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Showing results for "preterm birth lungs"
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
Key messages from the abstracts presented at the European Respiratory Society International Congress
This report summarizes techniques available for ventilated and spontaneously breathing infants and children in the ICU
Recent technological advances in equipment design have produced gains in popularity for this test among cystic fibrosis (CF) researchers and clinicians...
Recent studies have demonstrated that some children with acute bronchiolitis can be successfully managed using home oxygen therapy.
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.
Advances in statistical modelling have allowed the creation of smoothly changing spirometry reference ranges that apply across a wide age range and better...