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Preview	Issue Date	Title	Author(s)
	2004	Glycosaminoglycan degradation fragments in mucopolysaccharidosis I	Fuller, M.; Meikle, P.; Hopwood, J.
	2001	A novel missense mutation in lysosomal sulfamidase is the basis of MPS III A in a spontaneous mouse mutant	Bhattacharyya, R.; Gliddon, B.; Beccari, T.; Hopwood, J.; Stanley, P.
	2003	Identification and characterization of 13 new mutations in mucopolysaccharidosis type I patients	Matte, U.; Yogalingam, G.; Brooks, D.; Leistner, S.; Schwartz, I.; Lima, L.; Norato, D.; Brum, J.; Beesley, C.; Winchester, B.; Giugliani, R.; Hopwood, J.
	2000	Mucopolysaccharidosis type IIIB: characterisation and expression of wild-type and mutant recombinant a-N-acetylglocosaminidase and relationship with Sanfilippo phenotype in an attenuated patient	Yogalingam, G.; Weber, B.; Meehan, J.; Rogers, J.; Hopwood, J.
	2006	Galsulfase	Hopwood, J.; Bate, G.; Kirkpatrick, P.
	2005	Analysis of normal and mutant iduronate-2-sulphatase conformation	Parkinson-Lawrence, E.; Turner, C.; Hopwood, J.; Brooks, D.
	2005	Replacing acid ∝-glucosidase in Pompe disease: recombinant and transgenic enzymes are equipotent, but neither completely clears glycogen from type II muscle fibers	Raben, N.; Fukuda, T.; Gilbert, A.; de Jong, D.; Thurberg, B.; Mattaliano, R.; Meikle, P.; Hopwood, J.; Nagashima, K.; Nagaraju, K.; Plotz, P.
	1995	Isolation and characterisation of a recombinant precursor form of lysosomal acid α-glucosidase	Fuller, M.; Van der Ploeg, A.; Reuser, A.; Anson, D.; Hopwood, J.
	1998	Mild feline mucopolysaccharidosis type VI. Identification of an N-acetylgalactosamine-4-sulfatase mutation causing instability and increased specific activity	Yogalingam, G.; Hopwood, J.; Crawley, A.; Anson, D.
	1996	Enzyme replacement therapy in a feline model of Maroteaux-Lamy syndrome	Crawley, A.; Brooks, D.; Muller, V.; Petersen, B.; Isaac, E.; Bielicki, J.; King, B.; Boulter, C.; Moore, A.; Fazzalari, N.; Anson, D.; Byers, S.; Hopwood, J.