Coppens M - Search Results

1

Relevance of the JAK2V617F mutation in patients with deep vein thrombosis of the leg.

Lauw MN, Bus EW, van Wulfften Palthe AF, Coppens M, Homburg CH, Middeldorp S, van der Schoot CE, Koene HR, Biemond BJ. Lauw MN, et al. Among authors: coppens m. Ann Hematol. 2012 Jan;91(1):103-7. doi: 10.1007/s00277-011-1233-0. Epub 2011 Apr 12. Ann Hematol. 2012. PMID: 21484303 Free PMC article.

2

A prospective cohort study on the absolute incidence of venous thromboembolism and arterial cardiovascular disease in asymptomatic carriers of the prothrombin 20210A mutation.

Coppens M, van de Poel MH, Bank I, Hamulyak K, van der Meer J, Veeger NJ, Prins MH, Buller HR, Middeldorp S. Coppens M, et al. Blood. 2006 Oct 15;108(8):2604-7. doi: 10.1182/blood-2006-04-016527. Epub 2006 Jun 15. Blood. 2006. PMID: 16778142 Free article.

3

Inherited thrombophilias.

Coppens M, Kaandorp SP, Middeldorp S. Coppens M, et al. Obstet Gynecol Clin North Am. 2006 Sep;33(3):357-74. doi: 10.1016/j.ogc.2006.05.011. Obstet Gynecol Clin North Am. 2006. PMID: 16962914 Review.

4

Outcome of the subsequent pregnancy after a first loss in women with the factor V Leiden or prothrombin 20210A mutations.

Coppens M, Folkeringa N, Teune MJ, Hamulyák K, van der Meer J, Prins MH, Büller HR, Middeldorp S. Coppens M, et al. J Thromb Haemost. 2007 Jul;5(7):1444-8. doi: 10.1111/j.1538-7836.2007.02586.x. Epub 2007 Apr 16. J Thromb Haemost. 2007. PMID: 17439630 Free article.

5

The risk of venous and arterial thrombosis in hyperhomocysteinaemia is low and mainly depends on concomitant thrombophilic defects.

Lijfering WM, Coppens M, van de Poel MH, Middeldorp S, Hamulyák K, Bank I, Veeger NJ, Prins MH, Büller HR, van der Meer J. Lijfering WM, et al. Among authors: coppens m. Thromb Haemost. 2007 Aug;98(2):457-63. Thromb Haemost. 2007. PMID: 17721631

6

Absolute annual incidences of first events of venous thromboembolism and arterial vascular events in individuals with elevated FVIII:c. A prospective family cohort study.

Bank I, van de Poel MH, Coppens M, Hamulyák K, Prins MH, van der Meer J, Veeger NJ, Büller HR, Middeldorp S. Bank I, et al. Among authors: coppens m. Thromb Haemost. 2007 Nov;98(5):1040-4. Thromb Haemost. 2007. PMID: 18000609

7

Hyperhomocysteinemia is not a risk factor for venous and arterial thrombosis, and is associated with elevated factor VIII levels.

Lijfering WM, Coppens M, Veeger NJ, Middeldorp S, Hamulyák K, Prins MH, Büller HR, van der Meer J. Lijfering WM, et al. Among authors: coppens m. Thromb Res. 2008;123(2):244-50. doi: 10.1016/j.thromres.2007.12.010. Epub 2008 Feb 14. Thromb Res. 2008. PMID: 18279917 No abstract available.

8

Testing for inherited thrombophilia does not reduce the recurrence of venous thrombosis.

Coppens M, Reijnders JH, Middeldorp S, Doggen CJ, Rosendaal FR. Coppens M, et al. J Thromb Haemost. 2008 Sep;6(9):1474-7. doi: 10.1111/j.1538-7836.2008.03055.x. Epub 2008 Jun 6. J Thromb Haemost. 2008. PMID: 18540999 Free article.

9

Absolute risk of venous and arterial thromboembolism in thrombophilic families is not increased by high thrombin-activatable fibrinolysis inhibitor (TAFI) levels.

Folkeringa N, Coppens M, Veeger NJ, Bom VJ, Middeldorp S, Hamulyak K, Prins MH, Büller HR, van der Meer J. Folkeringa N, et al. Among authors: coppens m. Thromb Haemost. 2008 Jul;100(1):38-44. doi: 10.1160/TH07-11-0659. Thromb Haemost. 2008. PMID: 18612536

10

Selective testing for thrombophilia in patients with first venous thrombosis: results from a retrospective family cohort study on absolute thrombotic risk for currently known thrombophilic defects in 2479 relatives.

Lijfering WM, Brouwer JL, Veeger NJ, Bank I, Coppens M, Middeldorp S, Hamulyák K, Prins MH, Büller HR, van der Meer J. Lijfering WM, et al. Among authors: coppens m. Blood. 2009 May 21;113(21):5314-22. doi: 10.1182/blood-2008-10-184879. Epub 2009 Jan 12. Blood. 2009. PMID: 19139080 Free article.

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