Enzyme replacement therapy with agalsidase alfa in children with Fabry disease
Author:
Publisher
Wiley
Subject
General Medicine,Pediatrics, Perinatology, and Child Health
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1651-2227.2007.00029.x/fullpdf
Reference19 articles.
1. Enzymatic defect in Fabry disease;Brady;New Engl J Med,1967
2. Anderson-Fabry disease: a histopathological study of three cases with observations on the mechanism of production of pain;Kahn;J Neurol Neurosurg Psychiatry,1973
3. Nervous system involvement in Fabry's disease: clinicopathological and biochemical correlation;Kaye;Ann Neurol,1988
4. Fabry disease: immunocytochemical characterization of neuronal involvement;deVeber;Ann Neurol,1992
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