d'Amati G - Search Results

1

Exogenous peptides are able to penetrate human cell and mitochondrial membranes, stabilize mitochondrial tRNA structures, and rescue severe mitochondrial defects.

Perli E, Pisano A, Pignataro MG, Campese AF, Pelullo M, Genovese I, de Turris V, Ghelli AM, Cerbelli B, Giordano C, Colotti G, Morea V, d'Amati G. Perli E, et al. FASEB J. 2020 Jun;34(6):7675-7686. doi: 10.1096/fj.201903270R. Epub 2020 Apr 18. FASEB J. 2020. PMID: 32304340

2

[Mitochondrial diseases].

D'Amati G, Casali C, Giordano C. D'Amati G, et al. Pathologica. 1999 Feb;91(1):49-50. Pathologica. 1999. PMID: 10396951 Review. Italian. No abstract available.

3

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. 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.

4

Pathogenic expression of homoplasmic mtDNA mutations needs a complex nuclear-mitochondrial interaction.

Carelli V, Giordano C, d'Amati G. Carelli V, et al. Trends Genet. 2003 May;19(5):257-62. doi: 10.1016/S0168-9525(03)00072-6. Trends Genet. 2003. PMID: 12711217 Review.

5

[Cardiomyopathies due to defective energy metabolism: morphological and functional features].

Giordano C, D'Amati G. Giordano C, et al. Pathologica. 2005 Dec;97(6):361-8. Pathologica. 2005. PMID: 16619977 Review. Italian.

6

Sudden cardiac death in younger adults: autopsy diagnosis as a tool for preventive medicine.

di Gioia CR, Autore C, Romeo DM, Ciallella C, Aromatario MR, Lopez A, Pagannone E, Giordano C, Gallo P, d'Amati G. di Gioia CR, et al. Hum Pathol. 2006 Jul;37(7):794-801. doi: 10.1016/j.humpath.2006.03.008. Epub 2006 Jun 5. Hum Pathol. 2006. PMID: 16784977

7

Gastrointestinal dysmotility in mitochondrial neurogastrointestinal encephalomyopathy is caused by mitochondrial DNA depletion.

Giordano C, Sebastiani M, De Giorgio R, Travaglini C, Tancredi A, Valentino ML, Bellan M, Cossarizza A, Hirano M, d'Amati G, Carelli V. Giordano C, et al. Am J Pathol. 2008 Oct;173(4):1120-8. doi: 10.2353/ajpath.2008.080252. Epub 2008 Sep 11. Am J Pathol. 2008. PMID: 18787099 Free PMC article.

8

Isolated distal myopathy of the upper limbs associated with mitochondrial DNA depletion and polymerase gamma mutations.

Giordano C, Pichiorri F, Blakely EL, Perli E, Orlandi M, Gallo P, Taylor RW, Inghilleri M, d'Amati G. Giordano C, et al. Arch Neurol. 2010 Sep;67(9):1144-6. doi: 10.1001/archneurol.2010.200. Arch Neurol. 2010. PMID: 20837862

9

Oestrogens ameliorate mitochondrial dysfunction in Leber's hereditary optic neuropathy.

Giordano C, Montopoli M, Perli E, Orlandi M, Fantin M, Ross-Cisneros FN, Caparrotta L, Martinuzzi A, Ragazzi E, Ghelli A, Sadun AA, d'Amati G, Carelli V. Giordano C, et al. Brain. 2011 Jan;134(Pt 1):220-34. doi: 10.1093/brain/awq276. Epub 2010 Oct 13. Brain. 2011. PMID: 20943885 Free PMC article.

10

Evaluation of gastrointestinal mtDNA depletion in mitochondrial neurogastrointestinal encephalomyopathy (MNGIE).

Giordano C, d'Amati G. Giordano C, et al. Methods Mol Biol. 2011;755:223-32. doi: 10.1007/978-1-61779-163-5_18. Methods Mol Biol. 2011. PMID: 21761307

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