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Issue Date
Title
Author(s)
2003
MJA Practice Essentials - 2: Recent advances in therapy of diabetes - Endocrinology
Couper, J.
;
Prins, J.
1998
Transcranial correction of orbital neurofibromatosis
Snyder, B.
;
Hanieh, A.
;
Trott, J.
;
David, D.
1997
A unique point mutation in the fibroblast growth factor receptor 3 gene (FGFR3) defines a new craniosynostosis syndrome
Muenke, M.
;
Gripp, K.
;
McDonald-McGinn, D.
;
Gaudenz, K.
;
Whitaker, L.
;
Bartlett, S.
;
Markowitz, R.
;
Robin, N.
;
Nwokoro, N.
;
Mulvihill, J.
;
Losken, H.
;
Mulliken, J.
;
Guttmacher, A.
;
Wilroy, R.
;
Clarke, L.
;
Hollway, G.
;
Ades, L.
;
Haan, E.
;
Mulley, J.
;
Cohen, M.
;
et al.
2006
A pilot study of SRL 172 (killed Mycobacterium vaccae) in healthy chronic hepatitis B carriers and hepatitis B vaccine non-responders
Goldwater, P.
2003
Management of fertility issues in cancer survivors
Tremellen, K.
;
Petrucco, O.
2009
ASPREN surveillance system for influenza-like illness: a comparison with FluTracking and the National Notifiable Diseases Surveillance System
Parrella, A.
;
Dalton, C.B.
;
Pearce, R.
;
Litt, J.C.B.
;
Stocks, N.
2005
Funnel-web spider bite: a systematic review of recorded clinical cases
Isbister, G.
;
Gray, M.
;
Balit, C.
;
Raven, R.
;
Stokes, B.
;
Porges, K.
;
Tankel, A.
;
Turner, E.
;
White, J.
;
Fisher, M.
2000
Saposins A,B,C, and D in plasma of patients with lysosomal storage disorders
Chang, M.
;
Bindloss, C.
;
Grabowski, G.
;
Qi, X.
;
Winchester, B.
;
Hopwood, J.
;
Meikle, P.
1998
Evaluation of the lysosome-associated membrane protein LAMP-2 as a marker for lysosomal storage disorders
Hua, C.
;
Hopwood, J.
;
Carlsson, S.
;
Harris, R.
;
Meikle, P.
1998
Identification of a common mutation (R245h) in Sanfilippo A patients from the Netherlands
Weber, B.
;
Vandekamp, J.
;
Kleijer, W.
;
Guo, X.H.
;
Blanch, L.
;
van Diggelen, O.
;
Wevers, R.
;
Poorthuis, B.
;
Hopwood, J.
Discover
Author
13
et al.
12
Hopwood, J.
11
Gecz, J.
11
Haan, E.
6
Berkovic, S.
6
Ketteridge, D.
6
Scheffer, I.
5
Giugliani, R.
5
Gold, M.
5
Guffon, N.
.
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Subject
19
Mutation
18
Pedigree
13
Young Adult
12
Aged
11
Intellectual Disability
11
Phenotype
10
Syndrome
9
DNA Mutational Analysis
9
Follow-Up Studies
8
Australia
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Date issued
4
2020 - 2023
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2010 - 2019
47
2000 - 2009
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1995 - 1999