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Journal of Comparative Effectiveness Research|April 10, 2026
Advancements from the EVOLVE study for assessing real-world experience with eteplirsen, golodirsen and casimersen for the treatment of DMDCuixia Tian, Shannon Grabich, Aravindhan Veerapandiyan, et al.
International Journal of Molecular Sciences|November 13, 2025
Elevated Levels of Active GSK3β in the Blood of Patients with Myotonic Dystrophy Type 1 Correlate with Muscle WeaknessKatherine Jennings, Cuixia Tian, Rebeccah L Brown, et al.
Neuromuscular Disorders : NMD|September 12, 2016
Bone health measures in glucocorticoid-treated ambulatory boys with Duchenne muscular dystrophyCuixia Tian, Brenda L Wong, Lindsey Hornung, et al.
Muscle & Nerve|October 26, 2019
Neurodevelopmental, behavioral, and emotional symptoms in Becker muscular dystrophyJoshua T Lambert, Andrew J Darmahkasih, Paul S Horn, et al.
Muscle & Nerve|January 8, 2020
Neurodevelopmental, behavioral, and emotional symptoms common in Duchenne muscular dystrophyAndrew J Darmahkasih, Irina Rybalsky, Cuixia Tian, et al.
Muscle & Nerve|November 29, 2022
A longitudinal study of creatine kinase and creatinine levels in Duchenne muscular dystrophyAlexander M Zygmunt, Brenda L Wong, Paul S Horn, et al.
Journal of Cachexia, Sarcopenia and Muscle|October 25, 2023
Appendicular lean mass index changes in patients with Duchenne muscular dystrophy and Becker muscular dystrophyBrenda L Wong, Suzanne Summer, Paul S Horn, et al.
Journal of Pediatric Nursing|August 27, 2021
Emergency Planning as Part of Healthcare Transition Preparation for Patients with Duchenne Muscular DystrophyWendy A Chouteau, Carolyn Burrows, Samuel G Wittekind, et al.
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