Reitsma PH - Search Results

1

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 Free article.

2

Arterial wall thickness and the risk of recurrent ischemic events in carriers of the prothrombin G20210A mutation with clinical manifestations of atherosclerosis.

Gerdes VE, ten Cate H, de Groot E, Kwa VI, Prins MH, Reitsma PH, Büller HR, Brandjes DP; Amsterdam Vascular Medicine Group. Gerdes VE, et al. Among authors: reitsma ph. Atherosclerosis. 2002 Jul;163(1):135-40. doi: 10.1016/s0021-9150(01)00759-6. Atherosclerosis. 2002. PMID: 12048131

3

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 Free article.

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

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 Free article. Review. No abstract available.

6

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 Free article.

7

Thrombospondin-2 polymorphism is associated with a reduced risk of premature myocardial infarction.

Boekholdt SM, Trip MD, Peters RJ, Engelen M, Boer JM, Feskens EJ, Zwinderman AH, Kastelein JJ, Reitsma PH. Boekholdt SM, et al. Among authors: reitsma ph. Arterioscler Thromb Vasc Biol. 2002 Dec 1;22(12):e24-7. doi: 10.1161/01.atv.0000046235.22451.66. Arterioscler Thromb Vasc Biol. 2002. PMID: 12482844

8

The effect of a common methylenetetrahydrofolate reductase mutation on levels of homocysteine, folate, vitamin B12 and on the risk of premature atherosclerosis.

Verhoeff BJ, Trip MD, Prins MH, Kastelein JJ, Reitsma PH. Verhoeff BJ, et al. Among authors: reitsma ph. Atherosclerosis. 1998 Nov;141(1):161-6. doi: 10.1016/s0021-9150(98)00156-7. Atherosclerosis. 1998. PMID: 9863549

9

High plasma concentration of factor VIIIc is a major risk factor for venous thromboembolism.

Kraaijenhagen RA, in't Anker PS, Koopman MM, Reitsma PH, Prins MH, van den Ende A, Büller HR. Kraaijenhagen RA, et al. Among authors: reitsma ph. Thromb Haemost. 2000 Jan;83(1):5-9. Thromb Haemost. 2000. PMID: 10669145

10

The in vivo kinetics of tissue factor messenger RNA expression during human endotoxemia: relationship with activation of coagulation.

Franco RF, de Jonge E, Dekkers PE, Timmerman JJ, Spek CA, van Deventer SJ, van Deursen P, van Kerkhoff L, van Gemen B, ten Cate H, van der Poll T, Reitsma PH. Franco RF, et al. Among authors: reitsma ph. Blood. 2000 Jul 15;96(2):554-9. Blood. 2000. PMID: 10887118 Free article.

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