Reports and Findings
Research
Privacy or public good? Why not obtaining consent may be best practiceUsing medical and other data from private citizens without obtaining the consent of those citizens has been a taboo of statisticians and of society
Research
Aboriginal practitioners speak out: contextualising child protection interventionsThis paper reports on how the summit was designed and on some of the ideas and concerns that emerged within this dialogical space of cooperative inquiry.
Research
Dahlem ConferenceThere is increasing evidence that the functional state of the immune system at birth is predictive of the kinetics of immune maturation in early infancy.
Research
Lung volume and ventilation inhomogeneity in preterm infants at 15-18 months corrected ageTo assess whether lung volume and ventilation inhomogeneity in preterm infants at 15-18 months corrected age
Research
Antimicrobial susceptibility of Moraxella catarrhalis isolated from children in Kalgoorlie-BoulderTo investigate antimicrobial susceptibility of Moraxella catarrhalis isolated from a cohort of children being followed in a study of the natural history of OM
Research
Age at diagnosis of birth defectsMany birth defects surveillance programs ascertain cases of birth defects diagnosed beyond 1 year of age.
Research
TLR2 mediates recognition of live staphylococus epidermidisStaphylococcus epidermidis is a nosocomial pathogen that causes catheter-associated bacteremia in the immunocompromised, including those at the extremes of age
Research
Nothing but fear itself: parental fear as a determinant of child physical activity and independent mobilityOver the past decade we have seen declining rates in child engagement in physical activity with escalating health problems ensuing.
Research
Cell phone use by adolescents with Asperger SyndromeWhile young people have generally been at the forefront of the adoption and use of new communications technologies, little is known of uses by exceptional youth
Research
Updating the profile of C-terminal MECP2 deletions in Rett syndromeThis study aimed to compare the phenotype of Rett syndrome cases with C-terminal deletions to that of cases with different MECP2 mutations