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- 2022
-
Mark
Diagnosis and management of severe congenital protein C deficiency (SCPCD) : Communication from the SSC of the ISTH
(
- Contribution to journal › Article
- 2007
-
Mark
Coagulation factorV and thrombophilia: Background and mechanisms
(
- Contribution to journal › Article
- 2003
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Mark
Factor VI359T: a novel mutation associated with thrombosis and resistance to activated protein C
(
- Contribution to journal › Article
- 2002
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Mark
Multicentre evaluation of IL Test (TM) Free PS: A fully automated assay to quantify Free Protein S
(
- Contribution to journal › Article
- 2001
-
Mark
Three-dimensional model of the SHBG-like region of anticoagulant protein S: New structure-function insights
(
- Contribution to journal › Article
- 1998
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Mark
A common 4G allele in the promoter of the plasminogen activator inhibitor-1 (PAI-1) gene as a risk factor for pulmonary embolism and arterial thrombosis in hereditary protein S deficiency
(
- Contribution to journal › Article
- 1997
-
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
Activated protein C resistance : Clinical implications
(
- Contribution to journal › Scientific review
- 1996
-
Mark
Prevalence of factor V gene mutation amongst myocardial infarction patients and healthy controls is higher in Sweden than in other countries
(
- Contribution to journal › Article
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Mark
Resistance to activated protein C, the FV:Q506 allele, and venous thrombosis
(
- Contribution to journal › Scientific review