Vicente V - Search Results

1

Hereditary thrombophilia: identification of nonsense and missense mutations in the protein C gene.

Romeo G, Hassan HJ, Staempfli S, Roncuzzi L, Cianetti L, Leonardi A, Vicente V, Mannucci PM, Bertina R, Peschle C, et al. Romeo G, et al. Among authors: vicente v. Proc Natl Acad Sci U S A. 1987 May;84(9):2829-32. doi: 10.1073/pnas.84.9.2829. Proc Natl Acad Sci U S A. 1987. PMID: 2437584 Free PMC article.

2

Effects of oral anticoagulant therapy and haplotype 1 of the endothelial protein C receptor gene on activated protein C levels.

Medina P, Bonet E, Navarro S, Martos L, Estellés A, Ferrando F, Vicente V, Bertina RM, España F. Medina P, et al. Among authors: vicente v. Thromb Haemost. 2012 Mar;107(3):448-57. doi: 10.1160/TH11-07-0510. Epub 2012 Jan 25. Thromb Haemost. 2012. PMID: 22273845

3

Serum phospholipids are the main environmental determinants of activated factor VII in the most common FVII genotype. European Union Concerted Action "Clotart".

Mariani G, Bernardi F, Bertina R, Vicente VV, Prydz H, Samama M, Sandset PM, Di Nucci GD, Testa MG, Bendz B, Chiarotti F, Ciarla MV, Strom R. Mariani G, et al. Among authors: vicente vv. Haematologica. 1999 Jul;84(7):620-6. Haematologica. 1999. PMID: 10406904

4

Association of the thrombomodulin gene c.1418C>T polymorphism with thrombomodulin levels and with venous thrombosis risk.

Navarro S, Medina P, Bonet E, Corral J, Martínez-Sales V, Martos L, Rivera M, Roselló-Lletí E, Alberca I, Roldán V, Mira Y, Ferrando F, Estellés A, Vicente V, Bertina RM, España F. Navarro S, et al. Among authors: vicente v. Arterioscler Thromb Vasc Biol. 2013 Jun;33(6):1435-40. doi: 10.1161/ATVBAHA.113.301360. Epub 2013 Mar 21. Arterioscler Thromb Vasc Biol. 2013. PMID: 23520161

5

AB0 blood group and risk of venous or arterial thrombosis in carriers of factor V Leiden or prothrombin G20210A polymorphisms.

Miñano A, Ordóñez A, España F, González-Porras JR, Lecumberri R, Fontcuberta J, Llamas P, Marín F, Estellés A, Alberca I, Vicente V, Corral J. Miñano A, et al. Among authors: vicente v. Haematologica. 2008 May;93(5):729-34. doi: 10.3324/haematol.12271. Epub 2008 Apr 2. Haematologica. 2008. PMID: 18387978 Free article.

6

Nonsense mutation in exon-19 of GPIIb associated with thrombasthenic phenotype. Failure of GPIIb(delta597-1008) to form stable complexes with GPIIIa.

Arias-Salgado EG, Tao J, González-Manchón C, Butta N, Vicente V, Ayuso MS, Parrilla R. Arias-Salgado EG, et al. Among authors: vicente v. Thromb Haemost. 2002 Apr;87(4):684-91. Thromb Haemost. 2002. PMID: 12008952

7

Prothrombin A19911G and G20210A polymorphisms' role in thrombosis.

Pérez-Ceballos E, Corral J, Alberca I, Vayá A, Llamas P, Montes R, González-Conejero R, Vicente V. Pérez-Ceballos E, et al. Among authors: vicente v. Br J Haematol. 2002 Aug;118(2):610-4. doi: 10.1046/j.1365-2141.2002.03624.x. Br J Haematol. 2002. PMID: 12139755 Free article.

8

Effect of factor XIII VAL34LEU polymorphism on thrombolytic therapy in premature myocardial infarction.

Roldán V, Corral J, Marín F, Rivera J, Vicente V. Roldán V, et al. Among authors: vicente v. Thromb Haemost. 2002 Aug;88(2):354-5. Thromb Haemost. 2002. PMID: 12195711 No abstract available.

9

A common polymorphism in the annexin V Kozak sequence (-1C>T) increases translation efficiency and plasma levels of annexin V, and decreases the risk of myocardial infarction in young patients.

González-Conejero R, Corral J, Roldán V, Martínez C, Marín F, Rivera J, Iniesta JA, Lozano ML, Marco P, Vicente V. González-Conejero R, et al. Among authors: vicente v. Blood. 2002 Sep 15;100(6):2081-6. Blood. 2002. PMID: 12200370 Free article.

10

Polymorphisms of platelet adhesive receptors: do they play a role in primary intracerebral hemorrhage?

Iniesta J, Corral J, González-Conejero R, Piqueras C, Vicente V. Iniesta J, et al. Among authors: vicente v. Cerebrovasc Dis. 2003;15(1-2):51-5. doi: 10.1159/000067126. Cerebrovasc Dis. 2003. PMID: 12499711

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