Impulse oscillometry in patients with cystic fibrosis: relationship to dynamic lung volumes Source: Eur Respir J 2001; 18: Suppl. 33, 537s Year: 2001
Usefulness of impulse oscillometry, single breath diffusion and bodypletysmography for lung function assessment in patients with cystic fibrosis Source: Eur Respir J 2006; 28: Suppl. 50, 715s Year: 2006
Impulse oscillometry compared to standard lung function testing in patients with idiopathic pulmonary fibrosis Source: International Congress 2018 – CTD-ILD and hypersensitivity pneumonitis: mechanistic insights and prognostic markers Year: 2018
Impulse oscillometry (IOS) in emphysema: relationship to conventional lung function indices Source: Eur Respir J 2003; 22: Suppl. 45, 100s Year: 2003
The assessment of respiratory status using impulsive oscillometry in children with cystic fibrosis Source: Eur Respir J 2004; 24: Suppl. 48, 387s Year: 2004
Is impulse oscillometry (IOS) better than spirometry for monitoring treatment outcomes in adult cystic fibrosis (CF) pulmonary exacerbations? A pilot study Source: International Congress 2019 – Physiology of cystic fibrosis Year: 2019
Differences in regional pulmonary function between children with cystic fibrosis and healthy children determined by electrical impedance tomography Source: Annual Congress 2013 –Cystic fibrosis: physiotherapy, exercise and lung function in adults and children Year: 2013
Relationship the impulse oscillometry parameters and the lung damage in idiopathic pulmonary fibrosis patients Source: Annual Congress 2013 –Airway calibre, airway challenge and assessment of oxygenation Year: 2013
The relationship between impulse oscillometry (IOS) and health status in patients with COPD Source: Eur Respir J 2003; 22: Suppl. 45, 423s Year: 2003
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
Longitudinal relationship between physical activity and lung health in patients with cystic fibrosis Source: Eur Respir J 2014; 43: 817-823 Year: 2014
Impulse oscillometry measurements in adult patients with CF: Focus on reactance Source: International Congress 2015 – Functional and imaging techniques for assessing lung, airway and respiratory muscles 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
Impulse oscillometry parameters in patients with idiopathic pulmonary fibrosis (IPF) with different severity grades of restrictive disorders Source: Annual Congress 2009 - A wide spectrum of idiopathic pulmonary fibrosis Year: 2009
The value of lung function monitoring by means of a home monitor in patients with cystic fibrosis Source: Annual Congress 2011 - Cystic fibrosis: New aspects of diagnosis, inflammation and detecting exacerbation Year: 2011
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
“Lung clearence index”; Can it be a guide for long-term follow up of children with cystic fibrosis who have normal spirometric values? Source: Virtual Congress 2020 – Clinical monitoring and new therapies for cystic fibrosis Year: 2020
Performance of impulse oscillometry and spirometry for the diagnosis of acute exacerbations of cystic fibrosis in adults Source: Virtual Congress 2020 – Clinical monitoring and new therapies for cystic fibrosis Year: 2020
Effect of positive expiratory pressure (PEP) on breathing pattern characteristics in cystic fibrosis children Source: International Congress 2014 – Multidimensional analysis of respiratory problems Year: 2014
Utility of impulse oscillometry in prediction of annual decline of pulmonary function in patients with COPD Source: Eur Respir J 2004; 24: Suppl. 48, 59s Year: 2004