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Results 31-40 of 112 (Search time: 0.007 seconds).
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PreviewIssue DateTitleAuthor(s)
2023Understanding the pathways between prenatal and postnatal factors and overweight outcomes in early childhood: a pooled analysis of seven cohortsZheng, M.; Hesketh, K.D.; Vuillermin, P.; Dodd, J.; Wen, L.M.; Baur, L.A.; Taylor, R.; Byrne, R.; Mihrshahi, S.; Burgner, D.; Tang, M.L.K.; Campbell, K.J.
2023Prenatal iodine supplementation and early childhood neurodevelopment: the PoppiE trial - study protocol for a multicentre randomised controlled trialBest, K.P.; Gould, J.F.; Makrides, M.; Sullivan, T.; Cheong, J.; Zhou, S.J.; Kane, S.; Safa, H.; Sparks, A.; Doyle, L.W.; McPhee, A.J.; Nippita, T.A.C.; Afzali, H.H.A.; Grivell, R.; Mackerras, D.; Knight, E.; Wood, S.; Green, T.
2022The Australian Feeding Infants and Toddlers Study (OzFITS) 2021: Highlights and Future DirectionsNetting, M.J.; Moumin, N.A.; Makrides, M.; Green, T.J.
2010Immunogenicity of a monovalent 2009 influenza A(H1N1) vaccine in infants and children: A randomized trialNolan, T.; McVernon, J.; Skeljo, M.; Richmond, P.; Wadia, U.; Lambert, S.; Nissen, M.; Marshall, H.; Booy, R.; Heron, L.; Hartel, G.; Lai, M.; Basser, R.; Gittleson, C.; Greenberg, M.
2006Hepatocellular carcinoma in ten children under five years of age with bile salt export pump deficiencyKnisely, 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.
1996Maternal Immunization With Haemophilus Influenzae Type b Polysaccharide-Tetanus Protein Conjugate Vaccine in the GambiaMulholland, K.; Suara, R.; Siber, G.; Roberton, D.; Jaffar, S.; N'jie, J.; Baden, L.; Thompson, C.; Anwaruddin, R.; Dinan, L.; Glezen, W.; Francis, N.; Fritzell, B.; Greenwood, B.
2004Twenty-two novel mutations in the lysosomal a-glucosidase gene (GAA) underscore the genotype-phenotype correlation in glycogen storage disease type IIHermans, 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.
2002The molecular basis of cystathionine b-synthase deficiency in Australian patients: Genotype-phenotype correlations and response to treatmentGaustadnes, M.; Wilcken, B.; Oliveriusova, J.; McGill, J.; Fletcher, J.; Kraus, J.; Wilcken, D.
2019Managing asthma in pregnancy: effects on future child healthClifton, V.L.
2013Gain-of-function mutations in RIT1 cause Noonan syndrome, a RAS/MAPK pathway syndromeAoki, Y.; Niihori, T.; Banjo, T.; Okamoto, N.; Mizuno, S.; Kurosawa, K.; Ogata, T.; Takada, F.; Yano, M.; Ando, T.; Hoshika, T.; Barnett, C.; Ohashi, H.; Kawame, H.; Hasegawa, T.; Okutani, T.; Nagashima, T.; Hasegawa, S.; Funayama, R.; Nagashima, T.; et al.

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