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Volumn 181, Issue , 2013, Pages 185-193

C3 glomerulopathy

Author keywords

[No Author keywords available]

Indexed keywords

COMPLEMENT COMPONENT C3; IMMUNOSUPPRESSIVE AGENT;

EID: 84958675582     PISSN: 03025144     EISSN: None     Source Type: Book Series    
DOI: 10.1159/000348654     Document Type: Article
Times cited : (29)

References (32)
  • 1
    • 34249112293 scopus 로고    scopus 로고
    • Dense deposit disease is not a membranoproliferative glomerulonephritis
    • DOI 10.1038/modpathol.3800773, PII 3800773
    • Walker PD, Ferrario F, Joh K, et al: Dense deposit disease is not a membranoprolifera-tive glomerulonephritis. Mod Pathol 2007; 20: 605-616. (Pubitemid 46788867)
    • (2007) Modern Pathology , vol.20 , Issue.6 , pp. 605-616
    • Walker, P.D.1    Ferrario, F.2    Joh, K.3    Bonsib, S.M.4
  • 3
    • 84864554927 scopus 로고    scopus 로고
    • Acquired and genetic complement abnormalities play a critical role in dense deposit disease and other C3 glomerulopathies
    • Servais A, Noel L-H, Roumenina LT, et al: Acquired and genetic complement abnormalities play a critical role in dense deposit disease and other C3 glomerulopathies. Kidney Int 2012; 82:454-464.
    • (2012) Kidney Int , vol.82 , pp. 454-464
    • Servais, A.1    Noel, L.-H.2    Roumenina, L.T.3
  • 4
    • 0016142804 scopus 로고
    • Complement deposition in the kidney
    • Hamburger J, Crosnier J, Maxwell MH (eds) Chicago, Year Book Medical Publishers
    • Berger J, Noel L-H, Yaneva H: Complement deposition in the kidney; in Hamburger J, Crosnier J, Maxwell MH (eds): Advances in Nephrology. Chicago, Year Book Medical Publishers, 1974, vol 4, pp 37-48.
    • (1974) Advances in Nephrology , vol.4 , pp. 37-48
    • Berger, J.1    Noel, L.-H.2    Yaneva, H.3
  • 5
    • 79957858528 scopus 로고    scopus 로고
    • Prolif-erative glomerulonephritis secondary to dysfunction of the alternative pathway of complement
    • Sethi S, Fervenza FC, Zhang Y, et al: Prolif-erative glomerulonephritis secondary to dysfunction of the alternative pathway of complement. Clin J Am Soc Nephrol 2011; 6: 1009-1017.
    • (2011) Clin J Am Soc Nephrol , vol.6 , pp. 1009-1017
    • Sethi, S.1    Fervenza, F.C.2    Zhang, Y.3
  • 6
    • 84863512960 scopus 로고    scopus 로고
    • Pathology after eculizumab in dense deposit disease and C3 GN
    • Herlitz LC, Bomback AS, Markowitz GS, et al: Pathology after eculizumab in dense deposit disease and C3 GN. J Am Soc Nephrol 2012; 23:1229-1237.
    • (2012) J Am Soc Nephrol , vol.23 , pp. 1229-1237
    • Herlitz, L.C.1    Bomback, A.S.2    Markowitz, G.S.3
  • 8
    • 84864564017 scopus 로고    scopus 로고
    • C3 glo-merulonephritis: Clinicopathological findings, complement abnormalities, glomerular pro-teomic profile, treatment, and follow-up
    • Sethi S, Fervenza FC, Zhang Y, et al: C3 glo-merulonephritis: clinicopathological findings, complement abnormalities, glomerular pro-teomic profile, treatment, and follow-up. Kidney Int 2012; 82:465-473.
    • (2012) Kidney Int , vol.82 , pp. 465-473
    • Sethi, S.1    Fervenza, F.C.2    Zhang, Y.3
  • 9
    • 84863115476 scopus 로고    scopus 로고
    • Causes of alternative pathway dysregulation in dense deposit disease
    • Zhang Y, Meyer NC, Wang K, et al: Causes of alternative pathway dysregulation in dense deposit disease. Clin J Am Soc Nephrol 2012; 7:265-274.
    • (2012) Clin J Am Soc Nephrol , vol.7 , pp. 265-274
    • Zhang, Y.1    Meyer, N.C.2    Wang, K.3
  • 10
    • 64049119966 scopus 로고    scopus 로고
    • Dense deposit disease: Clinicopathologic study of 32 pediatric and adult patients
    • Nasr SH, Valeri AM, Appel GB, et al: Dense deposit disease: clinicopathologic study of 32 pediatric and adult patients. Clin J Am Soc Nephrol 2009; 4:22-32.
    • (2009) Clin J Am Soc Nephrol , vol.4 , pp. 22-32
    • Nasr, S.H.1    Valeri, A.M.2    Appel, G.B.3
  • 11
    • 31544450767 scopus 로고    scopus 로고
    • Severity of primary MPGN, rather than MPGN type, determines renal survival and post-transplantation recurrence risk
    • DOI 10.1038/sj.ki.5000084, PII 5000084
