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Results 31-39 of 39 (Search time: 0.003 seconds).
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PreviewIssue DateTitleAuthor(s)
1998Two mutations within a feline mucopolysaccharidosis type VI colony cause three different clinical phenotypesCrawley, A.; Yogalingam, G.; Muller, V.; Hopwood, J.
1998Genotype-phenotype correlations in mucopolysaccharidosis type I using enzyme kinetics, immunoquantification and in vitro turnover studiesBunge, S.; Clements, P.; Byers, S.; Kleijer, W.; Brooks, D.; Hopwood, J.
1996Cloning and Expression of the Gene Involved in Sanfilippo B Syndrome (Mucopolysaccharidosis III B)Weber, B.; Blanch, L.; Clements, P.; Scott, H.; Hopwood, J.
1997Lysosomal biogenesis in lysosomal storage disordersKarageorgos, L.; Isaac, E.; Brooks, D.; Ravenscroft, E.; Davey, R.; Hopwood, J.; Meikle, P.
1998Receptor Mediated Binding of Two Glycosylation Forms of N-Acetylgalactosamine-4-SulphataseFuller, M.; Hopwood, J.; Anson, D.
1998Molecular genetics of mucopolysaccharidosis type I - mutation analysis among the patients of the former Soviet UnionVoskoboeva, E.; Krasnopolskaya, X.; Mirenburg, T.; Weber, B.; Hopwood, J.
1999Altered trafficking and turnover of LAMP-1 in Pompe disease-affected cellsMeikle, P.; Yan, M.; Ravenscroft, E.; Isaac, E.; Hopwood, J.; Brooks, D.
1997Enzyme replacement therapy in Mucopolysaccharidosis VI: evidence for immune responses and altered efficacy of treatment in animal modelsBrooks, D.; King, B.; Crawley, A.; Byers, S.; Hopwood, J.
1997Human mucopolysaccharidosis IIID: clinical, biochemical, morphological and immunohistochemical characteristicsJones, 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.