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Globally, ARF and RHD cause more than a quarter of a million deaths and substantial disability each year.
We begin to bridge this knowledge gap by assessing evidence on social gradients in indigenous health in Australia.
We identified several novel candidate genes which warrant further analysis in cohorts matched more precisely for clinical phenotypes.
Investigation of this rare mixed lineage leukemia cytogenetic abnormality aims to provide further evidence of the genetic changes that underpin this leukemia.
IL8RA and IL8RB, encoded by CXCR1 and CXCR2, are receptors for interleukin (IL)-8 and other CXC chemokines involved in chemotaxis and activation of...
High consumption of sugar sweetened beverages (SSBs) has been linked to unhealthy weight gain and nutrition related chronic disease.
The cure rate for pediatric patients with B precursor acute lymphoblastic leukemia (pre-B ALL) is steadily improving, however relapses do occur despite...
This study aimed to investigate the trajectories over time of health status and health service use in Rett syndrome by mutation...
Otitis media (OM) is among the most common illnesses of early childhood, characterised by the presence of inflammation in the middle ear cavity...
Genome wide linkage studies (GWLS) have provided evidence for loci controlling visceral leishmaniasis on Chromosomes 1p22, 6q27, 22q12 in Sudan...