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PreviewIssue DateTitleAuthor(s)
2007Mutational analysis of 105 mucopolysaccharidosis type VI patientsKarageorgos, L.; Brooks, D.; Pollard, A.; Melville, E.; Hein, L.; Clements, P.; Ketteridge, D.; Swiedler, S.; Beck, M.; Giugliani, R.; Harmatz, P.; Wraith, J.; Guffon, N.; Teles, E.; Miranda, C.; Hopwood, J.
2003The a-L-iduronidase mutations R89Q and R89W result in an attenuated mucopolysaccharidosis type I clinical presentationHein, L.; Hopwood, J.; Clements, P.; Brooks, D.
2004Mutational analysis of mucopolysaccharidosis type VI patients undergoing a trial of enzyme replacement therapyKarageorgos, L.; Harmatz, P.; Simon, J.; Pollard, A.; Clements, P.; Brooks, D.; Hopwood, J.
2004Identification and molecular characterization of α-L-iduronidase mutations present in mucopolysaccharidosis type I patients undergoing enzyme replacement therapyYogalingam, G.; Guo, X.; Muller, V.; Brooks, D.; Clements, P.; Kakkis, E.; Hopwood, J.
2005Profiling oligosaccharidurias by electrospray tandem mass spectrometry: Quantifying reducing oligosaccharidesRamsay, S.; Meikle, P.; Hopwood, J.; Clements, P.
1995Crystallization and preliminary characterisation of human recombinant N-acetylpgalactosamine-4-sulfataseAshby, S.; Clements, P.; Guss, J.; Harvey, J.; Hopwood, J.
2007Mutational analysis of mucopolysaccharidosis type VI patients undergoing a phase II trial of enzyme replacement therapyKarageorgos, L.; Brooks, D.; Harmatz, P.; Ketteridge, D.; Pollard, A.; Melville, E.; Parkinson-Lawrence, E.; Clements, P.; Hopwood, J.
1997Structure of a human lysosomal sulfataseBond, C.; Clements, P.; Ashby, S.; Collyer, C.; Harrop, S.; Hopwood, J.; Guss, 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.