Fontcuberta J - Search Results

1

Laboratory evaluation and clinical characteristics of 2,132 consecutive unselected patients with venous thromboembolism--results of the Spanish Multicentric Study on Thrombophilia (EMET-Study).

Mateo J, Oliver A, Borrell M, Sala N, Fontcuberta J. Mateo J, et al. Among authors: fontcuberta j. Thromb Haemost. 1997 Mar;77(3):444-51. Thromb Haemost. 1997. PMID: 9065991

2

Association after linkage analysis indicates that homozygosity for the 46C-->T polymorphism in the F12 gene is a genetic risk factor for venous thrombosis.

Tirado I, Soria JM, Mateo J, Oliver A, Souto JC, Santamaria A, Felices R, Borrell M, Fontcuberta J. Tirado I, et al. Among authors: fontcuberta j. Thromb Haemost. 2004 May;91(5):899-904. doi: 10.1160/TH03-10-0620. Thromb Haemost. 2004. PMID: 15116249

3

The ABO blood group genotype and factor VIII levels as independent risk factors for venous thromboembolism.

Tirado I, Mateo J, Soria JM, Oliver A, Martínez-Sánchez E, Vallvé C, Borrell M, Urrutia T, Fontcuberta J. Tirado I, et al. Among authors: fontcuberta j. Thromb Haemost. 2005 Mar;93(3):468-74. doi: 10.1160/TH04-04-0251. Thromb Haemost. 2005. PMID: 15735796

4

Increased risk of venous thrombosis in carriers of natural anticoagulant deficiencies. Results of the family studies of the Spanish Multicenter Study on Thrombophilia (EMET study).

Mateo J, Oliver A, Borrell M, Sala N, Fontcuberta J. Mateo J, et al. Among authors: fontcuberta j. Blood Coagul Fibrinolysis. 1998 Jan;9(1):71-8. doi: 10.1097/00001721-199801000-00009. Blood Coagul Fibrinolysis. 1998. PMID: 9607121

5

The prothrombin 20210A allele is the most prevalent genetic risk factor for venous thromboembolism in the Spanish population.

Souto JC, Coll I, Llobet D, del Río E, Oliver A, Mateo J, Borrell M, Fontcuberta J. Souto JC, et al. Among authors: fontcuberta j. Thromb Haemost. 1998 Sep;80(3):366-9. Thromb Haemost. 1998. PMID: 9759610

6

Fibrinolytic abnormalities. A Spanish multicenter study ebt.I on 443 patients with venous thromboembolic disease.

Falkon L, Borrell M, Sala N, Felez J, Martín S, Grau E, Fontcuberta J. Falkon L, et al. Among authors: fontcuberta j. Thromb Res. 1992 May 15;66(4):455-60. doi: 10.1016/0049-3848(92)90295-l. Thromb Res. 1992. PMID: 1412209 No abstract available.

7

Thromboplastin-thrombomodulin-mediated time and serum folate levels are genetically correlated with the risk of thromboembolic disease: results from the GAIT project.

Souto JC, Almasy L, Borrell M, Stone WH, Blanco-Vaca F, Soria JM, Blangero J, Fontcuberta J. Souto JC, et al. Among authors: fontcuberta j. Thromb Haemost. 2002 Jan;87(1):68-73. Thromb Haemost. 2002. PMID: 11848458

8

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

9

Successful suppression using Rituximab of a factor VIII inhibitor in a boy with severe congenital haemophilia: an example of a significant decrease of treatment costs.

Mateo J, Badell I, Forner R, Borrell M, Tizzano E, Fontcuberta J. Mateo J, et al. Among authors: fontcuberta j. Thromb Haemost. 2006 Feb;95(2):386-7. Thromb Haemost. 2006. PMID: 16493502 No abstract available.

10

VAMP8 and serotonin transporter levels are associated with venous thrombosis risk in a Spanish female population. Results from the RETROVE Project.

Llobet D, Vallvé C, Tirado I, Vilalta N, Murillo J, Cuevas B, Román L, Carrasco M, Oliver A, Mateo J, Fontcuberta J, Souto JC. Llobet D, et al. Among authors: fontcuberta j. Thromb Res. 2019 Sep;181:99-105. doi: 10.1016/j.thromres.2019.07.023. Epub 2019 Jul 26. Thromb Res. 2019. PMID: 31382081

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