Faioni EM - Search Results

1

A proteomic analysis of changes in prothrombin and plasma proteins associated with the G20210A mutation.

Gelfi C, Viganò A, Ripamonti M, Wait R, Begum S, Biguzzi E, Castaman G, Faioni EM. Gelfi C, et al. Among authors: faioni em. Proteomics. 2004 Jul;4(7):2151-9. doi: 10.1002/pmic.200300724. Proteomics. 2004. PMID: 15221775

2

Mutations in the thrombomodulin gene are rare in patients with severe thrombophilia.

Faioni EM, Franchi F, Castaman G, Biguzzi E, Rodeghiero F. Faioni EM, et al. Br J Haematol. 2002 Aug;118(2):595-9. doi: 10.1046/j.1365-2141.2002.03644.x. Br J Haematol. 2002. PMID: 12139752 Free article.

3

Association of protein S p.Pro667Pro dimorphism with plasma protein S levels in normal individuals and patients with inherited protein S deficiency.

Castaman G, Biguzzi E, Razzari C, Tosetto A, Fontana G, Asti D, Brancaccio V, Castori D, Lane DA, Faioni EM; ProSIT (Protein S Italian Team). Castaman G, et al. Among authors: faioni em. Thromb Res. 2007;120(3):421-6. doi: 10.1016/j.thromres.2006.10.014. Epub 2006 Dec 15. Thromb Res. 2007. PMID: 17157360

4

Association of factor V deficiency with factor V HR2.

Faioni EM, Castaman G, Asti D, Lussana F, Rodeghiero F. Faioni EM, et al. Haematologica. 2004 Feb;89(2):195-200. Haematologica. 2004. PMID: 15003895

5

Molecular diversity and thrombotic risk in protein S deficiency: the PROSIT study.

Biguzzi E, Razzari C, Lane DA, Castaman G, Cappellari A, Bucciarelli P, Fontana G, Margaglione M, D'Andrea G, Simmonds RE, Rezende SM, Preston R, Prisco D, Faioni EM; Protein S Italian Team. Biguzzi E, et al. Among authors: faioni em. Hum Mutat. 2005 Mar;25(3):259-69. doi: 10.1002/humu.20136. Hum Mutat. 2005. PMID: 15712227

6

Identification and computationally-based structural interpretation of naturally occurring variants of human protein C.

Rovida E, Merati G, D'Ursi P, Zanardelli S, Marino F, Fontana G, Castaman G, Faioni EM. Rovida E, et al. Among authors: faioni em. Hum Mutat. 2007 Apr;28(4):345-55. doi: 10.1002/humu.20445. Hum Mutat. 2007. PMID: 17152060

7

A novel G-to-A mutation in the intron-N of the protein S gene leading to abnormal RNA splicing in a patient with protein S deficiency.

D'Andrea G, Di Perna P, Brancaccio V, Faioni EM, Castaman G, Cibelli G, Di Minno G, Margaglione M; Protein S Italian Team. D'Andrea G, et al. Among authors: faioni em. Haematologica. 2003 Apr;88(4):459-64. Haematologica. 2003. PMID: 12681974

8

The factor V HR2 haplotype and the risk of venous thrombosis: a meta-analysis.

Castaman G, Faioni EM, Tosetto A, Bernardi F. Castaman G, et al. Among authors: faioni em. Haematologica. 2003 Oct;88(10):1182-9. Haematologica. 2003. PMID: 14555316

9

c.301C > T (p.Arg101Cys): a novel mutation in the thrombin-sensitive region of protein S associated with a dysfunctional protein.

Franchi F, Viscardi Y, Razzari C, Faioni EM, Bonara P, Biguzzi E, Mannucci PM. Franchi F, et al. Among authors: faioni em. Thromb Haemost. 2006 Sep;96(3):381-3. doi: 10.1160/TH06-01-0053. Thromb Haemost. 2006. PMID: 16953283 No abstract available.

10

Expression of endothelial protein C receptor and thrombomodulin in human coronary atherosclerotic plaques.

Merlini PA, Rossi ML, Faioni EM, Franchi F, Bramucci E, Lucreziotti S, Biguzzi E, Mannucci PM, Ardissino D. Merlini PA, et al. Among authors: faioni em. Ital Heart J. 2004 Jan;5(1):42-7. Ital Heart J. 2004. PMID: 15080580

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