The global aHUS registry: methodology and initial patient characteristics

Atypical hemolytic uremic syndrome (aHUS) is a rare, genetically-mediated systemic disease most often caused by chronic, uncontrolled complement activation that leads to systemic thrombotic microangiopathy (TMA) and renal and other end-organ damage.

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Bibliographische Detailangaben
Hauptverfasser: Licht, Christoph (VerfasserIn) , Ardissino, Gianluigi (VerfasserIn) , Ariceta, Gema (VerfasserIn) , Cohen, David (VerfasserIn) , Cole, J. Alexander (VerfasserIn) , Gasteyger, Christoph (VerfasserIn) , Greenbaum, Larry A. (VerfasserIn) , Johnson, Sally (VerfasserIn) , Ogawa, Masayo (VerfasserIn) , Schaefer, Franz (VerfasserIn) , Vande Walle, Johan (VerfasserIn) , Frémeaux-Bacchi, Véronique (VerfasserIn)
Dokumenttyp: Article (Journal)
Sprache:Englisch
Veröffentlicht: 10 December 2015
In: BMC nephrology
Year: 2015, Jahrgang: 16, Pages: 1-8
ISSN:1471-2369
DOI:10.1186/s12882-015-0195-1
Online-Zugang:Resolving-System, lizenzpflichtig, Volltext: https://doi.org/10.1186/s12882-015-0195-1
Verlag, lizenzpflichtig, Volltext: https://bmcnephrol.biomedcentral.com/articles/10.1186/s12882-015-0195-1
Volltext
Verfasserangaben:Christoph Licht, Gianluigi Ardissino, Gema Ariceta, David Cohen, J. Alexander Cole, Christoph Gasteyger, Larry A. Greenbaum, Sally Johnson, Masayo Ogawa, Franz Schaefer, Johan Vande Walle and Véronique Frémeaux-Bacchi

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