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Results 31-40 of 50 (Search time: 0.003 seconds).
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Issue Date
Title
Author(s)
2013
Gastroesophageal reflux, esophageal function, gastric emptying, and the relationship to dysphagia before and after antireflux surgery in children
Loots, C.
;
Van Herwaarden, M.
;
Benninga, M.
;
VanderZee, D.
;
van Wijk, M.
;
Omari, T.
2013
Parental perspectives of vaccine safety and experience of adverse events following immunisation
Parrella, A.
;
Gold, M.
;
Marshall, H.
;
Braunack-Mayer, A.
;
Baghurst, P.
1997
The spectrum of primary immundeficiency disorders in Australia
Baumgart, K.
;
Britton, W.
;
Kemp, A.
;
French, M.
;
Roberton, D.
2000
Analysis of the breath hydrogen test for carbohydrate malabsorption: Validation of a pocket-sized breath test analysier
Lee, W.
;
Davidson, G.
;
Moore, D.
;
Butler, R.
1995
Longitudinal evaluation of serum trypsinogen measurement in pancreatic-insufficient and pancreatic-sufficient patients with cystic fibrosis
Couper, R.
;
Corey, M.
;
Durie, P.
;
Forstner, G.
;
Moore, D.
2005
Early onset seizures and Rett-like features associated with mutations in CDKL5
Evans, J.
;
Archer, H.
;
Colley, J.
;
Ravn, K.
;
Nielsen, J.
;
Kerr, A.
;
Williams, E.
;
Christodoulou, J.
;
Gecz, J.
;
Jardine, P.
;
Wright, M.
;
Pilz, D.
;
Lazarou, L.
;
Cooper, D.
;
Sampson, J.
;
Butler, R.
;
Whatley, S.
;
Clarke, A.
2005
Enzyme replacement therapy for Gaucher disease in Australia
Goldblatt, J.
;
Szer, J.
;
Fletcher, J.
;
McGill, J.
;
Rowell, J.
;
Wilson, M.
2001
Nationwide study of haemolytic uraemic syndrome: clinical, microbiological, and epidemiological features
Elliott, E.
;
Robins-Browne, R.
;
O'Loughlin, E.
;
Bennett-Wood, V.
;
Bourke, J.
;
Henning, P.
;
Hogg, G.
;
Knight, J.
;
Powell, H.
;
Redmond, D.
2012
Molecular diagnosis of infantile mitochondrial disease with targeted next-generation sequencing
Calvo, S.
;
Compton, A.
;
Hershman, S.
;
Lim, S.
;
Lieber, D.
;
Tucker, E.
;
Laskowski, A.
;
Garone, C.
;
Liu, S.
;
Jaffe, D.
;
Christodoulou, J.
;
Fletcher, J.
;
Bruno, D.
;
Goldblatt, J.
;
DiMauro, S.
;
Thorburn, D.
;
Mootha, V.
2011
De novo SCN1A mutations in migrating partial seizures of infancy
Carranza Rojo, D.
;
Hamiwka, L.
;
McMahon, J.
;
Dibbens, L.
;
Arsov, T.
;
Suls, A.
;
Stodberg, T.
;
Kelley, K.
;
Wirrell, E.
;
Appleton, B.
;
Mackay, M.
;
Freeman, J.
;
Yendle, S.
;
Berkovic, S.
;
Bienvenu, T.
;
De Jonghe, P.
;
Thorburn, D.
;
Mulley, J.
;
Mefford, H.
;
Scheffer, I.
Discover
Author
5
Gold, M.
4
Anderson, P.J.
4
Fletcher, J.
4
Gecz, J.
4
Haan, E.
3
Cheong, J.L.Y.
3
Davidson, G.
3
Doyle, L.W.
3
et al.
3
Revesz, T.
.
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Subject
47
Female
42
Child, Preschool
33
Adolescent
21
Infant, Newborn
18
Adult
12
Australia
10
Mutation
8
Follow-Up Studies
7
Middle Aged
7
Prospective Studies
.
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Date issued
2
2020 - 2022
17
2010 - 2019
23
2000 - 2009
8
1995 - 1999