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Preview	Issue Date	Title	Author(s)
	2005	An index case for the attenuated end of the mucopolysaccharidosis type VI clinical spectrum	Brooks, D.; Gibson, G.; Karageorgos, L.; Hein, L.; Robertson, E.; Hopwood, J.
	2002	Mucopolysaccharidosis type VI (Maroteaux-Lamy syndrome): A Y210C mutation causes either altered protein handling or altered protein function of N-acetylgalactosamine 4-sulfatase at multiple points in the vacuolar network	Bradford, T.; Litjens, T.; Parkinson, E.; Hopwood, J.; Brooks, D.
	2001	Gentamicin-mediated suppression of Hurler syndrome stop mutations restores a low level of a-L-iduronidase activity and reduces lysosomal glycosaminoglycan accumulation	Keeling, K.; Brooks, D.; Hopwood, J.; Li, P.; Thompson, J.; Bedwell, D.
	2003	Replacement therapy in Mucopolysaccharidosis type VI: advantages of early onset of therapy	Auclair, D.; Hopwood, J.; Brooks, D.; Lemontt, J.; Crawley, A.
	1997	A membrane protein primarily associated with the lysosomal compartment	Brooks, D.; Bradford, T.; Carlsson, S.; Hopwood, J.
	2002	Immune response to enzyme replacement therapy: single epitope control of antigen distribution from circulation	Glaros, E.; Turner, C.; Parkinson, E.; Hopwood, J.; Brooks, 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.
	1997	Lysosomal biogenesis in lysosomal storage disorders	Karageorgos, L.; Isaac, E.; Brooks, D.; Ravenscroft, E.; Davey, R.; Hopwood, J.; Meikle, P.
	1999	Altered trafficking and turnover of LAMP-1 in Pompe disease-affected cells	Meikle, P.; Yan, M.; Ravenscroft, E.; Isaac, E.; Hopwood, J.; Brooks, D.
	2000	Regulation of the lysosome-associated membrane protein in a sucrose model of lysosomal storage	Isaac, E.; Karageorgos, L.; Brooks, D.; Hopwood, J.; Meikle, P.