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Results 111-120 of 123 (Search time: 0.002 seconds).
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PreviewIssue DateTitleAuthor(s)
2009Delivery of recombinant proteins via the cerebrospinal fluid as a therapy option for neurodegenerative lysosomal storage diseasesHemsley, K.; Hopwood, J.
2001Expression and characterization of human recombinant and a-N-actylglucosaminidaseWeber, B.; Hopwood, J.; Yogalingam, G.
2001Prediction of Sanfilippo phenotype severity from immunoquantification of heparan-N-sulfamidase in cultured fibroblasts from mucopolysaccharidosis type IIIA patientsPerkins, K.; Muller, V.; Weber, B.; Hopwood, J.
2000Caprine mucopolysaccharidosis IIID. A preliminary trial of enzyme replacement therapyDown-Kelly, E.; Jones, M.; Alroy, J.; Cavanagh, K.; King, B.; Lucas, R.; Baker, J.; Kraemer, S.; Hopwood, J.
2000Recombinant canine a-L-fucosidase: expression, purification, and characterizationBielicki, J.; Muller, V.; Fuller, M.; Hopwood, J.; Anson, D.
2003Lysosomal storage disorders: emerging therapeutic options require early diagnosisMeikle, P.; 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.
2001Purification and characterization of recombinant human lysosomal a-mannosidaseBerg, T.; King, B.; Meikle, P.; Nilssen, O.; Tollersrud, O.; Hopwood, J.
2000Regulation of the lysosome-associated membrane protein in a sucrose model of lysosomal storageIsaac, E.; Karageorgos, L.; Brooks, D.; Hopwood, J.; Meikle, P.
2004Diagnosis of lysosomal storage disorders: current techniques and future directionsMeikle, P.; Fietz, M.; Hopwood, J.

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