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PreviewIssue DateTitleAuthor(s)
2008Behavioural characterisation of the alpha-mannosidosis guinea pigRobinson, A.; Crawley, A.; Auclair, D.; Weston, P.; Hirte, C.; Hemsley, K.; Hopwood, J.
2007Functional correction of CNS lesions in an MPS-IIIA mouse model by intracerebral AAV-mediated delivery of sulfamidase and SUMF1 genesFraldi, A.; Hemsley, K.; Crawley, A.; Lombardi, A.; Lau, A.; Sutherland, L.; Auricchio, A.; Ballabio, A.; Hopwood, J.
2003Replacement therapy in Mucopolysaccharidosis type VI: advantages of early onset of therapyAuclair, D.; Hopwood, J.; Brooks, D.; Lemontt, J.; Crawley, A.
2005Survival and engraftment of mouse embryonic stem cell-derived implants in the guinea pig brainRobinson, A.; Meedeniya, A.; Hemsley, K.; Auclair, D.; Crawley, A.; Hopwood, J.
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.
2000Enzyme replacement therapy in a feline model of MPS VI: Modification of enzyme structure and dose frequencyByers, S.; Crawley, A.; Brumfield, L.; Nuttall, J.; Hopwood, J.
1999Evaluation of fibroblast-mediated gene therapy in a feline model of mucopolysaccharidosis type VIYogalingam, G.; Crawley, A.; Hopwood, J.; Anson, D.

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