Coagulation studies in thrombotic thrombocytopenic purpura, with special reference to von willebrand factor and protein S
Author:
Publisher
Wiley
Subject
Hematology
Reference35 articles.
1. 7 Thrombotic Thrombocytopenic Purpura and the Haemolytic-Uraemic Syndrome: Evolving Concepts of Pathogenesis and Therapy
2. Presence of a platelet aggregating factor in the plasma of patients with thrombotic thrombocytopenic purpura (TTP) and its inhibition by normal plasma
3. Novel platelet-agglutinating protein from a thrombotic thrombocytopenic purpura plasma.
4. Inhibition of platelet-aggregating activity in thrombotic thrombocytopenic purpura plasma by normal adult immunoglobulin G.
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1. A Case of Severe Thrombotic Thrombocytopenic Purpura With Concomitant Legionella Pneumonia: Review of Pathogenesis and Treatment;American Journal of Therapeutics;2011-09
2. Platelet Count and Prothrombin Time Help Distinguish Thrombotic Thrombocytopenic Purpura–Hemolytic Uremic Syndrome From Disseminated Intravascular Coagulation in Adults;American Journal of Clinical Pathology;2010-03
3. Effects of endothelin-1 and phenylephrine on plasma levels of von Willebrand factor and protein S;Thrombosis Research;2010-01
4. Molecular basis of ADAMTS13 dysfunction in thrombotic thrombocytopenic purpura;Pediatric Nephrology;2009-03
5. Antiphospholipid antibodies: Paradigm in transition;Journal of Neuroinflammation;2009-01-20
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