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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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Opis bibliograficzny
Wydane w:Blood Res
Główni autorzy: Oh, Jisu, Oh, Doyeun, Lee, Seon Ju, Kim, Jeong Oh, Kim, Nam Keun, Chong, So Young, Huh, Ji Young, Baker, Ross I.
Format: Artigo
Język:Inglês
Wydane: Korean Society of Hematology; Korean Society of Blood and Marrow Transplantation; Korean Society of Pediatric Hematology-Oncology; Korean Society on Thrombosis and Hemostasis 2019
Hasła przedmiotowe:
Dostęp online: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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