메뉴 건너뛰기




Volumn 5, Issue 10, 2010, Pages 1844-1859

Relative role of genetic complement abnormalities in sporadic and familial aHUS and their impact on clinical phenotype

Author keywords

[No Author keywords available]

Indexed keywords

COMPLEMENT FACTOR H; COMPLEMENT FACTOR I; MEMBRANE COFACTOR PROTEIN; THROMBOMODULIN;

EID: 77958587405     PISSN: 15559041     EISSN: 1555905X     Source Type: Journal    
DOI: 10.2215/CJN.02210310     Document Type: Article
Times cited : (813)

References (48)
  • 1
    • 0035722282 scopus 로고    scopus 로고
    • Thrombotic microangiopathy, hemolytic uremic syndrome, and thrombotic thrombocytopenic purpura
    • DOI 10.1046/j.1523-1755.2001.060003831.x
    • Ruggenenti P, Noris M, Remuzzi G: Thrombotic microangiopathy, hemolytic uremic syndrome, and thrombotic thrombocytopenic purpura. Kidney Int 60: 831-846, 2001 (Pubitemid 34205784)
    • (2001) Kidney International , vol.60 , Issue.3 , pp. 831-846
    • Ruggenenti, P.1    Noris, M.2    Remuzzi, G.3
  • 3
    • 51549116628 scopus 로고    scopus 로고
    • Treatment and outcome of Shiga-toxin-associated hemolytic uremic syndrome (HUS)
    • Scheiring J, Andreoli SP, Zimmerhackl LB: Treatment and outcome of Shiga-toxin-associated hemolytic uremic syndrome (HUS). Pediatr Nephrol 23: 1749-1760, 2008
    • (2008) Pediatr Nephrol , vol.23 , pp. 1749-1760
    • Scheiring, J.1    Andreoli, S.P.2    Zimmerhackl, L.B.3
  • 4
    • 70350279315 scopus 로고    scopus 로고
    • Atypical hemolytic-uremic syndrome
    • Noris M, Remuzzi G: Atypical hemolytic-uremic syndrome. N Engl J Med 361: 1676-1687, 2009
    • (2009) N Engl J Med , vol.361 , pp. 1676-1687
    • Noris, M.1    Remuzzi, G.2
  • 5
    • 37349077580 scopus 로고    scopus 로고
    • Update on evaluating complement in hemolytic uremic syndrome
    • DOI 10.1097/MNH.0b013e3282f0872f, PII 0004155220071100000013
    • Kavanagh D, Goodship TH: Update on evaluating complement in hemolytic uremic syndrome. Curr Opin Nephrol Hypertens 16: 565-571, 2007 (Pubitemid 350293750)
    • (2007) Current Opinion in Nephrology and Hypertension , vol.16 , Issue.6 , pp. 565-571
    • Kavanagh, D.1    Goodship, T.H.2
  • 12
    • 38949155911 scopus 로고    scopus 로고
    • Factor H autoantibodies in atypical hemolytic uremic syndrome correlate with CFHR1/CFHR3 deficiency
    • Jozsi M, Licht C, Strobel S, Zipfel SL, Richter H, Heinen S, Zipfel PF, Skerka C: Factor H autoantibodies in atypical hemolytic uremic syndrome correlate with CFHR1/CFHR3 deficiency. Blood 111: 1512-1514, 2008
    • (2008) Blood , vol.111 , pp. 1512-1514
    • Jozsi, M.1    Licht, C.2    Strobel, S.3    Zipfel, S.L.4    Richter, H.5    Heinen, S.6    Zipfel, P.F.7    Skerka, C.8
  • 14
    • 76949087440 scopus 로고    scopus 로고
    • Characterization of complement factor H-related (CFHR) proteins in plasma reveals novel genetic variations of CFHR1 associated with atypical hemolytic uremic syndrome
    • Abarrategui-Garrido C, Martinez-Barricarte R, Lopez-Trascasa M, de Cordoba SR, Sanchez-Corral P: Characterization of complement factor H-related (CFHR) proteins in plasma reveals novel genetic variations of CFHR1 associated with atypical hemolytic uremic syndrome. Blood 114: 4261-4271, 2009
    • (2009) Blood , vol.114 , pp. 4261-4271
    • Abarrategui-Garrido, C.1    Martinez-Barricarte, R.2    Lopez-Trascasa, M.3    De Cordoba, S.R.4    Sanchez-Corral, P.5
  • 21
    • 0242601270 scopus 로고    scopus 로고
    • 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
    • Caprioli J, Castelletti F, Bucchioni S, Bettinaglio P, Bresin E, Pianetti G, Gamba S, Brioschi S, Daina E, Remuzzi G, Noris M: 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. Hum Mol Genet 12: 3385-3395, 2003
