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Preview	Issue Date	Title	Author(s)
	2006	Intra-articular enzyme administration for joint disease in feline mucopolysaccharidosis VI: Enzyme dose and interval	Auclair, D.; Hein, L.; Hopwood, J.; Byers, S.
	2004	Monitoring dose response of enzyme replacement therapy in feline mucopolysaccharidosis type VI by tandem mass spectrometry	Crawley, A.; Ramsay, S.; Byers, S.; Hopwood, J.; Meikle, P.
	2004	Enzyme-replacement therapy from birth delays the development of behavior and learning problems in mucopolysaccharidosis type IIIA mice	Gliddon, B.; Hopwood, J.
	2004	Caprine mucopolysaccharidosis IIID - Fetal and neonatal brain and liver glycosaminoglycan and morphological perturbations	Jones, M.; Alroy, J.; Downs-Kelly, E.; Lucas, R.; Kraemer, S.; Cavanagh, K.; King, B.; Hopwood, J.
	1999	Alpha-mannosidosis in the guinea pig: A new animal model for lysosomal storage disorders	Crawley, A.; Jones, M.; Bonning, L.; Finnie, J.; Hopwood, J.
	2004	Disease-specific markers for the mucopolysaccharidoses	Fuller, M.; Rozaklis, T.; Ramsay, S.; Hopwood, J.; Meikle, P.
	2000	Enzyme replacement therapy in a feline model of MPS VI: Modification of enzyme structure and dose frequency	Byers, S.; Crawley, A.; Brumfield, L.; Nuttall, J.; Hopwood, J.
	2005	Direct 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-sulfatase	Harmatz, P.; Ketteridge, D.; Giugliani, R.; Guffon, N.; Teles, E.; Miranda, C.; Yu, Z.; Swiedler, S.; Hopwood, J.
	2008	Diagnosis of metachromatic leukodystrophy by immune quantification of arylsulphatase A protein and activity in dried blood spots	Tan, M.; Dean, C.; Hopwood, J.; Meikle, P.
	2006	Immunochemistry of lysosomal storage disorders	Parkinson-Lawrence, E.; Fuller, M.; Hopwood, J.; Meikle, P.; Brooks, D.