Disease Progression Stages and Burden in Patients with Duchenne Muscular Dystrophy Using Administrative Claims Supplemented by Electronic Medical Records
Author:
Funder
Sarepta Therapeutics
Publisher
Springer Science and Business Media LLC
Subject
Pharmacology (medical),General Medicine
Link
https://link.springer.com/content/pdf/10.1007/s12325-022-02117-1.pdf
Reference33 articles.
1. Duan D, Goemans N, Takeda S, Mercuri E, Aartsma-Rus A. Duchenne muscular dystrophy. Nat Rev Dis Primers. 2021;7(1):13.
2. Al-Zaidy SA, Lloyd-Puryear M, Kennedy A, Lopez V, Mendell JR. A roadmap to newborn screening for Duchenne muscular dystrophy. Int J Neonatal Screen. 2017;3(2):8.
3. Connolly AM, Zaidman CM, Golumbek PT, et al. Twice-weekly glucocorticosteroids in infants and young boys with Duchenne muscular dystrophy. Muscle Nerve. 2019;59(6):650–7.
4. Spehrs-Ciaffi V, Fitting JW, Cotting J, Jeannet PY. Respiratory surveillance of patients with Duchenne and Becker muscular dystrophy. J Pediatr Rehabil Med. 2009;2(2):115–22.
5. Landfeldt E, Lindgren P, Bell CF, et al. The burden of Duchenne muscular dystrophy: an international, cross-sectional study. Neurology. 2014;83(6):529–36.
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