The standard of care for immune thrombotic thrombocytopenic purpura today
Author:
Affiliation:
1. Department of Pathology and Laboratory Medicine University of Kansas Medical Center Kansas City Kansas USA
Funder
National Institutes of Health
Publisher
Wiley
Subject
Hematology
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1111/jth.15406
Reference89 articles.
1. Structure of von Willebrand Factor-cleaving Protease (ADAMTS13), a Metalloprotease Involved in Thrombotic Thrombocytopenic Purpura
2. Mutations in a member of the ADAMTS gene family cause thrombotic thrombocytopenic purpura
3. ADAMTS-13 rapidly cleaves newly secreted ultralarge von Willebrand factor multimers on the endothelial surface under flowing conditions
4. Physiologic cleavage of von Willebrand factor by a plasma protease is dependent on its conformation and requires calcium ion
5. Biosynthesis of von Willebrand protein by human megakaryocytes.
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1. Plasma cell‐directed therapy strategies in immune‐mediated thrombotic thrombocytopenic purpura (iTTP);Transfusion;2024-01-18
2. Identify the influences of systemic lupus erythematosus on acquired ADAMTS13-deficient thrombotic thrombocytopenic purpura using comprehensive bioinformatics analysis;Lupus;2023-10-17
3. Effectiveness and safety of caplacizumab in acquired thrombotic thrombocytopenic purpura: health technology assessment and classification according to the methodology established in Colombia;International Journal of Technology Assessment in Health Care;2023
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5. Assay for ADAMTS-13 Activity with Flow Cytometric Readout;ACS Omega;2022-08-24
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