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- 2019
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Mark
A Heterozygous FGB Variant Causing Hypofibrinogenemia in a Swedish Family
(2019) The XXVII Congress of the International Society on Thrombosis and Haemostasis (ISTH) In Research and practice in thrombosis and haemostasis 3(S1). p.367-369
- Contribution to journal › Published meeting abstract
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Mark
Outcome of an enhanced diagnostic pipeline for patients suspected of inherited thrombocytopenia
- Contribution to journal › Letter
- 2018
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Mark
Evaluation of prophylactic therapy in haemophilia with global coagulation tests
- Contribution to journal › Letter
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Mark
A novel variant glanzmann thrombasthenia due to co-inheritance of a loss-and a gain-of-function mutation of ITGB3 : Evidence of a dominant effect of gain-of-function mutations
- Contribution to journal › Letter
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Mark
Impact of Exercise on Hemophilia
- Contribution to journal › Article
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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
- 2017
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Mark
Correlation to FVIII : C in two thrombin generation tests: TGA-CAT and INNOVANCE ETP
- Contribution to journal › Article
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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
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Mark
Low agreement between fresh and frozen-thawed platelet-rich plasma in the calibrated automated thrombogram assay
- Contribution to journal › Article
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Mark
Indications of underdiagnosis of atypical haemolytic uraemic syndrome in a cohort referred to the Coagulation Unit in Malmo, Sweden, for analysis of ADAMTS13 2007–2012
- Contribution to journal › Article
