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Research
N-3 fatty acid supplementation and leukocyte telomere length in patients with chronic kidney diseaseReducing oxidative stress, could modify telomere erosion during cell replication, and cardiovascular disease risk in patients with chronic kidney disease
Research
Schizophrenia Spectrum Disorders and Autism Spectrum DisorderWe examine the level of comorbidity found between Autism spectrum disorder and Schizophrenia spectrum disorders at a clinical and trait level
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Limited impact of neonatal or early infant schedules of 7-valent pneumococcal conjugate vaccinationEarly 7vPCV schedules have limited impact on pneumococcal vaccine type carriage in PNG
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Key findings from the second Australian Child and Adolescent Survey of Mental Health and WellbeingThe prevalence of mental disorders in children and adolescents in Australia, and the severity and impact of those mental disorders
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An observational study of febrile seizures: The importance of viral infection and immunizationDetermine the frequency of detection of specific viral pathogens in children with febrile seizures
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CATALISE: A multinational and multidisciplinary Delphi consensus study. Identifying language impairments in childrenDelayed or impaired language development is a common developmental concern, yet there is little agreement about the criteria used to identify and classify...
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Community Development Coordinator Role Consultation: Consultation ReportThis report will outline the theory and evidence base for Community Development and Community Engagement, report on consultation activities and findings
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Using theory to improve low back pain care in Australian Aboriginal primary care: A mixed method single cohort pilot studyLow back pain (LBP) care is frequently discordant with research evidence.
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Health of adolescent refugees resettling in high-income countriesEarly identification and management of the healthcare issues faced by adolescent refugees resettling in countries are key to improving long-term health outcomes
Research
Mutation Update for Kabuki Syndrome Genes KMT2D and KDM6A and Further Delineation of X-Linked Kabuki Syndrome Subtype 2Overview of all published mutations for the two Kabuki syndrome genes and point out possible mutation hot spots and strategies for molecular genetic testing