Prognostic utility of ADAMTS13 activity for the atypical hemolytic uremic syndrome (aHUS) and comparison of complement serology between aHUS and thrombotic thrombocytopenic purpura

BACKGROUND: Atypical hemolytic uremic syndrome (aHUS) involves dysregulation of the complement system, but whether this also occurs in thrombotic thrombocytopenic purpura (TTP) remains unclear. Although these conditions are difficult to differentiate clinically, TTP can be distinguished by low (<...

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Vydáno v:Blood Res
Hlavní autoři: Oh, Jisu, Oh, Doyeun, Lee, Seon Ju, Kim, Jeong Oh, Kim, Nam Keun, Chong, So Young, Huh, Ji Young, Baker, Ross I.
Médium: Artigo
Jazyk:Inglês
Vydáno: Korean Society of Hematology; Korean Society of Blood and Marrow Transplantation; Korean Society of Pediatric Hematology-Oncology; Korean Society on Thrombosis and Hemostasis 2019
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Original Article
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC6779945/
https://ncbi.nlm.nih.gov/pubmed/31730685
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.5045/br.2019.54.3.218
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