Understanding the relationship between secondhand smoke exposure and lung function in children with cystic fibrosis
Results from a clinical trial of the natural therapeutic alginate OligoG against Burkholderia lung infection in people with cystic fibrosis.
Is Body Mass Index Associated with Better Lung Function in Children with Pancreatic-Sufficient Cystic Fibrosis?
Is hyperpolarised gas magnetic resonance imaging a valid and reliable tool to detect lung health in cystic fibrosis patients? A COSMIN systematic review.
Predictive Effects of Low Birth Weight and Small for Gestational Age Status on Respiratory and Nutritional Outcomes in Cystic Fibrosis
Quantitative chest computerized tomography and FEV1 equally identify pulmonary exacerbation risk in children with cystic fibrosis.
Higher Interleukin-7 serum concentrations in patients with cystic fibrosis correlate with impaired lung function
