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Preview	Issue Date	Title	Author(s)
	2003	The a-L-iduronidase mutations R89Q and R89W result in an attenuated mucopolysaccharidosis type I clinical presentation	Hein, L.; Hopwood, J.; Clements, P.; Brooks, D.
	2003	Induction of tolerance to a recombinant human enzyme, acid alpha-glucosidase, in enzyme deficient knockout mice	Raben, N.; Nagaraju, K.; Lee, A.; Lu, N.; Rivera, Y.; Jatkar, T.; Hopwood, J.; Plotz, P.
	2003	Late-onset visceral presentation with cardiomyopathy and without neurological symptoms of adult Sanfilippo A syndrome	Van Hove, J.; Wevers, R.; Van Cleemput, J.; Moerman, P.; Sciot, R.; Matthijs, G.; Schollen, E.; de Jonge, J.; Carey, W.; Muller, V.; Nicholls, C.; Perkins, K.; Hopwood, J.
	2003	Family 39 a-L-iduronidases and b-D-xylosidases react through similar glycosyl-enzyme intermediates: Identification of the human iduronidase nucleophile	Nieman, C.; Wong, A.; He, S.; Clarke, L.; Hopwood, J.; Withers, S.
	2003	Significance of immune response to enzyme-replacement therapy for patients with a lysosomal storage disorder	Brooks, D.; Kakavanos, R.; Hopwood, J.
	2003	Mouse sulphamidase gene: characterization of the promoter region of the gene and expression in mouse tissues	Costanzi, E.; Beccari, T.; Aisa, M.; Tiribuzi, R.; Hopwood, J.; Orlacchio, A.
	2003	Usefulness of bone marrow transplantation in the Hurler syndrome	Braunlin, E.; Stauffer, N.; Peters, C.; Bass, J.; Berry, J.; Hopwood, J.; Krivit, W.
	2003	Replacement therapy in Mucopolysaccharidosis type VI: advantages of early onset of therapy	Auclair, D.; Hopwood, J.; Brooks, D.; Lemontt, J.; Crawley, A.
	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.
	2003	Determination of monosaccharides and disaccharides in mucopolysaccharidoses patients by electrospray ionisation mass spectrometry	Ramsay, S.; Meikle, P.; Hopwood, J.