ADAMTS‐13 and bleeding phenotype in von Willebrand disease-Reference-Cited by-同舟云学术

ADAMTS‐13 and bleeding phenotype in von Willebrand disease

Published:2020-10-31 Issue:8 Volume:4 Page:1331-1339
ISSN:2475-0379
Container-title:Research and Practice in Thrombosis and Haemostasis
language:en
Short-container-title:Res Pract Thromb Haemost

Author:

Boender Johan¹^ORCID,Nederlof Angelique¹²,Meijer Karina³,Mauser‐Bunschoten Evelien P.⁴,Cnossen Marjon H.²,Fijnvandraat Karin⁵⁶,Bom Johanna G.⁷⁸,Meris Joke⁹,Laros‐van Gorkom Britta A. P.¹⁰,Galen Karin P. M.⁴,Eikenboom Jeroen¹¹¹²^ORCID,Maat Moniek P. M¹^ORCID,Leebeek Frank W. G.¹^ORCID,Coppens M.,Nieuwenhuizen L.,Tamminga R.Y.J.,Ypma P.F.,Smiers F.J.W.,Beckers E.,Brons P.,Atiq F.,

Affiliation:

1. Department of Hematology Erasmus MC, University Medical Center Rotterdam Rotterdam The Netherlands

2. Department of Pediatric Hematology Erasmus MC, University Medical Center RotterdamSophia Children's Hospital Rotterdam The Netherlands

3. Department Hematology University Medical Center Groningen Groningen The Netherlands

4. van Creveld kliniek/Department Benign Hematology University Medical Center Utrecht Utrecht The Netherlands

5. Department of Pediatric Hematology Emma Children’s HospitalAmsterdam UMCUniversity of Amsterdam Amsterdam The Netherlands

6. Department of Plasma Proteins Sanquin Research Amsterdam Netherlands

7. Department Clinical Epidemiology Leiden University Medical Center Leiden The Netherlands

8. Jon J van Rood Center for Clinical Transfusion Medicine Sanquin Research Leiden The Netherlands

9. Netherlands Hemophilia Society Nijkerk The Netherlands

10. Department Hematology Radboud University Medical Center Nijmegen The Netherlands

11. Department Internal Medicine division Thrombosis and Hemostasis Leiden University Medical Center Leiden The Netherlands

12. Einthoven Laboratory for Vascular and Regenerative Medicine Leiden University Medical Center Leiden The Netherlands

Funder

CSL Behring

European Association for Haemophilia and Allied Disorders

Publisher

Wiley

Subject

Hematology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/rth2.12442

Reference28 articles.

1. Pathophysiology of thrombotic thrombocytopenic purpura

2. Low ADAMTS13 activity is associated with an increased risk of ischemic stroke

3. Low ADAMTS-13 activity and the risk of coronary heart disease - a prospective cohort study: the Rotterdam Study

4. Von Willebrand’s Disease

5. Determinants of bleeding phenotype in adult patients with moderate or severe von Willebrand disease

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1. Compound heterozygosity for novel von Willebrand factor genetic variants associated with von Willebrand disease in two Chinese patients;Blood Coagulation & Fibrinolysis;2022-10-18

2. Platelet degranulation and bleeding phenotype in a large cohort of Von Willebrand disease patients;British Journal of Haematology;2022-03-22

3. The trypsin inhibitor-like domain is required for a serine protease inhibitor of Haemonchus contortus to inhibit host coagulation;International Journal for Parasitology;2021-11