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Results 11-20 of 25 (Search time: 0.002 seconds).
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Issue Date
Title
Author(s)
2004
Cord-blood transplants from unrelated donors in patients with Hurler's Syndrome
Staba, S.
;
Escolar, M.
;
Poe, M.
;
Kim, Y.
;
Martin, P.
;
Szabolcs, P.
;
Allison-Thacker, J.
;
Wood, S.
;
Wenger, D.
;
Rubenstein, P.
;
Hopwood, J.
;
Krivit, W.
;
Kurtzberg, J.
1998
Two-dimensional mapping and microsequencing of lysosomal proteins from human placenta
Chataway, T.
;
Whittle, A.
;
Lewis, M.
;
Bindloss, C.
;
Davey, R.
;
Moritz, R.
;
Simpson, R.
;
Hopwood, J.
;
Meikle, P.
1995
In vivo delivery of human α-L-iduronidase in mice implanted with neo-organs
Salvetti, A.
;
Moullier, P.
;
Cornet, V.
;
Brooks, D.
;
Hopwood, J.
;
Danos, O.
;
Heard, J.M.
2002
In utero injection of a-L-iduronidase-carrying retrovirus in canine mucopolysaccharidosis type I: Infection of multiple tissues and neonatal gene expression
Meertens, L.
;
Zhao, Y.
;
Rosic-Kablar, S.
;
Li, L.
;
Chan, K.
;
Dobson, H.
;
Gartley, C.
;
Lutzko, C.
;
Hopwood, J.
;
Kohn, D.
;
Kruth, S.
;
Hough, M.
;
Dube, I.
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.
2004
Determination of oligosaccharides and glycolipids in amniotic fluid by electrospray ionisation tandem mass spectrometry: in utero indicators of lysosomal storage diseases
Ramsay, S.
;
Maire, I.
;
Bindloss, C.
;
Fuller, M.
;
Whitfield, P.
;
Piraud, M.
;
Hopwood, J.
;
Meikle, P.
2006
Galsulfase
Hopwood, J.
;
Bate, G.
;
Kirkpatrick, P.
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.
1998
Two mutations within a feline mucopolysaccharidosis type VI colony cause three different clinical phenotypes
Crawley, A.
;
Yogalingam, G.
;
Muller, V.
;
Hopwood, J.
Discover
Author
6
Harmatz, P.
5
Ketteridge, D.
4
Giugliani, R.
4
Guffon, N.
4
Meikle, P.
4
Miranda, C.
4
Swiedler, S.
4
Teles, E.
3
Beck, M.
3
Braunlin, E.
.
next >
Subject
17
Male
11
Child
10
Adolescent
10
Mucopolysaccharidosis VI
9
N-Acetylgalactosamine-4-Sulfatase
8
Adult
7
Child, Preschool
7
Recombinant Proteins
6
Glycosaminoglycans
5
Animals
.
next >
Date issued
2
2010 - 2013
16
2000 - 2009
7
1995 - 1999