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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,...
In infants and children with chronic respiratory disease, hypoxia is a potential risk of aircraft travel.
Advances in statistical modelling have allowed the creation of smoothly changing spirometry reference ranges that apply across a wide age range and better...
The aim of our study was to determine the contribution of secular trends and sample size to lung function reference equations, and establish the number...
In children, the ratio of forced expiratory volume in 1 s (FEV₁) to forced vital capacity (FVC) is reportedly constant or falls linearly with age...
Research question: Are asthma and allergies more common in adolescents conceived with assisted reproductive technologies (ART) compared with adolescents conceived without?
Cystic fibrosis (CF) is characterized by small airway disease; but central airways may also be affected. We hypothesized that airway resistance estimated from computational fluid dynamic (CFD) methodology in infants with CF was higher than controls and that early airway inflammation in infants with CF is associated with airway resistance.
Early viral infections were associated with greater neutrophilic inflammation and bacterial pathogens