메뉴 건너뛰기




Volumn 63, Issue 1, 2014, Pages 40-48

Insights from the use in clinical practice of eculizumab in adult patients with atypical hemolytic uremic syndrome affecting the native kidneys: An analysis of 19 cases

(18)  Fakhouri, Fadi a   Delmas, Yahsou b   Provot, François c   Barbet, Christelle d   Karras, Alexandre e   Makdassi, Raifah f   Courivaud, Cécile g   Rifard, Khair h   Servais, Aude i   Allard, Catherine j   Besson, Virginie k   Cousin, Maud k   Châtelet, Valérie l   Goujon, Jean Michel m   Coindre, Jean Philippe h   Laurent, Guillaume h   Loirat, Chantal n   Frémeaux Bacchi, Véronique n  

a INSERM   (France)

Author keywords

[No Author keywords available]

Indexed keywords

COMPLEMENT FACTOR H; CREATININE; ECULIZUMAB;

EID: 84896101449     PISSN: 02726386     EISSN: 15236838     Source Type: Journal    
DOI: 10.1053/j.ajkd.2013.07.011     Document Type: Article
Times cited : (77)

References (18)
  • 1
    • 36349034631 scopus 로고    scopus 로고
    • Does hemolytic uremic syndrome differ from thrombotic thrombocytopenic purpura?
    • F. Fakhouri, and V. Fremeaux-Bacchi Does hemolytic uremic syndrome differ from thrombotic thrombocytopenic purpura? Nat Clin Pract Nephrol 3 12 2007 679 687
    • (2007) Nat Clin Pract Nephrol , vol.3 , Issue.12 , pp. 679-687
    • Fakhouri, F.1    Fremeaux-Bacchi, V.2
  • 2
    • 84876044818 scopus 로고    scopus 로고
    • Genetics and outcome of atypical hemolytic uremic syndrome: A nationwide French series comparing children and adults
    • V. Fremeaux-Bacchi, F. Fakhouri, and A. Garnier et al. Genetics and outcome of atypical hemolytic uremic syndrome: a nationwide French series comparing children and adults Clin J Am Soc Nephrol 8 4 2012 554 562
    • (2012) Clin J Am Soc Nephrol , vol.8 , Issue.4 , pp. 554-562
    • Fremeaux-Bacchi, V.1    Fakhouri, F.2    Garnier, A.3
  • 3
    • 77958587405 scopus 로고    scopus 로고
    • Relative role of genetic complement abnormalities in sporadic and familial aHUS and their impact on clinical phenotype
    • M. Noris, J. Caprioli, and E. Bresin 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 10 2010 1844 1859
    • (2010) Clin J Am Soc Nephrol , vol.5 , Issue.10 , pp. 1844-1859
    • Noris, M.1    Caprioli, J.2    Bresin, E.3
  • 4
    • 84870534251 scopus 로고    scopus 로고
    • Eculizumab for atypical hemolytic uremic syndrome recurrence in renal transplantation
    • J. Zuber, M. Le Quintrec, and S. Krid et al. Eculizumab for atypical hemolytic uremic syndrome recurrence in renal transplantation Am J Transplant 12 12 2012 3337 3354
    • (2012) Am J Transplant , vol.12 , Issue.12 , pp. 3337-3354
    • Zuber, J.1    Le Quintrec, M.2    Krid, S.3
  • 5
    • 34548400755 scopus 로고    scopus 로고
    • Outcome of renal transplantation in patients with non-Shiga toxin-associated hemolytic uremic syndrome: Prognostic significance of genetic background
    • E. Bresin, E. Daina, and M. Noris 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 1 2006 88 99
    • (2006) Clin J Am Soc Nephrol , vol.1 , Issue.1 , pp. 88-99
    • Bresin, E.1    Daina, E.2    Noris, M.3
  • 6
    • 84874417661 scopus 로고    scopus 로고
    • Complement genes strongly predict recurrence and graft outcome in adult renal transplant recipients with atypical hemolytic and uremic syndrome
    • M. Le Quintrec, J. Zuber, and B. Moulin et al. Complement genes strongly predict recurrence and graft outcome in adult renal transplant recipients with atypical hemolytic and uremic syndrome Am J Transplant 13 3 2013 663 675
    • (2013) Am J Transplant , vol.13 , Issue.3 , pp. 663-675
    • Le Quintrec, M.1    Zuber, J.2    Moulin, B.3
  • 7
    • 70350279315 scopus 로고    scopus 로고
    • Atypical hemolytic-uremic syndrome
    • M. Noris, and G. Remuzzi Atypical hemolytic-uremic syndrome N Engl J Med 361 17 2009 1676 1687
    • (2009) N Engl J Med , vol.361 , Issue.17 , pp. 1676-1687
    • Noris, M.1    Remuzzi, G.2
  • 8
    • 84867993256 scopus 로고    scopus 로고
    • Use of eculizumab for atypical haemolytic uraemic syndrome and C3 glomerulopathies
    • J. Zuber, F. Fakhouri, L.T. Roumenina, C. Loirat, and V. Fremeaux-Bacchi Use of eculizumab for atypical haemolytic uraemic syndrome and C3 glomerulopathies Nat Rev Nephrol 8 11 2012 643 657
    • (2012) Nat Rev Nephrol , vol.8 , Issue.11 , pp. 643-657
