Challenges in diagnosing thrombotic thrombocytopenic purpura-Reference-Cited by-同舟云学术

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Challenges in diagnosing thrombotic thrombocytopenic purpura

Published:2025-07 Issue:3 Volume:47 Page:103842
ISSN:2531-1379
Container-title:Hematology, Transfusion and Cell Therapy
language:en
Short-container-title:Hematology, Transfusion and Cell Therapy

Author:

Jacobs Jeremy W.^ORCID,Booth Garrett S.^ORCID,Adkins Brian D.

Publisher

Elsevier BV

Reference11 articles.

1. Thrombotic thrombocytopenic purpura;Joly;Blood,2017

2. Unusually large plasma factor VIII: von Willebrand factor multimers in chronic relapsing thrombotic thrombocytopenic purpura;Moake;N Engl J Med,1982

3. Mutations in a member of the ADAMTS gene family cause thrombotic thrombocytopenic purpura;Levy;Nature,2001

4. Assessing treatment response in thrombotic thrombocytopenic purpura: beyond the platelet count;Martins de Oliveira Filho;Hematol Transfus Cell Ther,2024

5. Acquired thrombotic thrombocytopenic purpura without detectable anti-ADAMTS13 antibodies: a possible underlying autoimmune mechanism;Simon;Haematologica,2024

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