Dahlbäck B - Search Results

1

Genetic and phenotypic analysis of a large (122-member) protein S-deficient kindred provides an explanation for the familial coexistence of type I and type III plasma phenotypes.

Simmonds RE, Zöller B, Ireland H, Thompson E, de Frutos PG, Dahlbäck B, Lane DA. Simmonds RE, et al. Among authors: dahlback b. Blood. 1997 Jun 15;89(12):4364-70. Blood. 1997. PMID: 9192759 Free article.

2

Genetic and phenotypic variability between families with hereditary protein S deficiency.

Rezende SM, Lane DA, Zöller B, Mille-Baker B, Laffan M, Dahlbäck B, Simmonds RE. Rezende SM, et al. Among authors: dahlback b. Thromb Haemost. 2002 Feb;87(2):258-65. doi: 10.1055/s-0037-1612982. Thromb Haemost. 2002. PMID: 11858485

3

Clarification of the risk for venous thrombosis associated with hereditary protein S deficiency by investigation of a large kindred with a characterized gene defect.

Simmonds RE, Ireland H, Lane DA, Zöller B, García de Frutos P, Dahlbäck B. Simmonds RE, et al. Among authors: dahlback b. Ann Intern Med. 1998 Jan 1;128(1):8-14. doi: 10.7326/0003-4819-128-1-199801010-00002. Ann Intern Med. 1998. PMID: 9424998

4

Evaluation of the relationship between protein S and C4b-binding protein isoforms in hereditary protein S deficiency demonstrating type I and type III deficiencies to be phenotypic variants of the same genetic disease.

Zöller B, García de Frutos P, Dahlbäck B. Zöller B, et al. Among authors: dahlback b. Blood. 1995 Jun 15;85(12):3524-31. Blood. 1995. PMID: 7780139 Free article.

5

Activated protein C resistance: from phenotype to genotype and clinical practice.

Hillarp A, Dahlbäck B, Zöller B. Hillarp A, et al. Among authors: dahlback b. Blood Rev. 1995 Dec;9(4):201-12. doi: 10.1016/s0268-960x(95)90011-x. Blood Rev. 1995. PMID: 8839395 Review.

6

Protein S secretion differences of missense mutants account for phenotypic heterogeneity.

Espinosa-Parrilla Y, Yamazaki T, Sala N, Dahlbäck B, de Frutos PG. Espinosa-Parrilla Y, et al. Among authors: dahlback b. Blood. 2000 Jan 1;95(1):173-9. Blood. 2000. PMID: 10607700 Free article.

7

Deficient APC-cofactor activity of protein S Heerlen in degradation of factor Va Leiden: a possible mechanism of synergism between thrombophilic risk factors.

Giri TK, Yamazaki T, Sala N, Dahlbäck B, de Frutos PG. Giri TK, et al. Among authors: dahlback b. Blood. 2000 Jul 15;96(2):523-31. Blood. 2000. PMID: 10887114 Free article.

8

Differential regulation of alpha and beta chains of C4b-binding protein during acute-phase response resulting in stable plasma levels of free anticoagulant protein S.

García de Frutos P, Alim RI, Härdig Y, Zöller B, Dahlbäck B. García de Frutos P, et al. Among authors: dahlback b. Blood. 1994 Aug 1;84(3):815-22. Blood. 1994. PMID: 7519078 Free article.

9

Resistance to activated protein C as an additional genetic risk factor in hereditary deficiency of protein S.

Zöller B, Berntsdotter A, García de Frutos P, Dahlbäck B. Zöller B, et al. Among authors: dahlback b. Blood. 1995 Jun 15;85(12):3518-23. Blood. 1995. PMID: 7780138 Free article.

10

The A20210 allele of the prothrombin gene is frequently associated with the factor V Arg 506 to Gln mutation but not with protein S deficiency in thrombophilic families.

Zoller B, Svensson PJ, Dahlback B, Hillarp A. Zoller B, et al. Among authors: dahlback b. Blood. 1998 Mar 15;91(6):2210-1. Blood. 1998. PMID: 9490712 Free article. No abstract available.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

424 results

Search Page

Filters