Björn Dahlbäck
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- 1998
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Mark
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
- Contribution to journal › Letter
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Mark
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 [3]
- Contribution to journal › Letter
- 1997
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Mark
Presence of vitamin K dependent coagulation proteins in isolated lipoproteins from human plasma.
- Contribution to journal › Article
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Mark
The factor VR5O6Q mutation causing APC resistance is highly prevalent amongst unselected outpatients with clinically suspected deep venous thrombosis
- Contribution to journal › Article
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Mark
The 20210 A allele of the prothrombin gene is a common risk factor among Swedish outpatients with verified deep venous thrombosis
- Contribution to journal › Debate/Note/Editorial
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Mark
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
- Contribution to journal › Article
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Mark
Activated protein C resistance caused by a common factor V mutation has a single origin
- Contribution to journal › Article
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Mark
The factor VR506Q mutation causing APC resistance is highly prevalent amongst unselected outpatients with clinically suspected deep venous thrombosis
- Contribution to journal › Article
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Mark
Evaluation of original and modified APC-resistance tests in unselected outpatients with clinically suspected thrombosis and in healthy controls
- Contribution to journal › Article
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Mark
Activated protein C resistance due to a common factor V gene mutation is a major risk factor for venous thrombosis
- Contribution to journal › Article
