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Page 1
LGMD2E patients risk developing dilated cardiomyopathy.
Fanin M, Melacini P, Boito C, Pegoraro E, Angelini C. Fanin M, et al. Neuromuscul Disord. 2003 May;13(4):303-9. doi: 10.1016/s0960-8966(02)00280-8. Neuromuscul Disord. 2003. PMID: 12868499
Genomic organization of the dysferlin gene and novel mutations in Miyoshi myopathy.
Aoki M, Liu J, Richard I, Bashir R, Britton S, Keers SM, Oeltjen J, Brown HE, Marchand S, Bourg N, Beley C, McKenna-Yasek D, Arahata K, Bohlega S, Cupler E, Illa I, Majneh I, Barohn RJ, Urtizberea JA, Fardeau M, Amato A, Angelini C, Bushby K, Beckmann JS, Brown RH Jr. Aoki M, et al. Neurology. 2001 Jul 24;57(2):271-8. doi: 10.1212/wnl.57.2.271. Neurology. 2001. PMID: 11468312
Cardiac transplantation in a Duchenne muscular dystrophy carrier.
Melacini P, Fanin M, Angelini A, Pegoraro E, Livi U, Danieli GA, Hoffman EP, Thiene G, Dalla Volta S, Angelini C. Melacini P, et al. Neuromuscul Disord. 1998 Dec;8(8):585-90. doi: 10.1016/s0960-8966(98)00071-6. Neuromuscul Disord. 1998. PMID: 10093066
16 results