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Results 1-10 of 70 (Search time: 0.002 seconds).
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Issue Date
Title
Author(s)
2012
Gastroesophageal reflux in pediatrics: (patho)physiology and new insights in diagnostics and treatment
Loots, C.
;
Benninga, M.
;
Omari, T.
2010
Complications of childhood diabetes and the role of technology
Cho, Y.
;
Couper, J.
;
Donaghue, K.
2010
The minimum frequency of glucose measurements from which glycemic variation can be consistently assessed
Baghurst, P.
;
Rodbard, D.
;
Cameron, F.
2013
Dietary n-3 LC-PUFA during the perinatal period as a strategy to minimize childhood allergic disease
Makrides, M.
;
Gunaratne, A.
;
Collins, C.
;
Makrides, M.
;
Ochoa, J.
;
Szajewska, H.
;
The 77th NNI Workshop (28 Oct 2012 - 1 Nov 2012 : Panama City, FL)
2013
Short report: care for children and adolescents with diabetes in Australia and New Zealand: have we achieved the defined goals?
Cameron, F.
;
Cotterill, A.
;
Couper, J.
;
Craig, M.
;
Davis, E.
;
Donaghue, K.
;
Jones, T.
;
King, B.
;
Sheil, B.
2015
Novel IL1RAPL1 mutations associated with intellectual disability impair synaptogenesis
Ramos-Brossier, M.
;
Montani, C.
;
Lebrun, N.
;
Gritti, L.
;
Martin, C.
;
Seminatore-Nole, C.
;
Toussaint, A.
;
Moreno, S.
;
Poirier, K.
;
Dorseuil, O.
;
Chelly, J.
;
Hackett, A.
;
Gecz, J.
;
Bieth, E.
;
Faudet, A.
;
Heron, D.
;
Kooy, R.
;
Loeys, B.
;
Humeau, Y.
;
Sala, C.
;
et al.
2016
Prenatal fish oil supplementation and allergy: 6-year follow-up of a randomized controlled trial
Best, K.P.
;
Sullivan, T.
;
Palmer, D.
;
Gold, M.
;
Kennedy, D.J.
;
Martin, J.
;
Makrides, M.
2016
HUWE1 mutations in Juberg-Marsidi and Brooks syndromes: the results of an X-chromosome exome sequencing study
Friez, M.
;
Brooks, S.
;
Stevenson, R.
;
Field, M.
;
Basehore, M.
;
Adès, L.
;
Sebold, C.
;
Mcgee, S.
;
Saxon, S.
;
Skinner, C.
;
Craig, M.
;
Murray, L.
;
Simensen, R.
;
Yap, Y.
;
Shaw, M.
;
Gardner, A.
;
Corbett, M.
;
Kumar, R.
;
Bosshard, M.
;
Van Loon, B.
;
et al.
2014
Refining analyses of copy number variation identifies specific genes associated with developmental delay
Coe, B.
;
Witherspoon, K.
;
Rosenfeld, J.
;
van Bon, B.
;
Vulto-van Silfhout, A.
;
Bosco, P.
;
Friend, K.
;
Baker, C.
;
Buono, S.
;
Vissers, L.
;
Schuurs-Hoeijmakers, J.
;
Hoischen, A.
;
Pfundt, R.
;
Krumm, N.
;
Carvill, G.
;
Li, D.
;
Amaral, D.
;
Brown, N.
;
Lockhart, P.
;
Scheffer, I.
;
et al.
2013
Enzyme replacement therapy for mucopolysaccharidosis VI: long-term cardiac effects of galsulfase (Naglazyme®) therapy
Braunlin, E.
;
Rosenfeld, H.
;
Kampmann, C.
;
Johnson, J.
;
Beck, M.
;
Giugliani, R.
;
Guffon, N.
;
Ketteridge, D.
;
Miranda, C.
;
Scarpa, M.
;
Schwartz, I.
;
Teles, E.
;
Wraith, J.
;
Barrios, P.
;
Dias da Silva, E.
;
Kurio, G.
;
Richardson, M.
;
Gildengorin, G.
;
Hopwood, J.
;
Imperiale, M.
;
et al.
Discover
Author
4
Couper, J.
4
Gold, M.
4
Haan, E.
4
Marshall, H.
3
Baghurst, P.
3
Griffiths, A.
3
Hopwood, J.
3
Inder, T.E.
3
Makrides, M.
3
Mulley, J.
.
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Subject
69
Humans
55
Male
50
Female
32
Child, Preschool
29
Adolescent
19
Adult
16
Infant
13
Infant, Newborn
12
Mutation
10
Australia
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2011
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2010