clinic Therapy for Adults After Stroke: A Randomized Clinical TrialSteven C Cramer, Lucy Dodakian, Vu Le, et al.Muscle & Nerve|May 24, 2026
Optimizing Care for Growth and Puberty in Duchenne Muscular Dystrophy: A Survey of Clinical Practice in the OPTIMIZE DMD ConsortiumClaire L Wood, Funmbi Babalola, Robert W Benjamin, et al.Journal of the Endocrine Society|January 9, 2026
Adrenal Suppression in Duchenne Muscular Dystrophy: Management Strategies Incorporating Novel Steroid VamoroloneAnne Marie Sbrocchi, Kathi Kinnett, Maria-Elena Lautatzis, et al.Neurology|February 16, 2021
Intense Arm Rehabilitation Therapy Improves the Modified Rankin Scale Score: Association Between Gains in Impairment and FunctionSteven C Cramer, Vu Le, Jeffrey L Saver, et al.Journal of Child Neurology|March 21, 2012
Consensus statement on standard of care for congenital myopathiesChing H Wang, James J Dowling, Kathryn North, et al.Lancet (London, England)|July 29, 2026
Deramiocel heart-derived cellular therapy in advanced Duchenne muscular dystrophy (HOPE-3): a phase 3, randomised, double-blind, placebo-controlled trialCraig M McDonald, Chet Villa, Jonathan H Soslow, et al.Pageof 16