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Volumn 13, Issue 11, 1998, Pages 2934-2936

Should living related kidney transplantation be considered for patients with renal failure due to Fabry's disease?

Author keywords

galactosidase A; Fabry's disease; Living related donation; Transplantation

Indexed keywords

GLYCOSPHINGOLIPID;

EID: 0031754865     PISSN: 09310509     EISSN: None     Source Type: Journal    
DOI: 10.1093/ndt/13.11.2934     Document Type: Article
Times cited : (9)

References (12)
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    • Desnick RJ, Ioannou YA, Eng CM. α-Galactosidase A deficiency: Fabry disease. In: Scriver R, Beaudet AL, Sly WS, Valle D. The Metabolic and Molecular Basis of Inherited Disease. McGraw-Hill, New York, 7th edn, 1995; 2741 2784
    • (1995) The Metabolic and Molecular Basis of Inherited Disease , pp. 2741-2784
    • Desnick, R.J.1    Ioannou, Y.A.2    Eng, C.M.3
  • 2
    • 0024487020 scopus 로고
    • Fabry disease: Molecular genetics of the inherited nephropathy
    • Desnick RJ, Astrin KH, Bishop DF. Fabry disease: molecular genetics of the inherited nephropathy. Adv Nephrol 1989; 18: 113-127
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    • Desnick, R.J.1    Astrin, K.H.2    Bishop, D.F.3
  • 3
    • 0014055398 scopus 로고
    • Angiokeratoma corporis diffusum universale (Fabry's disease) in female subjects
    • Burda CD, Winder PR. Angiokeratoma corporis diffusum universale (Fabry's disease) in female subjects. Am J Med 1967; 42: 293 301
    • (1967) Am J Med , vol.42 , pp. 293-301
    • Burda, C.D.1    Winder, P.R.2
  • 4
  • 7
    • 0025346987 scopus 로고
    • Renal changes in heterozygous Fabry's disease - A family study
    • Chen HC, Tsai JH, Lai YH, Guh JY. Renal changes in heterozygous Fabry's disease - a family study. Am J Kidney Dis 1990; 15: 180 183
    • (1990) Am J Kidney Dis , vol.15 , pp. 180-183
    • Chen, H.C.1    Tsai, J.H.2    Lai, Y.H.3    Guh, J.Y.4
  • 8
    • 0028866658 scopus 로고
    • A female heterozygous patient with Fabry's disease with renal accumulation of trihexosylceramide detected with a monoclonal antibody
    • Fukushima M, Tsuchiyama Y, Nakato T et al. A female heterozygous patient with Fabry's disease with renal accumulation of trihexosylceramide detected with a monoclonal antibody. Am J Kidney Dis 1995; 26: 952-955
    • (1995) Am J Kidney Dis , vol.26 , pp. 952-955
    • Fukushima, M.1    Tsuchiyama, Y.2    Nakato, T.3
  • 9
    • 9244220588 scopus 로고    scopus 로고
    • Novel frameshift mutation in a heterozygous woman with Fabry disease and endstage renal failure
    • Van Loo A, Vanholder R, Madsen K et al. Novel frameshift mutation in a heterozygous woman with Fabry disease and endstage renal failure. Am J Nephrol 1996; 16: 352-357
    • (1996) Am J Nephrol , vol.16 , pp. 352-357
    • Van Loo, A.1    Vanholder, R.2    Madsen, K.3
  • 10
    • 0016802543 scopus 로고
    • La transplantation rénale chez les sujets atteints de maladie de Fabry: Transplantation du rein d'un sujet hétérozygote à un sujet sain
    • Grünfeld J-P, Le Porrier M, Droz D, Bensaude I, Hinglais N, Crosnier J. La transplantation rénale chez les sujets atteints de maladie de Fabry: transplantation du rein d'un sujet hétérozygote à un sujet sain. Presse Med 1975; 4: 2081-2085
    • (1975) Presse Med , vol.4 , pp. 2081-2085
    • Grünfeld, J.-P.1    Le Porrier, M.2    Droz, D.3    Bensaude, I.4    Hinglais, N.5    Crosnier, J.6
  • 11
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    • Rare diseases in renal replacement therapy in the ERA-EDTA registry
    • Tsakiris D, Simpson HKL, Jones EHP et al. Rare diseases in renal replacement therapy in the ERA-EDTA registry. Nephrol Dial Transplant 1996; 11 [Suppl 7]: 4-20
    • (1996) Nephrol Dial Transplant , vol.11 , Issue.7 SUPPL. , pp. 4-20
    • Tsakiris, D.1    Simpson, H.K.L.2    Jones, E.H.P.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.