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Results 31-39 of 39 (Search time: 0.003 seconds).
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PreviewIssue DateTitleAuthor(s)
2005Profiling oligosaccharidurias by electrospray tandem mass spectrometry: Quantifying reducing oligosaccharidesRamsay, S.; Meikle, P.; Hopwood, J.; Clements, P.
2006Immunochemistry of lysosomal storage disordersParkinson-Lawrence, E.; Fuller, M.; Hopwood, J.; Meikle, P.; Brooks, D.
2005Urinary lipid profiling for the identification of Fabry hemizygotes and heterozygotesFuller, M.; Sharp, P.; Rozaklis, T.; Whitfield, P.; Blacklock, D.; Hopwood, J.; Meikle, P.
2001Determination of acid a-glucosidase activity in blood spots as a diagnostic test for Pompe diseaseUmapathysivam, K.; Hopwood, J.; Meikle, P.
2000Determination of acid a-glucosidase protein: evaluation as a screening marker for pompe disease and other lysosomal storage disordersUmapathysivam, K.; Whittle, A.; Ranieri, E.; Bindloss, C.; Ravenscroft, E.; Van Diggelen, O.; Hopwood, J.; Meikle, P.
2000Saposins A,B,C, and D in plasma of patients with lysosomal storage disordersChang, M.; Bindloss, C.; Grabowski, G.; Qi, X.; Winchester, B.; Hopwood, J.; Meikle, P.
2002Determination of oligosaccharides in Pompe disease by electrospray ionization tandem mass spectrometryRozaklis, T.; Ramsay, S.; Whitfield, P.; Ranieri, E.; Hopwood, J.; Meikle, P.
2004Immunoquantification of a-galactosidase: Evaluation for the diagnosis of Fabry DiseaseFuller, M.; Lovejoy, M.; Brooks, D.; Harkin, M.; Hopwood, J.; Meikle, P.
2006Detection of mucopolysaccharidosis type II by measurement of iduronate-2-sulfatase in dried blood spots and plasma samplesDean, C.; Bockmann, M.; Hopwood, J.; Brooks, D.; Meikle, P.