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References
Eng CM et al. (2001) Safety and efficacy of recombinant human α-galactosidase A replacement therapy in Fabry's disease. N Engl J Med 345: 9–16
Wilcox WR et al. (2004) Long-term safety and efficacy of enzyme replacement therapy for Fabry disease. Am J Hum Genet 75: 65–74
Desnick RJ (online 7 September 2005) The phase 4 clinical trial demonstrates clinical benefit of Fabrazyme® (agalsidase beta) [http://www.acmg.net/resources/ACMG/2005/abs-group-04.pdf] (accessed 7 September 2005)
Nakao S et al. (2003) Fabry disease: Detection of undiagnosed hemodialysis patients and identification of a “renal variant” phenotype. Kidney Int 64: 801–807
Kosch M et al. (2004) Enzyme replacement therapy administered during hemodialysis in patients with Fabry disease. Kidney Int 66: 1279–1282
Acknowledgements
The synopsis was written by Chloe Harman, Associate Editor, Nature Clinical Practice.
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Dr. Desnick is a consultant to the Genzyme Corporation and an inventor on intellectual property licensed to the Genzyme Corporation. He is also a founder of, consultant to, and holder of options in Amicus Therapeutics, Inc. Dr Banikazemi has no competing interests.
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Banikazemi, M., Desnick, R. Does enzyme replacement therapy improve symptoms of Fabry disease in patients undergoing dialysis?. Nat Rev Nephrol 2, 72–73 (2006). https://doi.org/10.1038/ncpneph0100
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DOI: https://doi.org/10.1038/ncpneph0100
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