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Volumn 21, Issue 2, 2006, Pages 547-548

Gentamicin-induced diffuse renal tubular dysfunction [3]

Author keywords

[No Author keywords available]

Indexed keywords

ADENOSINE TRIPHOSPHATE; BICARBONATE; GENTAMICIN; SODIUM POTASSIUM CHLORIDE COTRANSPORTER; SULTAMICILLIN;

EID: 31544476846     PISSN: 09310509     EISSN: 14602385     Source Type: Journal    
DOI: 10.1093/ndt/gfi179     Document Type: Letter
Times cited : (8)

References (7)
  • 1
    • 14844361715 scopus 로고    scopus 로고
    • Acquired Bartter-like syndrome associated with gentamicin administration
    • Chou CL, Chen YH, Chau T, Lin SH. Acquired Bartter-like syndrome associated with gentamicin administration. Am J Med Sci 2005; 329: 144-149
    • (2005) Am J Med Sci , vol.329 , pp. 144-149
    • Chou, C.L.1    Chen, Y.H.2    Chau, T.3    Lin, S.H.4
  • 2
    • 0033868928 scopus 로고    scopus 로고
    • Phenotypic variability in Bartter syndrome type I
    • Bettinelli A, Ciarmatori S, Cesareo L et al. Phenotypic variability in Bartter syndrome type I. Pediatr Nephrol 2000; 14: 940-945
    • (2000) Pediatr Nephrol , vol.14 , pp. 940-945
    • Bettinelli, A.1    Ciarmatori, S.2    Cesareo, L.3
  • 3
    • 0030745876 scopus 로고    scopus 로고
    • Cell biology of aminoglycoside nephrotoxicity: Newer aspects
    • Molitoris BA. Cell biology of aminoglycoside nephrotoxicity: Newer aspects. Curr Opin Nephrol Hypertens 1997; 6: 384-388
    • (1997) Curr Opin Nephrol Hypertens , vol.6 , pp. 384-388
    • Molitoris, B.A.1
  • 4
    • 0043022120 scopus 로고    scopus 로고
    • Renal disease and mitochondrial genetics
    • Rotig A. Renal disease and mitochondrial genetics. J Nephrol 2003; 16: 286-292
    • (2003) J Nephrol , vol.16 , pp. 286-292
    • Rotig, A.1
  • 6
    • 0344167734 scopus 로고    scopus 로고
    • Cosegregation of C-insertion at position 961 with the A1555G mutation of the mitochondrial 12S rRNA gene in a large Chinese family with maternally inherited hearing loss
    • Li R, Xing G, Yan M et al. Cosegregation of C-insertion at position 961 with the A1555G mutation of the mitochondrial 12S rRNA gene in a large Chinese family with maternally inherited hearing loss. Am J Med Genet A 2004; 124: 113-117
    • (2004) Am J Med Genet A , vol.124 , pp. 113-117
    • Li, R.1    Xing, G.2    Yan, M.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.