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Volumn 19, Issue 3, 2004, Pages 727-730

Factor H deficiency and fibrillary glomerulopathy

Author keywords

Cyclosporine A; Factor H; Fibrillary glomerulopathy; Nephrotic proteinuria

Indexed keywords

ATENOLOL; CHOLESTEROL; COMPLEMENT FACTOR H; CYCLOPHOSPHAMIDE; CYCLOSPORIN A; ENALAPRIL; METHYLPREDNISOLONE; NIFEDIPINE; PREDNISOLONE; PREDNISONE;

EID: 1342263687     PISSN: 09310509     EISSN: None     Source Type: Journal    
DOI: 10.1093/ndt/gfg605     Document Type: Article
Times cited : (15)

References (11)
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    • Ault BH. Factor H and the pathogenesis of renal diseases. Pediatr Nephrol 2000; 14: 1045-1053
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    • Ault, B.H.1
  • 3
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    • Familial relapsing haemolytic uraemic syndrome and complement factor H deficiency
    • Warwicker P, Donne RL, Goodship JA et al. Familial relapsing haemolytic uraemic syndrome and complement factor H deficiency. Nephrol Dial Transplant 1999; 14: 1229-1233
    • (1999) Nephrol. Dial. Transplant. , vol.14 , pp. 1229-1233
    • Warwicker, P.1    Donne, R.L.2    Goodship, J.A.3
  • 4
    • 0031693194 scopus 로고    scopus 로고
    • Hypocomplementemic autosomal recessive hemolytic uremic syndrome with decreased factor H
    • Ohali M, Shalev H, Schlesinger M et al. Hypocomplementemic autosomal recessive hemolytic uremic syndrome with decreased factor H. Pediatr Nephrol 1998; 12: 619-624
    • (1998) Pediatr. Nephrol. , vol.12 , pp. 619-624
    • Ohali, M.1    Shalev, H.2    Schlesinger, M.3
  • 5
    • 0035143299 scopus 로고    scopus 로고
    • The molecular basis of familial hemolytic uremic syndrome: Mutation analysis of factor H gene reveals a hot spot in short consensus repeat 20
    • and the Italian Registry of Familial and Recurrent HUS/TTP
    • Caprioli J, Bettinaglio P, Zipfel PF et al. and the Italian Registry of Familial and Recurrent HUS/TTP. The molecular basis of familial hemolytic uremic syndrome: mutation analysis of factor H gene reveals a hot spot in short consensus repeat 20. J Am Soc Nephrol 2001; 12: 297-307
    • (2001) J. Am. Soc. Nephrol. , vol.12 , pp. 297-307
    • Caprioli, J.1    Bettinaglio, P.2    Zipfel, P.F.3
  • 6
    • 0022904646 scopus 로고
    • Factor H deficiency in two brothers with atypical dense intramembranous deposit disease
    • Levy M, Halbwachs-Mecarelli L, Gubler MC et al. Factor H deficiency in two brothers with atypical dense intramembranous deposit disease. Kidney Int 1986; 30: 949-956
    • (1986) Kidney Int. , vol.30 , pp. 949-956
    • Levy, M.1    Halbwachs-Mecarelli, L.2    Gubler, M.C.3
  • 9
    • 0032986645 scopus 로고    scopus 로고
    • Long term effects of cyclosporine A in Alport's syndrome
    • Callis L, Vila A, Carrera M, Nieto J. Long term effects of cyclosporine A in Alport's syndrome. Kidney Int 1999; 55: 1051-1056
    • (1999) Kidney Int. , vol.55 , pp. 1051-1056
    • Callis, L.1    Vila, A.2    Carrera, M.3    Nieto, J.4
  • 10
    • 0347418134 scopus 로고    scopus 로고
    • Cyclosporine A slows the progressive renal disease of Alport Syndrome (X-Linked Hereditary Nephritis): Results of a canine model
    • Chen D, Jefferson B, Harvey SC et al. Cyclosporine A slows the progressive renal disease of Alport Syndrome (X-Linked Hereditary Nephritis): results of a canine model. J Am Soc Nephrol 2003; 14: 690-698
    • (2003) J. Am. Soc. Nephrol. , vol.14 , pp. 690-698
    • Chen, D.1    Jefferson, B.2    Harvey, S.C.3
  • 11
    • 0036699540 scopus 로고    scopus 로고
    • Uncontrolled C3 activation causes membranoproliferative glomerulonephritis in mice deficient in complement factor H
    • Pickering MC, Cook HT, Warren J et al. Uncontrolled C3 activation causes membranoproliferative glomerulonephritis in mice deficient in complement factor H. Nature Genet 2002; 31: 424-428
    • (2002) Nature Genet. , vol.31 , pp. 424-428
    • Pickering, M.C.1    Cook, H.T.2    Warren, J.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.