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Preview	Issue Date	Title	Author(s)
	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.
	1998	Two-dimensional mapping and microsequencing of lysosomal proteins from human placenta	Chataway, T.; Whittle, A.; Lewis, M.; Bindloss, C.; Davey, R.; Moritz, R.; Simpson, R.; Hopwood, J.; Meikle, P.
	2001	Conditional tissue-specific expression of the acid α-glucosidase (GAA) gene in the GAA knockout mice: implications for therapy	Raben, N.; Lu, N.; Nagaraju, K.; Rivera, Y.; Lee, A.; Yan, B.; Byrne, B.; Meikle, P.; Umapathysivam, K.; Hopwood, J.; Plotz, P.
	2004	Glycosaminoglycan degradation fragments in mucopolysaccharidosis I	Fuller, M.; Meikle, P.; Hopwood, J.
	2005	Prediction of neuropathology in mucopolysaccharidosis I patients	Fuller, M.; Brooks, D.; Evangelista, M.; Hein, L.; Hopwood, J.; Meikle, P.
	2007	Secondary sphingolipid accumulation in a macrophage model of Gaucher disease	Hein, L.; Meikle, P.; Hopwood, J.; Fuller, M.
	2004	Determination of oligosaccharides and glycolipids in amniotic fluid by electrospray ionisation tandem mass spectrometry: in utero indicators of lysosomal storage diseases	Ramsay, S.; Maire, I.; Bindloss, C.; Fuller, M.; Whitfield, P.; Piraud, M.; Hopwood, J.; Meikle, P.
	2008	Effect of lysosomal storage on bis(monoacylglycero)phosphate	Meikle, P.; Duplock, S.; Blacklock, D.; Whitfield, P.; Macintosh, G.; Hopwood, J.; Fuller, M.
	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.