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Page 1
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.
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.
Left ventricular dysfunction in Duchenne muscular dystrophy.
James KA, Gralla J, Ridall LA, Do TN, Czaja AS, Mourani PM, Ciafaloni E, Cunniff C, Donnelly J, Oleszek J, Pandya S, Price E, Yang ML, Auerbach SR. James KA, et al. Cardiol Young. 2020 Feb;30(2):171-176. doi: 10.1017/S1047951119002610. Epub 2020 Jan 22. Cardiol Young. 2020. PMID: 31964455 Free PMC article.
20 results