d'Amati G - Search Results

1

Mitochondrial neurogastrointestinal encephalomyopathy: evidence of mitochondrial DNA depletion in the small intestine.

Giordano C, Sebastiani M, Plazzi G, Travaglini C, Sale P, Pinti M, Tancredi A, Liguori R, Montagna P, Bellan M, Valentino ML, Cossarizza A, Hirano M, d'Amati G, Carelli V. Giordano C, et al. Gastroenterology. 2006 Mar;130(3):893-901. doi: 10.1053/j.gastro.2006.01.004. Gastroenterology. 2006. PMID: 16530527

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

Myocyte transdifferentiation: a possible pathogenetic mechanism for arrhythmogenic right ventricular cardiomyopathy.

d'Amati G, di Gioia CR, Giordano C, Gallo P. d'Amati G, et al. Arch Pathol Lab Med. 2000 Feb;124(2):287-90. doi: 10.5858/2000-124-0287-MT. Arch Pathol Lab Med. 2000. PMID: 10656741 Free article.

4

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.

5

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

6

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.

7

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. 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.

8

Detection of deleted mitochondrial DNA in Kearns-Sayre syndrome using laser capture microdissection.

Pistilli D, di Gioia CR, D'Amati G, Sciacchitano S, Quaglione R, Quitadamo R, Casali C, Gallo P, Santorelli FM. Pistilli D, et al. Hum Pathol. 2003 Oct;34(10):1058-61. doi: 10.1053/s0046-8177(03)00344-7. Hum Pathol. 2003. PMID: 14608542

9

Blue rubber bleb nevus syndrome and pulmonary hypertension: an unusual association.

Giordano C, Battagliese A, di Gioia CR, Campagna D, Benedetti F, Travaglini C, Gallo P, d' Amati G. Giordano C, et al. Cardiovasc Pathol. 2004 Nov-Dec;13(6):317-22. doi: 10.1016/j.carpath.2004.07.004. Cardiovasc Pathol. 2004. PMID: 15556778

10

[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.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

238 results

Search Page

Filters