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PreviewIssue DateTitleAuthor(s)
2016TBC1D24 genotype-phenotype correlationBalestrini, S.; Milh, M.; Castiglioni, C.; Lüthy, K.; Finelli, M.; Verstreken, P.; Cardon, A.; Stražišar, B.; Holder, J.; Lesca, G.; Mancardi, M.; Poulat, A.; Repetto, G.; Banka, S.; Bilo, L.; Birkeland, L.; Bosch, F.; Brockmann, K.; Cross, J.; Doummar, D.; et al.
2014Trends in hospital admissions for conditions associated with child maltreatment, Northern Territory, 1999-2010Guthridge, S.; Ryan, P.; Condon, J.; Moss, J.; Lynch, J.
2014Effects of simulated interventions to improve school entry academic skills on socioeconomic inequalities in educational achievementChittleborough, C.; Mittinty, M.; Lawlor, D.; Lynch, J.
2014Renal replacement therapy associated with lithium nephrotoxicity in AustraliaRoxanas, M.; Grace, B.; George, C.
2014Validation of self-reported information on dental caries in a birth cohort at 18 years of ageRibeiro Silva, A.; Baptista Menezes, A.; Formoso Assuncao, M.; Goncalves, H.; Demarco, F.; Vargas-Ferreira, F.; Peres, M.; Milgrom, P.M.
2014Neonatal brain pathology predicts adverse attention and processing speed outcomes in very preterm and/or very low birth weight childrenMurray, A.L.; Scratch, S.E.; Thompson, D.K.; Inder, T.E.; Doyle, L.W.; Anderson, J.F.I.; Anderson, P.J.
2014Longitudinal study of sleep behavior in normal infants during the first year of lifeBruni, O.; Baumgartner, E.; Sette, S.; Ancona, M.; Caso, G.; Di Cosimo, M.; Mannini, A.; Ometto, M.; Pasquini, A.; Ulliana, A.; Ferri, R.
2013Bed-sharing and risk of hospitalisation due to pneumonia and diarrhoea in infancy: the 2004 Pelotas Birth CohortNgale, K.; Santos, I.; González-Chica, D.; De Barros, A.; Matijasevich, A.
2013Comparison of stool microbiota compositions, stool alpha1-antitrypsin and calprotectin concentrations, and diarrhoeal morbidity of Indonesian infants fed breast milk or probiotic/prebiotic-supplemented formulaOswari, H.; Prayitno, L.; Dwipoerwantoro, P.; Firmansyah, A.; Makrides, M.; Lawley, B.; Kuhn-Sherlock, B.; Cleghorn, G.; Tannock, G.
2013Mutations in DEPDC5 cause familial focal epilepsy with variable fociDibbens, L.; de Vries, B.; Donatello, S.; Heron, S.; Hodgson, B.; Chintawar, S.; Crompton, D.; Hughes, J.; Bellows, S.; Klein, K.; Callenbach, P.; Corbett, M.; Gardner, A.; Kivity, S.; Iona, X.; Regan, B.; Weller, C.; Crimmins, D.; O'Brien, T.; Guerrero-Lopez, R.; et al.