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Preview	Issue Date	Title	Author(s)
	2007	Mutational analysis of 105 mucopolysaccharidosis type VI patients	Karageorgos, L.; Brooks, D.; Pollard, A.; Melville, E.; Hein, L.; Clements, P.; Ketteridge, D.; Swiedler, S.; Beck, M.; Giugliani, R.; Harmatz, P.; Wraith, J.; Guffon, N.; Teles, E.; Miranda, C.; Hopwood, J.
	1997	Diagnosis of lysosomal storage disorders: evaluation of lysosome-associated membrane protein LAMP-1 as a diagnostic marker	Meikle, P.; Brooks, D.; Ravenscroft, E.; Yan, M.; Williams, R.; Jaunzems, A.; Chataway, T.; Karageorgos, L.; Davey, R.; Boulter, C.; Carlsson, S.; Hopwood, J.
	2004	Mutational analysis of mucopolysaccharidosis type VI patients undergoing a trial of enzyme replacement therapy	Karageorgos, L.; Harmatz, P.; Simon, J.; Pollard, A.; Clements, P.; Brooks, D.; Hopwood, J.
	2007	Mutational analysis of mucopolysaccharidosis type VI patients undergoing a phase II trial of enzyme replacement therapy	Karageorgos, L.; Brooks, D.; Harmatz, P.; Ketteridge, D.; Pollard, A.; Melville, E.; Parkinson-Lawrence, E.; Clements, P.; Hopwood, J.
	2005	An index case for the attenuated end of the mucopolysaccharidosis type VI clinical spectrum	Brooks, D.; Gibson, G.; Karageorgos, L.; Hein, L.; Robertson, E.; Hopwood, J.
	2014	Aminoglycoside-induced premature stop codon read-through of mucopolysaccharidosis type I patient Q70X and W402X mutations in cultured cells	Kamei, M.; Kasperski, K.; Fuller, M.; Parkinson-Lawrence, E.; Karageorgos, L.; Belakhov, V.; Baasov, T.; Hopwood, J.; Brooks, D.; Zschocke, J.; Gibson, K.; BRown, G.; Morava, E.; Peters, V.
	1997	Lysosomal biogenesis in lysosomal storage disorders	Karageorgos, L.; Isaac, E.; Brooks, D.; Ravenscroft, E.; Davey, R.; Hopwood, J.; Meikle, P.
	2000	Regulation of the lysosome-associated membrane protein in a sucrose model of lysosomal storage	Isaac, E.; Karageorgos, L.; Brooks, D.; Hopwood, J.; Meikle, P.