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Volumn 12, Issue 4, 2014, Pages 266-268

Atypical hemolytic uremic syndrome: The role of complement pathway gene mutation analysis

Author keywords

[No Author keywords available]

Indexed keywords

ALTERNATIVE COMPLEMENT PATHWAY C3 C5 CONVERTASE; COMPLEMENT FACTOR H; COMPLEMENT FACTOR I; DIACYLGLYCEROL KINASE; ECULIZUMAB; MEMBRANE COFACTOR PROTEIN; NEPHRITIC FACTOR; THROMBIN ACTIVATABLE FIBRINOLYSIS INHIBITOR; THROMBOMODULIN; COMPLEMENT;

EID: 84900010039     PISSN: 15430790     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Note
Times cited : (2)

References (9)
  • 1
    • 84894213708 scopus 로고    scopus 로고
    • Atypical haemolytic-uraemic syndrome due to heterozygous mutations of CFH/CFHR1-3 and complement factor H 479
    • [published online November 15, doi: 10.2450/2013.0107-13
    • Chaudhary P, Hepgur M, Sarkissian S, Smith RJ, Weitz IC. Atypical haemolytic-uraemic syndrome due to heterozygous mutations of CFH/CFHR1-3 and complement factor H 479 [published online November 15, 2013]. Blood Transfus. doi: 10.2450/2013.0107-13.
    • (2013) Blood Transfus
    • Chaudhary, P.1    Hepgur, M.2    Sarkissian, S.3    Smith, R.J.4    Weitz, I.C.5
  • 2
    • 84900010983 scopus 로고    scopus 로고
    • Eculizumab (ECU) inhibits throm-botic microangiopathy (TMA) and improves renal function in adult patients (pts) with atypical hemolytic uremic syndrome (aHUS)
    • ASH abstract 2179
    • Fakhouri F, Hourmant M, Cataland SR, et al. Eculizumab (ECU) inhibits throm-botic microangiopathy (TMA) and improves renal function in adult patients (pts) with atypical hemolytic uremic syndrome (aHUS) [ASH abstract 2179]. Blood. 2013;122(21)(suppl).
    • (2013) Blood , vol.122 , Issue.21 SUPPL.
    • Fakhouri, F.1    Hourmant, M.2    Cataland, S.R.3
  • 3
    • 57649241639 scopus 로고    scopus 로고
    • Factor H, membrane cofactor protein, and factor I mutations in patients with hemolysis, elevated liver enzymes, and low platelet count syndrome
    • Fakhouri F, Jablonski M, Lepercq J, et al. Factor H, membrane cofactor protein, and factor I mutations in patients with hemolysis, elevated liver enzymes, and low platelet count syndrome. Blood. 2008;112(12):4542-4545.
    • (2008) Blood , vol.112 , Issue.12 , pp. 4542-4545
    • Fakhouri, F.1    Jablonski, M.2    Lepercq, J.3
  • 4
    • 77952556624 scopus 로고    scopus 로고
    • Pregnancy-associated hemolytic uremic syndrome revisited in the era of complement gene mutations
    • Fakhouri F, Roumenina L, Provot F, et al. Pregnancy-associated hemolytic uremic syndrome revisited in the era of complement gene mutations. J Am Soc Nephrol. 2010;21(5):859-867.
    • (2010) J Am Soc Nephrol , vol.21 , Issue.5 , pp. 859-867
    • Fakhouri, F.1    Roumenina, L.2    Provot, F.3
  • 5
    • 84875860574 scopus 로고    scopus 로고
    • Zimmerman Program Investigators. Collagen binding provides a sensitive screen for variant von Willebrand disease
    • Flood VH, Gill JC, Friedman KD, et al; Zimmerman Program Investigators. Collagen binding provides a sensitive screen for variant von Willebrand disease. Clin Chem. 2013;59(4):684-691.
    • (2013) Clin Chem , vol.59 , Issue.4 , pp. 684-691
    • Flood, V.H.1    Gill, J.C.2    Friedman, K.D.3
  • 6
    • 84885717017 scopus 로고    scopus 로고
    • Abnormalities in the alternative pathway of complement in children with hematopoietic stem cell transplant-associated throm-botic microangiopathy
    • Jodele S, Licht C, Goebel J, et al. Abnormalities in the alternative pathway of complement in children with hematopoietic stem cell transplant-associated throm-botic microangiopathy. Blood. 2013;122(12):2003-2007.
    • (2013) Blood , vol.122 , Issue.12 , pp. 2003-2007
    • Jodele, S.1    Licht, C.2    Goebel, J.3
  • 7
    • 84883049968 scopus 로고    scopus 로고
    • Atypical hemolytic uremic syndrome (aHUS): Making the diagnosis
    • Laurence J. Atypical hemolytic uremic syndrome (aHUS): making the diagnosis. Clin Adv Hematol Oncol. 2012;10(10)(suppl 17):1-12.
    • (2012) Clin Adv Hematol Oncol. , vol.10 , Issue.10 SUPPL. 17 , pp. 1-12
    • Laurence, J.1
  • 8
    • 83055187115 scopus 로고    scopus 로고
    • Von Willebrand disease (VWD): Evidence-based diagnosis and management guidelines, the National Heart, Lung, and Blood Institute (NHLBI) Expert Panel report (USA)
    • Nichols WL, Hultin MB, James AH, et al. von Willebrand disease (VWD): evidence-based diagnosis and management guidelines, the National Heart, Lung, and Blood Institute (NHLBI) Expert Panel report (USA). Haemophilia. 2008;14(2):171-232.
    • (2008) Haemophilia , vol.14 , Issue.2 , pp. 171-232
    • Nichols, W.L.1    Hultin, M.B.2    James, A.H.3
  • 9
    • 34548491156 scopus 로고    scopus 로고
    • Dense Deposit Disease Focus Group. New approaches to the treatment of dense deposit disease
    • Smith RJ, Alexander J, Barlow PN, et al; Dense Deposit Disease Focus Group. New approaches to the treatment of dense deposit disease. J Am Soc Nephrol. 2007;18(9):2447-2456.
    • (2007) J Am Soc Nephrol , vol.18 , Issue.9 , pp. 2447-2456
    • Smith, R.J.1    Alexander, J.2    Barlow, P.N.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.