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Preview	Issue Date	Title	Author(s)
	2004	Spontaneous and engineered mammalian storage disease models	Hopwood, J.; Crawley, A.; Taylor, R.; Platt, F.; Walkley, S.
	2004	Enzyme replacement therapy in mucopolysaccharidosis VI (Maroteaux-Lamy Syndrome)	Harmatz, P.; Whitley, C.; Waber, L.; Pais, R.; Steiner, R.; Plecko, B.; Kaplan, P.; Simon, J.; Butensky, E.; Hopwood, J.
	2004	Mutational analysis of mucopolysaccharidosis type VI patients undergoing a trial of enzyme replacement therapy	Karageorgos, L.; Harmatz, P.; Simon, J.; Pollard, A.; Clements, P.; Brooks, D.; Hopwood, J.
	2004	Transport, enzymatic activity, and stability of mutant sulfamidise (SGSH) identified in patients with mucopolysaccharidosis type III A	Muschol, N.; Storch, S.; Balhausen, D.; Beesley, C.; Westermann, J.; Gal, A.; Ullrich, K.; Hopwood, J.; Winchester, B.; Braulke, T.
	2004	Identification and molecular characterization of α-L-iduronidase mutations present in mucopolysaccharidosis type I patients undergoing enzyme replacement therapy	Yogalingam, G.; Guo, X.; Muller, V.; Brooks, D.; Clements, P.; Kakkis, E.; Hopwood, J.
	2004	Intracerebral injection of sulfamidase delays neuropathology in murine MPS-IIIA	Savas, P.; Hemsley, K.; Hopwood, J.
	2004	Iduronate-2-sulphatase protein detection in plasma from mucopolysaccharidosis type II patients	Parkinson, E.; Muller, V.; Hopwood, J.; Brooks, D.
	2004	Cord-blood transplants from unrelated donors in patients with Hurler's Syndrome	Staba, S.; Escolar, M.; Poe, M.; Kim, Y.; Martin, P.; Szabolcs, P.; Allison-Thacker, J.; Wood, S.; Wenger, D.; Rubenstein, P.; Hopwood, J.; Krivit, W.; Kurtzberg, J.
	2004	In vitro characterization of genetically modified embryonic stem cells as a therapy for murine mucopolysaccharidosis type IIIA	Lau, A.; Hemsley, K.; Meedeniya, A.; Hopwood, J.
	2004	Purification and characterization of recombinant murine sulfamidase	Gliddon, B.; Yogalingam, G.; Hopwood, J.