Fijnvandraat K - Search Results

1

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.

2

Estrogens reduce plasma histidine-rich glycoprotein (HRG) levels in a dose-dependent way.

Hennis BC, Boomsma DI, Fijnvandraat K, Gevers Leuven JA, Peters M, Kluft C. Hennis BC, et al. Among authors: fijnvandraat k. Thromb Haemost. 1995 Mar;73(3):484-7. Thromb Haemost. 1995. PMID: 7667832 Clinical Trial.

3

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

4

Endotoxin induced coagulation activation and protein C reduction in meningococcal septic shock.

Fijnvandraat K, Peters M, Derkx B, van Deventer S, ten Cate JW. Fijnvandraat K, et al. Prog Clin Biol Res. 1994;388:247-54. Prog Clin Biol Res. 1994. PMID: 7831362 Review. No abstract available.

5

Inter-individual variation in half-life of infused recombinant factor VIII is related to pre-infusion von Willebrand factor antigen levels.

Fijnvandraat K, Peters M, ten Cate JW. Fijnvandraat K, et al. Br J Haematol. 1995 Oct;91(2):474-6. doi: 10.1111/j.1365-2141.1995.tb05325.x. Br J Haematol. 1995. PMID: 8547097 Clinical Trial.

6

Activation of the intrinsic pathway of coagulation in children with meningococcal septic shock.

Wuillemin WA, Fijnvandraat K, Derkx BH, Peters M, Vreede W, ten Cate H, Hack CE. Wuillemin WA, et al. Among authors: fijnvandraat k. Thromb Haemost. 1995 Dec;74(6):1436-41. Thromb Haemost. 1995. PMID: 8772216

7

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.

8

The missense mutation Arg593 --> Cys is related to antibody formation in a patient with mild hemophilia A.

Fijnvandraat K, Turenhout EA, van den Brink EN, ten Cate JW, van Mourik JA, Peters M, Voorberg J. Fijnvandraat K, et al. Blood. 1997 Jun 15;89(12):4371-7. Blood. 1997. PMID: 9192760 Free article.

9

A human alloantibody interferes with binding of factor IXa to the factor VIII light chain.

Fijnvandraat K, Celie PH, Turenhout EA, ten Cate JW, van Mourik JA, Mertens K, Peters M, Voorberg J. Fijnvandraat K, et al. Blood. 1998 Apr 1;91(7):2347-52. Blood. 1998. PMID: 9516133 Free article.

10

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

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