The global aHUS registry: methodology and initial patient characteristics

BACKGROUND: 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. METHODS: The global aHUS Registry, ini...

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Detalles Bibliográficos
Autores principales: Licht, Christoph, Ardissino, Gianluigi, Ariceta, Gema, Cohen, David, Cole, J. Alexander, Gasteyger, Christoph, Greenbaum, Larry A., Johnson, Sally, Ogawa, Masayo, Schaefer, Franz, Vande Walle, Johan, Frémeaux-Bacchi, Véronique
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4674928/
https://www.ncbi.nlm.nih.gov/pubmed/26654630
http://dx.doi.org/10.1186/s12882-015-0195-1

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4674928/
https://www.ncbi.nlm.nih.gov/pubmed/26654630
http://dx.doi.org/10.1186/s12882-015-0195-1

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