Eva Zetterberg
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- 2021
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Mark
The Copenhagen founder variant GP1BA c.58T>G is the most frequent cause of inherited thrombocytopenia in Denmark
- Contribution to journal › Article
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Mark
Highly impaired platelet ultrastructure in two families with novel IKZF5 variants
- Contribution to journal › Article
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Mark
Severe Congenital Thrombocytopenia Characterized by Decreased Platelet Sialylation and Moderate Complement Activation Caused by Novel Compound Heterozygous Variants in GNE
- Contribution to journal › Article
- 2020
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Mark
Bleeding symptoms in patients diagnosed as type 3 von Willebrand disease : Results from 3WINTERS-IPS, an international and collaborative cross-sectional study
- 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
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Mark
Collagen Turnover and Plasma Ascorbic Acid Levels in Patients Suspected of Inherited Bleeding Disorders Harboring Variants in Collagen-related Genes
(2020) The XXVIII Congress of the International Society on Thrombosis and Haemostasis (ISTH) In Research and practice in thrombosis and haemostasis 4(S1). p.599-599
- Contribution to journal › Published meeting abstract
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Mark
Genetic screening of children with suspected inherited bleeding disorders
- 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
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Mark
Coagulation factor VIII is vital for increasing global coagulation after physical exercise
- Contribution to journal › Article
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Mark
Evaluation of a standardized protocol for thrombin generation using the calibrated automated thrombogram : A Nordic study
- Contribution to journal › Article
