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Page 1
Mitochondrial DNA mutations and pathogenesis.
Schon EA, Bonilla E, DiMauro S. Schon EA, et al. Among authors: dimauro s. J Bioenerg Biomembr. 1997 Apr;29(2):131-49. doi: 10.1023/a:1022685929755. J Bioenerg Biomembr. 1997. PMID: 9239539 Review.
Pathogenesis of the deafness-associated A1555G mitochondrial DNA mutation.
Giordano C, Pallotti F, Walker WF, Checcarelli N, Musumeci O, Santorelli F, d'Amati G, Schon EA, DiMauro S, Hirano M, Davidson MM. Giordano C, et al. Among authors: dimauro s. Biochem Biophys Res Commun. 2002 Apr 26;293(1):521-9. doi: 10.1016/S0006-291X(02)00256-5. Biochem Biophys Res Commun. 2002. PMID: 12054632
Mitochondrial respiratory-chain diseases.
DiMauro S, Schon EA. DiMauro S, et al. N Engl J Med. 2003 Jun 26;348(26):2656-68. doi: 10.1056/NEJMra022567. N Engl J Med. 2003. PMID: 12826641 Review. No abstract available.
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: dimauro s. Lancet. 2004 Aug 14-20;364(9434):592-6. doi: 10.1016/S0140-6736(04)16851-7. Lancet. 2004. PMID: 15313359
Mitochondrial mutations: genotype to phenotype.
Schon EA, DiMauro S. Schon EA, et al. Among authors: dimauro s. Novartis Found Symp. 2007;287:214-25; discussion 226-33. doi: 10.1002/9780470725207.ch15. Novartis Found Symp. 2007. PMID: 18074641 Review.
Mitochondrial disorders in the nervous system.
DiMauro S, Schon EA. DiMauro S, et al. Annu Rev Neurosci. 2008;31:91-123. doi: 10.1146/annurev.neuro.30.051606.094302. Annu Rev Neurosci. 2008. PMID: 18333761 Review.
735 results