Giordano C - Search Results

1

A novel LAMP2 mutation associated with severe cardiac hypertrophy and microvascular remodeling in a female with Danon disease: a case report and literature review.

Bottillo I, Giordano C, Cerbelli B, D'Angelantonio D, Lipari M, Polidori T, Majore S, Bertini E, D'Amico A, Giannarelli D, De Bernardo C, Masuelli L, Musumeci F, Avella A, Re F, Zachara E, d'Amati G, Grammatico P. Bottillo I, et al. Among authors: giordano c. Cardiovasc Pathol. 2016 Sep-Oct;25(5):423-31. doi: 10.1016/j.carpath.2016.07.005. Epub 2016 Jul 25. Cardiovasc Pathol. 2016. PMID: 27497751 Review.

2

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. Among authors: giordano c. 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.

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. 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.

4

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

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

5

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

6

[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.

7

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. Among authors: giordano c. 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

8

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.

9

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

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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