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Diagnosis of Bacterial Bloodstream Infections: A 16S Metagenomics Approach16S metagenomics is a powerful approach for the diagnosis and understanding of Bacterial bloodstream infection
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Change in residential remoteness during the first 5 years of life in an Australian cerebral palsy cohortTo determine if families of children with cerebral palsy living in Australia move to less remote areas between birth and 5 years.
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Rhinovirus-induced asthma exacerbations and risk populationsAsthma exacerbations are heterogeneous conditions that involve the complex interplay between environmental exposures and innate and adaptive immune function
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The establishment of DOHaD working groups in Australia and New ZealandThis report introduces the DOHaD ANZ Working Groups and summarizes their plans and activities
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Evidence of a reduction over time in the behavioral severity of autistic disorder diagnosesWe examined whether there were changes over time in the qualitative and quantitative phenotype of individuals who received the diagnosis of Autistic Disorder.
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Knowledge translation lessons from an audit of Aboriginal Australians with acute coronary syndrome presenting to a regional hospitalThis audit is used as a case study of translating knowledge processes in order to identify the factors that support equity-oriented knowledge translation.
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Respiratory viruses in young South African children with acute lower respiratory infections and interactions with HIVRV-A and RV-C are endemic in South African children and HIV infection may be protective against RSV and bronchiolitis.
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Gross motor performance in children prenatally exposed to alcohol and living in remote AustraliaA higher than expected proportion of children with fetal alcohol spectrum disorders had gross motor scores that indicated impairment and need for therapy
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Lipidomics reveals associations of phospholipids with obesity and insulin resistance in young adultsLipidomic biomarkers associated with obesity and IR using plasma samples from a population-based cohort of young adults
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Somatic activating mutations in Pik3ca cause sporadic venous malformations in mice and humansOur data demonstrate a causal relationship between activating Pik3ca mutations and the genesis of venous malformations