Inherited ADAMTS13 mutations associated with Thrombotic Thrombocytopenic Purpura: a short review and update
Author:
Affiliation:
1. School of Pharmacy, Centre for Biomolecular Sciences, University of Nottingham, Nottingham, UK and
2. Institute of Cardiovascular Sciences, College of Medical and Dental Sciences, University of Birmingham, Birmingham, UK
Funder
Medical Research Council
Publisher
Informa UK Limited
Subject
Hematology,General Medicine
Link
https://www.tandfonline.com/doi/pdf/10.1080/09537104.2022.2138306
Reference33 articles.
1. von Willebrand factor, Jedi knight of the bloodstream
2. Regional UK TTP Registry: correlation with laboratory ADAMTS 13 analysis and clinical features
3. Stroke and myocardial infarction in hereditary thrombotic thrombocytopenic purpura: similarities to sickle cell anemia
4. Updates on thrombotic thrombocytopenic purpura: Recent developments in pathogenesis, treatment and survivorship
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1. Long‐term follow‐up of patients with congenital thrombotic thrombocytopenia purpura receiving a plasma‐derived factor VIII (Koate) that contains ADAMTS13;Haemophilia;2023-10-19
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