    • (2003) Hum Mol Genet , vol.12 , pp. 3385-3395
    • Caprioli, J.1    Castelletti, F.2    Bucchioni, S.3    Bettinaglio, P.4    Bresin, E.5    Pianetti, G.6    Gamba, S.7    Brioschi, S.8    Daina, E.9    Remuzzi, G.10    Noris, M.11
  • 23
    • 65649106258 scopus 로고    scopus 로고
    • Liver-kidney transplantation to cure atypical hemolytic uremic syndrome
    • Saland JM, Ruggenenti P, Remuzzi G: Liver-kidney transplantation to cure atypical hemolytic uremic syndrome. J Am Soc Nephrol 20: 940-949, 2009
    • (2009) J Am Soc Nephrol , vol.20 , pp. 940-949
    • Saland, J.M.1    Ruggenenti, P.2    Remuzzi, G.3
  • 25
    • 67650508077 scopus 로고    scopus 로고
    • The high frequency of complement factor H-related CFHR1 gene deletion is restricted to specific subgroups of patients with atypical haemolytic uraemic syndrome
    • Dragon-Durey MA, Blanc C, Marliot F, Loirat C, Blouin J, Sautes-Fridman C, Fridman WH, Fremeaux-Bacchi V: The high frequency of complement factor H-related CFHR1 gene deletion is restricted to specific subgroups of patients with atypical haemolytic uraemic syndrome. J Med Genet 46: 447-450, 2009
    • (2009) J Med Genet , vol.46 , pp. 447-450
    • Dragon-Durey, M.A.1    Blanc, C.2    Marliot, F.3    Loirat, C.4    Blouin, J.5    Sautes-Fridman, C.6    Fridman, W.H.7    Fremeaux-Bacchi, V.8
  • 27
    • 53749084348 scopus 로고    scopus 로고
    • Complement and the atypical hemolytic uremic syndrome in children
    • Loirat C, Noris M, Fremeaux-Bacchi V: Complement and the atypical hemolytic uremic syndrome in children. Pediatr Nephrol 23: 1957-1972, 2008
    • (2008) Pediatr Nephrol , vol.23 , pp. 1957-1972
    • Loirat, C.1    Noris, M.2    Fremeaux-Bacchi, V.3
  • 28
    • 22544486255 scopus 로고    scopus 로고
    • The complement system in the pathophysiology of pregnancy
    • Girardi G, Bulla R, Salmon JE, Tedesco F: The complement system in the pathophysiology of pregnancy. Mol Immunol 43: 68-77, 2006
    • (2006) Mol Immunol , vol.43 , pp. 68-77
    • Girardi, G.1    Bulla, R.2    Salmon, J.E.3    Tedesco, F.4
  • 29
    • 42149106183 scopus 로고    scopus 로고
    • Complement and renal transplantation: From donor to recipient
    • Damman J, Schuurs TA, Ploeg RJ, Seelen MA: Complement and renal transplantation: From donor to recipient. Transplantation 85: 923-927, 2008
    • (2008) Transplantation , vol.85 , pp. 923-927
    • Damman, J.1    Schuurs, T.A.2    Ploeg, R.J.3    Seelen, M.A.4
  • 30
    • 62449129937 scopus 로고    scopus 로고
    • Hereditary and acquired complement dysregulation in membranoproliferative glomerulonephritis
    • Licht C, Fremeaux-Bacchi V: Hereditary and acquired complement dysregulation in membranoproliferative glomerulonephritis. Thromb Haemost 101: 271-278, 2009
    • (2009) Thromb Haemost , vol.101 , pp. 271-278
    • Licht, C.1    Fremeaux-Bacchi, V.2
  • 31
    • 0031740383 scopus 로고    scopus 로고
    • Secondary membranoproliferative glomerulonephritis due to hemolytic uremic syndrome: An unusual presentation
    • Jha V, Murthy MS, Kohli HS, Sud K, Gupta KL, Joshi K, Sakhuja V: Secondary membranoproliferative glomerulonephritis due to hemolytic uremic syndrome: An unusual presentation. Ren Fail 20: 845-850, 1998
    • (1998) Ren Fail , vol.20 , pp. 845-850
    • Jha, V.1    Murthy, M.S.2    Kohli, H.S.3    Sud, K.4    Gupta, K.L.5    Joshi, K.6    Sakhuja, V.7
  • 33
    • 0024388999 scopus 로고
    • Complement receptors and regulatory proteins in human atherosclerotic lesions
    • Seifert PS, Hansson GK: Complement receptors and regulatory proteins in human atherosclerotic lesions. Arteriosclerosis 9: 802-811, 1989
