Aznar J - Search Results

1

Upper extremity deep vein thrombosis in a young patient double heterozygous for factor V Leiden and prothrombin G20210A mutation.

Vayá A, Todolí J, Ricart J, Estellés T, Mira Y, Villa P, Calabuig JR, Aznar J. Vayá A, et al. Among authors: aznar j. Clin Appl Thromb Hemost. 2001 Jan;7(1):72-4. doi: 10.1177/107602960100700114. Clin Appl Thromb Hemost. 2001. PMID: 11190909 Free article.

2

Hemorheological alterations and hypercoagulable state in deep vein thrombosis.

Mira Y, Vayá A, Martínez M, Villa P, Santaolaria ML, Ferrando F, Aznar J. Mira Y, et al. Among authors: aznar j. Clin Hemorheol Microcirc. 1998 Dec;19(4):265-70. Clin Hemorheol Microcirc. 1998. PMID: 9972663

3

Factor V Leiden and antibodies against phospholipids and protein S in a young woman with recurrent thromboses and abortion.

España F, Villa P, Mira Y, Grancha S, Royo M, Estellés A, Vayá A, Aznar J. España F, et al. Among authors: aznar j. Haematologica. 1999 Jan;84(1):80-4. Haematologica. 1999. PMID: 10091395

4

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

5

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. Among authors: aznar j. Clin Appl Thromb Hemost. 1999 Jul;5(3):190-1. doi: 10.1177/107602969900500310. Clin Appl Thromb Hemost. 1999. PMID: 10726008 Free article.

6

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. Among authors: aznar j. Haematologica. 2000 Apr;85(4):425-8. Haematologica. 2000. PMID: 10756370

7

Acute myocardial infarction associated with the prothrombin G20210A mutation.

Vayá A, Trenor R, Molla S, Estellés A, Mira Y, Villa P, Aznar J. Vayá A, et al. Among authors: aznar j. Clin Appl Thromb Hemost. 2000 Apr;6(2):111-2. doi: 10.1177/107602960000600213. Clin Appl Thromb Hemost. 2000. PMID: 10775034 Free article. No abstract available.

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. Among authors: aznar j. Clin Appl Thromb Hemost. 2000 Jul;6(3):162-8. doi: 10.1177/107602960000600308. Clin Appl Thromb Hemost. 2000. PMID: 10898277 Free article.

9

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: aznar j. Clin Appl Thromb Hemost. 2000 Jul;6(3):179-80. doi: 10.1177/107602960000600311. Clin Appl Thromb Hemost. 2000. PMID: 10898280 Free article.

10

PAI-1 promoter 4G/5G genotype as an additional risk factor for venous thrombosis in subjects with genetic thrombophilic defects.

Seguí R, Estellés A, Mira Y, España F, Villa P, Falcó C, Vayá A, Grancha S, Ferrando F, Aznar J. Seguí R, et al. Among authors: aznar j. Br J Haematol. 2000 Oct;111(1):122-8. doi: 10.1046/j.1365-2141.2000.02321.x. Br J Haematol. 2000. PMID: 11091191 Free article.

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