Bleeding phenotype of patients with moderate haemophilia A and B assessed by thromboelastometry and thrombin generation-Reference-Cited by-同舟云学术

Bleeding phenotype of patients with moderate haemophilia A and B assessed by thromboelastometry and thrombin generation

Published:2021-06-09 Issue:5 Volume:27 Page:793-801
ISSN:1351-8216
Container-title:Haemophilia
language:en
Short-container-title:Haemophilia

Author:

Måseide Ragnhild J.¹²³^ORCID,Berntorp Erik⁴^ORCID,Nummi Vuokko⁵^ORCID,Lassila Riitta⁵,Tjønnfjord Geir E.¹³,Holme Pål A.¹²³

Affiliation:

1. Department of Haematology Oslo University Hospital Oslo Norway

2. Research Institute of Internal Medicine Oslo University Hospital Oslo Norway

3. Institute of Clinical Medicine University of Oslo Oslo Norway

4. Department of Translational Medicine Lund University Malmö Sweden

5. Coagulation Disorders Unit, Haematology, Comprehensive Cancer Centre, Helsinki University Hospital and Research Program in Systems Oncology, Faculty of Medicine, Helsinki University Helsinki Finland

Publisher

Wiley

Subject

Genetics(clinical),Hematology,General Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/hae.14355

Reference33 articles.

1. A longitudinal study of orthopaedic outcomes for severe factor-VIII-deficient haemophiliacs

2. Thrombin functions during tissue factor–induced blood coagulation

3. Calibrated Automated Thrombin Generation Measurement in Clotting Plasma

4. Whole blood coagulation thrombelastographic profiles employing minimal tissue factor activation

5. Whole blood clot formation phenotypes in hemophilia A and rare coagulation disorders. Patterns of response to recombinant factor VIIa

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