Source: Annual Congress 2007 - Cystic fibrosis lung disease: what do we measure? What do we know?
Disease area: Paediatric lung diseases



Rating:

Share or cite this content

Citations should be made in the following way:
J. De Backer, W. Vos, A. Devolder, S. Verhust, K. Desager, W. De Backer (Antwerp, Belgium). Assessment of regional resistance distribution using computational fluid dynamics in cystic fibrosis patients. Eur Respir J 2007; 30: Suppl. 51, 349

Member's Comments

No comment yet.

Related content which might interest you: 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 Longitudinal changes in lung function and the association with pulmonary structure and infection in infants with cystic fibrosis Source: Annual Congress 2008 - Cystic fibrosis: novel aspects of airway function and inflammation Year: 2008 Single-breath washout and association with structural lung changes in children with cystic fibrosis Source: International Congress 2016 – Advanced lung function testing in childhood respiratory and sleep disease Year: 2016 Lung clearance Index changes over time among patients with cystic fibrosis Source: International Congress 2015 – New findings in paediatric respiratory physiology Year: 2015 Ability of lung clearance index to track changes in a routine clinical CF setting Source: International Congress 2015 – Paediatric respiratory physiology Year: 2015 Longitudinal course of clinically measured lung clearance index in children with cystic fibrosis Source: Virtual Congress 2020 – New frontiers in cystic fibrosis imaging and lung physiology Year: 2020 Underestimation of lung clearance index values in infants with cystic fibrosis due to software analysis algorithms Source: International Congress 2015 – Respiratory physiology in children: technical and clinical aspects Year: 2015 Lung function parameters influence serum concentration after antibiotic inhalation in patients with cystic fibrosis Source: Eur Respir J 2001; 18: Suppl. 33, 537s Year: 2001 A mathematical model to understand the airway clearance in cystic fibrosis Source: International Congress 2019 – New developments in sleep-disordered breathing, gas exchange and lung function in children Year: 2019 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 Relationship between airflow limitation and lung volume in cystic fibrosis patients Source: Eur Respir J 2002; 20: Suppl. 38, 301s Year: 2002 Changes in ventilatory mechanics with increasing disease severity in children and adolesecents with cystic fibrosis (CF) Source: Eur Respir J 2002; 20: Suppl. 38, 209s Year: 2002 Long-term course of lung clearance index among patients with cystic fibrosis Source: Virtual Congress 2020 – Respiratory physiology and sleep: new approaches to diagnosis and treatment Year: 2020 Assessment of the work of breathing (sWOB) within different functional and genetic groups in patients with cystic fibrosis (CF) Source: Annual Congress 2013 –New perspectives of lung function assessment in children Year: 2013 Clinical characteristics and disease severity of adults with cystic fibrosis with at least one residual function mutation Source: International Congress 2018 – Cystic fibrosis in adults: current research Year: 2018 Global burden of non-cystic fibrosis bronchiectasis: A simple epidemiological analysis Source: Annual Congress 2012 - Epidemiology of various respiratory diseases Year: 2012 Improvement in pulmonary function after IV antibiotic treatment in cystic fibrosis patients Source: Eur Respir J 2002; 20: Suppl. 38, 342s Year: 2002 Molecular detection of complex microbial communities in sputa of patients with cystic fibrosis and non cystic fibrosis bronchiectasis Source: Annual Congress 2010 - Cystic fibrosis: lung disease infection and more Year: 2010 New algorithm of antibiotic selection reveals the abundance and reduces bacterial load in sputum of adult patients with cystic fibrosis. Source: Virtual Congress 2021 – Cystic fibrosis Year: 2021 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