Bertina RM - 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: 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.

2

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.

3

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.

4

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.

5

Three novel mutations in five unrelated subjects with hereditary protein S deficiency type I.

Reitsma PH, Ploos van Amstel HK, Bertina RM. Reitsma PH, et al. Among authors: bertina rm. J Clin Invest. 1994 Feb;93(2):486-92. doi: 10.1172/JCI116997. J Clin Invest. 1994. PMID: 8113388 Free PMC article.

6

Twelve novel and two recurrent mutations in 14 Austrian families with hereditary protein C deficiency.

Poort SR, Pabinger-Fasching I, Mannhalter C, Reitsma PH, Bertina RM. Poort SR, et al. Among authors: bertina rm. Blood Coagul Fibrinolysis. 1993 Apr;4(2):273-80. doi: 10.1097/00001721-199304000-00009. Blood Coagul Fibrinolysis. 1993. PMID: 8499565

7

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. Among authors: bertina rm. Thromb Haemost. 1991 May 6;65(5):511-3. Thromb Haemost. 1991. PMID: 1651567

8

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: bertina rm. Thromb Haemost. 1990 Oct 22;64(2):239-44. Thromb Haemost. 1990. PMID: 1702905

9

A CCA/CCG neutral dimorphism in the codon for Pro 626 of the human protein S gene PS alpha (PROS1).

Diepstraten CM, van Amstel JK, Reitsma PH, Bertina RM. Diepstraten CM, et al. Among authors: bertina rm. Nucleic Acids Res. 1991 Sep 25;19(18):5091. doi: 10.1093/nar/19.18.5091. Nucleic Acids Res. 1991. PMID: 1923788 Free PMC article.

10

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.

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