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Volumn 3, Issue 8, 2003, Pages 1030-1032

Fabry disease in a renal allograft

Author keywords

Alpha galactosidase A; Fabry disease; Focal sclerosis; Heterozygote; Kidney transplantation; Proteinuria

Indexed keywords

ALPHA GALACTOSIDASE; AZATHIOPRINE; BETA ADRENERGIC RECEPTOR BLOCKING AGENT; CREATININE; CYCLOSPORIN; IMMUNOSUPPRESSIVE AGENT; LABETALOL; MYCOPHENOLIC ACID 2 MORPHOLINOETHYL ESTER; PREDNISONE; STEROID;

EID: 0042265153     PISSN: 16006135     EISSN: None     Source Type: Journal    
DOI: 10.1034/j.1600-6143.2003.00139.x     Document Type: Article
Times cited : (12)

References (10)
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  • 3
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    • Alpha galactosidase A deficiency: Fabry disease
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    • Desnick R. Alpha galactosidase A deficiency: Fabry disease. In: Scriver CR, Sly WS, eds. Scriver's: The Metabolic Bases of Inherited Diseases 8th edn. Columbus: McGraw-Hill Professional, 2000; 3: 3733-3774.
    • (2000) Scriver's: The Metabolic Bases of Inherited Diseases 8th Edn. , vol.3 , pp. 3733-3774
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  • 4
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    • Renal pathology
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  • 5
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    • Early renal changes in hemizygous and heterozygous patients with Fabry's disease
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  • 7
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    • Enzyme replacement therapy in Fabry disease: A randomized controlled trial
    • Schiffmann R, Kopp JB, Austin HA 3rd et al. Enzyme replacement therapy in Fabry disease: a randomized controlled trial. JAMA 2001; 285: 2743-2749.
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    • Schiffmann, R.1    Kopp, J.B.2    Austin H.A. III3
  • 8
    • 0035811624 scopus 로고    scopus 로고
    • Safety and efficacy of recombinant human alpha-galactosidase A - Replacement therapy in Fabry's disease
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.