1Caprioli J, Castclletti F, Bucchioni S,et al. Complement factor H mutations and gene polymorphisms in haemolytic uraemic syndrome:The C - 257T,the A2089G and the G2881T polymorphisms are strongly associated with the disease[J]. Hum Mol Genet,2003,12(24) :3385 -3395.
2Dragon - Durey MA, Fremeaux - Bacchi V, Loirat C, et al. Heterozygous and homozygoas factor h deficiencies associated with hemolytic uremic syndrome or membranoproliferative glomerulonephrit s : Report and genetic analysis of 16 cases [ J ]. J Am Soc Nephro1,2004,15 ( 3 ) :787 - 795.
3Roy V, Rizvi MA, Vesely SK, et al. Thrombotic thrombocytopenic purpura - like syndromes following bone marrow transplantation : An analysis of associated conditions and clinical outcomes [ J ]. Bone Marrow Transplant, 2001,27 ( 6 ) : 641 - 646.
4Ruggenerlti P, Noris M, Remuzzi G. Thrombotic microangiopathy, hemolytic uremic syndrome, and thrombotic thrombocytopenic purpura [ J ]. Kidney lnt,2001,60 ( 3 ) : 831 - 846.
5Tarr PI, Gordon CA, Chahdler WL. Shiga - toxin - producing Escherichia coil and haemolytic uraemic syndrome [ J ]. Lancet, 2005,365 ( 9464 ) : 1073 - 1086.
6Gianviti A ,Tozzi AE, de Petris L, et al. Risk factors for poor renal prognosis in children with hemolytic hi'emic syndrome [ J ]. Pediatr Nephrol, 2003,18(12) :1229 - 1235.
7Rock G. The nmnagement of thrombotic thrombocytopenic purpura in 20(15 [ J ]. Semin Thromb He most,2005,31 ( 6 ) : 709 - 716.
8Wong CS, Jelacic S, Habeeb RL,et al. The risk of the hemolytic - uremic syndrome after antibiotic treatment of Escherlchia coli 0157 : H7 infections [ J ]. N Engl J Med,2000 ,342 (26) :1930 - 1936.
9Safdar N, Said A, Gangnon RE, et al. Risk of hemolytic uremic syndrome after antibiotic treatment of Escherichia coli 0157:H7 enteritis :A meta- analysis [ J ].JAMA.2002.288 ( 8 } :996 - 1001.
10Panos GZ, Betsi GI, Falagas ME. Systematic review:Are antibiotics detrimental or beneficial for the treatment of patients with Escheriehia coli O157 : H7 infection [ J ] . Aliment Pharmacol Ther, 2006,24 ( 5 ) : 731 - 742.
