Results 171 to 180 of about 22,042 (204)
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Thrombotic Thrombocytopenic Purpura
Archives of Internal Medicine, 1966This SYNDROME was first described by Moschcowitz in 1925 1 as an acute, febrile pleomorphic anemia with hyaline thrombosis of terminal arterioles and capillaries. Since then over 150 cases have been described. The predominant features are thrombocytopenia, hemolytic anemia, transient mental and focal neurological phenomena, pyrexia, and a variable ...
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Integrative oncology: Addressing the global challenges of cancer prevention and treatment
Ca-A Cancer Journal for Clinicians, 2022Jun J Mao,, Msce +2 more
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Thrombotic thrombocytopenic purpura
The Hematology Journal, 2004Bernhard, Lämmle +4 more
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Thrombotic Thrombocytopenic Purpura
2009Thrombotic 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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Hereditary Thrombotic Thrombocytopenic Purpura
New England Journal of Medicine, 2020Yahsou, Delmas +2 more
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Duodenal Thrombotic Thrombocytopenic Purpura
Clinical Gastroenterology and Hepatology, 2007David J, Owens, Barbara, Jung
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Multidisciplinary standards of care and recent progress in pancreatic ductal adenocarcinoma
Ca-A Cancer Journal for Clinicians, 2020Aaron J Grossberg +2 more
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Thrombotic Thrombocytopenic Purpura-2005
Seminars in Thrombosis and Hemostasis, 2005Hau C, Kwaan, Charles L, Bennett
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