Ventilation distribution is not influenced by structural lung disease in infants with cystic fibrosis (CF) diagnosed following newborn screening (NBS) Source: Annual Congress 2009 - Cystic fibrosis: disease progression and novel therapies Year: 2009
Improvement in lung function during the 1st year of life in infants diagnosed with CF through newborn screening (NBS) Source: Annual Congress 2011 - Cystic fibrosis: detection and monitoring of early lung disease Year: 2011
Stable lung function is maintained over 2 years in newborn screened (NBS) CF infants Source: Annual Congress 2013 –Cystic fibrosis: lung function and change of lung function in infants and children before and after treatment Year: 2013
Microbiological yield of oropharyngeal swab compared to induced sputum in children with cystic fibrosis (CF) < 5 years of age Source: Annual Congress 2013 –Cystic fibrosis: clinical problems, genetics and microbiology in children Year: 2013
Within-subject variability of lung function in newborn screened (NBS) CF infants Source: International Congress 2016 – Cystic fibrosis: inflammation, microbiology, management and monitoring Year: 2016
Evaluation of the pulmonary function of patients with cystic fibrosis aged 3-18 year old by using impulse oscillometry and spirometry Source: International Congress 2015 – Cystic fibrosis: microbiology, immunology and assessment Year: 2015
Development of lung function in children born preterm with and without bronchopulmonary dysplasia - a follow-up study at 12 years of age. Source: International Congress 2019 – Molecular and experimental paediatric lung disease Year: 2019
Tracking of lung function obtained by whole-body plethysmography in infants and children with cystic fibrosis (CF) Source: Annual Congress 2011 - Advances in lung function testing from infancy to adulthood Year: 2011
Preschool lung clearance index (LCI) predicts adolescent lung function in cystic fibrosis (CF) Source: International Congress 2015 – Cystic fibrosis: physiology, biomarkers, microbiology and miscellaneous Year: 2015
The impact of Achromobacter xylosoxidans on lung function and hospital admissions in adult patients with cystic fibrosis (CF) Source: Annual Congress 2009 - Cystic fibrosis: understanding a complex disease Year: 2009
Outcomes at 6 months following NIV in adults with cystic fibrosis (CF): experience of a large UK centre Source: International Congress 2019 – Physiology of cystic fibrosis Year: 2019
Variability of the lung clearance index (LCI) assessed pre and post physiotherapy in patients with cystic fibrosis (CF) Source: Annual Congress 2008 - Clinical applications of ventilatory function tests in paediatric pulmonology Year: 2008
Lung clearance index (LCI) at age 1-4 years vs lung function and chest X-ray (CXR) scores at age 7 years in children with CF Source: Annual Congress 2011 - Cystic fibrosis: new basic, clinical and bacteriological knowledge Year: 2011
Normal lung function in infants with cystic fibrosis shortly after birth Source: Annual Congress 2013 –Cystic fibrosis: lung function and change of lung function in infants and children before and after treatment Year: 2013
Lung function abnormalities in asthmatic children (a 3-5 year follow-up study) Source: Eur Respir J 2001; 18: Suppl. 33, 120s Year: 2001
Progression of lung involvement in patients with cystic fibrosis (CF), assessed by longitudinal respiratory function measurements Source: Eur Respir J 2002; 20: Suppl. 38, 20s Year: 2002
Breathing pattern during rest and exercise in patients with cystic fibrosis (CF), pulmonary fibrosis (PF) and COPD before lung transplantation Source: Eur Respir J 2005; 26: Suppl. 49, 685s Year: 2005
A borderline, or negative sweat test, leads to a diagnostic delay in hypertrypsinaemic cystic fibrosis (CF) infants with mild CFTR mutations Source: Eur Respir J 2001; 18: Suppl. 33, 124s Year: 2001
Exercise capacity in patients with cystic fibrosis at 6 and 12 months after lung transplantation Source: International Congress 2018 – Latest developments in cystic fibrosis Year: 2018
Predictors of pulmonary function test (Spirometry) values for Pakistani children, aged 5-14 years Source: International Congress 2018 – Insights in primary ciliary dyskinesia, asthma and lung function testing Year: 2018