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Results 21-30 of 33 (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.
2006GalsulfaseHopwood, J.; Bate, G.; Kirkpatrick, P.
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.
2003Prevalence of mucopolysaccharidosis type VI mutations in Siamese catsCrawley, A.; Muntz, F.; Haskins, M.; Jones, B.; Hopwood, J.
2011Screening patients referred to a metabolic clinic for lysosomal storage disordersFuller, M.; Tucker, J.; Lang, D.; Dean, C.; Fietz, M.; Meikle, P.; Hopwood, J.
1998Two mutations within a feline mucopolysaccharidosis type VI colony cause three different clinical phenotypesCrawley, A.; Yogalingam, G.; Muller, V.; Hopwood, J.
2006Intra-articular enzyme administration for joint disease in feline mucopolysaccharidosis VI: Enzyme dose and intervalAuclair, D.; Hein, L.; Hopwood, J.; Byers, S.
1999Alpha-mannosidosis in the guinea pig: A new animal model for lysosomal storage disordersCrawley, A.; Jones, M.; Bonning, L.; Finnie, J.; 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.
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.

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