Case Report: Von Willebrand Factor Abnormalities and Endothelial Cell Perturbation in a Patient with Acute Thrombotic Thrombocytopenic Purpura-Reference-Cited by-同舟云学术

Case Report: Von Willebrand Factor Abnormalities and Endothelial Cell Perturbation in a Patient with Acute Thrombotic Thrombocytopenic Purpura

Published:1986-01 Issue:1 Volume:291 Page:47-50
ISSN:0002-9629
Container-title:The American Journal of the Medical Sciences
language:en
Short-container-title:The American Journal of the Medical Sciences

Author:

Moake Joel L.,Rudy Christine K.,Troll Joseph H.,Weinstein Mark J.,Colannino Noreen M.,Hong Suchen L.,Koutcher Jason A.,Melaragno Anthony J.,Manner Charles E.

Publisher

Elsevier BV

Subject

General Medicine

Reference19 articles.

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

2. von Willebrand factor multimer forms produced by human endothelial cells;Hong;Blood,1985

3. A new method for the quantitative detection of platelet aggregates in patients with arterial insufficiency;Wu;Lancet,1974

4. Presence of a platelet aggregating factor in the plasma of patients with thrombotic thrombocytopenic purpura (TTP) and its inhibition by normal plasma;Lian;Blood,1979

5. Synthesis of antihemophilic factor antigen by cultured human endothelial cells;Jaffe;J Clin Invest,1973

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