Atypical hemolytic uremic syndrome: a syndrome in need of clarity

Atypical hemolytic uremic syndrome (aHUS) is a thrombotic microangiopathy (TMA) originally understood to be limited to renal and hematopoietic involvement. Whereas aberrations in complement regulatory proteins (CRPs), C3 or complement factor B (CFB) are detected in ∼60% of patients, a complement-der...

Descripción completa

Detalles Bibliográficos
Autor principal: Berger, Bruce E
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2018
Materias:
Thrombotic Microangiopathies
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6543964/
https://www.ncbi.nlm.nih.gov/pubmed/31198222
http://dx.doi.org/10.1093/ckj/sfy066

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6543964/
https://www.ncbi.nlm.nih.gov/pubmed/31198222
http://dx.doi.org/10.1093/ckj/sfy066

Ejemplares similares