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Results 1-10 of 12 (Search time: 0.005 seconds).
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PreviewIssue DateTitleAuthor(s)
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.
2003Significance of immune response to enzyme-replacement therapy for patients with a lysosomal storage disorderBrooks, D.; Kakavanos, R.; Hopwood, J.
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.
2006Common antigenicity for two glycosidasesKakavanos, R.; Lehn, P.; Callebaut, I.; Meikle, P.; Parkinson-Lawrence, E.; Hopwood, J.; Brooks, D.
2006Stop-codon read-through for patients affected by a lysosomal storage disorderBrooks, D.; Muller, V.; Hopwood, J.
2006Immunochemistry of lysosomal storage disordersParkinson-Lawrence, E.; Fuller, M.; Hopwood, J.; Meikle, P.; Brooks, D.
2009Delivery of recombinant proteins via the cerebrospinal fluid as a therapy option for neurodegenerative lysosomal storage diseasesHemsley, K.; Hopwood, J.
2001Expression and characterization of human recombinant and a-N-actylglucosaminidaseWeber, B.; Hopwood, J.; Yogalingam, G.

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