Voorberg J - Search Results

1

Variation in baseline factor VIII concentration in a retrospective cohort of mild/moderate hemophilia A patients carrying identical F8 mutations.

Loomans JI, van Velzen AS, Eckhardt CL, Peters M, Mäkipernaa A, Holmstrom M, Brons PP, Dors N, Haya S, Voorberg J, van der Bom JG, Fijnvandraat K. Loomans JI, et al. Among authors: voorberg j. J Thromb Haemost. 2017 Feb;15(2):246-254. doi: 10.1111/jth.13581. Epub 2017 Feb 3. J Thromb Haemost. 2017. PMID: 27943580 Free article.

2

Quantitative analysis of von Willebrand factor propeptide release in vivo: effect of experimental endotoxemia and administration of 1-deamino-8-D-arginine vasopressin in humans.

Borchiellini A, Fijnvandraat K, ten Cate JW, Pajkrt D, van Deventer SJ, Pasterkamp G, Meijer-Huizinga F, Zwart-Huinink L, Voorberg J, van Mourik JA. Borchiellini A, et al. Among authors: voorberg j. Blood. 1996 Oct 15;88(8):2951-8. Blood. 1996. PMID: 8874191 Free article.

3

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. Among authors: voorberg j. Blood. 1997 Jun 15;89(12):4371-7. Blood. 1997. PMID: 9192760 Free article.

4

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. Among authors: voorberg j. Blood. 1998 Apr 1;91(7):2347-52. Blood. 1998. PMID: 9516133 Free article.

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: voorberg j. Thromb Haemost. 1999 May;81(5):723-6. Thromb Haemost. 1999. PMID: 10365744

6

Human antibodies with specificity for the C2 domain of factor VIII are derived from VH1 germline genes.

van Den Brink EN, Turenhout EA, Davies J, Bovenschen N, Fijnvandraat K, Ouwehand WH, Peters M, Voorberg J. van Den Brink EN, et al. Among authors: voorberg j. Blood. 2000 Jan 15;95(2):558-63. Blood. 2000. PMID: 10627462 Free article.

7

Intracellular accumulation of factor VIII induced by missense mutations Arg593-->Cys and Asn618-->Ser explains cross-reacting material-reduced haemophilia A.

Roelse JC, De Laaf RT, Timmermans SM, Peters M, Van Mourik JA, Voorberg J. Roelse JC, et al. Among authors: voorberg j. Br J Haematol. 2000 Feb;108(2):241-6. doi: 10.1046/j.1365-2141.2000.01834.x. Br J Haematol. 2000. PMID: 10691849 Free article.

8

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: voorberg j. Blood. 2000 Jul 15;96(2):540-5. Blood. 2000. PMID: 10887116 Free article.

9

Multiple VH genes are used to assemble human antibodies directed toward the A3-C1 domains of factor VIII.

van den Brink EN, Turenhout EA, Bovenschen N, Heijnen BG, Mertens K, Peters M, Voorberg J. van den Brink EN, et al. Among authors: voorberg j. Blood. 2001 Feb 15;97(4):966-72. doi: 10.1182/blood.v97.4.966. Blood. 2001. PMID: 11159524 Free article.

10

Two classes of germline genes both derived from the V(H)1 family direct the formation of human antibodies that recognize distinct antigenic sites in the C2 domain of factor VIII.

van den Brink EN, Bril WS, Turenhout EA, Zuurveld M, Bovenschen N, Peters M, Yee TT, Mertens K, Lewis DA, Ortel TL, Lollar P, Scandella D, Voorberg J. van den Brink EN, et al. Among authors: voorberg j. Blood. 2002 Apr 15;99(8):2828-34. doi: 10.1182/blood.v99.8.2828. Blood. 2002. PMID: 11929772 Free article.

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