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Enzyme Replacement Therapy With Agalsidase Alfa in Patients With Fabrys Disease: An Analysis of Registry Data
Lancet 374:1986-1996, 1950, Mehta,A.,et al, 2009
See this aricle in Pubmed
Article Abstract
By comparison with historical natural history data for patients with Fabry�s disease who were not treated with enzyme replacement therapy, long-term treatment with agalsidase alfa leads to substantial and sustained clinical benefits.
Related Tags
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agalsidase alfa
efficacy
enzyme treatment
enzyme,defect
Fabry's disease
lipid storage disorder of CNS
lysosomal storage disease
treatment of neurologic disorder
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