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Results 31-40 of 221 (Search time: 0.008 seconds).
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PreviewIssue DateTitleAuthor(s)
2005Over-expression of human lysosomal -mannosidae in mouse embryonic stem cellsRobinson, A.; Crawley, A.; Hopwood, J.
2005Direct comparison of measures of endurance, mobility, and joint function during enzyme-replacement therapy of mucopolysaccharidosis VI (Maroteaux-Lamy syndrome): results after 48 weeks in a phase 2 open-label clinical study of recombinant human n-acetylgalactosamine 4-sulfataseHarmatz, P.; Ketteridge, D.; Giugliani, R.; Guffon, N.; Teles, E.; Miranda, C.; Yu, Z.; Swiedler, S.; Hopwood, J.
2004Purification and characterization of recombinant murine sulfamidaseGliddon, B.; Yogalingam, G.; Hopwood, J.
2005Correlation of acid a-glucosidase and glycogen content in skin fibroblasts with age of onset in Pompe diseaseUmapathysivam, K.; Hopwood, J.; Meikle, P.
2007Bovine mucopolysaccharidosis type IIIBKarageorgos, L.; Hill, B.; Bawden, M.; Hopwood, J.
2003Lysosomal storage disorders: emerging therapeutic options require early diagnosisMeikle, P.; Hopwood, J.
2003Prevalence of mucopolysaccharidosis type VI mutations in Siamese catsCrawley, A.; Muntz, F.; Haskins, M.; Jones, B.; Hopwood, J.
2004Diagnosis of lysosomal storage disorders: current techniques and future directionsMeikle, P.; Fietz, M.; 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.
2005Pharmacokinetic profile of recombinant human N-acetylgalactosamine 4-sulphatase enzyme replacement therapy in patients with mucopolysaccharidosis VI (Maroteaux-Lamy syndrome): a phase I/II studyHarmatz, P.; Kramer, W.; Hopwood, J.; Simon, J.; Butensky, E.; Swiedler, S.