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What’s new in the diagnosis and pathophysiology of thrombotic thrombocytopenic purpura

Severe ADAMTS13 (a disintegrin and metalloproteinase with a thrombospondin type 1 motif, member 13) deficiency causes thrombotic thrombocytopenic purpura (TTP), which is characterized by microangiopathic hemolytic anemia, thrombocytopenia, and the absence of oliguric or anuric renal failure. However...

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Detalhes bibliográficos
Publicado no:Hematology Am Soc Hematol Educ Program
Autor principal: Sadler, J. Evan
Formato: Artigo
Idioma:Inglês
Publicado em: 2015
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4777280/
https://ncbi.nlm.nih.gov/pubmed/26637781
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1182/asheducation-2015.1.631
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