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PreviewIssue DateTitleAuthor(s)
2004Determination of oligosaccharides and glycolipids in amniotic fluid by electrospray ionisation tandem mass spectrometry: in utero indicators of lysosomal storage diseasesRamsay, S.; Maire, I.; Bindloss, C.; Fuller, M.; Whitfield, P.; Piraud, M.; Hopwood, J.; Meikle, P.
2004Newborn screening for lysosomal storage disorders: Clinical evaluation of a two-tier strategyMeikle, P.; Ranieri, E.; Simonsen, H.; Rozaklis, T.; Ramsay, S.; Whitfield, P.; Fuller, M.; Christensen, E.; Skovby, F.; Hopwood, J.
2008Plasma lipids are altered in Gaucher disease: Biochemical markers to evaluate therapeutic interventionMeikle, P.; Whitfield, P.; Rozaklis, T.; Blacklock, D.; Duplock, S.; Elstein, D.; Zimran, A.; Mengel, E.; Cannell, P.; Hopwood, J.; Fuller, M.
2008Effect of lysosomal storage on bis(monoacylglycero)phosphateMeikle, P.; Duplock, S.; Blacklock, D.; Whitfield, P.; Macintosh, G.; Hopwood, J.; Fuller, M.
2008Minimum substrate requirements of endoglycosidase activities toward dermatan sulfate by electrospray ionization-tandem mass spectrometryNielsen, T.; Meikle, P.; Hopwood, J.; Fuller, M.
2008Glucosylceramide accumulation is not confined to the lysosome in fibroblasts from patients with Gaucher diseaseFuller, M.; Rozaklis, T.; Lovejoy, M.; Zarrinkalam, K.; Hopwood, J.; Meikle, P.
2004Glycosaminoglycan degradation fragments in mucopolysaccharidosis IFuller, M.; Meikle, P.; Hopwood, J.
2007Secondary sphingolipid accumulation in a macrophage model of Gaucher diseaseHein, L.; Meikle, P.; Hopwood, J.; Fuller, M.
2004Disease-specific markers for the mucopolysaccharidosesFuller, M.; Rozaklis, T.; Ramsay, S.; Hopwood, J.; Meikle, P.
2006Characterization of sulfated oligosaccharides in mucopolysaccharidosis type IIIA by electrospray ionization mass spectrometryMason, K.; Meikle, P.; Hopwood, J.; Fuller, M.