Margaglione M - Search Results

1

Bafunno V, Margaglione M. Bafunno V, et al. Among authors: margaglione m. Clin Chem Lab Med. 2010 Dec;48 Suppl 1:S41-51. doi: 10.1515/CCLM.2010.361. Epub 2010 Oct 29. Clin Chem Lab Med. 2010. PMID: 21034258 Review.

2

Fibrinogen and mechanisms of thrombosis. A difficult link.

Di Minno G, Cerbone A, Margaglione M, Vecchione G, Grandone E, Mancini M. Di Minno G, et al. Among authors: margaglione m. Eur J Epidemiol. 1992 May;8 Suppl 1:88-91. doi: 10.1007/BF00145357. Eur J Epidemiol. 1992. PMID: 1505658 Review.

3

Arterial thrombosis in women. Pathogenesis.

Margaglione M. Margaglione M. Thromb Res. 2005 Feb;115 Suppl 1:63-5. Thromb Res. 2005. PMID: 15790158 No abstract available.

4

Low protein Z levels and risk of occurrence of deep vein thrombosis.

Santacroce R, Sarno M, Cappucci F, Sessa F, Colaizzo D, Brancaccio V, Grandone E, Margaglione M. Santacroce R, et al. Among authors: margaglione m. J Thromb Haemost. 2006 Nov;4(11):2417-22. doi: 10.1111/j.1538-7836.2006.02186.x. Epub 2006 Aug 25. J Thromb Haemost. 2006. PMID: 16938126 Free article. Clinical Trial.

5

A novel mutation in human ether-a-go-go-related gene, alanine to proline at position 490, found in a large family with autosomal dominant long QT syndrome.

Pellegrino PL, Bafunno V, Ieva R, Brunetti ND, Mavilio G, Sessa F, Grimaldi M, Margaglione M, Di Biase M. Pellegrino PL, et al. Among authors: margaglione m. Am J Cardiol. 2007 Jun 15;99(12):1737-40. doi: 10.1016/j.amjcard.2007.01.056. Epub 2007 Apr 30. Am J Cardiol. 2007. PMID: 17560885

6

A beta3 Asp217-->Val substitution in a patient with variant Glanzmann Thrombasthenia severely affects integrin alphaIIBbeta3 functions.

D'Andrea G, Bafunno V, Del Vecchio L, Amoriello A, Morabito P, Vecchione G, Grandone E, Margaglione M. D'Andrea G, et al. Among authors: margaglione m. Blood Coagul Fibrinolysis. 2008 Oct;19(7):657-62. doi: 10.1097/MBC.0b013e3283048e42. Blood Coagul Fibrinolysis. 2008. PMID: 18832906

7

Detection of new deletions in a group of Italian patients with Hemophilia A by multiplex ligation-dependent probe amplification.

Santacroce R, Longo V, Bafunno V, Sessa F, Chetta M, Sarno M, Bukvic N, D'Andrea G, Tomaiuolo M, Margaglione M. Santacroce R, et al. Among authors: margaglione m. Genet Test Mol Biomarkers. 2009 Oct;13(5):573-6. doi: 10.1089/gtmb.2009.0015. Genet Test Mol Biomarkers. 2009. PMID: 19715469

8

The JAK2 rs12343867 CC genotype frequently occurs in patients with splanchnic venous thrombosis without the JAK2V617F mutation: a retrospective study.

Colaizzo D, Tiscia GL, Bafunno V, Amitrano L, Vergura P, Grandone E, Guardascione MA, Margaglione M. Colaizzo D, et al. Among authors: margaglione m. J Thromb Haemost. 2010 Feb;8(2):413-6. doi: 10.1111/j.1538-7836.2009.03691.x. Epub 2009 Nov 17. J Thromb Haemost. 2010. PMID: 19922437 Free article. No abstract available.

9

A platelet defect modulates bleeding in mild hemophilia: the tale of 2 brothers.

Lapecorella M, Santacroce R, Napolitano M, Bafunno V, Favuzzi G, Longo V, Grandone E, Mariani G, Margaglione M. Lapecorella M, et al. Among authors: margaglione m. Clin Appl Thromb Hemost. 2009 Dec;15(6):715-6. doi: 10.1177/1076029609333676. Clin Appl Thromb Hemost. 2009. PMID: 19926614 Free article. No abstract available.

10

Polymorphisms in genes involved in autoimmune disease and the risk of FVIII inhibitor development in Italian patients with haemophilia A.

Bafunno V, Santacroce R, Chetta M, D'Andrea G, Pisanelli D, Sessa F, Trotta T, Tagariello G, Peyvandi F, Margaglione M. Bafunno V, et al. Among authors: margaglione m. Haemophilia. 2010 May;16(3):469-73. doi: 10.1111/j.1365-2516.2009.02150.x. Epub 2009 Dec 14. Haemophilia. 2010. PMID: 20015215

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