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Preview	Issue Date	Title	Author(s)
	1998	Coexistence of Gaucher-Disease Type 1 and Joubert-Syndrome	Van Royen-Kerkhof, A.; Pollthe, B.; Kleijer, W.; van Diggelen, O.; Aerts, J.; Hopwood, J.; Beemer, F.
	1998	Identification of a common mutation (R245h) in Sanfilippo A patients from the Netherlands	Weber, B.; Vandekamp, J.; Kleijer, W.; Guo, X.H.; Blanch, L.; van Diggelen, O.; Wevers, R.; Poorthuis, B.; Hopwood, J.
	1998	Molecular heterogeneity in mucopolysaccharidosis IVA in Australia and Northern Ireland: nine novel mutations including T312S, a common allele that confers a mild phenotype	Yamada, N.; Fukuda, S.; Tomatsu, S.; Muller, V.; Hopwood, J.; Nelson, J.; Kato, Z.; Yamagishi, A.; Sukegawa, K.; Kondo, M.; Orii, T.
	1997	Mutations among Italian mucopolysaccharidosis Type I patients	Gatti, R.; Di Natale, P.; Villani, G.; Filocamo, M.; Muller, V.; Guo, X.H.; Nelson, P.; Scott, H.; Hopwood, J.
	1997	Canine fucosidosis: a model for retroviral gene transfer into haematopoietic stem cells	Ferrara, M.; Occhiodoro, T.; Fuller, M.; Hawthorne, W.; Teutsch, S.; Tucker, V.; Hopwood, J.; Stewart, G.; Anson, D.
	1998	Two mutations within a feline mucopolysaccharidosis type VI colony cause three different clinical phenotypes	Crawley, A.; Yogalingam, G.; Muller, V.; 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.
	1998	Receptor Mediated Binding of Two Glycosylation Forms of N-Acetylgalactosamine-4-Sulphatase	Fuller, M.; Hopwood, J.; Anson, D.
	1997	Human mucopolysaccharidosis IIID: clinical, biochemical, morphological and immunohistochemical characteristics	Jones, M.; Alroy, J.; Rutledge, J.; Taylor, J.; Alvord Jnr., E.; Toone, J.; Applegarth, D.; Hopwood, J.; Skutelsky, E.; Ianelli, C.; Thorley Lawson, D.; Mitchell Herpolsheimer, C.; Arias, A.; Sharp, P.; Evans, W.; Sillence, D.; Cavanagh, K.