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Volumn 362, Issue 9395, 2003, Pages 1514-1515

Complement dysregulation in haemolytic uraemic syndrome

Author keywords

[No Author keywords available]

Indexed keywords

COMPLEMENT COMPONENT C3B; MEMBRANE PROTEIN;

EID: 0242486444     PISSN: 01406736     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0140-6736(03)14777-0     Document Type: Note
Times cited : (20)

References (9)
  • 1
    • 0041411081 scopus 로고    scopus 로고
    • Long-term renal prognosis of diarrhea-associated hemolytic uremic syndrome: A systematic review, meta-analysis, and meta-regression
    • Garg A.X., Suri R.S., Barrowman N., et al. Long-term renal prognosis of diarrhea-associated hemolytic uremic syndrome: a systematic review, meta-analysis, and meta-regression. JAMA. 290:2003;1360-1370.
    • (2003) JAMA , vol.290 , pp. 1360-1370
    • Garg, A.X.1    Suri, R.S.2    Barrowman, N.3
  • 2
    • 0035722282 scopus 로고    scopus 로고
    • Thrombotic microangiopathy, hemolytic uremic syndrome, and thrombotic thrombocytopenic purpura
    • Ruggenenti P., Noris M., Remuzzi G. Thrombotic microangiopathy, hemolytic uremic syndrome, and thrombotic thrombocytopenic purpura. Kidney Int. 60:2001;831-846.
    • (2001) Kidney Int , vol.60 , pp. 831-846
    • Ruggenenti, P.1    Noris, M.2    Remuzzi, G.3
  • 3
    • 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
    • Oct 28
    • Caprioli J, Castelletti F, Bucchioni S, et al. 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 2003: Oct 28.
    • (2003) Hum Mol Genet
    • Caprioli, J.1    Castelletti, F.2    Bucchioni, S.3
  • 4
    • 0037339175 scopus 로고    scopus 로고
    • Severe deficiency of the specific von Willebrand factor-cleaving protease (ADAMTS 13) activity in a subgroup of children with atypical hemolytic uremic syndrome
    • Veyradier A., Obert B., Haddad E., et al. Severe deficiency of the specific von Willebrand factor-cleaving protease (ADAMTS 13) activity in a subgroup of children with atypical hemolytic uremic syndrome. J Pediatr. 142:2003;310-317.
    • (2003) J Pediatr , vol.142 , pp. 310-317
    • Veyradier, A.1    Obert, B.2    Haddad, E.3
  • 5
    • 0242331610 scopus 로고    scopus 로고
    • Mutations in human complement regulator, membrane cofactor protein (CD46), predispose to development of familial hemolytic uremic syndrome
    • Richards A., Kemp E.J., Liszewski M.K., et al. Mutations in human complement regulator, membrane cofactor protein (CD46), predispose to development of familial hemolytic uremic syndrome. Proc Natl Acad Sci USA. 100:2003;12966-12971.
    • (2003) Proc Natl Acad Sci USA , vol.100 , pp. 12966-12971
    • Richards, A.1    Kemp, E.J.2    Liszewski, M.K.3
  • 7
    • 0036419401 scopus 로고    scopus 로고
    • Post-transplant hemolytic-uremic syndrome
    • Ruggenenti P. Post-transplant hemolytic-uremic syndrome. Kidney Int. 62:2002;1093-1104.
    • (2002) Kidney Int , vol.62 , pp. 1093-1104
    • Ruggenenti, P.1
  • 8
    • 0242694369 scopus 로고    scopus 로고
    • The risk of recurrence of hemolytic uremic syndrome after renal transplantation in children
    • Loirat C., Niaudet P. The risk of recurrence of hemolytic uremic syndrome after renal transplantation in children. Pediatr Nephrol. 17:2003;1095-1101.
    • (2003) Pediatr Nephrol , vol.17 , pp. 1095-1101
    • Loirat, C.1    Niaudet, P.2
  • 9
    • 18744377731 scopus 로고    scopus 로고
    • Recurrence of hemolytic uremic syndrome after live related renal transplantation associated with subsequent de novo disease in the donor
    • Donne R.L., Abbs I., Barany P., et al. Recurrence of hemolytic uremic syndrome after live related renal transplantation associated with subsequent de novo disease in the donor. Am J Kidney Dis. 40:2002;E22.
    • (2002) Am J Kidney Dis , vol.40 , pp. 22
    • Donne, R.L.1    Abbs, I.2    Barany, P.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.