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PreviewIssue DateTitleAuthor(s)
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.
2001Determination of acid a-glucosidase activity in blood spots as a diagnostic test for Pompe diseaseUmapathysivam, K.; Hopwood, J.; Meikle, P.
1998Evaluation of the lysosome-associated membrane protein LAMP-2 as a marker for lysosomal storage disordersHua, C.; Hopwood, J.; Carlsson, S.; Harris, R.; Meikle, P.
1998Two-dimensional mapping and microsequencing of lysosomal proteins from human placentaChataway, T.; Whittle, A.; Lewis, M.; Bindloss, C.; Davey, R.; Moritz, R.; Simpson, R.; Hopwood, J.; Meikle, P.
2005Prediction of neuropathology in mucopolysaccharidosis I patientsFuller, M.; Brooks, D.; Evangelista, M.; Hein, L.; Hopwood, J.; Meikle, P.
2003Determination of monosaccharides and disaccharides in mucopolysaccharidoses patients by electrospray ionisation mass spectrometryRamsay, S.; Meikle, P.; Hopwood, J.
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.
2004Immunoquantification of a-galactosidase: Evaluation for the diagnosis of Fabry DiseaseFuller, M.; Lovejoy, M.; Brooks, D.; Harkin, M.; Hopwood, J.; Meikle, P.
2005Laronidase treatment of mucopolysaccharidosis IWraith, J.; Hopwood, J.; Fuller, M.; Meikle, P.; Brooks, D.
2002Correlation among genotype, phenotype, and biochemical markers in Gaucher disease: Implications for the prediction of disease severityWhitfield, P.; Nelson, P.; Sharp, P.; Bindloss, C.; Dean, C.; Ravenscroft, E.; Fong, B.; Fietz, M.; Hopwood, J.; Meikle, P.

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