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Results 1-10 of 11 (Search time: 0.015 seconds).
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PreviewIssue DateTitleAuthor(s)
2010Enzyme replacement therapy for mucopolysaccharidosis VI from 8 weeks of age - a sibling control studyMcGill, J.; Inwood, A.; Coman, D.; Lipke, M.; de Lore, D.; Swiedler, S.; Hopwood, J.
2010Enzyme replacement therapy for mucopolysaccharidosis VI: evaluation of long-term pulmonary function in patients treated with recombinant human N-acetylgalactosamine 4-sulfataseHarmatz, P.; Yu, Z.; Giugliani, R.; Schwartz, I.; Guffon, N.; Teles, E.; Miranda, C.; Wraith, J.; Beck, M.; Arash, L.; Scarpa, M.; Ketteridge, D.; Hopwood, J.; Plecko, B.; Steiner, R.; Whitley, C.; Kaplan, P.; Swiedler, S.; Hardy, K.; Berger, K.; et al.
2010Determination of urinary oligosaccharides by high-performance liquid chromatography/electrospray ionization-tandem mass spectrometry: Application to Hunter syndromeNielsen, T.; Rozek, T.; Hopwood, J.; Fuller, M.
2010Functional analysis of the HGSNAT gene in patients with Mucopolysaccharidosis IIIC (Sanfilippo C Syndrome)Fedele, A.; Hopwood, J.
2010Biochemical profiling to predict disease severity in metachromatic leukodystrophyTan, M.; Fuller, M.; Zabidi-Hussin, Z.; Hopwood, J.; Meikle, P.
2010Allogeneic stem cell transplantation does not improve neurological deficits in mucopolysaccharidosis type IIIA miceLau, A.; Hannouche, H.; Rozaklis, T.; Hassiotis, S.; Hopwood, J.; Hemsley, K.
2010SGSH gene transfer in mucopolysaccharidosis type IIIA mice using canine adenovirus vectorsLau, A.; Hopwood, J.; Kremer, E.; Hemsley, K.
2010Embryonic stem cell-derived glial precursors as a vehicle for sulfamidase production in the MPS-IIIA mouse brainRobinson, A.; Zhao, G.; Rathjen, J.; Rathjen, P.; Hutchinson, R.; Eyre, H.; Hemsley, K.; Hopwood, J.
2010Genetic manipulation of murine embryonic stem cells with enhanced green fluorescence protein and sulfatase-modifying factor I genesZhao, G.; Karageorgos, L.; Hutchinson, R.; Hopwood, J.; Hemsley, K.
2010Enzyme replacement therapy for mucopolysaccharidosis VI: Growth and pubertal development in patients treated with recombinant human N-acetylgalactosamine 4-sulfataseDecker, C.; Yu, Z.; Giugliani, R.; Schwartz, I.; Guffon, N.; Teles, E.; Miranda, C.; Wraith, J.; Beck, M.; Arash, L.; Scarpa, M.; Ketteridge, D.; Hopwood, J.; Plecko, B.; Steiner, R.; Whitley, C.; Kaplan, P.; Swiedler, S.; Conrad, S.; Harmatz, P.