Purpura, thrombotic thrombocytopenic

Results 191 to 200 of about 36,176 (202)

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The Journal of Pediatrics, 1962
Summary Thrombotic thrombocytopenic purpura is a relatively uncommon clinical syndrome characterized by thrombocytopenia, hemolytic anemia, and neurologic abnormalities. The case presented followed an infection with rubeola. The patient had a complete remission for 6 months.
Mildred Schaffhausen, William Krivit, Kenneth F. Swaiman +2 more
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Thrombotic thrombocytopenic purpura

JAAPA, 2021
Lauren Collin, Zachary Lavender
openaire +3 more sources

Thrombotic Thrombocytopenic Purpura

2009
Thrombotic thrombocytopenic purpura (TTP) is a thrombotic microangiopathy that leads to microangiopathic hemolytic anemia and thrombocytopenia. Idiopathic TTP results from autoantibodies binding to ADAMTS13, an enzyme that cleaves high-molecular weight von Willebrand factor (vWF) multimers.
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Human medicines European public assessment report (EPAR): Cablivi, caplacizumab, Purpura, Thrombotic Thrombocytopenic, Date of authorisation: 30/08/2018, Revision: 2, Status: Authorised

Case Medical Research, 2019

semanticscholar +1 more source

Purpura, Thrombotic Thrombocytopenic (TTP)

, 2011
E. Pivalizza, Omonele O. Nwokolo
semanticscholar +1 more source

Thrombotic thrombocytopenic purpura