Leebeek FWG - Search Results

1

Joint assessment in von Willebrand disease. Validation of the Haemophilia Joint Health score and Haemophilia Activities List.

van Galen KPM, Timmer MA, de Kleijn P, Fischer K, Foppen W, Schutgens REG, Eikenboom J, Meijer K, Cnossen MH, Fijnvandraat K, van der Bom JG, Laros-van Gorkom BAP, Leebeek FWG, Mauser-Bunschoten EP, Win Study Group OBOT. van Galen KPM, et al. Among authors: leebeek fwg. Thromb Haemost. 2017 Aug 1;117(8):1465-1470. doi: 10.1160/TH16-12-0967. Epub 2017 May 11. Thromb Haemost. 2017. PMID: 28492695

2

Recombinant factor VIIa improves clot formation but not fibrolytic potential in patients with cirrhosis and during liver transplantation.

Lisman T, Leebeek FW, Meijer K, Van Der Meer J, Nieuwenhuis HK, De Groot PG. Lisman T, et al. Hepatology. 2002 Mar;35(3):616-21. doi: 10.1053/jhep.2002.31771. Hepatology. 2002. PMID: 11870375

3

In vitro studies, pharmacokinetic studies and clinical use of a high purity double virus inactivated FVIII/VWF concentrate (Immunate) in the treatment of von Willebrand disease.

Ver Elst KM, van Vliet HD, Kappers-Klunne MC, Leebeek FW. Ver Elst KM, et al. Thromb Haemost. 2004 Jul;92(1):67-74. doi: 10.1160/TH04-02-0107. Thromb Haemost. 2004. PMID: 15213847

4

Variations in glycosylation of von Willebrand factor with O-linked sialylated T antigen are associated with its plasma levels.

van Schooten CJ, Denis CV, Lisman T, Eikenboom JC, Leebeek FW, Goudemand J, Fressinaud E, van den Berg HM, de Groot PG, Lenting PJ. van Schooten CJ, et al. Blood. 2007 Mar 15;109(6):2430-7. doi: 10.1182/blood-2006-06-032706. Epub 2006 Nov 7. Blood. 2007. PMID: 17090649 Free article.

5

PFA-100 monitoring of von Willebrand factor (VWF) responses to desmopressin (DDAVP) and factor VIII/VWF concentrate substitution in von Willebrand disease type 1 and 2.

van Vliet HH, Kappers-Klunne MC, Leebeek FW, Michiels JJ. van Vliet HH, et al. Thromb Haemost. 2008 Sep;100(3):462-8. Thromb Haemost. 2008. PMID: 18766263

6

Diagnosis and management of von Willebrand disease in The Netherlands.

de Wee EM, Leebeek FW, Eikenboom JC. de Wee EM, et al. Semin Thromb Hemost. 2011 Jul;37(5):480-7. doi: 10.1055/s-0031-1281032. Epub 2011 Nov 18. Semin Thromb Hemost. 2011. PMID: 22102190 Review.

7

Coronary artery calcification in hemophilia A: no evidence for a protective effect of factor VIII deficiency on atherosclerosis.

Tuinenburg A, Rutten A, Kavousi M, Leebeek FW, Ypma PF, Laros-van Gorkom BA, Nijziel MR, Kamphuisen PW, Mauser-Bunschoten EP, Roosendaal G, Biesma DH, van der Lugt A, Hofman A, Witteman JC, Bots ML, Schutgens RE. Tuinenburg A, et al. Arterioscler Thromb Vasc Biol. 2012 Mar;32(3):799-804. doi: 10.1161/ATVBAHA.111.238162. Epub 2011 Dec 15. Arterioscler Thromb Vasc Biol. 2012. PMID: 22173226

8

Inhibitor incidence after intensive FVIII replacement for surgery in mild and moderate haemophilia A: a prospective national study in the Netherlands.

Eckhardt CL, Mauser-Bunschoten EP, Peters M, Leebeek FW, van der Meer FJ, Fijnvandraat K. Eckhardt CL, et al. Br J Haematol. 2012 Jun;157(6):747-52. doi: 10.1111/j.1365-2141.2012.09119.x. Epub 2012 Apr 26. Br J Haematol. 2012. PMID: 22533635 Free article. Clinical Trial.

9

Diagnosis and management of haemophilia.

Fijnvandraat K, Cnossen MH, Leebeek FW, Peters M. Fijnvandraat K, et al. BMJ. 2012 May 2;344:e2707. doi: 10.1136/bmj.e2707. BMJ. 2012. PMID: 22551712 Free article. Review. No abstract available.

10

Determinants of bleeding phenotype in adult patients with moderate or severe von Willebrand disease.

de Wee EM, Sanders YV, Mauser-Bunschoten EP, van der Bom JG, Degenaar-Dujardin ME, Eikenboom J, de Goede-Bolder A, Laros-van Gorkom BA, Meijer K, Hamulyák K, Nijziel MR, Fijnvandraat K, Leebeek FW; WiN study group. de Wee EM, et al. Thromb Haemost. 2012 Oct;108(4):683-92. doi: 10.1160/TH12-04-0244. Epub 2012 Aug 23. Thromb Haemost. 2012. PMID: 22918553

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