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Issue Date
Title
Author(s)
2006
Effect of baclofen on esophagogastric motility and gastroesophageal reflux in children with gastroesophageal reflux disease: A randomized controlled trial
Omari, T.
;
Benninga, M.
;
Sansom, L.
;
Butler, R.
;
Dent, J.
;
Davidson, G.
2000
Escherichia coli 'O' group serology of a haemolytic uraemic syndrome (HUS) epidemic
Goldwater, P.
;
Bettelheim, K.
2005
Threshold effect of urinary glycosaminoglycans and the walk test as indicators of disease progression in a survey of subjects with mucopolysaccharidosis VI (Maroteaux-Lamy syndrome)
Swiedler, S.
;
Beck, M.
;
Bajbouj, M.
;
Giugliani, R.
;
Schwartz, I.
;
Harmatz, P.
;
Wraith, J.
;
Roberts, J.
;
Ketteridge, D.
;
Hopwood, J.
;
Guffon, N.
;
Miranda, C.
;
Teles, E.
;
Berger, K.
;
Piscia-Nichols, C.
2006
Hepatocellular carcinoma in ten children under five years of age with bile salt export pump deficiency
Knisely, A.
;
Strautnieks, S.
;
Meier, Y.
;
Stieger, B.
;
Byrne, J.
;
Portmann, B.
;
Bull, L.
;
Pawlikowska, L.
;
Bilezikci, B.
;
Ozcay, F.
;
Laszlo, A.
;
Tiszlavicz, L.
;
Moore, L.
;
Raftos, J.
;
Arnell, H.
;
Fischler, B.
;
Nemeth, A.
;
Papadogiannakis, N.
;
Cielecka-Kuszyk, J.
;
Jankowska, I.
;
et al.
2004
Twenty-two novel mutations in the lysosomal a-glucosidase gene (GAA) underscore the genotype-phenotype correlation in glycogen storage disease type II
Hermans, M.
;
van Leenen, D.
;
Kroos, M.
;
Beesley, C.
;
Van der Ploeg, A.
;
Sakuraba, H.
;
Wevers, R.
;
Kleijer, W.
;
Mikelakakis, H.
;
Kirk, E.
;
Fletcher, J.
;
Bosshard, N.
;
Basel-Vanagaite, L.
;
Besley, G.
;
Reuser, A.
2002
The molecular basis of cystathionine b-synthase deficiency in Australian patients: Genotype-phenotype correlations and response to treatment
Gaustadnes, M.
;
Wilcken, B.
;
Oliveriusova, J.
;
McGill, J.
;
Fletcher, J.
;
Kraus, J.
;
Wilcken, D.
2006
Intracellular cytokies in peripheral blood leucocytes in children with chronic renal failure
Nairn, J.
;
Hodge, G.
;
Henning, P.
2008
SLC9A6 mutations cause X-linked mental retardation, microcephaly, epilepsy, and ataxia, a phenotype mimicking Angelman syndrome
Gilfillan, G.
;
Selmer, K.
;
Roxrud, I.
;
Smith, R.
;
Kyllerman, M.
;
Eiklid, K.
;
Kroken, M.
;
Mattingsdal, M.
;
Egeland, T.
;
Stenmark, H.
;
Sjoholm, H.
;
Server, A.
;
Samuelsson, L.
;
Christianson, A.
;
Tarpey, P.
;
Whibley, A.
;
Stratton, M.
;
Futreal, P.
;
Teague, J.
;
Edkins, S.
;
et al.
2008
Glucose control, organ failure, and mortality in pediatric intensive care
Yung, M.
;
Wilkins, B.
;
Norton, L.
;
Slater, A.
2000
Neuroblastoma associated with seizures and arrested development
White, A.
;
Manson, J.
;
Toogood, I.
Discover
Author
11
Davidson, G.
10
Hopwood, J.
8
Gecz, J.
8
Omari, T.
7
Gold, M.
6
Baghurst, P.
6
Fletcher, J.
5
et al.
5
Martin, A.
4
Benninga, M.
.
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Subject
95
Humans
64
Child
62
Male
57
Female
55
Infant
44
Adolescent
30
Adult
26
Infant, Newborn
18
Australia
16
Mutation
.
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Date issued
10
2009
9
2008
11
2007
7
2006
11
2005
7
2004
10
2003
9
2002
10
2001
11
2000
.
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