Value of ADAMTS13 activity and inhibitor in the postmortem diagnosis of thrombotic thrombocytopenic purpura
Author:
Publisher
Wiley
Subject
Hematology,General Medicine
Reference21 articles.
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2. Is severe deficiency of ADAMTS-13 specific for thrombotic thrombocytopenic purpura? Yes;Tsai;J Thromb Haemost,2003
3. Fatal congenital thrombotic thrombocytopenic purpura with apparent ADAMTS13 inhibitor: in vitro inhibition of ADAMTS13 activity by hemoglobin;Studt;Blood,2005
4. Mutations in a member of the ADAMTS gene family cause thrombotic thrombocytopenic purpura;Levy;Nature,2001
5. Assay of von Willebrand factor (vWF)-cleaving protease based upon decreased collagen binding affinity of degraded vWF;Gerritsen;Thromb Haemost,1999
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1. Update on ADAMTS13 and VWF in cardiovascular and hematological disorders;Clinica Chimica Acta;2016-12
2. Response to ‘Death during pregnancy: Thrombotic thrombocytopenic purpura or septic shock?’;Journal of Obstetrics and Gynaecology Research;2013-11-18
3. ADAMTS13 endopeptidase 3.4.24.87;Class 3.4–6 Hydrolases, Lyases, Isomerases, Ligases;2013
4. Autopsy case of sudden maternal death from thrombotic thrombocytopenic purpura;Journal of Obstetrics and Gynaecology Research;2012-07-06
5. A high LDH to AST ratio helps to differentiate pregnancy-associated thrombotic thrombocytopenic purpura (TTP) from HELLP syndrome;The Journal of Maternal-Fetal & Neonatal Medicine;2011-10-14
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