1Zhang T, Lu J, Liang S, et al. Comprehensive analysis of complement genes in patients with atypical hemolytic uremic syndrome [ J ]. Am J Nephro1,2016,43 ( 3 ) : 160 - 169. DOI : 10.1159/000445127.
2Loirat C, Fr6meaux-Bacchi V. Anti-factor H autoantibody-associated he- molytic uremic syndrome:the earlier diagnosed and treated, the better [J]. Kidney Int,2014,85 (5) : 1019 - 1022. DOI: 10. 1038/ki. 2013. 447.
3Ariceta G, Besbas N, Johnson S, et al. Guideline for the investigation and initial therapy of diarrhea-negative hemolytic uremic syndrome [ J ]. Pediatr Nephrol,2009,24 (4) :687 - 696. DOI: 10. 1007/s00467-008- 0964-1.
4Loirat C, Noris M, Fremeaux-Bacehi V. Complement and the atypical he- molytic uremic syndrome in children [ J ]. Pediatr Nephrol, 2008,23 ( 11 ) : 1957 - 1972. DOI : 10. 1007/s00467-008-0872-4.
5Bhattacharjee A, Lehtinen MJ, Kajander T, et al. Both domain 19 and domain 20 of factor H are involved in binding to complement C3b and C3d [ J ]. Mol Immunol, 2010,47 ( 9 ) : 1686 - 1691. DOI : 10. 1016/j.molimm. 2010.03. 007.
6Bhattacharjee A, Pteuter S, Trojnar E, et al. The major autoantibody epitope on factor H in atypical hemolytic uremic syndrome is structurally different from its homologous site in factor H-related protein 1, suppor- ting a novel model for induction of autoimmunity in this disease [ J ]. J Biol Chem,2015,290 ( 15 ) :9500 - 9510. DOI: 10. 1074/jbc. M114. 630871.
7Sansbury FH, Cordell H J, Bingham C, et al. Factors determining pene- trance in familial atypical haemolytic uraemie syndrome [ J ]. J Med Genet,2014, 51 ( 11 ) : 756 - 764. DOI: 10. 1136/jmedgenet-2014- 102498.
8Lee JM, Park YS, Lee JH, et al. Atypical hemolytic uremic syndrome : Korean pediatric series [ J ]. Pediatr Int, 2015,57 ( 3 ) : 431 - 438. DOI : 10.1111/ped. 12549.
9Vieira-Martins P, E1 Sissy 12, Bordereau P, et al. Defining the genetics of thrombotic mieroangiopathies [ J ]. Transfus Apher Sci, 2016,54 ( 2 ) : 212 - 219. DOI : 10. 1016/j. transei. 2016.04.011.
10Valoti E, Alberti M, Tortajada A, et al. A novel atypical hemolytic ure- mic syndrome-associated hybrid CFHR1/CFH gene encoding a fusion protein that antagonizes factor H-dependent complement regulation [ J]. J Am Soc Nephrol, 2015,26 ( 1 ) : 209 - 219. DOI : 10. 1681/ ASN. 2013121339.
