D'Angelo A - Search Results

1

The role of vitamin B12 in fasting hyperhomocysteinemia and its interaction with the homozygous C677T mutation of the methylenetetrahydrofolate reductase (MTHFR) gene. A case-control study of patients with early-onset thrombotic events.

D'Angelo A, Coppola A, Madonna P, Fermo I, Pagano A, Mazzola G, Galli L, Cerbone AM. D'Angelo A, et al. Thromb Haemost. 2000 Apr;83(4):563-70. Thromb Haemost. 2000. PMID: 10780318

2

Gene-gene and gene-environment interactions in mild hyperhomocysteinemia.

D'Angelo A, Mazzola G, Fermo I. D'Angelo A, et al. Pathophysiol Haemost Thromb. 2003 Sep-2004 Dec;33(5-6):337-41. doi: 10.1159/000083824. Pathophysiol Haemost Thromb. 2003. PMID: 15692239 Free article. Review.

3

Hyperhomocysteinemia and venous thromboembolic disease.

D'Angelo A, Mazzola G, Crippa L, Fermo I, Viganò D'Angelo S. D'Angelo A, et al. Haematologica. 1997 Mar-Apr;82(2):211-9. Haematologica. 1997. PMID: 9175329 Review.

4

Contribution of the cystathionine beta-synthase gene (844ins68) polymorphism to the risk of early-onset venous and arterial occlusive disease and of fasting hyperhomocysteinemia.

de Franchis R, Fermo I, Mazzola G, Sebastio G, Di Minno G, Coppola A, Andria G, D'Angelo A. de Franchis R, et al. Thromb Haemost. 2000 Oct;84(4):576-82. Thromb Haemost. 2000. PMID: 11057853

5

Prevalence of moderate hyperhomocysteinemia in patients with early-onset venous and arterial occlusive disease.

Fermo I, Vigano' D'Angelo S, Paroni R, Mazzola G, Calori G, D'Angelo A. Fermo I, et al. Ann Intern Med. 1995 Nov 15;123(10):747-53. doi: 10.7326/0003-4819-123-10-199511150-00002. Ann Intern Med. 1995. PMID: 7574192

6

Moderate hyperhomocysteinemia and central retinal vein occlusion.

D'Angelo A, Tavola A, Fermo I, Mazzola G, Brancato R. D'Angelo A, et al. Thromb Haemost. 2002 Jun;87(6):1078-9. Thromb Haemost. 2002. PMID: 12083491 No abstract available.

7

Reduced in vivo oxidative stress following 5-methyltetrahydrofolate supplementation in patients with early-onset thrombosis and 677TT methylenetetrahydrofolate reductase genotype.

Coppola A, D'Angelo A, Fermo I, Mazzola G, Di Minno MN, Cajani A, Sala A, Folco G, Tremoli E, Di Minno G. Coppola A, et al. Br J Haematol. 2005 Oct;131(1):100-8. doi: 10.1111/j.1365-2141.2005.05732.x. Br J Haematol. 2005. PMID: 16173969 Free article.

8

Homozygous C677T mutation of the 5,10 methylenetetrahydrofolate reductase gene and hyperhomocysteinemia in Italian patients with a history of early-onset ischemic stroke.

Soriente L, Coppola A, Madonna P, Cerbone AM, Di Minno G, Orefice G, D'Angelo A. Soriente L, et al. Stroke. 1998 Apr;29(4):869-71. doi: 10.1161/01.str.29.4.869. Stroke. 1998. PMID: 9550528 No abstract available.

9

Genotype-independent in vivo oxidative stress following a methionine loading test: maximal platelet activation in subjects with early-onset thrombosis.

Di Minno MN, Pezzullo S, Palmieri V, Coppola A, D'Angelo A, Sampietro F, Cavalca V, Tremoli E, Di Minno G. Di Minno MN, et al. Thromb Res. 2011 Oct;128(4):e43-8. doi: 10.1016/j.thromres.2011.05.017. Epub 2011 Jun 12. Thromb Res. 2011. PMID: 21669453

10

Protein S and protein C anticoagulant activity in acute and chronic cardiac ischemic syndromes. Relationship to inflammation, complement activation and in vivo thrombin activity.

D'Angelo A, Gerosa S, D'Angelo SV, Mailhac A, Colombo A, Agazzi A, Mazzola G, Chierchia S. D'Angelo A, et al. Thromb Res. 1994 Jul 15;75(2):133-42. doi: 10.1016/0049-3848(94)90062-0. Thromb Res. 1994. PMID: 7974387

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