Fijnvandraat K - Search Results

1

The factor VIII treatment history of non-severe hemophilia A.

Abdi A, Kloosterman FR, Eckhardt CL, Male C, Castaman G, Fischer K, Beckers EAM, Kruip MJHA, Peerlinck K, Mancuso ME, Santoro C, Hay CR, Platokouki H, van der Bom JG, Gouw SC, Fijnvandraat K, Hart DP; INSIGHT Study Group. Abdi A, et al. Among authors: fijnvandraat k. J Thromb Haemost. 2020 Dec;18(12):3203-3210. doi: 10.1111/jth.15076. Epub 2020 Sep 28. J Thromb Haemost. 2020. PMID: 32877570 Free PMC article.

2

Coagulation activation and tissue necrosis in meningococcal septic shock: severely reduced protein C levels predict a high mortality.

Fijnvandraat K, Derkx B, Peters M, Bijlmer R, Sturk A, Prins MH, van Deventer SJ, ten Cate JW. Fijnvandraat K, et al. Thromb Haemost. 1995 Jan;73(1):15-20. Thromb Haemost. 1995. PMID: 7740486

3

Recombinant, B-domain deleted factor VIII (r-VIII SQ): pharmacokinetics and initial safety aspects in hemophilia A patients.

Fijnvandraat K, Berntorp E, ten Cate JW, Johnsson H, Peters M, Savidge G, Tengborn L, Spira J, Stahl C. Fijnvandraat K, et al. Thromb Haemost. 1997 Feb;77(2):298-302. Thromb Haemost. 1997. PMID: 9157585 Clinical Trial.

4

Factor VIII inhibitors in mild and moderate-severity haemophilia A. UK Haemophilia Centre Directors Organisation.

Hay CR, Ludlam CA, Colvin BT, Hill FG, Preston FE, Wasseem N, Bagnall R, Peake IR, Berntorp E, Mauser Bunschoten EP, Fijnvandraat K, Kasper CK, White G, Santagostino E. Hay CR, et al. Among authors: fijnvandraat k. Thromb Haemost. 1998 Apr;79(4):762-6. Thromb Haemost. 1998. PMID: 9569189

5

Longitudinal analysis of factor VIII inhibitors in a previously untreated mild haemophilia A patient with an Arg593-->Cys substitution.

van den Brink EN, Timmermans SM, Turenhout EA, Bank CM, Fijnvandraat K, Voorberg J, Peters M. van den Brink EN, et al. Among authors: fijnvandraat k. Thromb Haemost. 1999 May;81(5):723-6. Thromb Haemost. 1999. PMID: 10365744

6

Immunobiology of inhibitor development in hemophilia A.

Fijnvandraat K, Bril WS, Voorberg J. Fijnvandraat K, et al. Semin Thromb Hemost. 2003 Feb;29(1):61-8. doi: 10.1055/s-2003-37940. Semin Thromb Hemost. 2003. PMID: 12640567 Review.

7

Tolerance to factor VIII in a transgenic mouse expressing human factor VIII cDNA carrying an Arg(593) to Cys substitution.

Bril WS, van Helden PM, Hausl C, Zuurveld MG, Ahmad RU, Hollestelle MJ, Reitsma PH, Fijnvandraat K, van Lier RA, Schwarz HP, Mertens K, Reipert BM, Voorberg J. Bril WS, et al. Among authors: fijnvandraat k. Thromb Haemost. 2006 Feb;95(2):341-7. doi: 10.1160/TH05-08-0559. Thromb Haemost. 2006. PMID: 16493498

8

Intensive peri-operative use of factor VIII and the Arg593-->Cys mutation are risk factors for inhibitor development in mild/moderate hemophilia A.

Eckhardt CL, Menke LA, van Ommen CH, van der Lee JH, Geskus RB, Kamphuisen PW, Peters M, Fijnvandraat K. Eckhardt CL, et al. Among authors: fijnvandraat k. J Thromb Haemost. 2009 Jun;7(6):930-7. doi: 10.1111/j.1538-7836.2009.03357.x. J Thromb Haemost. 2009. PMID: 19548904 Free article.

9

Inhibitors of factor VIII in hemophilia.

Eckhardt CL, Kamphuisen PW, Fijnvandraat K. Eckhardt CL, et al. Among authors: fijnvandraat k. N Engl J Med. 2009 Jul 16;361(3):309; author reply 310. N Engl J Med. 2009. PMID: 19610163 No abstract available.

10

Health-related quality of life among adult patients with moderate and severe von Willebrand disease.

de Wee EM, Mauser-Bunschoten EP, Van Der Bom JG, Degenaar-Dujardin ME, Eikenboom HC, Fijnvandraat K, de Goede-Bolder A, Laros-van Gorkom BA, Meijer K, Raat H, Leebeek FW; Win Study Group. de Wee EM, et al. Among authors: fijnvandraat k. J Thromb Haemost. 2010 Jul;8(7):1492-9. doi: 10.1111/j.1538-7836.2010.03864.x. Epub 2010 Mar 23. J Thromb Haemost. 2010. PMID: 20345712 Free article.

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