van der Velden PA - Search Results

1

Molecular basis of hereditary protein C and protein S deficiency.

Reitsma PH, van Amstel HK, Poort BR, van der Velden PA, Bertina RM. Reitsma PH, et al. Among authors: van der velden pa, van amstel hk. Curr Stud Hematol Blood Transfus. 1991;(58):94-9. doi: 10.1159/000419345. Curr Stud Hematol Blood Transfus. 1991. PMID: 1835438 Review. No abstract available.

2

A frequent thrombomodulin amino acid dimorphism is not associated with thrombophilia.

van der Velden PA, Krommenhoek-Van Es T, Allaart CF, Bertina RM, Reitsma PH. van der Velden PA, et al. Thromb Haemost. 1991 May 6;65(5):511-3. Thromb Haemost. 1991. PMID: 1651567

3

Application of two neutral MspI DNA polymorphisms in the analysis of hereditary protein C deficiency.

Reitsma PH, te Lintel Hekkert W, Koenhen E, van der Velden PA, Allaart CF, Deutz-Terlouw PP, Poort SR, Bertina RM. Reitsma PH, et al. Among authors: van der velden pa. Thromb Haemost. 1990 Oct 22;64(2):239-44. Thromb Haemost. 1990. PMID: 1702905

4

Factor VII and fibrinogen levels as risk factors for venous thrombosis. A case-control study of plasma levels and DNA polymorphisms--the Leiden Thrombophilia Study (LETS).

Koster T, Rosendaal FR, Reitsma PH, van der Velden PA, Briët E, Vandenbroucke JP. Koster T, et al. Among authors: van der velden pa. Thromb Haemost. 1994 Jun;71(6):719-22. Thromb Haemost. 1994. PMID: 7974338

5

Instability of repeats of the von Willebrand factor gene variable number tandem repeat sequence in intron 40.

Eikenboom JC, Reitsma PH, van der Velden PA, Briët E. Eikenboom JC, et al. Among authors: van der velden pa. Br J Haematol. 1993 Jul;84(3):533-5. doi: 10.1111/j.1365-2141.1993.tb03114.x. Br J Haematol. 1993. PMID: 8105872

6

Mutation in blood coagulation factor V associated with resistance to activated protein C.

Bertina RM, Koeleman BP, Koster T, Rosendaal FR, Dirven RJ, de Ronde H, van der Velden PA, Reitsma PH. Bertina RM, et al. Among authors: van der velden pa. Nature. 1994 May 5;369(6475):64-7. doi: 10.1038/369064a0. Nature. 1994. PMID: 8164741 Free article.

7

Use of the direct RNA amplification technique NASBA to detect factor V Leiden, a point mutation associated with APC resistance.

Reitsma PH, van der Velden PA, Vogels E, van Strijp D, Tacken N, Adriaansen H, van Gemen B. Reitsma PH, et al. Among authors: van der velden pa, van gemen b, van strijp d. Blood Coagul Fibrinolysis. 1996 Sep;7(6):659-63. doi: 10.1097/00001721-199609000-00012. Blood Coagul Fibrinolysis. 1996. PMID: 8899156

8

Homozygotes for CDKN2 (p16) germline mutation in Dutch familial melanoma kindreds.

Gruis NA, van der Velden PA, Sandkuijl LA, Prins DE, Weaver-Feldhaus J, Kamb A, Bergman W, Frants RR. Gruis NA, et al. Among authors: van der velden pa. Nat Genet. 1995 Jul;10(3):351-3. doi: 10.1038/ng0795-351. Nat Genet. 1995. PMID: 7670475

9

Familial melanoma; CDKN2A and beyond.

Gruis NA, van der Velden PA, Bergman W, Frants RR. Gruis NA, et al. Among authors: van der velden pa. J Investig Dermatol Symp Proc. 1999 Sep;4(1):50-4. doi: 10.1038/sj.jidsp.5640181. J Investig Dermatol Symp Proc. 1999. PMID: 10537008 Free article. Review.

10

Genetics of familial atypical multiple mole-melanoma (FAMMM) syndrome in The Netherlands: how far have we come?

Gruis NA, Van der Velden PA, Bergman W, Frants RR. Gruis NA, et al. Among authors: van der velden pa. Bull Cancer. 1998 Jul;85(7):627-30. Bull Cancer. 1998. PMID: 9752270 Free article.

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