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Preview	Issue Date	Title	Author(s)
	2005	Replacing acid ∝-glucosidase in Pompe disease: recombinant and transgenic enzymes are equipotent, but neither completely clears glycogen from type II muscle fibers	Raben, N.; Fukuda, T.; Gilbert, A.; de Jong, D.; Thurberg, B.; Mattaliano, R.; Meikle, P.; Hopwood, J.; Nagashima, K.; Nagaraju, K.; Plotz, P.
	2003	Determination of monosaccharides and disaccharides in mucopolysaccharidoses patients by electrospray ionisation mass spectrometry	Ramsay, S.; Meikle, P.; Hopwood, J.
	2006	Common antigenicity for two glycosidases	Kakavanos, R.; Lehn, P.; Callebaut, I.; Meikle, P.; Parkinson-Lawrence, E.; Hopwood, J.; Brooks, D.
	2005	Immunochemical analysis of CD107a (LAMP-1)	Parkinson-Lawrence, E.; Dean, C.; Chang, M.; Hopwood, J.; Meikle, P.; Brooks, D.
	2006	Stabilising normal and mis-sense variant α-glucosidase	Kakavanos, R.; Hopwood, J.; Lang, D.; Meikle, P.; Brooks, D.
	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.
	2004	Monitoring dose response of enzyme replacement therapy in feline mucopolysaccharidosis type VI by tandem mass spectrometry	Crawley, A.; Ramsay, S.; Byers, S.; Hopwood, J.; Meikle, P.
	2004	Disease-specific markers for the mucopolysaccharidoses	Fuller, M.; Rozaklis, T.; Ramsay, S.; Hopwood, J.; Meikle, P.
	2008	Diagnosis of metachromatic leukodystrophy by immune quantification of arylsulphatase A protein and activity in dried blood spots	Tan, M.; Dean, C.; Hopwood, J.; Meikle, P.
	2006	Immunochemistry of lysosomal storage disorders	Parkinson-Lawrence, E.; Fuller, M.; Hopwood, J.; Meikle, P.; Brooks, D.