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Purpura, Thrombotic Thrombocytopenic
Known as:
Purpura, Thrombotic Thrombocytopenic [Disease/Finding]
, Disease, Moschkowitz
, Thrombopenic Purpura, Thrombotic
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An acquired, congenital, or familial disorder caused by PLATELET AGGREGATION with THROMBOSIS in terminal arterioles and capillaries. Clinical…
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National Institutes of Health
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Related topics
Related topics
20 relations
ADAMTS13 gene
Blood Vessel
Disseminated Intravascular Coagulation
Hematopoietic and Lymphoid Cell
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Narrower (4)
Congenital Thrombotic Thrombocytopenic Purpura
Familial Thrombotic Thrombocytopenic Purpura
Hemolytic-Uremic Syndrome
Thrombotic thrombocytopenic purpura, acquired
Broader (3)
Thrombotic Microangiopathies
Vascular Diseases
circulatory disorders
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Review
2008
Review
2008
Von Willebrand factor, ADAMTS13, and thrombotic thrombocytopenic purpura.
J. Sadler
Blood
2008
Corpus ID: 206868424
Discoveries during the past decade have revolutionized our understanding of idiopathic thrombotic thrombocytopenic purpura (TTP…
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Review
2005
Review
2005
Blood and marrow transplant clinical trials network toxicity committee consensus summary: thrombotic microangiopathy after hematopoietic stem cell transplantation.
V. Ho
,
C. Cutler
,
+6 authors
S. Giralt
Biology of Blood and Marrow Transplantation
2005
Corpus ID: 4768712
Review
2004
Review
2004
Recent advances in thrombotic thrombocytopenic purpura.
J. Sadler
,
J. Moake
,
T. Miyata
,
J. George
Hematology. American Society of Hematology…
2004
Corpus ID: 41637075
Thrombotic thrombocytopenic purpura (TTP) is characterized by microangiopathic hemolytic anemia and thrombocytopenia, accompanied…
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Highly Cited
2004
Highly Cited
2004
Epitope mapping of ADAMTS13 autoantibodies in acquired thrombotic thrombocytopenic purpura.
C. Klaus
,
B. Plaimauer
,
+4 authors
F. Scheiflinger
Blood
2004
Corpus ID: 1876981
Severe deficiency of the von Willebrand factor (VWF)-cleaving protease ADAMTS13 can lead to thrombotic thrombocytopenic purpura…
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Highly Cited
2003
Highly Cited
2003
Nonneutralizing IgM and IgG antibodies to von Willebrand factor-cleaving protease (ADAMTS-13) in a patient with thrombotic thrombocytopenic purpura.
F. Scheiflinger
,
P. Knöbl
,
+5 authors
M. Rieger
Blood
2003
Corpus ID: 26067421
Acquired thrombotic thrombocytopenic purpura (TTP) has been linked to severe deficiency of ADAMTS-13 activity caused by…
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Review
2003
Review
2003
Thrombotic thrombocytopenic purpura and hemolytic uremic syndrome are distinct pathologic entities. A review of 56 autopsy cases.
G. Hosler
,
A. Cusumano
,
G. Hutchins
Archives of Pathology & Laboratory Medicine
2003
Corpus ID: 26057298
CONTEXT Thrombotic thrombocytopenic purpura (TTP) and the hemolytic uremic syndrome (HUS) share many clinical features and have…
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Review
1991
Review
1991
Escherichia coli O157:H7 and its significance in foods.
M. P. Doyle
Journal of food microbiology
1991
Corpus ID: 4202806
Review
1988
Review
1988
Clinical and neuropathological findings in systemic lupus erythematosus: The role of vasculitis, heart emboli, and thrombotic thrombocytopenic purpura
O. Devinsky
,
C. Petito
,
D. Alonso
Annals of Neurology
1988
Corpus ID: 36272377
We reviewed the medical records and autopsy reports of 50 patients with systemic lupus erythematosus to determine the clinical…
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Highly Cited
1982
Highly Cited
1982
Autoimmune thrombocytopenic purpura in homosexual men.
L. Morris
,
A. Distenfeld
,
E. Amorosi
,
S. Karpatkin
Annals of Internal Medicine
1982
Corpus ID: 37780352
Since November 1980 we have diagnosed 11 cases of severe autoimmune thrombocytopenic purpura in homosexual men; their mean…
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Highly Cited
1977
Highly Cited
1977
Treatment of thrombotic thrombocytopenic purpura with plasma.
J. Byrnes
,
M. Khurana
New England Journal of Medicine
1977
Corpus ID: 23092616
Thrombotic thrombocytopenic purpura, the acute form of which is usually fatal, is characterized clinically by thrombocytopenia…
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