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Results 1-10 of 28 (Search time: 0.002 seconds).
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Issue Date
Title
Author(s)
2010
Enzyme replacement therapy for mucopolysaccharidosis VI: Growth and pubertal development in patients treated with recombinant human N-acetylgalactosamine 4-sulfatase
Decker, 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.
2013
Enzyme replacement therapy for mucopolysaccharidosis VI: long-term cardiac effects of galsulfase (Naglazyme®) therapy
Braunlin, E.
;
Rosenfeld, H.
;
Kampmann, C.
;
Johnson, J.
;
Beck, M.
;
Giugliani, R.
;
Guffon, N.
;
Ketteridge, D.
;
Miranda, C.
;
Scarpa, M.
;
Schwartz, I.
;
Teles, E.
;
Wraith, J.
;
Barrios, P.
;
Dias da Silva, E.
;
Kurio, G.
;
Richardson, M.
;
Gildengorin, G.
;
Hopwood, J.
;
Imperiale, M.
;
et al.
2010
Functional analysis of the HGSNAT gene in patients with Mucopolysaccharidosis IIIC (Sanfilippo C Syndrome)
Fedele, A.
;
Hopwood, J.
2013
Heparan sulfate proteoglycans containing a glypican 5 core and 2-O-sulfo-induronic acid function as Sonic Hedgehog co-receptors to promote proliferation
Witt, R.
;
Hecht, M.
;
Pazyra-Murphy, M.
;
Cohen, S.
;
Noti, C.
;
van Kuppevelt, T.
;
Fuller, M.
;
Chan, J.
;
Hopwood, J.
;
Seeberger, P.
;
Segal, R.
2010
Lessons learnt from animal models: pathophysiology of neuropathic lysosomal storage disorders
Hemsley, K.
;
Hopwood, J.
2010
Enzyme replacement therapy for mucopolysaccharidosis VI: evaluation of long-term pulmonary function in patients treated with recombinant human N-acetylgalactosamine 4-sulfatase
Harmatz, 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.
2011
Gaucher disease in sheep
Karageorgos, L.
;
Lancaster, M.
;
Nimmo, J.
;
Hopwood, J.
2012
Mass spectrometric quantification of glycogen to assess primary substrate accumulation in the Pompe mouse
Fuller, M.
;
Duplock, S.
;
Turner, C.
;
Davey, P.
;
Brooks, D.
;
Hopwood, J.
;
Meikle, P.
2012
Abnormal gangliosides are localized in lipid rafts in Sanfilippo (MPS3a) mouse brain
Dawson, G.
;
Fuller, M.
;
Hemsley, K.
;
Hopwood, J.
2011
Emerging therapies for neurodegenerative lysosomal storage disorders - from concept to reality
Hemsley, K.
;
Hopwood, J.
Discover
Author
3
Teles, E.
3
Wraith, J.
2
Arash, L.
2
et al.
2
Fedele, A.
2
Harmatz, P.
2
Hutchinson, R.
2
Jolly, R.
2
Kaplan, P.
2
Kremer, E.
.
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Subject
7
Humans
5
Animals
5
Mucopolysaccharidosis VI
5
Sanfilippo syndrome
4
Lysosomal storage disease
4
Mucopolysaccharidosis
4
N-Acetylgalactosamine-4-Sulfatase
3
Cats
3
Child
3
Female
.
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Date issued
2
2014
3
2013
6
2012
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2011
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2010