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[Mitochondrial diseases].
D'Amati G, Casali C, Giordano C. D'Amati G, et al. Among authors: giordano c. Pathologica. 1999 Feb;91(1):49-50. Pathologica. 1999. PMID: 10396951 Review. Italian. No abstract available.
Is apoptosis a diagnostic marker of acute myocardial infarction?
Piro FR, di Gioia CR, Gallo P, Giordano C, d'Amati G. Piro FR, et al. Among authors: giordano c. Arch Pathol Lab Med. 2000 Jun;124(6):827-31. doi: 10.5858/2000-124-0827-IAADMO. Arch Pathol Lab Med. 2000. PMID: 10835514 Free article.
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. 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
A homoplasmic mitochondrial transfer ribonucleic acid mutation as a cause of maternally inherited hypertrophic cardiomyopathy.
Taylor RW, Giordano C, Davidson MM, d'Amati G, Bain H, Hayes CM, Leonard H, Barron MJ, Casali C, Santorelli FM, Hirano M, Lightowlers RN, DiMauro S, Turnbull DM. Taylor RW, et al. Among authors: giordano c. J Am Coll Cardiol. 2003 May 21;41(10):1786-96. doi: 10.1016/s0735-1097(03)00300-0. J Am Coll Cardiol. 2003. PMID: 12767666 Free article.
1,375 results