Mira Y - Search Results

1

Contribution of polymorphisms in the endothelial protein C receptor gene to soluble endothelial protein C receptor and circulating activated protein C levels, and thrombotic risk.

Medina P, Navarro S, Estellés A, Vayá A, Woodhams B, Mira Y, Villa P, Migaud-Fressart M, Ferrando F, Aznar J, Bertina RM, España F. Medina P, et al. Among authors: mira y. Thromb Haemost. 2004 May;91(5):905-11. doi: 10.1160/TH03-10-0657. Thromb Haemost. 2004. PMID: 15116250

2

Prothrombin G20210A mutation and oral contraceptive use increase upper-extremity deep vein thrombotic risk.

Vayá A, Mira Y, Mateo J, Falco C, Villa P, Estelles A, Corella D, Fontcuberta J, Aznar J. Vayá A, et al. Among authors: mira y. Thromb Haemost. 2003 Mar;89(3):452-7. Thromb Haemost. 2003. PMID: 12624627

3

Factor V Leiden and prothrombin G20210A mutations in young adults with cryptogenic ischemic stroke.

Aznar J, Mira Y, Vayá A, Corella D, Ferrando F, Villa P, Estellés A. Aznar J, et al. Among authors: mira y. Thromb Haemost. 2004 May;91(5):1031-4. doi: 10.1160/TH03-11-0690. Thromb Haemost. 2004. PMID: 15116266

4

Influence of lipids and obesity on haemorheological parameters in patients with deep vein thrombosis.

Vayá A, Falcó C, Simó M, Ferrando F, Mira Y, Todolí J, España F, Corella D. Vayá A, et al. Among authors: mira y. Thromb Haemost. 2007 Sep;98(3):621-6. Thromb Haemost. 2007. PMID: 17849051 Free article.

5

Haplotypes of the EPCR gene, prothrombin levels, and the risk of venous thrombosis in carriers of the prothrombin G20210A mutation.

Navarro S, Medina P, Mira Y, Estellés A, Villa P, Ferrando F, Vayá A, Bertina RM, España F. Navarro S, et al. Among authors: mira y. Haematologica. 2008 Jun;93(6):885-91. doi: 10.3324/haematol.12448. Epub 2008 Apr 9. Haematologica. 2008. PMID: 18403391 Free article.

6

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: mira y. 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

7

Hereditary homozygous heparin cofactor II deficiency and the risk of developing venous thrombosis.

Villa P, Aznar J, Vaya A, España F, Ferrando F, Mira Y, Estellés A. Villa P, et al. Among authors: mira y. Thromb Haemost. 1999 Sep;82(3):1011-4. Thromb Haemost. 1999. PMID: 10494755

8

Congenital and acquired thrombotic risk factors in women using oral contraceptives: clinical aspects.

Mira Y, Aznar J, Estellés A, Vayá A, Villa P, Ferrando F. Mira Y, et al. Clin Appl Thromb Hemost. 2000 Jul;6(3):162-8. doi: 10.1177/107602960000600308. Clin Appl Thromb Hemost. 2000. PMID: 10898277 Free article.

9

Low level of circulating activated protein C is a risk factor for venous thromboembolism.

España F, Vayá A, Mira Y, Medina P, Estellés A, Villa P, Falcó C, Aznar J. España F, et al. Among authors: mira y. Thromb Haemost. 2001 Dec;86(6):1368-73. Thromb Haemost. 2001. PMID: 11776301

10

Cerebral venous thrombosis associated to homozygous factor V Leiden mutation in a female of Syrian origin.

Mira Y, Alfaro A, Estellés A, Vayá A, Ferrando F, Villa P. Mira Y, et al. Haematologica. 2002 Jan;87(1):ELT02. Haematologica. 2002. PMID: 11801486 No abstract available.

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