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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
Genetic screening of children with suspected inherited bleeding disorders
(
- Contribution to journal › Article
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Mark
A rare heterozygous variant in FGB (Fibrinogen Merivale) causing hypofibrinogenemia in a Swedish family
(
- 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
- 2018
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Mark
Germline heterozygous variants in genes associated with familial hemophagocytic lymphohistiocytosis as a cause of increased bleeding
(
- Contribution to journal › Article
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Mark
Platelet-derived microparticles regulates thrombin generation via phophatidylserine in abdominal sepsis
(
- 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
- 2016
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Mark
Rac1 regulates bacterial toxin-induced thrombin generation.
2016) In Inflammation Research(
- Contribution to journal › Article
- 2015
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Mark
Monocytes regulate systemic coagulation and inflammation in abdominal sepsis.
(
- Contribution to journal › Article
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Mark
Quantification of sphingosine 1-phosphate by validated LC-MS/MS method revealing strong correlation with apolipoprotein M in plasma but not in serum due to platelet activation during blood coagulation.
(
- Contribution to journal › Article