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- 2021
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Mark
Validation of factor VIII activity for monitoring standard and extended half-life products and correlation to thrombin generation assays
(
- Contribution to journal › Article
- 2020
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Mark
A rare heterozygous variant in FGB (Fibrinogen Merivale) causing hypofibrinogenemia in a Swedish family
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- Contribution to journal › Article
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Mark
Genetic screening of children with suspected inherited bleeding disorders
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- Contribution to journal › Article
- 2019
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Mark
A simplified flow cytometric method for detection of inherited platelet disorders—A comparison to the gold standard light transmission aggregometry
(
- Contribution to journal › Article
- 2017
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Mark
Application of whole-exome sequencing to direct the specific functional testing and diagnosis of rare inherited bleeding disorders in patients from the Öresund Region, Scandinavia
(
- Contribution to journal › Article
- 2011
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Mark
Activated protein C cofactor function of protein S: a novel role for a gamma-carboxyglutamic acid residue
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- Contribution to journal › Article
- 2004
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Mark
Functional characterization of Factor V-Ile359Thr, a novel mutation associated with thrombosis.
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- Contribution to journal › Article
- 2003
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Mark
Factor VI359T: a novel mutation associated with thrombosis and resistance to activated protein C
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- Contribution to journal › Article
- 2002
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Mark
Functional characterization of recombinant FV Hong Kong and FV Cambridge.
(
- Contribution to journal › Article