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Preview	Issue Date	Title	Author(s)
	1999	Prevalence of lysosomal storage disorders	Meikle, P.; Hopwood, J.; Clague, A.; Carey, W.
	2010	Enzyme replacement therapy for mucopolysaccharidosis VI: evaluation of long-term pulmonary function in patients treated with recombinant human N-acetylgalactosamine 4-sulfatase	Harmatz, P.; Yu, Z.; Giugliani, R.; Schwartz, I.; Guffon, N.; Teles, E.; Miranda, C.; Wraith, J.; Beck, M.; Arash, L.; Scarpa, M.; Ketteridge, D.; Hopwood, J.; Plecko, B.; Steiner, R.; Whitley, C.; Kaplan, P.; Swiedler, S.; Hardy, K.; Berger, K.; et al.
	2000	Gene encoding the mouse sulphamidase: cDNA cloning, structure, and chromosomal mapping	Costanzi, E.; Beccari, T.; Stinchi, S.; Bibi, L.; Hopwood, J.; Orlacchio, A.
	2011	Gaucher disease in sheep	Karageorgos, L.; Lancaster, M.; Nimmo, J.; Hopwood, J.
	2005	Profiling oligosaccharidurias by electrospray tandem mass spectrometry: Quantifying reducing oligosaccharides	Ramsay, S.; Meikle, P.; Hopwood, J.; Clements, P.
	2011	Emerging therapies for neurodegenerative lysosomal storage disorders - from concept to reality	Hemsley, K.; Hopwood, J.
	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.
	2007	N-acetylgalactosamine-6-sulfatase protein detection in MPS IVA patient and unaffected control samples	Parkinson-Lawrence, E.; Muller, V.; Hopwood, J.; Brooks, D.
	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.