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Volumn 25, Issue 4, 2014, Pages 653-655

Fabry disease: Dose matters

Author keywords

[No Author keywords available]

Indexed keywords

AGALSIDASE ALFA; AGALSIDASE BETA; ALBUMIN; ALPHA GALACTOSIDASE; CREATININE; GLOBOTRIAOSYLCERAMIDE; VASCULOTROPIN; ISOENZYME;

EID: 84901434009     PISSN: 10466673     EISSN: 15333450     Source Type: Journal    
DOI: 10.1681/ASN.2013121322     Document Type: Editorial
Times cited : (21)

References (23)
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    • edited by Scriver C, Beaudet A, Sly W, Valle D, 8th Ed., New York, McGraw-Hill
    • Desnick RJ, Ioannou YA, Eng CM: Alpha-galactosidase A deficiency: Fabry disease. In: The Metabolic Bases of Inherited Disease, edited by Scriver C, Beaudet A, Sly W, Valle D, 8th Ed., New York, McGraw-Hill, 2001, pp 3733-3774
    • (2001) The Metabolic Bases of Inherited Disease , pp. 3733-3774
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  • 3
    • 44449143398 scopus 로고    scopus 로고
    • Nephropathy in males and females with Fabry disease: Cross-sectional description of patients before treatment with enzyme replacement therapy
    • Ortiz A, Oliveira JP, Waldek S, Warnock DG, Cianciaruso B, Wanner C; Fabry Registry: Nephropathy in males and females with Fabry disease: Cross-sectional description of patients before treatment with enzyme replacement therapy. Nephrol Dial Transplant 23: 1600-1607, 2008
    • (2008) Nephrol Dial Transplant , vol.23 , pp. 1600-1607
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  • 6
    • 31544456336 scopus 로고    scopus 로고
    • Long-term therapy with agalsidase alfa for Fabry disease: Safety and effects on renal function in a home infusion setting
    • Schiffmann R, Ries M, Timmons M, Flaherty JT, Brady RO: Long-term therapy with agalsidase alfa for Fabry disease: Safety and effects on renal function in a home infusion setting. Nephrol Dial Transplant 21: 345-354, 2006
    • (2006) Nephrol Dial Transplant , vol.21 , pp. 345-354
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  • 9
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    • Antiproteinuric therapy and Fabry nephropathy: Sustained reduction of proteinuria in patients receiving enzyme replacement therapy with agalsidase-beta
    • Tahir H, Jackson LL, Warnock DG: Antiproteinuric therapy and Fabry nephropathy: Sustained reduction of proteinuria in patients receiving enzyme replacement therapy with agalsidase-beta. J Am Soc Nephrol 18: 2609-2617, 2007
    • (2007) J Am Soc Nephrol , vol.18 , pp. 2609-2617
    • Tahir, H.1    Jackson, L.L.2    Warnock, D.G.3
  • 10
    • 3142737171 scopus 로고    scopus 로고
    • Enzyme replacement therapy for Fabry disease: Lessons from two alpha-galactosidase A orphan products and one FDA approval
    • Desnick RJ: Enzyme replacement therapy for Fabry disease: Lessons from two alpha-galactosidase A orphan products and one FDA approval. Expert Opin Biol Ther 4: 1167-1176, 2004
    • (2004) Expert Opin Biol Ther , vol.4 , pp. 1167-1176
    • Desnick, R.J.1
  • 11
    • 4644316602 scopus 로고    scopus 로고
    • Enzyme therapy for Fabry disease: Neutralizing antibodies toward agalsidase alpha and beta
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  • 12
    • 34248138939 scopus 로고    scopus 로고
    • Weekly enzyme replacement therapy may slow decline of renal function in patients with Fabry disease who are on long-term biweekly dosing
    • Schiffmann R, Askari H, Timmons M, Robinson C, Benko W, Brady RO, Ries M: Weekly enzyme replacement therapy may slow decline of renal function in patients with Fabry disease who are on long-term biweekly dosing. J Am Soc Nephrol 18: 1576-1583, 2007
    • (2007) J Am Soc Nephrol , vol.18 , pp. 1576-1583
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  • 13
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  • 15
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    • Tsuboi K, Yamamoto H: Clinical observation of patients with Fabry disease after switching from agalsidase beta (Fabrazyme) to agalsidase alfa (Replagal). Genet Med 14: 779-786, 2012
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    • Tsuboi, K.1    Yamamoto, H.2
  • 17
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    • (2011) Kidney Int , vol.79 , pp. 663-670
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  • 23
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    • Long-term enzyme replacement therapy is associated with reduced proteinuria and preserved proximal tubular function in women with fabry disease [Published Online Ahead of Print November 8, 2013]
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    • Nephrol Dial Transplant
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.