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Volumn 27, Issue 3, 2001, Pages 185-190

Hemolytic-uremic syndrome and complement factor H deficiency: Clinical aspects

Author keywords

Complement factor H; Enterocolitis; Hemolytic uremic syndrome; HUS; Hypertension; International registry

Indexed keywords

COMPLEMENT FACTOR H;

EID: 0034972837     PISSN: 00946176     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2001-15247     Document Type: Conference Paper
Times cited : (26)

References (28)
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    • (1980) Klin Wochenschr , vol.58 , pp. 173-184
    • Thoenes, W.1    John, H.D.2
  • 22
    • 0031759886 scopus 로고    scopus 로고
    • Complement regulatory proteins in glomerular diseases
    • (1998) Kidney Int , vol.54 , pp. 1419-1428
    • Nanaku, M.1
  • 24
    • 0032950690 scopus 로고    scopus 로고
    • Hypocomplementemia discloses genetic predisposition to hemolytic uremic syndrome and thrombotic thrombocytopenic purpura: Role of factor H abnormalities
    • (1999) J Am Soc Nephrol , vol.10 , pp. 281-293
    • Noris, M.1    Ruggenenti, P.2    Perna, A.3
  • 25
    • 0032526881 scopus 로고    scopus 로고
    • Complement activation occurs on subendothelial extracellular matrix in vitro and is initiated by retraction or removal of overlying endothelial cells
    • (1998) J Immunol , vol.12 , pp. 6128-6136
    • Hindmarsh, E.J.1    Marks, R.M.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.