Fijnvandraat K - Search Results

1

Major differences in clinical presentation, diagnosis and management of men and women with autosomal inherited bleeding disorders.

Atiq F, Saes JL, Punt MC, van Galen KPM, Schutgens REG, Meijer K, Cnossen MH, Laros-Van Gorkom BAP, Peters M, Nieuwenhuizen L, Kruip MJHA, de Meris J, van der Bom JG, van der Meer FJM, Fijnvandraat K, Kruis IC, van Heerde WL, Eikenboom HCJ, Leebeek FWG, Schols SEM; WiN, RBiN and TiN study groups. Atiq F, et al. Among authors: fijnvandraat k. EClinicalMedicine. 2021 Jan 29;32:100726. doi: 10.1016/j.eclinm.2021.100726. eCollection 2021 Feb. EClinicalMedicine. 2021. PMID: 33554093 Free PMC article.

2

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.

3

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.

4

Acquired protein S deficiency caused by estrogen treatment of tall stature.

van Ommen CH, Fijnvandraat K, Vulsma T, Delemarre-Van De Waal HA, Peters M. van Ommen CH, et al. Among authors: fijnvandraat k. J Pediatr. 1999 Oct;135(4):477-81. doi: 10.1016/s0022-3476(99)70171-x. J Pediatr. 1999. PMID: 10518082

5

Molecular analysis of human anti-factor VIII antibodies by V gene phage display identifies a new epitope in the acidic region following the A2 domain.

van den Brink EN, Turenhout EA, Bank CM, Fijnvandraat K, Peters M, Voorberg J. van den Brink EN, et al. Among authors: fijnvandraat k. Blood. 2000 Jul 15;96(2):540-5. Blood. 2000. PMID: 10887116 Free article.

6

The impact of unaware carriership on the clinical presentation of haemophilia.

MacLean PE, Fijnvandraat K, Beijlevelt M, Peters M. MacLean PE, et al. Among authors: fijnvandraat k. Haemophilia. 2004 Sep;10(5):560-4. doi: 10.1111/j.1365-2516.2004.00955.x. Haemophilia. 2004. PMID: 15357784

7

Identifying children with sickle cell anaemia in a non-endemic country: age at diagnosis and presenting symptoms.

van den Tweel X, Heijboer H, Fijnvandraat K, Peters M. van den Tweel X, et al. Among authors: fijnvandraat k. Eur J Pediatr. 2006 Aug;165(8):581-2. doi: 10.1007/s00431-006-0102-7. Epub 2006 Apr 29. Eur J Pediatr. 2006. PMID: 16649026 No abstract available.

8

Quality of life of female caregivers of children with sickle cell disease: a survey.

van den Tweel XW, Hatzmann J, Ensink E, van der Lee JH, Peters M, Fijnvandraat K, Grootenhuis M. van den Tweel XW, et al. Among authors: fijnvandraat k. Haematologica. 2008 Apr;93(4):588-93. doi: 10.3324/haematol.11610. Epub 2008 Mar 5. Haematologica. 2008. PMID: 18322259 Free article.

9

[Glucose-6-phosphate dehydrogenase deficiency: clinical presentation and eliciting factors].

Dors N, Rodrigues Pereira R, van Zwieten R, Fijnvandraat K, Peters M. Dors N, et al. Among authors: fijnvandraat k. Ned Tijdschr Geneeskd. 2008 May 3;152(18):1029-33. Ned Tijdschr Geneeskd. 2008. PMID: 18547022 Dutch.

10

Obesity: a new disaster for haemophilic patients? A nationwide survey.

Hofstede FG, Fijnvandraat K, Plug I, Kamphuisen PW, Rosendaal FR, Peters M. Hofstede FG, et al. Among authors: fijnvandraat k. Haemophilia. 2008 Sep;14(5):1035-8. doi: 10.1111/j.1365-2516.2008.01806.x. Epub 2008 Jul 15. Haemophilia. 2008. PMID: 18637967

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