    • Zuber, J.1    Fakhouri, F.2    Roumenina, L.T.3    Loirat, C.4    Fremeaux-Bacchi, V.5
  • 9
    • 77957562699 scopus 로고    scopus 로고
    • Anti-factor H autoantibody-associated hemolytic uremic syndrome: Review of literature of the autoimmune form of HUS
    • M.A. Dragon-Durey, C. Blanc, A. Garnier, J. Hofer, S.K. Sethi, and L.B. Zimmerhackl Anti-factor H autoantibody-associated hemolytic uremic syndrome: review of literature of the autoimmune form of HUS Semin Thromb Hemost 36 6 2010 633 640
    • (2010) Semin Thromb Hemost , vol.36 , Issue.6 , pp. 633-640
    • Dragon-Durey, M.A.1    Blanc, C.2    Garnier, A.3    Hofer, J.4    Sethi, S.K.5    Zimmerhackl, L.B.6
  • 10
    • 60649118722 scopus 로고    scopus 로고
    • Eculizumab for paroxysmal nocturnal haemoglobinuria
    • C. Parker Eculizumab for paroxysmal nocturnal haemoglobinuria Lancet 373 9665 2009 759 767
    • (2009) Lancet , vol.373 , Issue.9665 , pp. 759-767
    • Parker, C.1
  • 11
    • 84878589219 scopus 로고    scopus 로고
    • Terminal complement inhibitor eculizumab in atypical hemolytic-uremic syndrome
    • C.M. Legendre, C. Licht, and P. Muus et al. Terminal complement inhibitor eculizumab in atypical hemolytic-uremic syndrome N Engl J Med 368 23 2013 2169 2181
    • (2013) N Engl J Med , vol.368 , Issue.23 , pp. 2169-2181
    • Legendre, C.M.1    Licht, C.2    Muus, P.3
  • 12
    • 77952556624 scopus 로고    scopus 로고
    • Pregnancy-associated hemolytic uremic syndrome revisited in the era of complement gene mutations
    • F. Fakhouri, L. Roumenina, and F. Provot et al. Pregnancy-associated hemolytic uremic syndrome revisited in the era of complement gene mutations J Am Soc Nephrol 21 5 2010 859 867
    • (2010) J Am Soc Nephrol , vol.21 , Issue.5 , pp. 859-867
    • Fakhouri, F.1    Roumenina, L.2    Provot, F.3
  • 13
    • 0032569884 scopus 로고    scopus 로고
    • Von Willebrand factor-cleaving protease in thrombotic thrombocytopenic purpura and the hemolytic-uremic syndrome
    • M. Furlan, R. Robles, and M. Galbusera et al. von Willebrand factor-cleaving protease in thrombotic thrombocytopenic purpura and the hemolytic-uremic syndrome N Engl J Med 339 22 1998 1578 1584
    • (1998) N Engl J Med , vol.339 , Issue.22 , pp. 1578-1584
    • Furlan, M.1    Robles, R.2    Galbusera, M.3
  • 14
    • 80955168000 scopus 로고    scopus 로고
    • Epidemic profile of Shiga-toxin-producing Escherichia coli O104:H4 outbreak in Germany
    • C. Frank, D. Werber, and J.P. Cramer et al. Epidemic profile of Shiga-toxin-producing Escherichia coli O104:H4 outbreak in Germany N Engl J Med 365 19 2011 1771 1780
    • (2011) N Engl J Med , vol.365 , Issue.19 , pp. 1771-1780
    • Frank, C.1    Werber, D.2    Cramer, J.P.3
  • 15
    • 40849130173 scopus 로고    scopus 로고
    • VEGF inhibition and renal thrombotic microangiopathy
    • V. Eremina, J.A. Jefferson, and J. Kowalewska et al. VEGF inhibition and renal thrombotic microangiopathy N Engl J Med 358 11 2008 1129 1136
    • (2008) N Engl J Med , vol.358 , Issue.11 , pp. 1129-1136
    • Eremina, V.1    Jefferson, J.A.2    Kowalewska, J.3
  • 16
    • 84863719861 scopus 로고    scopus 로고
    • Cancer-related microangiopathic hemolytic anemia: Clinical and laboratory features in 168 reported cases
    • K. Lechner, and H.L. Obermeier Cancer-related microangiopathic hemolytic anemia: clinical and laboratory features in 168 reported cases Medicine 91 4 2012 195 205
    • (2012) Medicine , vol.91 , Issue.4 , pp. 195-205
    • Lechner, K.1    Obermeier, H.L.2
  • 17
    • 33749627378 scopus 로고    scopus 로고
    • Thrombotic thrombocytopenic purpura in systemic lupus erythematosus: A frequent and severe consequence of active disease
    • V. Majithia, and V. Harisdangkul Thrombotic thrombocytopenic purpura in systemic lupus erythematosus: a frequent and severe consequence of active disease Rheumatology 45 9 2006 1170 1171
    • (2006) Rheumatology , vol.45 , Issue.9 , pp. 1170-1171
    • Majithia, V.1    Harisdangkul, V.2
  • 18
    • 84871942008 scopus 로고    scopus 로고
    • Thrombocytopenia is not mandatory to diagnose haemolytic and uremic syndrome
    • M. Sallee, K. Ismail, and F. Fakhouri et al. Thrombocytopenia is not mandatory to diagnose haemolytic and uremic syndrome BMC Nephrol 14 2013 3
    • (2013) BMC Nephrol , vol.14 , pp. 3
    • Sallee, M.1    Ismail, K.2    Fakhouri, F.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.