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PreviewIssue DateTitleAuthor(s)
1996Feline mucopolysaccharidosis type VI - characterization of recombinant N-acetylgalactosamine 4-sulfatase and identification of a mutation causing the diseaseYogalingam, G.; Litjens, T.; Bielicki, J.; Crawley, A.; Muller, V.; Anson, D.; Hopwood, J.
1999Advantages of using same species enzyme for replacement therapy in a feline model of mucopolysaccharidosis type VIBielicki, J.; Crawley, A.; Davey, R.; Varnai, J.; Hopwood, J.
1997Effect of enzyme replacement therapy on bone formation in a feline model of mucopolysaccharidosis Type VIByers, S.; Nuttall, J.; Crawley, A.; Hopwood, J.; Smith, K.; Fazzalari, N.
1998Mild feline mucopolysaccharidosis type VI. Identification of an N-acetylgalactosamine-4-sulfatase mutation causing instability and increased specific activityYogalingam, G.; Hopwood, J.; Crawley, A.; Anson, D.
1996Enzyme replacement therapy in a feline model of Maroteaux-Lamy syndromeCrawley, A.; Brooks, D.; Muller, V.; Petersen, B.; Isaac, E.; Bielicki, J.; King, B.; Boulter, C.; Moore, A.; Fazzalari, N.; Anson, D.; Byers, S.; Hopwood, J.
1997Enzyme replacement therapy from birth in a feline model of mucopolysaccharidosis type VICrawley, A.; Niedzielski, K.; Isaac, E.; Davey, R.; Byers, S.; Hopwood, J.
1998Two mutations within a feline mucopolysaccharidosis type VI colony cause three different clinical phenotypesCrawley, A.; Yogalingam, G.; Muller, V.; Hopwood, J.
1999Alpha-mannosidosis in the guinea pig: A new animal model for lysosomal storage disordersCrawley, A.; Jones, M.; Bonning, L.; Finnie, J.; Hopwood, J.
1999Evaluation of fibroblast-mediated gene therapy in a feline model of mucopolysaccharidosis type VIYogalingam, G.; Crawley, A.; Hopwood, J.; Anson, D.
1997Enzyme replacement therapy in Mucopolysaccharidosis VI: evidence for immune responses and altered efficacy of treatment in animal modelsBrooks, D.; King, B.; Crawley, A.; Byers, S.; Hopwood, J.