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Results 11-20 of 23 (Search time: 0.003 seconds).
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Issue Date
Title
Author(s)
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.
2007
Mutational analysis of mucopolysaccharidosis type VI patients undergoing a phase II trial of enzyme replacement therapy
Karageorgos, L.
;
Brooks, D.
;
Harmatz, P.
;
Ketteridge, D.
;
Pollard, A.
;
Melville, E.
;
Parkinson-Lawrence, E.
;
Clements, P.
;
Hopwood, J.
1997
Molecular defects in Sanfilippo syndrome type A
Blanch, L.
;
Weber, B.
;
Guo, X.H.
;
Scott, H.
;
Hopwood, J.
2005
Prediction of neuropathology in mucopolysaccharidosis I patients
Fuller, M.
;
Brooks, D.
;
Evangelista, M.
;
Hein, L.
;
Hopwood, J.
;
Meikle, P.
2003
Usefulness of bone marrow transplantation in the Hurler syndrome
Braunlin, E.
;
Stauffer, N.
;
Peters, C.
;
Bass, J.
;
Berry, J.
;
Hopwood, J.
;
Krivit, W.
2008
Long-term follow-up of endurance and safety outcomes during enzyme replacement therapy for mucopolysaccharidosis VI: Final results of three clinical studies of recombinant human N-acetylgalactosamine 4-sulfatase
Harmatz, P.
;
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.
;
Yu, Z.
;
Swiedler, S.
;
Decker, C.
2003
Determination of monosaccharides and disaccharides in mucopolysaccharidoses patients by electrospray ionisation mass spectrometry
Ramsay, S.
;
Meikle, P.
;
Hopwood, J.
2011
Screening patients referred to a metabolic clinic for lysosomal storage disorders
Fuller, M.
;
Tucker, J.
;
Lang, D.
;
Dean, C.
;
Fietz, M.
;
Meikle, P.
;
Hopwood, J.
2005
Direct comparison of measures of endurance, mobility, and joint function during enzyme-replacement therapy of mucopolysaccharidosis VI (Maroteaux-Lamy syndrome): results after 48 weeks in a phase 2 open-label clinical study of recombinant human n-acetylgalactosamine 4-sulfatase
Harmatz, P.
;
Ketteridge, D.
;
Giugliani, R.
;
Guffon, N.
;
Teles, E.
;
Miranda, C.
;
Yu, Z.
;
Swiedler, S.
;
Hopwood, J.
2006
Detection of mucopolysaccharidosis type II by measurement of iduronate-2-sulfatase in dried blood spots and plasma samples
Dean, C.
;
Bockmann, M.
;
Hopwood, J.
;
Brooks, D.
;
Meikle, P.
Discover
Author
7
Harmatz, P.
7
Meikle, P.
6
Ketteridge, D.
5
Giugliani, R.
5
Guffon, N.
5
Miranda, C.
5
Swiedler, S.
5
Teles, E.
4
Beck, M.
4
Brooks, D.
.
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Subject
23
Humans
20
Adolescent
14
Child, Preschool
14
Male
13
Adult
13
Female
8
Infant
8
Mucopolysaccharidosis VI
8
Recombinant Proteins
7
N-Acetylgalactosamine-4-Sulfatase
.
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Date issued
4
2010 - 2015
13
2000 - 2009
6
1996 - 1999