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Preview	Issue Date	Title	Author(s)
	2009	Examination of intravenous and intra-CSF protein delivery for treatment of neurological disease	Hemsley, K.; Luck, A.; Crawley, A.; Hassiotis, S.; Beard, H.; King, B.; Rozek, T.; Rozaklis, T.; Fuller, M.; Hopwood, J.
	1995	Isolation and characterisation of a recombinant precursor form of lysosomal acid α-glucosidase	Fuller, M.; Van der Ploeg, A.; Reuser, A.; Anson, D.; Hopwood, J.
	2011	Screening patients referred to a metabolic clinic for lysosomal storage disorders	Fuller, M.; Tucker, J.; Lang, D.; Dean, C.; Fietz, M.; Meikle, P.; Hopwood, J.
	2010	Sphingolipids: the nexus between Gaucher disease and insulin resistance	Fuller, M.
	2008	Lipid composition of microdomains is altered in a cell model of Gaucher disease	Hein, L.; Duplock, S.; Hopwood, J.; Fuller, M.
	2013	Selective reduction of bis(monoacylglycero)phosphate ameliorates the storage burden in a THP-1 macrophage model of Gaucher disease	Hein, L.; Duplock, S.; Fuller, M.
	2014	Liquid chromatography/electrospray ionisation-tandem mass spectrometry quantification of GM2 gangliosides in human peripheral cells and plasma	Fuller, M.; Duplock, S.; Hein, L.; Rigat, B.; Mahuran, D.
	2004	Disease-specific markers for the mucopolysaccharidoses	Fuller, M.; Rozaklis, T.; Ramsay, S.; Hopwood, J.; Meikle, P.
	2006	Immunochemistry of lysosomal storage disorders	Parkinson-Lawrence, E.; Fuller, M.; Hopwood, J.; Meikle, P.; Brooks, D.
	2004	Immunoquantification of a-galactosidase: Evaluation for the diagnosis of Fabry Disease	Fuller, M.; Lovejoy, M.; Brooks, D.; Harkin, M.; Hopwood, J.; Meikle, P.