Vayá A - Search Results

1

Portal vein thrombosis associated to prothrombin G20210A mutation and protein C deficiency.

Mira Y, García del Castillo G, Estellés A, Villa P, Vayá A, Ortuño C, Aznar J. Mira Y, et al. Among authors: vaya a. Clin Appl Thromb Hemost. 2000 Jul;6(3):179-80. doi: 10.1177/107602960000600311. Clin Appl Thromb Hemost. 2000. PMID: 10898280 Free article.

2

Is family history sufficient to identify women with risk of venous thromboembolism before commencing the contraceptive pill?

Aznar J, Mira Y, Vayá A, Ferrando F, Villa P. Aznar J, et al. Among authors: vaya a. Clin Appl Thromb Hemost. 2002 Apr;8(2):139-41. doi: 10.1177/107602960200800209. Clin Appl Thromb Hemost. 2002. PMID: 12121054 Free article.

3

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. Thromb Haemost. 2003 Mar;89(3):452-7. Thromb Haemost. 2003. PMID: 12624627

4

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: vaya a. Thromb Haemost. 2004 May;91(5):1031-4. doi: 10.1160/TH03-11-0690. Thromb Haemost. 2004. PMID: 15116266

5

Spontaneous renal subcapsular hematoma in an anticoagulated patient.

Ferrando F, Budía A, Mira Y, Vayá A, Aznar J. Ferrando F, et al. Among authors: vaya a. Clin Appl Thromb Hemost. 2006 Jan;12(1):89-92. doi: 10.1177/107602960601200114. Clin Appl Thromb Hemost. 2006. PMID: 16444440 Free article.

6

Sialic acid is an inflammation marker associated with a history of deep vein thrombosis.

Reganon E, Vila V, Martínez-Sales V, Vayá A, Mira Y, Ferrando F, Aznar J. Reganon E, et al. Among authors: vaya a. Thromb Res. 2007;119(1):73-8. doi: 10.1016/j.thromres.2005.12.017. Epub 2006 Feb 28. Thromb Res. 2007. PMID: 16500696

7

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: vaya a. Haematologica. 2008 Jun;93(6):885-91. doi: 10.3324/haematol.12448. Epub 2008 Apr 9. Haematologica. 2008. PMID: 18403391 Free article.

8

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: vaya a. Thromb Haemost. 1999 Sep;82(3):1011-4. Thromb Haemost. 1999. PMID: 10494755

9

Central retinal vein thrombosis associated with prothrombin 20210G/A gene variant.

Vayá A, López JM, Mira Y, Ricart JM, Villa P, España-Gregori E, Estellés A, Aznar J. Vayá A, et al. Clin Appl Thromb Hemost. 1999 Jul;5(3):190-1. doi: 10.1177/107602969900500310. Clin Appl Thromb Hemost. 1999. PMID: 10726008 Free article.

10

Intracardiac thrombosis in a case of Behcet's disease associated with the prothrombin 20210G-A mutation.

Vayá A, Forner MJ, Estellés A, Villa P, Mira Y, Ferrando F, García Fuster JM, Oliver V, Aznar J. Vayá A, et al. Haematologica. 2000 Apr;85(4):425-8. Haematologica. 2000. PMID: 10756370

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