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Results 1-10 of 47 (Search time: 0.008 seconds).
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PreviewIssue DateTitleAuthor(s)
2000Regulation of the lysosome-associated membrane protein in a sucrose model of lysosomal storageIsaac, E.; Karageorgos, L.; Brooks, D.; Hopwood, J.; Meikle, P.
2000Enzyme replacement therapy in mucopolysaccharidosis I: Altered distribution and targeting of a-L-induronidase in immunized ratsTurner, C.; Hopwood, J.; Brooks, D.
2003Immune tolerance after long-term enzyme-replacement therapy among patients who have mucopolysaccharidosis IKakavanos, R.; Turner, C.; Hopwood, J.; Kakkis, E.; Brooks, D.
2006Stop-codon read-through for patients affected by a lysosomal storage disorderBrooks, D.; Muller, V.; Hopwood, J.
2003Significance of immune response to enzyme-replacement therapy for patients with a lysosomal storage disorderBrooks, D.; Kakavanos, R.; Hopwood, J.
2003Replacement therapy in Mucopolysaccharidosis type VI: advantages of early onset of therapyAuclair, D.; Hopwood, J.; Brooks, D.; Lemontt, J.; Crawley, A.
2001Gentamicin-mediated suppression of Hurler syndrome stop mutations restores a low level of a-L-iduronidase activity and reduces lysosomal glycosaminoglycan accumulationKeeling, K.; Brooks, D.; Hopwood, J.; Li, P.; Thompson, J.; Bedwell, D.
2003Identification and characterization of 13 new mutations in mucopolysaccharidosis type I patientsMatte, U.; Yogalingam, G.; Brooks, D.; Leistner, S.; Schwartz, I.; Lima, L.; Norato, D.; Brum, J.; Beesley, C.; Winchester, B.; Giugliani, R.; Hopwood, J.
2005Development of an assay for the detection of mucopolysaccharidosis type VI patients using dried blood-spotsHein, L.; Meikle, P.; Dean, C.; Bockmann, M.; Auclair, D.; Hopwood, J.; Brooks, D.
2006Stabilising normal and mis-sense variant α-glucosidaseKakavanos, R.; Hopwood, J.; Lang, D.; Meikle, P.; Brooks, D.