van Heerde WL - Search Results

1

Thrombocytopenia in early malaria is associated with GP1b shedding in absence of systemic platelet activation and consumptive coagulopathy.

de Mast Q, de Groot PG, van Heerde WL, Roestenberg M, van Velzen JF, Verbruggen B, Roest M, McCall M, Nieman AE, Westendorp J, Syafruddin D, Fijnheer R, van Dongen-Lases EC, Sauerwein RW, van der Ven AJ. de Mast Q, et al. Among authors: van der ven aj, van velzen jf, van heerde wl, van dongen lases ec. Br J Haematol. 2010 Dec;151(5):495-503. doi: 10.1111/j.1365-2141.2010.08399.x. Epub 2010 Oct 19. Br J Haematol. 2010. PMID: 20955404 Free article.

2

The complexity of the phospholipid binding protein Annexin V.

van Heerde WL, de Groot PG, Reutelingsperger CP. van Heerde WL, et al. Thromb Haemost. 1995 Feb;73(2):172-9. Thromb Haemost. 1995. PMID: 7792726 Review. No abstract available.

3

Binding of recombinant annexin V to endothelial cells: effect of annexin V binding on endothelial-cell-mediated thrombin formation.

van Heerde WL, Poort S, van 't Veer C, Reutelingsperger CP, de Groot PG. van Heerde WL, et al. Among authors: van t veer c. Biochem J. 1994 Aug 15;302 ( Pt 1)(Pt 1):305-12. doi: 10.1042/bj3020305. Biochem J. 1994. PMID: 8068019 Free PMC article.

4

Annexin V inhibits the procoagulant activity of matrices of TNF-stimulated endothelium under blood flow conditions.

van Heerde WL, Sakariassen KS, Hemker HC, Sixma JJ, Reutelingsperger CP, de Groot PG. van Heerde WL, et al. Arterioscler Thromb. 1994 May;14(5):824-30. doi: 10.1161/01.atv.14.5.824. Arterioscler Thromb. 1994. PMID: 8172859

5

The presence of antiphospholipid antibodies is not related to increased levels of annexin A5 in plasma.

Van Heerde WL, Reutelingsperger CP, Maassen C, Lux P, Derksen RH, De Groot PG. Van Heerde WL, et al. J Thromb Haemost. 2003 Mar;1(3):532-6. doi: 10.1046/j.1538-7836.2003.00106.x. J Thromb Haemost. 2003. PMID: 12871462 Free article.

6

Thirteen novel mutations in the factor VIII gene in the Nijmegen haemophilia A patient population.

Boekhorst J, Verbruggen B, Lavergne JM, Costa JM, Schoormans SC, Brons PP, van Kraaij MG, Nováková IR, van Heerde WL. Boekhorst J, et al. Among authors: van heerde wl, van kraaij mg. Br J Haematol. 2005 Oct;131(1):109-17. doi: 10.1111/j.1365-2141.2005.05737.x. Br J Haematol. 2005. PMID: 16173970 Free article.

7

Annexin A5 polymorphism (-1C-->T) and the presence of anti-annexin A5 antibodies in the antiphospholipid syndrome.

de Laat B, Derksen RH, Mackie IJ, Roest M, Schoormans S, Woodhams BJ, de Groot PG, van Heerde WL. de Laat B, et al. Among authors: van heerde wl. Ann Rheum Dis. 2006 Nov;65(11):1468-72. doi: 10.1136/ard.2005.045237. Epub 2006 Jan 31. Ann Rheum Dis. 2006. PMID: 16449315 Free PMC article.

8

Methodological shortcomings in assessment of factor VIII concentrate inhibition.

Verbruggen B, van Heerde W, Budde U. Verbruggen B, et al. Haemophilia. 2007 Sep;13(5):680-1. doi: 10.1111/j.1365-2516.2007.01529.x. Haemophilia. 2007. PMID: 17880465 No abstract available.

9

Diagnosis of factor VIII deficiency.

Verbruggen B, Meijer P, Novákova I, Van Heerde W. Verbruggen B, et al. Haemophilia. 2008 Jul;14 Suppl 3:76-82. doi: 10.1111/j.1365-2516.2008.01715.x. Haemophilia. 2008. PMID: 18510526 Review.

10

Improvements in factor VIII inhibitor detection: From Bethesda to Nijmegen.

Verbruggen B, van Heerde WL, Laros-van Gorkom BA. Verbruggen B, et al. Among authors: van heerde wl. Semin Thromb Hemost. 2009 Nov;35(8):752-9. doi: 10.1055/s-0029-1245107. Epub 2010 Feb 18. Semin Thromb Hemost. 2009. PMID: 20169511 Review.

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