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Results 11-20 of 20 (Search time: 0.003 seconds).
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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.
2008Effect of lysosomal storage on bis(monoacylglycero)phosphateMeikle, P.; Duplock, S.; Blacklock, D.; Whitfield, P.; Macintosh, G.; Hopwood, J.; Fuller, M.
2011Screening patients referred to a metabolic clinic for lysosomal storage disordersFuller, M.; Tucker, J.; Lang, D.; Dean, C.; Fietz, M.; Meikle, P.; Hopwood, J.
2004Disease-specific markers for the mucopolysaccharidosesFuller, M.; Rozaklis, T.; Ramsay, S.; Hopwood, J.; Meikle, P.
2006Immunochemistry of lysosomal storage disordersParkinson-Lawrence, E.; Fuller, M.; Hopwood, J.; Meikle, P.; Brooks, D.
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.
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.
2005Laronidase treatment of mucopolysaccharidosis IWraith, J.; Hopwood, J.; Fuller, M.; Meikle, P.; Brooks, D.