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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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| Vydáno v: | Hematology Am Soc Hematol Educ Program |
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| Hlavní autor: | |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
2015
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| Témata: | |
| On-line přístup: | 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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