    • (1989) Arteriosclerosis , vol.9 , pp. 802-811
    • Seifert, P.S.1    Hansson, G.K.2
  • 36
    • 47749148096 scopus 로고    scopus 로고
    • Plasma therapy in atypical haemolytic uremic syndrome: Lessons from a family with a factor H mutation
    • Davin JC, Strain L, Goodship TH: Plasma therapy in atypical haemolytic uremic syndrome: Lessons from a family with a factor H mutation. Pediatr Nephrol 23: 1517-1521, 2008
    • (2008) Pediatr Nephrol , vol.23 , pp. 1517-1521
    • Davin, J.C.1    Strain, L.2    Goodship, T.H.3
  • 38
    • 34548400755 scopus 로고    scopus 로고
    • HUS/TTP ftIRoRaF: Outcome of renal transplantation in patients with non-Shiga toxin-associated haemolytic uremic syndrome: Prognostic significance of genetic background
    • Bresin E, Daina E, Noris M, Castelleti F, Stefanov R, Hill P, Goodship TM, Remuzzi G: HUS/TTP ftIRoRaF: Outcome of renal transplantation in patients with non-Shiga toxin-associated haemolytic uremic syndrome: Prognostic significance of genetic background. Clin J Am Soc Nephrol 1: 88-99, 2006
    • (2006) Clin J Am Soc Nephrol , vol.1 , pp. 88-99
    • Bresin, E.1    Daina, E.2    Noris, M.3    Castelleti, F.4    Stefanov, R.5    Hill, P.6    Goodship, T.M.7    Remuzzi, G.8
  • 42
    • 11144290605 scopus 로고    scopus 로고
    • Posttransplantation cytomegalovirus-induced recurrence of atypical hemolytic uremic syndrome associated with a factor H mutation: Successful treatment with intensive plasma exchanges and ganciclovir
    • Olie KH, Goodship TH, Verlaak R, Florquin S, Groothoff JW, Strain L, Weening JJ, Davin JC: Posttransplantation cytomegalovirus-induced recurrence of atypical hemolytic uremic syndrome associated with a factor H mutation: Successful treatment with intensive plasma exchanges and ganciclovir. Am J Kidney Dis 45: e12-e15, 2005
    • (2005) Am J Kidney Dis , vol.45
    • Olie, K.H.1    Goodship, T.H.2    Verlaak, R.3    Florquin, S.4    Groothoff, J.W.5    Strain, L.6    Weening, J.J.7    Davin, J.C.8
  • 45
    • 59449088846 scopus 로고    scopus 로고
    • Eculizumab for congenital atypical hemolytic-uremic syndrome
    • Gruppo RA, Rother RP: Eculizumab for congenital atypical hemolytic-uremic syndrome. N Engl J Med 360: 544-546, 2009
    • (2009) N Engl J Med , vol.360 , pp. 544-546
    • Gruppo, R.A.1    Rother, R.P.2
  • 47
    • 70350130833 scopus 로고    scopus 로고
    • Safety and long-term efficacy of eculizumab in a renal transplant patient with recurrent atypical hemolytic-uremic syndrome
    • Chatelet V, Fremeaux-Bacchi V, Lobbedez T, Ficheux M, de Ligny BH: Safety and long-term efficacy of eculizumab in a renal transplant patient with recurrent atypical hemolytic-uremic syndrome. Am J Transplant 9: 2644-2645, 2009
    • (2009) Am J Transplant , vol.9 , pp. 2644-2645
    • Chatelet, V.1    Fremeaux-Bacchi, V.2    Lobbedez, T.3    Ficheux, M.4    De Ligny, B.H.5
  • 48
    • 77949570344 scopus 로고    scopus 로고
    • Maintenance of kidney function following treatment with eculizumab and discontinuation of plasma exchange after a third kidney transplant for atypical hemolytic uremic syndrome associated with a CFH mutation
    • Davin JC, Gracchi V, Bouts A, Groothoff J, Strain L, Goodship T: Maintenance of kidney function following treatment with eculizumab and discontinuation of plasma exchange after a third kidney transplant for atypical hemolytic uremic syndrome associated with a CFH mutation. Am J Kidney Dis 55: 708-711, 2010
    • (2010) Am J Kidney Dis , vol.55 , pp. 708-711
    • Davin, J.C.1    Gracchi, V.2    Bouts, A.3    Groothoff, J.4    Strain, L.5    Goodship, T.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.