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Results 1-10 of 48 (Search time: 0.002 seconds).
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PreviewIssue DateTitleAuthor(s)
2008Diagnosis of metachromatic leukodystrophy by immune quantification of arylsulphatase A protein and activity in dried blood spotsTan, M.; Dean, C.; Hopwood, J.; Meikle, P.
2011Screening patients referred to a metabolic clinic for lysosomal storage disordersFuller, M.; Tucker, J.; Lang, D.; Dean, C.; Fietz, M.; Meikle, P.; Hopwood, J.
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.
2003Determination of monosaccharides and disaccharides in mucopolysaccharidoses patients by electrospray ionisation mass spectrometryRamsay, S.; Meikle, P.; Hopwood, J.
2006Enzyme replacement therapy in alpha-mannosidosis guinea-pigsCrawley, A.; King, B.; Berg, T.; Meikle, P.; Hopwood, J.
2007Secondary sphingolipid accumulation in a macrophage model of Gaucher diseaseHein, L.; Meikle, P.; Hopwood, J.; Fuller, M.
2005Correlation of acid a-glucosidase and glycogen content in skin fibroblasts with age of onset in Pompe diseaseUmapathysivam, K.; Hopwood, J.; Meikle, P.
2003Lysosomal storage disorders: emerging therapeutic options require early diagnosisMeikle, P.; Hopwood, J.
2004Diagnosis of lysosomal storage disorders: current techniques and future directionsMeikle, P.; Fietz, M.; Hopwood, J.
2004Monitoring dose response of enzyme replacement therapy in feline mucopolysaccharidosis type VI by tandem mass spectrometryCrawley, A.; Ramsay, S.; Byers, S.; Hopwood, J.; Meikle, P.