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PreviewIssue DateTitleAuthor(s)
2005Replacing acid ∝-glucosidase in Pompe disease: recombinant and transgenic enzymes are equipotent, but neither completely clears glycogen from type II muscle fibersRaben, N.; Fukuda, T.; Gilbert, A.; de Jong, D.; Thurberg, B.; Mattaliano, R.; Meikle, P.; Hopwood, J.; Nagashima, K.; Nagaraju, K.; Plotz, P.
2005Correlation of acid a-glucosidase and glycogen content in skin fibroblasts with age of onset in Pompe diseaseUmapathysivam, K.; Hopwood, J.; Meikle, P.
2005Immunoquantification of b-glucosidase: Diagnosis and prediction of severity in Gaucher diseaseFuller, M.; Lovejoy, M.; Hopwood, J.; Meikle, P.
2005Development of an assay for the detection of mucopolysaccharidosis type VI patients using dried blood-spotsHein, L.; Meikle, P.; Dean, C.; Bockmann, M.; Auclair, D.; Hopwood, J.; Brooks, D.
2005Prediction of neuropathology in mucopolysaccharidosis I patientsFuller, M.; Brooks, D.; Evangelista, M.; Hein, L.; Hopwood, J.; Meikle, P.
2005Laronidase treatment of mucopolysaccharidosis IWraith, J.; Hopwood, J.; Fuller, M.; Meikle, P.; Brooks, D.
2005Immunochemical analysis of CD107a (LAMP-1)Parkinson-Lawrence, E.; Dean, C.; Chang, M.; Hopwood, J.; Meikle, P.; Brooks, D.
2005Profiling oligosaccharidurias by electrospray tandem mass spectrometry: Quantifying reducing oligosaccharidesRamsay, S.; Meikle, P.; Hopwood, J.; Clements, P.
2005Urinary lipid profiling for the identification of Fabry hemizygotes and heterozygotesFuller, M.; Sharp, P.; Rozaklis, T.; Whitfield, P.; Blacklock, D.; Hopwood, J.; Meikle, P.