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Results 1-10 of 220 (Search time: 0.003 seconds).
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PreviewIssue DateTitleAuthor(s)
1996Long-term in vitro correction of alpha-L-iduronidase deficiency (Hurler syndrome) in human bone marrowFairbairn, L.; Lashford, L.; Spooncer, E.; McDermott, R.; Lebens, G.; Arrand, J.; Arrand, J.; Bellantuono, I.; Holt, R.; Hatton, C.; Cooper, A.; Besley, G.; Wraith, J.; Anson, D.; Hopwood, J.; Dexter, T.
1995Glucoronate-2-sulphataseBielicki, J.; Freeman, C.; Hopwood, J.
1998Coexistence of Gaucher-Disease Type 1 and Joubert-SyndromeVan Royen-Kerkhof, A.; Pollthe, B.; Kleijer, W.; van Diggelen, O.; Aerts, J.; Hopwood, J.; Beemer, F.
1996Identification, expression, and biochemical characterization of N-acetylgalactosamine-4-sulfatase mutations and relationship with clinical phenotype in MPS-VI patientsLitjens, T.; Brooks, D.; Peters, C.; Gibson, G.; Hopwood, J.
2007Pathology of mucopolysaccharidosis IIIA in huntaway dogsJolly, R.; Johnstone, A.; Norman, E.; Hopwood, J.; Walkley, S.
2007Mutational analysis of 105 mucopolysaccharidosis type VI patientsKarageorgos, L.; Brooks, D.; Pollard, A.; Melville, E.; Hein, L.; Clements, P.; Ketteridge, D.; Swiedler, S.; Beck, M.; Giugliani, R.; Harmatz, P.; Wraith, J.; Guffon, N.; Teles, E.; Miranda, C.; Hopwood, J.
1997Diagnosis of lysosomal storage disorders: evaluation of lysosome-associated membrane protein LAMP-1 as a diagnostic markerMeikle, P.; Brooks, D.; Ravenscroft, E.; Yan, M.; Williams, R.; Jaunzems, A.; Chataway, T.; Karageorgos, L.; Davey, R.; Boulter, C.; Carlsson, S.; Hopwood, J.
1998Caprine mucopolysaccharidosis-IIID: clinical, biochemical, morphological and immunohistochemical characteristicsJones, M.; Alroy, J.; Boyer, P.; Cavanagh, K.; Johnson, K.; Gage, D.; Vorro, J.; Render, J.; Common, R.; Leedle, R.; Lowrie, C.; Sharp, P.; Liour, S.S.; Levene, B.; Hoard, H.; Lucas, R.; Hopwood, J.
1999A mouse model for mucopolysaccharidosis type III A (Sanfilippo syndrome)Bhaumik, M.; Muller, V.; Rozaklis, T.; Johnson, L.; Dobrenis, K.; Bhattacharyya, R.; Wurzelmann, S.; Finamore, P.; Hopwood, J.; Walkley, S.; Stanley, P.
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.

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