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Results 21-30 of 31 (Search time: 0.003 seconds).
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PreviewIssue DateTitleAuthor(s)
2008Diagnosis of metachromatic leukodystrophy by immune quantification of arylsulphatase A protein and activity in dried blood spotsTan, M.; Dean, C.; Hopwood, J.; Meikle, P.
2006Immunochemistry of lysosomal storage disordersParkinson-Lawrence, E.; Fuller, M.; Hopwood, J.; Meikle, P.; Brooks, D.
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.
2005Urinary lipid profiling for the identification of Fabry hemizygotes and heterozygotesFuller, M.; Sharp, P.; Rozaklis, T.; Whitfield, P.; Blacklock, D.; Hopwood, J.; Meikle, P.
2005Immunoquantification of b-glucosidase: Diagnosis and prediction of severity in Gaucher diseaseFuller, M.; Lovejoy, 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.
2003Lysosomal storage disorders: emerging therapeutic options require early diagnosisMeikle, P.; Hopwood, J.
2001Purification and characterization of recombinant human lysosomal a-mannosidaseBerg, T.; King, B.; Meikle, P.; Nilssen, O.; Tollersrud, O.; Hopwood, J.

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