Bertina RM - Search Results

1

Partial protein S gene deletion in a family with hereditary thrombophilia.

Ploos van Amstel HK, Huisman MV, Reitsma PH, Wouter ten Cate J, Bertina RM. Ploos van Amstel HK, et al. Among authors: bertina rm. Blood. 1989 Feb;73(2):479-83. Blood. 1989. PMID: 2521801 Free article.

2

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: bertina rm. 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.

3

The spectrum of genetic defects in a panel of 40 Dutch families with symptomatic protein C deficiency type I: heterogeneity and founder effects.

Reitsma PH, Poort SR, Allaart CF, Briët E, Bertina RM. Reitsma PH, et al. Among authors: bertina rm. Blood. 1991 Aug 15;78(4):890-4. Blood. 1991. PMID: 1868249 Free article.

4

Heerlen polymorphism of protein S, an immunologic polymorphism due to dimorphism of residue 460.

Bertina RM, Ploos van Amstel HK, van Wijngaarden A, Coenen J, Leemhuis MP, Deutz-Terlouw PP, van der Linden IK, Reitsma PH. Bertina RM, et al. Blood. 1990 Aug 1;76(3):538-48. Blood. 1990. PMID: 2143091 Free article.

5

A mutation in the protein S pseudogene is linked to protein S deficiency in a thrombophilic family.

Ploos van Amstel HK, Reitsma PH, Hamulyák K, de Die-Smulders CE, Mannucci PM, Bertina RM. Ploos van Amstel HK, et al. Among authors: bertina rm. Thromb Haemost. 1989 Nov 24;62(3):897-901. Thromb Haemost. 1989. PMID: 2531940

6

Two novel point mutations correlate with an altered developmental expression of blood coagulation factor IX (hemophilia B Leyden phenotype).

Reitsma PH, Mandalaki T, Kasper CK, Bertina RM, Briët E. Reitsma PH, et al. Among authors: bertina rm. Blood. 1989 Feb 15;73(3):743-6. Blood. 1989. PMID: 2917196 Free article.

7

The human protein S locus: identification of the PS alpha gene as a site of liver protein S messenger RNA synthesis.

Ploos van Amstel HK, Reitsma PH, Bertina RM. Ploos van Amstel HK, et al. Among authors: bertina rm. Biochem Biophys Res Commun. 1988 Dec 30;157(3):1033-8. doi: 10.1016/s0006-291x(88)80978-1. Biochem Biophys Res Commun. 1988. PMID: 2974696

8

The putative factor IX gene promoter in hemophilia B Leyden.

Reitsma PH, Bertina RM, Ploos van Amstel JK, Riemens A, Briët E. Reitsma PH, et al. Among authors: bertina rm. Blood. 1988 Sep;72(3):1074-6. Blood. 1988. PMID: 3416069 Free article.

9

Identification of eight point mutations in protein S deficiency type I--analysis of 15 pedigrees.

Gómez E, Poort SR, Bertina RM, Reitsma PH. Gómez E, et al. Among authors: bertina rm. Thromb Haemost. 1995 May;73(5):750-5. Thromb Haemost. 1995. PMID: 7482398

10

Activated protein C resistance as an additional risk factor for thrombosis in protein C-deficient families.

Koeleman BP, Reitsma PH, Allaart CF, Bertina RM. Koeleman BP, et al. Among authors: bertina rm. Blood. 1994 Aug 15;84(4):1031-5. Blood. 1994. PMID: 8049422 Free article.

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