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Page 1
Prevalence of Duchenne and Becker muscular dystrophies in the United States.
Romitti PA, Zhu Y, Puzhankara S, James KA, Nabukera SK, Zamba GK, Ciafaloni E, Cunniff C, Druschel CM, Mathews KD, Matthews DJ, Meaney FJ, Andrews JG, Conway KM, Fox DJ, Street N, Adams MM, Bolen J; MD STARnet. Romitti PA, et al. Pediatrics. 2015 Mar;135(3):513-21. doi: 10.1542/peds.2014-2044. Epub 2015 Feb 16. Pediatrics. 2015. PMID: 25687144 Free PMC article.
Needs management in families affected by childhood-onset dystrophinopathies.
Conway KM, Eichinger K, Trout C, Romitti PA, Mathews KD, Pandya SK; Muscular Dystrophy Surveillance, Tracking and Research Network (MD STARnet). Conway KM, et al. SAGE Open Med. 2019 Mar 2;7:2050312119834470. doi: 10.1177/2050312119834470. eCollection 2019. SAGE Open Med. 2019. PMID: 30854202 Free PMC article.
Characterization of individuals with selected muscular dystrophies from the expanded pilot of the Muscular Dystrophy Surveillance, Tracking and Research Network (MD STARnet) in the United States.
Wallace B, Smith KT, Thomas S, Conway KM, Westfield C, Andrews JG, Weinert RO, Do TQN, Street N; Muscular Dystrophy Surveillance, Tracking, and Research Network (MD STARnet). Wallace B, et al. Birth Defects Res. 2021 Apr 15;113(7):560-569. doi: 10.1002/bdr2.1764. Epub 2020 Jul 24. Birth Defects Res. 2021. PMID: 32710484 Free PMC article.
Association of genetic mutations and loss of ambulation in childhood-onset dystrophinopathy.
Haber G, Conway KM, Paramsothy P, Roy A, Rogers H, Ling X, Kozauer N, Street N, Romitti PA, Fox DJ, Phan HC, Matthews D, Ciafaloni E, Oleszek J, James KA, Galindo M, Whitehead N, Johnson N, Butterfield RJ, Pandya S, Venkatesh S, Bhattaram VA. Haber G, et al. Muscle Nerve. 2021 Feb;63(2):181-191. doi: 10.1002/mus.27113. Epub 2020 Nov 17. Muscle Nerve. 2021. PMID: 33150975 Free PMC article.
34 results