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Preview	Issue Date	Title	Author(s)
	2000	Determination of acid a-glucosidase protein: evaluation as a screening marker for pompe disease and other lysosomal storage disorders	Umapathysivam, K.; Whittle, A.; Ranieri, E.; Bindloss, C.; Ravenscroft, E.; Van Diggelen, O.; Hopwood, J.; Meikle, P.
	2000	Saposins A,B,C, and D in plasma of patients with lysosomal storage disorders	Chang, M.; Bindloss, C.; Grabowski, G.; Qi, X.; Winchester, B.; Hopwood, J.; Meikle, P.
	2002	Determination of oligosaccharides in Pompe disease by electrospray ionization tandem mass spectrometry	Rozaklis, T.; Ramsay, S.; Whitfield, P.; Ranieri, E.; Hopwood, J.; Meikle, P.
	2001	Determination of acid a-glucosidase activity in blood spots as a diagnostic test for Pompe disease	Umapathysivam, K.; Hopwood, J.; Meikle, P.
	2005	Profiling oligosaccharidurias by electrospray tandem mass spectrometry: Quantifying reducing oligosaccharides	Ramsay, S.; Meikle, P.; Hopwood, J.; Clements, P.
	2008	Plasma lipids are altered in Gaucher disease: Biochemical markers to evaluate therapeutic intervention	Meikle, P.; Whitfield, P.; Rozaklis, T.; Blacklock, D.; Duplock, S.; Elstein, D.; Zimran, A.; Mengel, E.; Cannell, P.; Hopwood, J.; Fuller, M.
	2005	Development of an assay for the detection of mucopolysaccharidosis type VI patients using dried blood-spots	Hein, L.; Meikle, P.; Dean, C.; Bockmann, M.; Auclair, D.; Hopwood, J.; Brooks, D.
	2005	Correlation of acid a-glucosidase and glycogen content in skin fibroblasts with age of onset in Pompe disease	Umapathysivam, K.; Hopwood, J.; Meikle, P.
	2008	Glucosylceramide accumulation is not confined to the lysosome in fibroblasts from patients with Gaucher disease	Fuller, M.; Rozaklis, T.; Lovejoy, M.; Zarrinkalam, K.; Hopwood, J.; Meikle, P.
	2006	Enzyme replacement therapy in alpha-mannosidosis guinea-pigs	Crawley, A.; King, B.; Berg, T.; Meikle, P.; Hopwood, J.