Art
J-GLOBAL ID：200902107776137953
Reference number：01A0857183
Upshaw-Schulman Syndrome Revisited: A Concept of Congenital Thrombotic Thrombocytopenic Purpura.
Upshaw-Schulman症候群の再考 先天性血栓性血小板減少性紫斑病の一概念
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Material：
Volume：
74
Issue：
1
Page：
101-108
Publication year：
Jul. 2001
JST Material Number：
F0888A
ISSN：
0925-5710
CODEN：
IJHEEY
Document type：
Article
Article type：
原著論文
Country of issue：
Germany, Federal Republic of (DEU)
Language：
ENGLISH (EN)
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Semi thesaurus term：
Thesaurus term/Semi thesaurus term
Keywords indexed to the article.
All keywords is available on JDreamIII(charged).
On J-GLOBAL, this item will be available after more than half a year after the record posted. In addtion, medical articles require to login to MyJ-GLOBAL.
JST classification (2)：
JST classification
Category name(code) classified by JST.
Hematologic diseases
, Congenital diseases,deformities in general.
Reference (26)：
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SCHULMAN, I. Studies on thrombopoiesis. I. A factor in normal human plasma required for platelet production; chronic thrombocytopenia due to its deficiency. Blood. 1960, 14, 943-957
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UPSHAW, J. D. Congenital deficiency of a factor in normal plasma that reverses microangiopathic hemolysis and thrombocytopenia. N Engl J Med. 1978, 298, 1350-1352
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RENNARD, S. Decreased cold-insoluble globulin in congenital thrombocytopenia (Upshaw-Schulman syndrome). N Engl J Med. 1979, 300, 368
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KOIZUMI, S. Upshaw-Schulman syndrome and fibronectin (cold-insoluble globulin). N Engl J Med. 1981, 305, 1284-1285
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GOODNOUGH, L. T. Fibronectin levels in congenital thrombocytopenia: Schulman's syndrome. N Engl J Med. 1982, 306, 938-939
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