Does lung transplantation affect on the improvement of psychological status in patients with adult cystic fibrosis? Source: International Congress 2018 – Contemporary respiratory care: symptoms, the role of the nurse and the organisation of care Year: 2018
How much genotype influences cystic fibrosis associated liver disease? Source: Eur Respir J 2006; 28: Suppl. 50, 717s Year: 2006
Factors affecting lung function in adult cystic fibrosis patients after lung transplantation. Source: International Congress 2018 – Evolving approaches to differential diagnosis Year: 2018
Impact of CFTR modulator use on outcomes in people with severe cystic fibrosis lung disease Source: Eur Respir Rev, 29 (155) 190112; 10.1183/16000617.0112-2019 Year: 2020
Leveraging early markers of cystic fibrosis structural lung disease to improve outcomes Source: Eur Respir J, 55 (4) 2000105; 10.1183/13993003.00105-2020 Year: 2020
Do causes influence clinical, functional and quality of life aspects on patients with bronchiectasis not associated with cystic fibrosis? Source: International Congress 2019 – Chronic cough, a1-antitrypsin deficiency and other conditions Year: 2019
Patient reported quality of life in advanced cystic fibrosis (CF) lung disease assessed for lung transplantation Source: Annual Congress 2008 - Lung and bone marrow transplantation: miscellaneous Year: 2008
Lung function in children with cystic fibrosis liver disease Source: Virtual Congress 2021 – Cystic fibrosis in children: various aspects Year: 2021
Exercise tolerance in children with cystic fibrosis undergoing lung transplantation assessment Source: Eur Respir J 2001; 18: 293-297 Year: 2001
Early determinants of lung disease in children with cystic fibrosis Source: Virtual Congress 2020 – New frontiers in cystic fibrosis imaging and lung physiology Year: 2020
Difficult issues in the selection of cystic fibrosis patients for lung transplantation Source: ISSN=ISSN 1025-448x, ISBN=ISBN 1-904097-46-6, page=139 Year: 2006
Comparison of progression in lung structure and lung function in children and adolescents with cystic fibrosis Source: Eur Respir J 2006; 28: Suppl. 50, 714s Year: 2006
Relationship between nutritional and clinical status in adult cystic fibrosis patients Source: Eur Respir J 2006; 28: Suppl. 50, 58s Year: 2006
Inflammation and infection in infants with cystic fibrosis is associated with changes in lung function in the first year of life Source: Annual Congress 2008 - Respiratory physiology in health and disease Year: 2008
Long-term effects of a partially supervised conditioning programme in cystic fibrosis Source: Eur Respir J 2010; 35: 578-583 Year: 2010
Monitoring early lung disease in cystic fibrosis: where are we now? Source: Breathe 2014; 10: 34-47 Year: 2014
The lung clearance index correlates with markers of pulmonary deterioration in patients with cystic fibrosis Source: Annual Congress 2013 –Cystic fibrosis: physiotherapy, exercise and lung function in adults and children Year: 2013
What (and how) do we attain by performing surgical lung biopsy for interstitial lung disease? Source: International Congress 2015 – Interstitial lung diseases II Year: 2015
Lung clearance index and functional MRI outcomes to assess lung disease in preschool children with cystic fibrosis Source: Virtual Congress 2020 – New frontiers in cystic fibrosis imaging and lung physiology Year: 2020
Is lung function worsening during adolescence in cystic fibrosis? A retrospective study Source: Annual Congress 2012 - Cystic fibrosis (adults and children): new aspects of risk factors, treatments and diagnosis Year: 2012