Podocyte dysfunction in atypical haemolytic uraemic syndrome
Author:
Publisher
Springer Science and Business Media LLC
Subject
Nephrology
Link
http://www.nature.com/articles/nrneph.2014.250.pdf
Reference106 articles.
1. Noris, M. & Remuzzi, G. Atypical hemolytic-uremic syndrome. N. Engl. J. Med. 361, 1676–1687 (2009).
2. Mele, C., Remuzzi, G. & Noris, M. Hemolytic uremic syndrome. Semin. Immunopathol. 36, 399–420 (2014).
3. Valoti, E. et al. A novel atypical hemolytic uremic syndrome-associated hybrid CFHR1/CFH gene encoding a fusion protein that antagonizes factor H-dependent complement regulation. J. Am. Soc. Nephrol. http://dx.doi.org/10.1681/ASN.2013121339 .
4. Dragon-Durey, M. A. et al. Anti-Factor H autoantibodies associated with atypical hemolytic uremic syndrome. J. Am. Soc. Nephrol. 16, 555–563 (2005).
5. Noris, M., Mescia, F. & Remuzzi, G. STEC-HUS, atypical HUS and TTP are all diseases of complement activation. Nat. Rev. Nephrol. 8, 622–633 (2012).
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