Atypical hemolytic uremic syndrome and genetic aberrations in the complement factor H-related 5 gene-Reference-Cited by-同舟云学术

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Atypical hemolytic uremic syndrome and genetic aberrations in the complement factor H-related 5 gene

Published:2012-05-24 Issue:7 Volume:57 Page:459-464
ISSN:1434-5161
Container-title:Journal of Human Genetics
language:en
Short-container-title:J Hum Genet

Author:

Westra Dineke,Vernon Katherine A,Volokhina Elena B,Pickering Matthew C,van de Kar Nicole C A J,van den Heuvel Lambert P

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Genetics

Link

http://www.nature.com/articles/jhg201257.pdf

Reference24 articles.

1. Boyce, T. G., Swerdlow, D. L., Griffin, P. M. Escherichia coli O157:H7 and the hemolytic-uremic syndrome. N. Engl. J. Med. 333, 364–368 (1995).

2. Kaplan, B. S., Meyers, K. E., Schulman, S. L. The pathogenesis and treatment of hemolytic uremic syndrome. J. Am. Soc. Nephrol. 9, 1126–1133 (1998).

3. Noris, M., Brioschi, S., Caprioli, J., Todeschini, M., Bresin, E., Porrati, F. et al. Familial haemolytic uraemic syndrome and an MCP mutation. Lancet 362, 1542–1547 (2003).

4. Caprioli, J., Noris, M., Brioschi, S., Pianetti, G., Castelletti, F., Bettinaglio, P. et al. Genetics of HUS: the impact of MCP, CFH, and IF mutations on clinical presentation, response to treatment, and outcome. Blood 108, 1267–1279 (2006).

5. Fremeaux-Bacchi, V., Dragon-Durey, M. A., Blouin, J., Vigneau, C., Kuypers, D., Boudailliez, B. et al. Complement factor I: a susceptibility gene for atypical haemolytic uraemic syndrome. J. Med. Genet. 41, e84 (2004).

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