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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	Evaluation of the lysosome-associated membrane protein LAMP-2 as a marker for lysosomal storage disorders	Hua, C.; Hopwood, J.; Carlsson, S.; Harris, R.; Meikle, P.
	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.
	1998	Recombinant human sulphamidase: expression, amplification, purification and characterization	Bielicki, J.; Hopwood, J.; Melville, E.; Anson, D.
	1998	Development of a two-dimensional gel electrophoresis database of human lysosomal proteins	Chataway, T.; Whittle, A.; Lewis, M.; Bindloss, C.; Moritz, R.; Simpson, R.; Hopwood, J.; Meikle, P.
	1998	Two-dimensional mapping and microsequencing of lysosomal proteins from human placenta	Chataway, T.; Whittle, A.; Lewis, M.; Bindloss, C.; Davey, R.; Moritz, R.; Simpson, R.; Hopwood, J.; Meikle, P.
	1998	Two mutations within a feline mucopolysaccharidosis type VI colony cause three different clinical phenotypes	Crawley, A.; Yogalingam, G.; Muller, V.; Hopwood, J.
	1998	Genotype-phenotype correlations in mucopolysaccharidosis type I using enzyme kinetics, immunoquantification and in vitro turnover studies	Bunge, S.; Clements, P.; Byers, S.; Kleijer, W.; Brooks, D.; Hopwood, J.
	1998	Receptor Mediated Binding of Two Glycosylation Forms of N-Acetylgalactosamine-4-Sulphatase	Fuller, M.; Hopwood, J.; Anson, D.