Reitsma PH - Search Results

1

Factor XIII Val34Leu is a genetic factor involved in the etiology of venous thrombosis.

Franco RF, Reitsma PH, Lourenço D, Maffei FH, Morelli V, Tavella MH, Araújo AG, Piccinato CE, Zago MA. Franco RF, et al. Among authors: reitsma ph. Thromb Haemost. 1999 May;81(5):676-9. Thromb Haemost. 1999. PMID: 10365735

2

Factor XIII Val34Leu and the risk of venous thromboembolism in factor V Leiden carriers.

Franco RF, Middeldorp S, Meinardi JR, van Pampus EC, Reitsma PH. Franco RF, et al. Among authors: reitsma ph. Br J Haematol. 2000 Oct;111(1):118-21. doi: 10.1046/j.1365-2141.2000.02338.x. Br J Haematol. 2000. PMID: 11091190

3

Identification of polymorphisms in the 5'-untranslated region of the TAFI gene: relationship with plasma TAFI levels and risk of venous thrombosis.

Franco RF, Fagundes MG, Meijers JC, Reitsma PH, Lourenço D, Morelli V, Maffei FH, Ferrari IC, Piccinato CE, Silva WA Jr, Zago MA. Franco RF, et al. Among authors: reitsma ph. Haematologica. 2001 May;86(5):510-7. Haematologica. 2001. PMID: 11410415

4

Genetic risk factors of venous thrombosis.

Franco RF, Reitsma PH. Franco RF, et al. Among authors: reitsma ph. Hum Genet. 2001 Oct;109(4):369-84. doi: 10.1007/s004390100593. Hum Genet. 2001. PMID: 11702218 Review.

5

Prevalence of hereditary haemochromatosis in premature atherosclerotic vascular disease.

Franco RF, Zago MA, Trip MD, ten Cate H, van den Ende A, Prins MH, Kastelein JJ, Reitsma PH. Franco RF, et al. Among authors: reitsma ph. Br J Haematol. 1998 Sep;102(5):1172-5. doi: 10.1046/j.1365-2141.1998.00898.x. Br J Haematol. 1998. PMID: 9753040

6

A functional single nucleotide polymorphism in the thrombin-activatable fibrinolysis inhibitor (TAFI) gene associates with outcome of meningococcal disease.

Kremer Hovinga JA, Franco RF, Zago MA, Ten Cate H, Westendorp RG, Reitsma PH. Kremer Hovinga JA, et al. Among authors: reitsma ph. J Thromb Haemost. 2004 Jan;2(1):54-7. doi: 10.1111/j.1538-7836.2004.00557.x. J Thromb Haemost. 2004. PMID: 14717966 Free article.

7

The 20210 G-->A mutation in the 3'-untranslated region of the prothrombin gene and the risk for arterial thrombotic disease.

Franco RF, Trip MD, ten Cate H, van den Ende A, Prins MH, Kastelein JJ, Reitsma PH. Franco RF, et al. Among authors: reitsma ph. Br J Haematol. 1999 Jan;104(1):50-4. doi: 10.1046/j.1365-2141.1999.01149.x. Br J Haematol. 1999. PMID: 10027711

8

Gene polymorphisms of the haemostatic system and the risk of arterial thrombotic disease.

Franco RF, Reitsma PH. Franco RF, et al. Among authors: reitsma ph. Br J Haematol. 2001 Dec;115(3):491-506. doi: 10.1046/j.1365-2141.2001.03175.x. Br J Haematol. 2001. PMID: 11736929 Review. No abstract available.

9

Polymorphisms in the protein C gene as risk factor for venous thrombosis.

Pomp ER, Doggen CJ, Vos HL, Reitsma PH, Rosendaal FR. Pomp ER, et al. Among authors: reitsma ph. Thromb Haemost. 2009 Jan;101(1):62-7. Thromb Haemost. 2009. PMID: 19132190

10

Genetics of venous thrombosis.

Rosendaal FR, Reitsma PH. Rosendaal FR, et al. Among authors: reitsma ph. J Thromb Haemost. 2009 Jul;7 Suppl 1:301-4. doi: 10.1111/j.1538-7836.2009.03394.x. J Thromb Haemost. 2009. PMID: 19630821 Free article. Review.

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