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Issue Date
Title
Author(s)
2003
The a-L-iduronidase mutations R89Q and R89W result in an attenuated mucopolysaccharidosis type I clinical presentation
Hein, L.
;
Hopwood, J.
;
Clements, P.
;
Brooks, D.
2002
Sanfilippo syndrome in Turkey: Identification of novel mutations in subtypes A and B
Emre, S.
;
Terzioglu, M.
;
Tokatli, A.
;
Coskun, T.
;
Ozalp, I.
;
Weber, B.
;
Hopwood, J.
2007
Morphopathological features in tissues of α-mannosidosis guinea pigs at different gestational ages
Auclair, D.
;
Hopwood, J.
2004
Spontaneous and engineered mammalian storage disease models
Hopwood, J.
;
Crawley, A.
;
Taylor, R.
;
Platt, F.
;
Walkley, S.
2002
Biochemical and molecular analysis of mucopolysaccharidoses in Turkey
Emre, S.
;
Terzioglu, M.
;
Coskun, T.
;
Tokatli, A.
;
Ozalp, I.
;
Muller, V.
;
Hopwood, J.
1995
N-Acetylgalactosamine-6-sulphatase
Bielicki, J.
;
Hopwood, J.
1996
Two novel frameshift mutations causing premature stop codons in a patient with the severe form of Maroteaux-Lamy syndrome
Isbrandt, D.
;
Hopwood, J.
;
von Figura, K.
;
Peters, C.
2001
Selection of endpoints in clinical studies of enzyme replacement therapy in lysosomal storage disorders - Commentary
Hopwood, J.
1995
N-Acetylgalactosamine-4-sulphatase
Bielicki, J.
;
Hopwood, J.
2000
Determination of acid a-glucosidase protein: evaluation as a screening marker for pompe disease and other lysosomal storage disorders
Umapathysivam, K.
;
Whittle, A.
;
Ranieri, E.
;
Bindloss, C.
;
Ravenscroft, E.
;
Van Diggelen, O.
;
Hopwood, J.
;
Meikle, P.
Discover
Author
48
Meikle, P.
47
Brooks, D.
35
Fuller, M.
28
Hemsley, K.
24
Crawley, A.
17
Anson, D.
17
Muller, V.
16
King, B.
16
Rozaklis, T.
14
Weber, B.
.
next >
Subject
126
Humans
94
Animals
41
Recombinant Proteins
36
Cricetinae
36
Mucopolysaccharidosis VI
33
CHO Cells
33
Female
32
Molecular Sequence Data
32
Mucopolysaccharidosis III
31
Fibroblasts
.
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Date issued
28
2010 - 2014
122
2000 - 2009
70
1995 - 1999