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Mitochondrial encephalomyopathies.
DiMauro S, Zeviani M, Moraes CT, Nakase H, Rizzuto R, Lombes A, Shanske S, Schon EA. DiMauro S, et al. Among authors: zeviani m. Prog Clin Biol Res. 1989;306:117-28. Prog Clin Biol Res. 1989. PMID: 2544896 Review. No abstract available.
The mitochondrial DNA C3303T mutation can cause cardiomyopathy and/or skeletal myopathy.
Bruno C, Kirby DM, Koga Y, Garavaglia B, Duran G, Santorelli FM, Shield LK, Xia W, Shanske S, Goldstein JD, Iwanaga R, Akita Y, Carrara F, Davis A, Zeviani M, Thorburn DR, DiMauro S. Bruno C, et al. Among authors: zeviani m. J Pediatr. 1999 Aug;135(2 Pt 1):197-202. doi: 10.1016/s0022-3476(99)70022-3. J Pediatr. 1999. PMID: 10431114 Free article.
Risk of developing a mitochondrial DNA deletion disorder.
Chinnery PF, DiMauro S, Shanske S, Schon EA, Zeviani M, Mariotti C, Carrara F, Lombes A, Laforet P, Ogier H, Jaksch M, Lochmüller H, Horvath R, Deschauer M, Thorburn DR, Bindoff LA, Poulton J, Taylor RW, Matthews JN, Turnbull DM. Chinnery PF, et al. Among authors: zeviani m. Lancet. 2004 Aug 14-20;364(9434):592-6. doi: 10.1016/S0140-6736(04)16851-7. Lancet. 2004. PMID: 15313359
Deletions of mitochondrial DNA in Kearns-Sayre syndrome. 1988.
Zeviani M, Moraes CT, DiMauro S, Nakase H, Bonilla E, Schon EA, Rowland LP. Zeviani M, et al. Neurology. 1998 Dec;51(6):1525 and 8 pages following. doi: 10.1212/wnl.51.6.1525-a. Neurology. 1998. PMID: 9855494 No abstract available.
469 results