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The presence of Pseudomonas aeruginosa biofilms in lower airway specimens from cystic fibrosis (CF) patients is well established.
Stratification of monitoring protocols based on the risk profile of the patient can help us in the future to better care for people with Cystic Fibrosis.
This paper is a review of lung function tests best suited to use for early detection of lung disease in Cystic Fibrosis.
This study aimed to identify psychosocial predictors in cystic fibrosis that may inform intervention strategies.
Our work has identified a clinically relevant host-derived factor that may participate in shaping early events in the aetiology of CF respiratory disease
This study developed and tested a highly usable, and moderately acceptable, smartphone app to improve the psychosocial health of young people living with CF
Bile acid signalling is a leading trigger for the development of chronic phenotypes underlying the pathophysiology of chronic respiratory disease
Understanding early triggers of Cystic Fibrosis Lung Disease
The Kids Research Institute Australia researchers have been awarded more than $10 million in research funding from the National Health and Medical Research Council (NHMRC).
The lungs are one of the last organs in the body to develop as a baby grows. They're also one of the most important.