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PreviewIssue DateTitleAuthor(s)
2004Determination of oligosaccharides and glycolipids in amniotic fluid by electrospray ionisation tandem mass spectrometry: in utero indicators of lysosomal storage diseasesRamsay, S.; Maire, I.; Bindloss, C.; Fuller, M.; Whitfield, P.; Piraud, M.; Hopwood, J.; Meikle, P.
2004Newborn screening for lysosomal storage disorders: Clinical evaluation of a two-tier strategyMeikle, P.; Ranieri, E.; Simonsen, H.; Rozaklis, T.; Ramsay, S.; Whitfield, P.; Fuller, M.; Christensen, E.; Skovby, F.; Hopwood, J.
1995Isolation and characterisation of a recombinant precursor form of lysosomal acid α-glucosidaseFuller, M.; Van der Ploeg, A.; Reuser, A.; Anson, D.; Hopwood, J.
2000Recombinant canine a-L-fucosidase: expression, purification, and characterizationBielicki, J.; Muller, V.; Fuller, M.; Hopwood, J.; Anson, D.
1998Receptor Mediated Binding of Two Glycosylation Forms of N-Acetylgalactosamine-4-SulphataseFuller, M.; Hopwood, J.; Anson, D.
1995Expression, purification and characterization of recombinant human N-acetylgalactosamine-6-sulphataseBielicki, J.; Fuller, M.; Guo, X.; Morris, C.; Hopwood, J.; Anson, D.
1997Canine fucosidosis: a model for retroviral gene transfer into haematopoietic stem cellsFerrara, M.; Occhiodoro, T.; Fuller, M.; Hawthorne, W.; Teutsch, S.; Tucker, V.; Hopwood, J.; Stewart, G.; Anson, D.
2011Enzyme replacement reduces neuropathology in MPS IIIA dogsCrawley, A.; Marshall, N.; Beard, H.; Hassiotis, S.; Walsh, V.; King, B.; Hucker, N.; Fuller, M.; Jolly, R.; Hopwood, J.; Hemsley, K.
2010Enzyme replacement therapy for mucopolysaccharidosis VI from 8 weeks of age - a sibling control studyMcGill, J.; Inwood, A.; Coman, D.; Lipke, M.; de Lore, D.; Swiedler, S.; Hopwood, J.
2008Behavioural characterisation of the alpha-mannosidosis guinea pigRobinson, A.; Crawley, A.; Auclair, D.; Weston, P.; Hirte, C.; Hemsley, K.; Hopwood, J.