Reports and Findings
Research
Polymorphisms associated with normal memory variation also affect memory impairment in schizophreniaNeurocognitive dysfunction is a core feature of schizophrenia with particularly prominent deficits in verbal episodic memory.
Research
Ndrg1 in development and maintenance of the myelin sheathCMT4D disease is a severe autosomal recessive demyelinating neuropathy with extensive axonal loss leading to early disability
Research
Extent of metabolic risk in adolescent girls with features of polycystic ovary syndromeThe objective of this study was to determine prevalence of metabolic syndrome in adolescents with polycystic ovary syndrome (PCOS)
Research
Crowding and other strong predictors of upper respiratory tract carriage of otitis media-relatedWe investigated predictors of nasopharyngeal carriage in Australian Aboriginal and non-Aboriginal children.
Research
The over-estimation of risk in pregnancyThe concept of risk is especially salient to obstetric care. Unknown factors can still be responsible for peri-natal morbidity
Research
Researchers' experience with project management in health and medical research: Results from a post-project reviewProject management is widely used to deliver projects on time, within budget and of defined quality
Research
Obstetric profiles of foreign-born women in Western Australia using data linkage, 1998-2006Despite Western Australia (WA) having the highest proportion of overseas-born residents of any Australian state, no previous study has examined the general...
Research
Slam and dc-sign measles receptor polymorphisms and their impact on antibody and cytokine responses to measles vaccineDespite the use of measles vaccine, measles virus continues to circulate and cause severe disease
Research
The airway epithelium is a direct source of matrix degrading enzymes in bronchiolitis obliterans syndromeLong-term survival after lung transplantation is hindered by the development of bronchiolitis obliterans syndrome (BOS).
Research
Novel non-TCR chromosome translocations t(3;11)(q25;p13) and t(X;11)(q25;p13) activating LMO2In T-cell acute lymphoblastic leukemia (T-ALL) cytogenetic alterations juxtapose the LIM-domain-only-2 gene (LMO2) with T-cell receptor loci.