PubMed for id: 889445

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Year	Number of Results
2005	1
2010	1
2013	2
2014	1
2015	1
2023	0

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Page 1

Novel factor H mutation associated with familial membranoproliferative glomerulonephritis type I.

Alfandary H, Davidovits M. Alfandary H, et al. Pediatr Nephrol. 2015 Dec;30(12):2129-34. doi: 10.1007/s00467-015-3166-7. Epub 2015 Aug 20. Pediatr Nephrol. 2015. PMID: 26289290

A novel CFHR5 mutation associated with C3 glomerulonephritis in a Turkish girl.

Besbas N, Gulhan B, Gucer S, Korkmaz E, Ozaltin F. Besbas N, et al. J Nephrol. 2014 Aug;27(4):457-60. doi: 10.1007/s40620-013-0008-1. Epub 2013 Dec 5. J Nephrol. 2014. PMID: 24536001

Atypical haemolytic uraemic syndrome with underlying glomerulopathies. A case series and a review of the literature.

Manenti L, Gnappi E, Vaglio A, Allegri L, Noris M, Bresin E, Pilato FP, Valoti E, Pasquali S, Buzio C. Manenti L, et al. Nephrol Dial Transplant. 2013 Sep;28(9):2246-59. doi: 10.1093/ndt/gft220. Epub 2013 Jun 19. Nephrol Dial Transplant. 2013. PMID: 23787552 Review.

Pulse cyclophosphamide therapy and clinical remission in atypical hemolytic uremic syndrome with anti-complement factor H autoantibodies.

Boyer O, Balzamo E, Charbit M, Biebuyck-Gougé N, Salomon R, Dragon-Durey MA, Frémeaux-Bacchi V, Niaudet P. Boyer O, et al. Am J Kidney Dis. 2010 May;55(5):923-7. doi: 10.1053/j.ajkd.2009.12.026. Epub 2010 Mar 3. Am J Kidney Dis. 2010. PMID: 20202729

Late-onset thrombocytic microangiopathy caused by cblC disease: association with a factor H mutation.

Guigonis V, Frémeaux-Bacchi V, Giraudier S, Favier R, Borderie D, Massy Z, Mougenot B, Rosenblatt DS, Deschênes G. Guigonis V, et al. Am J Kidney Dis. 2005 Mar;45(3):588-95. doi: 10.1053/j.ajkd.2004.12.004. Am J Kidney Dis. 2005. PMID: 15754282

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