    • Little MA, Dupont P, Campbell E, et al: Severity of primary MPGN, rather than MPGN type, determines renal survival and posttransplantation recurrence risk. Kidney Int 2006; 69:504-511. (Pubitemid 43164442)
    • (2006) Kidney International , vol.69 , Issue.3 , pp. 504-511
    • Little, M.A.1    Dupont, P.2    Campbell, E.3    Dorman, A.4    Walshe, J.J.5
  • 12
    • 84862301748 scopus 로고    scopus 로고
    • Factor H autoantibodies in membranoprolif-erative glomerulonephritis
    • Goodship TH, Pappworth IY, Toth T, et al: Factor H autoantibodies in membranoprolif-erative glomerulonephritis. Mol Immunol 2012; 52:200-206.
    • (2012) Mol Immunol , vol.52 , pp. 200-206
    • Goodship, T.H.1    Pappworth, I.Y.2    Toth, T.3
  • 13
    • 77950628002 scopus 로고    scopus 로고
    • Antifactor B autoantibody in dense deposit disease
    • Strobel S, Zimmering M, Papp K, et al: Antifactor B autoantibody in dense deposit disease. Mol Immunol 2010; 47:1476-1483.
    • (2010) Mol Immunol , vol.47 , pp. 1476-1483
    • Strobel, S.1    Zimmering, M.2    Papp, K.3
  • 14
    • 84855161508 scopus 로고    scopus 로고
    • Combined C3b and factor B autoantibodies and MPGN type II
    • Chen Q, Muller D, Rudolph B, et al: Combined C3b and factor B autoantibodies and MPGN type II. N Engl J Med 2011; 365:2340-2342.
    • (2011) N Engl J Med , vol.365 , pp. 2340-2342
    • Chen, Q.1    Muller, D.2    Rudolph, B.3
  • 15
    • 79958793824 scopus 로고    scopus 로고
    • Heterogeneous pattern of renal disease associated with homozygous factor H deficiency
    • Servais A, Noel L-H, Dragon-Durey MA, et al: Heterogeneous pattern of renal disease associated with homozygous factor H deficiency. Hum Pathol 2011; 42:1305-1311.
    • (2011) Hum Pathol , vol.42 , pp. 1305-1311
    • Servais, A.1    Noel, L.-H.2    Dragon-Durey, M.A.3
  • 16
    • 77957827919 scopus 로고    scopus 로고
    • Human C3 mutation reveals a mechanism of dense deposit disease patho-genesis and provides insights into complement activation and regulation
    • Martinez-Barricarte R, Heurich M, Valdes-Canedo F, et al: Human C3 mutation reveals a mechanism of dense deposit disease patho-genesis and provides insights into complement activation and regulation. J Clin Invest 2010; 120:3702-3712.
    • (2010) J Clin Invest , vol.120 , pp. 3702-3712
    • Martinez-Barricarte, R.1    Heurich, M.2    Valdes-Canedo, F.3
  • 17
    • 41849110155 scopus 로고    scopus 로고
    • Genetic deficiency of complement factor H in a patient with age-related macular degeneration and membranoproliferative glomerulo-nephritis
    • Montes T, de Jorge EG, Ramos R, et al: Genetic deficiency of complement factor H in a patient with age-related macular degeneration and membranoproliferative glomerulo-nephritis. Mol Immunol 2008; 45:2897-2904.
    • (2008) Mol Immunol , vol.45 , pp. 2897-2904
    • Montes, T.1    De Jorge, E.G.2    Ramos, R.3
  • 19
    • 84860779074 scopus 로고    scopus 로고
    • Ecu-lizumab for dense deposit disease and C3 glo-merulonephritis
    • Bomback AS, Smith RJ, Barile GR, et al: Ecu-lizumab for dense deposit disease and C3 glo-merulonephritis. Clin J Am Soc Nephrol 2012; 7:748-756.
    • (2012) Clin J Am Soc Nephrol , vol.7 , pp. 748-756
    • Bomback, A.S.1    Smith, R.J.2    Barile, G.R.3
  • 20
    • 0028952777 scopus 로고
    • Hereditary porcine membranoproliferative glo-merulonephritis type II is caused by factor H deficiency
    • Hogasen K, Jansen JH, Mollnes TE, et al: Hereditary porcine membranoproliferative glo-merulonephritis type II is caused by factor H deficiency. J Clin Invest 1995; 95:1054-1061.
    • (1995) J Clin Invest , vol.95 , pp. 1054-1061
    • Hogasen, K.1    Jansen, J.H.2    Mollnes, T.E.3
  • 21
    • 0036699540 scopus 로고    scopus 로고
    • Uncontrolled C3 activation causes membranoproliferative glomerulonephritis in mice deficient in complement factor H
    • DOI 10.1038/ng912
    • Pickering MC, Cook HT, Warren J, et al: Uncontrolled C3 activation causes membranop-roliferative glomerulonephritis in mice deficient in complement factor H. Nat Genet 2002; 31:424-428. (Pubitemid 35154455)
    • (2002) Nature Genetics , vol.31 , Issue.4 , pp. 424-428
    • Pickering, M.C.1    Cook, H.T.2    Warren, J.3    Bygrave, A.E.4    Moss, J.5    Walport, M.J.6    Botto, M.7
