Case Report: Von Willebrand Factor Abnormalities and Endothelial Cell Perturbation in a Patient with Acute Thrombotic Thrombocytopenic Purpura
- 1 January 1986
- journal article
- case report
- Published by Elsevier in The American Journal of the Medical Sciences
- Vol. 291 (1), 47-50
- https://doi.org/10.1097/00000441-198601000-00009
Abstract
No abstract availableKeywords
This publication has 12 references indexed in Scilit:
- Therapy of chronic relapsing thrombotic thrombocytopenic purpura with prednisone and azathioprineAmerican Journal of Hematology, 1985
- Efficacy of several plasma components in a young boy with chronic thrombocytopenia and hemolytic anemia who responds repeatedly to normal plasma infusionsAmerican Journal of Hematology, 1984
- Detection of a Platelet-Agglutinating Factor in Thrombotic Thrombocytopenic PurpuraAnnals of Internal Medicine, 1984
- Unusually Large Plasma Factor VIII: von Willebrand Factor Multimers in Chronic Relapsing Thrombotic Thrombocytopenic PurpuraNew England Journal of Medicine, 1982
- Pathologic effects of plasma from patients with thrombotic thrombocytopenic purpura on platelets and cultured vascular endothelial cellsBlood, 1982
- THROMBOTIC THROMBOCYTOPENIC PURPURA: CONFLICTING RESULTS OF IN-VITRO STUDIESThe Lancet, 1980
- Human blood platelet adhesion to artery subendothelium is mediated by factor VIII–Von Willebrand factor bound to the subendotheliumNature, 1979
- Synthesis of Factor VIII Antigen by Cultured Guinea Pig MegakaryocytesJournal of Clinical Investigation, 1977
- A NEW METHOD FOR THE QUANTITATIVE DETECTION OF PLATELET AGGREGATES IN PATIENTS WITH ARTERIAL INSUFFICIENCYThe Lancet, 1974
- Synthesis of Antihemophilic Factor Antigen by Cultured Human Endothelial CellsJournal of Clinical Investigation, 1973