Fischer K - Search Results

1

Long-Term Outcome after Joint Bleeds in Von Willebrand Disease Compared to Haemophilia A: A Post Hoc Analysis.

van Galen KPM, Timmer M, de Kleijn P, Leebeek FWG, Foppen W, Schutgens REG, Eikenboom J, Meijer K, Fijnvandraat K, Laros-van Gorkom BAP, Twisk JW, Mauser-Bunschoten EP, Fischer K; WiN Studygroup. van Galen KPM, et al. Among authors: fischer k. Thromb Haemost. 2018 Oct;118(10):1690-1700. doi: 10.1055/s-0038-1670704. Epub 2018 Oct 1. Thromb Haemost. 2018. PMID: 30273954

2

The effects of postponing prophylactic treatment on long-term outcome in patients with severe hemophilia.

Fischer K, van der Bom JG, Mauser-Bunschoten EP, Roosendaal G, Prejs R, de Kleijn P, Grobbee DE, van den Berg M. Fischer K, et al. Blood. 2002 Apr 1;99(7):2337-41. doi: 10.1182/blood.v99.7.2337. Blood. 2002. PMID: 11895765 Free article.

3

Age at first treatment and immune tolerance to factor VIII in severe hemophilia.

van der Bom JG, Mauser-Bunschoten EP, Fischer K, van den Berg HM. van der Bom JG, et al. Among authors: fischer k. Thromb Haemost. 2003 Mar;89(3):475-9. Thromb Haemost. 2003. PMID: 12624630

4

Prophylaxis for severe hemophilia: experience from Europe and the United States.

van den Berg HM, Fischer K. van den Berg HM, et al. Among authors: fischer k. Semin Thromb Hemost. 2003 Feb;29(1):49-54. doi: 10.1055/s-2003-37971. Semin Thromb Hemost. 2003. PMID: 12640565 Review.

5

Do prothrombotic factors influence clinical phenotype of severe haemophilia? A review of the literature.

van Dijk K, van der Bom JG, Fischer K, Grobbee DE, van den Berg HM. van Dijk K, et al. Among authors: fischer k. Thromb Haemost. 2004 Aug;92(2):305-10. doi: 10.1160/TH04-02-0112. Thromb Haemost. 2004. PMID: 15269826

6

Hepatitis C and health-related quality of life among patients with hemophilia.

Posthouwer D, Plug I, van der Bom JG, Fischer K, Rosendaal FR, Mauser-Bunschoten EP. Posthouwer D, et al. Among authors: fischer k. Haematologica. 2005 Jun;90(6):846-50. Haematologica. 2005. PMID: 15951299

7

The natural history of childhood-acquired hepatitis C infection in patients with inherited bleeding disorders.

Posthouwer D, Fischer K, van Erpecum KJ, Mauser-Bunschoten EP. Posthouwer D, et al. Among authors: fischer k. Transfusion. 2006 Aug;46(8):1360-6. doi: 10.1111/j.1537-2995.2006.00903.x. Transfusion. 2006. PMID: 16934072

8

Progression to end-stage liver disease in patients with inherited bleeding disorders and hepatitis C: an international, multicenter cohort study.

Posthouwer D, Makris M, Yee TT, Fischer K, van Veen JJ, Griffioen A, van Erpecum KJ, Mauser-Bunschoten EP. Posthouwer D, et al. Among authors: fischer k. Blood. 2007 May 1;109(9):3667-71. doi: 10.1182/blood-2006-08-038349. Epub 2007 Jan 9. Blood. 2007. PMID: 17213288 Free article. Clinical Trial.

9

Models for prediction of factor VIII half-life in severe haemophiliacs: distinct approaches for blood group O and non-O patients.

Fischer K, Pendu R, van Schooten CJ, van Dijk K, Denis CV, van den Berg HM, Lenting PJ. Fischer K, et al. PLoS One. 2009 Aug 25;4(8):e6745. doi: 10.1371/journal.pone.0006745. PLoS One. 2009. PMID: 19707594 Free PMC article.

10

Non-fatal cardiovascular disease, malignancies, and other co-morbidity in adult haemophilia patients.

Fransen van de Putte DE, Fischer K, Pulles AE, Roosendaal G, Biesma DH, Schutgens RE, Mauser-Bunschoten EP. Fransen van de Putte DE, et al. Among authors: fischer k. Thromb Res. 2012 Aug;130(2):157-62. doi: 10.1016/j.thromres.2011.12.012. Epub 2011 Dec 30. Thromb Res. 2012. PMID: 22209337

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