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Participant’s interviews describe how the Cultural, Social and Emotional Well Being(CSEWB) Program significantly changed their lives and their families’ lives in various constructive and affirming ways to bring about positive outcomes.
The Rare and Undiagnosed Diseases Diagnostic Service refers to a genomic diagnostic platform operating within the Genetic Services of Western Australia
Overall results of this preliminary study suggest that supplementation with fish oil may only significantly increase DHA in minor allele carriers of FADS1 SNPs. Further research is required to confirm this novel finding.
These findings also suggest that variants in ERAP1 have a differential impact on the risk of AAU when compared with AS, and hence the genetic risk for AAU...
New initiatives to develop a standard reference method and the assignment of "true" values to samples provide a solution to these problems.
Identified an association between polymorphisms in a long intergenic non-coding RNA (lincRNA) gene (AC011288.2) and pneumococcal bacteremia
Reduced frontal power at 3 months may indicate increased risk for reduced expressive language skills at 12 months.
Here we examined single nucleotide polymorphisms (SNPs) in these genes as risk factors for cutaneous (CL) and mucosal leishmaniasis (ML), and leishmaniasis...
Refugee children have complex backgrounds with exposure to multiple traumatic events.
Research to further improve outcomes for people with CF is dependent upon well characterised, archived and accessible clinical specimens.
This is a retrospective study of 38 cases of infection by Babesia macropus, associated with a syndrome of anaemia and debility in hand-reared or free-ranging...
The present study aimed to clarify the effect of viral and bacterial co-detections on disease severity during paediatric acute respiratory infection (ARI).
Viruses, bacteria, and parasites have developed strategies to invade and establish long-term infections in their hosts.
To investigate survival up to early adulthood for children with intellectual disability and compare their risk of mortality with that of children without intellectual disability.
Uniformly low expression of IFN and IFNGR1 in PKDL skin biopsies could explain parasite persistence
We examined the association of maternal factors and infant nutrition, with the subsequent diagnosis of NAFLD in adolescents
The polygenic nature of childhood ALL predisposition together with the timing of environmental triggers may hold vital clues for disease etiology.
This genome-wide association study (GWAS) utilises data from the Western Australian Pregnancy Cohort (Raine) Study for 25-hydroxyvitamin D (25(OH)D) levels...
Dissecting how genetic and environmental influences impact on learning is helpful for maximizing numeracy and literacy.