Deficient Activity of von Willebrand Factor-Cleaving Protease in Patients With Upshaw-Schulman Syndrome
Author:
Publisher
Springer Science and Business Media LLC
Subject
Hematology
Link
http://link.springer.com/article/10.1007/BF02982559/fulltext.html
Reference20 articles.
1. Upshaw JDJ. Congenital deficiency of a factor in normal plasma that reverses microangiopathic hemolysis and thrombocytopenia.N Eng J Med. 1978;298:1350–1352.
2. Schulman I, Pierce M, Lukens A, Currimbhoy Z. Studies on thrombopoiesis. A factor in normal human plasma required for platelet production; chronic thrombocytopenia due to its deficiency.Blood. 1960;16:943–957.
3. Moake JL, Rudy CK, Troll JH, et al. Unusually large plasma factor VIII; von Willebrand factor multimers in chronic relapsing thrombotic thrombocytopenic purpura.N Eng J Med. 1982;307:1432–1435.
4. Chintagumpala MM, Hurwitz RL, Moake JL, Mahoney DH, Steuber CP. Chronic relapsing thrombotic thrombocytopenic purpura in infants with large von Willebrand factor multimers during remission.J Pediatr. 1992;120:49–53.
5. Shinohara T, Miyamura S, Suzuki E, Kobayashi K. Congenital microangiopathic hemolytic anemia: report of a Japanese girl.Eur J Pediatr. 1982;138:191–193.
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