  • 22
    • 67349180237 scopus 로고    scopus 로고
    • C3 deposition glomerulopathy due to a functional factor H defect
    • Habbig S, Mihatsch MJ, Heinen S, et al: C3 deposition glomerulopathy due to a functional factor H defect. Kidney Int 2009; 75:1230-1234.
    • (2009) Kidney Int , vol.75 , pp. 1230-1234
    • Habbig, S.1    Mihatsch, M.J.2    Heinen, S.3
  • 23
    • 79952280131 scopus 로고    scopus 로고
    • Complement factor H deficiency and endo-capillary glomerulonephritis due to paternal isodisomy and a novel factor H mutation
    • Schejbel L, Schmidt IM, Kirchhoff M, et al: Complement factor H deficiency and endo-capillary glomerulonephritis due to paternal isodisomy and a novel factor H mutation. Genes Immun 2011; 12:90-99.
    • (2011) Genes Immun , vol.12 , pp. 90-99
    • Schejbel, L.1    Schmidt, I.M.2    Kirchhoff, M.3
  • 24
    • 33847237272 scopus 로고    scopus 로고
    • The interactive factor H-atypical hemolytic uremic syndrome mutation database and website: Update and integration of membrane cofactor protein and factor i mutations with structural models
    • Saunders RE, Abarrategui-Garrido C, Fre-meaux-Bacchi V, et al: The interactive factor H-atypical hemolytic uremic syndrome mutation database and website: update and integration of membrane cofactor protein and factor I mutations with structural models. Hum Mutat 2007; 28:222-234.
    • (2007) Hum Mutat , vol.28 , pp. 222-234
    • Saunders, R.E.1    Abarrategui-Garrido, C.2    Fre-Meaux-Bacchi, V.3
  • 25
    • 74249114451 scopus 로고    scopus 로고
    • Mutations in complement factor i as found in atypical hemolytic uremic syndrome lead to either altered secretion or altered function of factor i
    • Nilsson SC, Kalchishkova N, Trouw LA, et al: Mutations in complement factor I as found in atypical hemolytic uremic syndrome lead to either altered secretion or altered function of factor I. Eur J Immunol 2010; 40:172-185.
    • (2010) Eur J Immunol , vol.40 , pp. 172-185
    • Nilsson, S.C.1    Kalchishkova, N.2    Trouw, L.A.3
  • 26
    • 77956394517 scopus 로고    scopus 로고
    • Identification of a mutation in complement factor H-related protein 5 in patients of Cypriot origin with glomerulonephritis
    • Gale DP, de Jorge EG, Cook HT, et al: Identification of a mutation in complement factor H-related protein 5 in patients of Cypriot origin with glomerulonephritis. Lancet 2010; 376:794-801.
    • (2010) Lancet , vol.376 , pp. 794-801
    • Gale, D.P.1    De Jorge, E.G.2    Cook, H.T.3
  • 27
    • 84863511490 scopus 로고    scopus 로고
    • A hybrid CFHR3-1 gene causes familial C3 glo-merulopathy
    • Malik TH, Lavin PJ, de Jorge EG, et al: A hybrid CFHR3-1 gene causes familial C3 glo-merulopathy. J Am Soc Nephrol 2012; 23: 1122.
    • (2012) J Am Soc Nephrol , vol.23 , pp. 1122
    • Malik, T.H.1    Lavin, P.J.2    De Jorge, E.G.3
  • 29
    • 79957858528 scopus 로고    scopus 로고
    • Prolif-erative glomerulonephritis secondary to dysfunction of the alternative pathway of complement
    • Sethi S, Fervenza FC, Zhang Y, et al: Prolif-erative glomerulonephritis secondary to dysfunction of the alternative pathway of complement. Clin J Am Soc Nephrol 2011; 5: 1009-1017.
    • (2011) Clin J Am Soc Nephrol , vol.5 , pp. 1009-1017
    • Sethi, S.1    Fervenza, F.C.2    Zhang, Y.3
  • 31
    • 78751637542 scopus 로고    scopus 로고
    • Allograft failure in kidney transplant recipients with membranoproliferative glomerulonephritis
    • Angelo JR, Bell CS, Braun MC: Allograft failure in kidney transplant recipients with membranoproliferative glomerulonephritis. Am J Kidney Dis 2012; 57:291-299.
    • (2012) Am J Kidney Dis , vol.57 , pp. 291-299
    • Angelo, J.R.1    Bell, C.S.2    Braun, M.C.3
  • 32
    • 84867993256 scopus 로고    scopus 로고
    • Use of eculizumab for atypical haemolytic uraemic syndrome and C3 glomerulopathies
    • Zuber J, Fakhouri F, Roumenina LT, et al: Use of eculizumab for atypical haemolytic uraemic syndrome and C3 glomerulopathies. Nat Rev Nephrol 2012; 8:643-657.
    • (2012) Nat Rev Nephrol , vol.8 , pp. 643-657
    • Zuber, J.1    Fakhouri, F.2    Roumenina, L.T.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.