Publication Genetic variation in PBMC-produced IFN-? and TNF-a associations with relapse in multiple sclerosis.
Publication Plasma vascular endothelial growth factor A and placental growth factor: novel biomarkers of pulmonary hypertension in congenital diaphragmatic hernia.
Publication MC1R variants increased the risk of sporadic cutaneous melanoma in darker-pigmented Caucasians: a pooled-analysis from the M-SKIP project.
Publication Aberrant mitochondria in a Bethlem myopathy patient with a homozygous amino acid substitution that destabilizes the collagen VI a2(VI) chain.
Publication Improving allied health professionals' research implementation behaviours for children with cerebral palsy: protocol for a before-after study.
Publication A shared framework for the common mental disorders and Non-Communicable Disease: key considerations for disease prevention and control.
Publication CLPB mutations cause 3-methylglutaconic aciduria, progressive brain atrophy, intellectual disability, congenital neutropenia, cataracts, movement disorder.
Publication Antimicrobial protein and Peptide concentrations and activity in human breast milk consumed by preterm infants at risk of late-onset neonatal sepsis.
Publication Phenotypic and molecular insights into spinal muscular atrophy due to mutations in BICD2.
Publication A systematic review of self-reported swallowing assessments in progressive neurological disorders.
