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Volumn 47, Issue 7, 2015, Pages 2258-2261

Thrombotic Microangiopathy as a Cause of Chronic Kidney Transplant Dysfunction: Case Report Demonstrating Successful Treatment with Eculizumab

Author keywords

[No Author keywords available]

Indexed keywords

ALEMTUZUMAB; ECULIZUMAB; MYCOPHENOLATE MOFETIL; PREDNISOLONE; TACROLIMUS; MONOCLONAL ANTIBODY;

EID: 84940991737     PISSN: 00411345     EISSN: 18732623     Source Type: Journal    
DOI: 10.1016/j.transproceed.2015.08.004     Document Type: Conference Paper
Times cited : (6)

References (9)
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    • Relative role of genetic complement abnormalities in sporadic and familial aHUS and their impact on clinical phenotype
    • M. Noris, J. Caprioli, E. Bresin, C. Mossali, G. Pianetti, S. Gamba, and et al. Relative role of genetic complement abnormalities in sporadic and familial aHUS and their impact on clinical phenotype Clin J Am Soc Nephrol 5 2010 1844 1859
    • (2010) Clin J Am Soc Nephrol , vol.5 , pp. 1844-1859
    • Noris, M.1    Caprioli, J.2    Bresin, E.3    Mossali, C.4    Pianetti, G.5    Gamba, S.6
  • 2
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    • Outcome of renal transplantation in patients with non-Shiga toxin-associated hemolytic uremic syndrome: Prognostic significance of genetic background
    • E. Bresin, E. Daina, M. Noris, F. Castelletti, R. Stefanov, P. Hill, and et al. Outcome of renal transplantation in patients with non-Shiga toxin-associated hemolytic uremic syndrome: prognostic significance of genetic background Clin J Am Soc Nephrol 1 2006 88 99
    • (2006) Clin J Am Soc Nephrol , vol.1 , pp. 88-99
    • Bresin, E.1    Daina, E.2    Noris, M.3    Castelletti, F.4    Stefanov, R.5    Hill, P.6
  • 3
    • 77954048044 scopus 로고    scopus 로고
    • Thrombotic microangiopathy after kidney transplantation
    • M. Noris, and G. Remuzzi Thrombotic microangiopathy after kidney transplantation Am J Transplant 10 2010 1517 1523
    • (2010) Am J Transplant , vol.10 , pp. 1517-1523
    • Noris, M.1    Remuzzi, G.2
  • 4
    • 33745767079 scopus 로고    scopus 로고
    • Favorable long-term outcome after liver-kidney transplant for recurrent hemolytic uremic syndrome associated with a factor H mutation
    • J.M. Saland, S.H. Emre, B.L. Shneider, C. Benchimol, S. Ames, J.S. Bromberg, and et al. Favorable long-term outcome after liver-kidney transplant for recurrent hemolytic uremic syndrome associated with a factor H mutation Am J Transplant 6 2006 1948 1952
    • (2006) Am J Transplant , vol.6 , pp. 1948-1952
    • Saland, J.M.1    Emre, S.H.2    Shneider, B.L.3    Benchimol, C.4    Ames, S.5    Bromberg, J.S.6
  • 5
    • 84878589219 scopus 로고    scopus 로고
    • Terminal complement inhibitor eculizumab in atypical hemolytic-uremic syndrome
    • C.M. Legendre, C. Licht, P. Muus, L.A. Greenbaum, S. Babu, C. Bedrosian, and et al. Terminal complement inhibitor eculizumab in atypical hemolytic-uremic syndrome N Engl J Med 368 2013 2169 2181
    • (2013) N Engl J Med , vol.368 , pp. 2169-2181
    • Legendre, C.M.1    Licht, C.2    Muus, P.3    Greenbaum, L.A.4    Babu, S.5    Bedrosian, C.6
  • 6
    • 84870534251 scopus 로고    scopus 로고
    • Eculizumab for atypical hemolytic uremic syndrome recurrence in renal transplantation
    • J. Zuber, M. le Quintrec, S. Krid, C. Bertoye, V. Gueutin, A. Lahoche, and et al. Eculizumab for atypical hemolytic uremic syndrome recurrence in renal transplantation Am J Transplant 12 2012 3337 3354
    • (2012) Am J Transplant , vol.12 , pp. 3337-3354
    • Zuber, J.1    Le Quintrec, M.2    Krid, S.3    Bertoye, C.4    Gueutin, V.5    Lahoche, A.6
  • 7
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    • Mutations in complement C3 predispose to development of atypical hemolytic uremic syndrome
    • V. Frémeaux-Bacchi, E. Miller, M. Liszewski, L. Strain, J. Blouin, A. Brown, and et al. Mutations in complement C3 predispose to development of atypical hemolytic uremic syndrome Blood 112 2008 4948 4952
    • (2008) Blood , vol.112 , pp. 4948-4952
    • Frémeaux-Bacchi, V.1    Miller, E.2    Liszewski, M.3    Strain, L.4    Blouin, J.5    Brown, A.6
  • 9
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    • A large family with a gain-of-function mutation of complement C3 predisposing to atypical hemolytic uremic syndrome, microhematuria, hypertension and chronic renal failure
    • K. Lhotta, A.R. Janecke, J. Scheiring, B. Petzlberger, T. Giner, V. Fally, and et al. A large family with a gain-of-function mutation of complement C3 predisposing to atypical hemolytic uremic syndrome, microhematuria, hypertension and chronic renal failure Clin J Am Soc Nephrol 4 2009 1356 1362
    • (2009) Clin J Am Soc Nephrol , vol.4 , pp. 1356-1362
    • Lhotta, K.1    Janecke, A.R.2    Scheiring, J.3    Petzlberger, B.4    Giner, T.5    Fally, V.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.