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PreviewIssue DateTitleAuthor(s)
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.
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.
2005Over-expression of human lysosomal -mannosidae in mouse embryonic stem cellsRobinson, A.; 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.
1998Two mutations within a feline mucopolysaccharidosis type VI colony cause three different clinical phenotypesCrawley, A.; Yogalingam, G.; Muller, V.; Hopwood, J.
2004Monitoring dose response of enzyme replacement therapy in feline mucopolysaccharidosis type VI by tandem mass spectrometryCrawley, A.; Ramsay, S.; Byers, S.; Hopwood, J.; Meikle, P.
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.
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.