Advances in understanding of pathogenesis of aHUS and HELLP

Both atypical haemolytic uraemic syndrome (aHUS) and the HELLP syndrome (haemolytic anaemia, elevated liver enzymes, and low platelets) are thrombotic microangiopathies characterized by microvascular endothelial activation, cell injury and thrombosis. aHUS is a disease of complement dysregulation, s...

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Main Authors: Celia J. Fang, Anna Richards, M. Kathryn Liszewski, David Kavanagh, John P. Atkinson
格式: Revisão
语言:英语
出版: 2008
在线阅读:https://doi.org/10.1111/j.1365-2141.2008.07324.x
https://onlinelibrary.wiley.com/doi/pdfdirect/10.1111/j.1365-2141.2008.07324.x
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