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Results 1-10 of 126 (Search time: 0.002 seconds).
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PreviewIssue DateTitleAuthor(s)
2007Pathology of mucopolysaccharidosis IIIA in huntaway dogsJolly, R.; Johnstone, A.; Norman, E.; Hopwood, J.; Walkley, S.
2007Mutational analysis of 105 mucopolysaccharidosis type VI patientsKarageorgos, L.; Brooks, D.; Pollard, A.; Melville, E.; Hein, L.; Clements, P.; Ketteridge, D.; Swiedler, S.; Beck, M.; Giugliani, R.; Harmatz, P.; Wraith, J.; Guffon, N.; Teles, E.; Miranda, C.; Hopwood, J.
2003The a-L-iduronidase mutations R89Q and R89W result in an attenuated mucopolysaccharidosis type I clinical presentationHein, L.; Hopwood, J.; Clements, P.; Brooks, D.
2002Sanfilippo syndrome in Turkey: Identification of novel mutations in subtypes A and BEmre, S.; Terzioglu, M.; Tokatli, A.; Coskun, T.; Ozalp, I.; Weber, B.; Hopwood, J.
2007Morphopathological features in tissues of α-mannosidosis guinea pigs at different gestational agesAuclair, D.; Hopwood, J.
2004Spontaneous and engineered mammalian storage disease modelsHopwood, J.; Crawley, A.; Taylor, R.; Platt, F.; Walkley, S.
2002Biochemical and molecular analysis of mucopolysaccharidoses in TurkeyEmre, S.; Terzioglu, M.; Coskun, T.; Tokatli, A.; Ozalp, I.; Muller, V.; Hopwood, J.
2001Selection of endpoints in clinical studies of enzyme replacement therapy in lysosomal storage disorders - CommentaryHopwood, J.
2000Determination of acid a-glucosidase protein: evaluation as a screening marker for pompe disease and other lysosomal storage disordersUmapathysivam, K.; Whittle, A.; Ranieri, E.; Bindloss, C.; Ravenscroft, E.; Van Diggelen, O.; 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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