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Early life lower respiratory tract illness impairs lung function at 1 year, independent of baseline lung function

Newborn screening (NBS) for cystic fibrosis (CF) provides an opportunity to commence management and therapeutic interventions significantly earlier

Preterm children have worse lung function than healthy controls

Lung function measures in a health, unsedated 1- and 2-year-old children in a South African birth cohort study

The Foundations of Lung Disease Team is focused on improving the diagnosis, treatment, and lifelong care of childhood lung disease.

We’ve heard from families that trustworthy information about preterm-associated lung disease is difficult to find. In response, we’ve created resources to empower families with the knowledge they need to manage these challenges.

The aim of this study was to document the likely interpretative effects of changing from commonly used current spirometry reference equations to the GLI2012...

Cystic fibrosis (CF) lung disease commences early in the disease progression and is the most common cause of mortality.

We aimed to ascertain the fit of the European Respiratory Society Global Lung Initiative 2012 reference ranges to contemporary Australasian spirometric data.

Prediction bias in spirometry reference equations can arise from combining equations for different age groups,...