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Results 1-10 of 221 (Search time: 0.005 seconds).
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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.
2000Recombinant canine a-L-fucosidase: expression, purification, and characterizationBielicki, J.; Muller, V.; Fuller, M.; Hopwood, J.; Anson, D.
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.
2008Maroteaux-Lamy syndrome: Functional characterization of pathogenic mutations and polymorphisms in the arylsulfatase B geneGarrido, E.; Cormand, B.; Hopwood, J.; Chabas, A.; Grinberg, D.; Vilageliu, L.
2008Lipid composition of microdomains is altered in a cell model of Gaucher diseaseHein, L.; Duplock, S.; Hopwood, J.; Fuller, M.
2008Long-term follow-up of endurance and safety outcomes during enzyme replacement therapy for mucopolysaccharidosis VI: Final results of three clinical studies of recombinant human N-acetylgalactosamine 4-sulfataseHarmatz, P.; Giugliani, R.; Schwartz, I.; Guffon, N.; Teles, E.; Miranda, C.; Wraith, J.; Beck, M.; Arash, L.; Scarpa, M.; Ketteridge, D.; Hopwood, J.; Plecko, B.; Steiner, R.; Whitley, C.; Kaplan, P.; Yu, Z.; Swiedler, S.; Decker, C.
2007Morphopathological features in tissues of α-mannosidosis guinea pigs at different gestational agesAuclair, D.; Hopwood, J.
2008Diagnosis of metachromatic leukodystrophy by immune quantification of arylsulphatase A protein and activity in dried blood spotsTan, M.; Dean, C.; Hopwood, J.; Meikle, P.
2003Induction of tolerance to a recombinant human enzyme, acid alpha-glucosidase, in enzyme deficient knockout miceRaben, N.; Nagaraju, K.; Lee, A.; Lu, N.; Rivera, Y.; Jatkar, T.; Hopwood, J.; Plotz, P.

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