1. Adelaide Research & Scholarship

Search


Current filters:

Start a new search
Add filters:

Use filters to refine the search results.

 | 
Results 111-120 of 129 (Search time: 0.005 seconds).
Item hits:
PreviewIssue DateTitleAuthor(s)
2001Coronary artery patency following long-term successful engraftment 14 years after bone marrow transplantation in the Hurler syndromeBraunlin, E.; Rose, A.; Hopwood, J.; Candel, R.; Krivit, W.
2009Delivery of recombinant proteins via the cerebrospinal fluid as a therapy option for neurodegenerative lysosomal storage diseasesHemsley, K.; Hopwood, J.
1997Lysosomal biogenesis in lysosomal storage disordersKarageorgos, L.; Isaac, E.; Brooks, D.; Ravenscroft, E.; Davey, R.; Hopwood, J.; Meikle, P.
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.
1998Receptor Mediated Binding of Two Glycosylation Forms of N-Acetylgalactosamine-4-SulphataseFuller, M.; Hopwood, J.; Anson, D.
2000Recombinant canine a-L-fucosidase: expression, purification, and characterizationBielicki, J.; Muller, V.; Fuller, M.; Hopwood, J.; Anson, D.
2002Correlation among genotype, phenotype, and biochemical markers in Gaucher disease: Implications for the prediction of disease severityWhitfield, P.; Nelson, P.; Sharp, P.; Bindloss, C.; Dean, C.; Ravenscroft, E.; Fong, B.; Fietz, M.; Hopwood, J.; Meikle, P.
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.

Discover