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
Impulse oscillometry in patients with cystic fibrosis: relationship to health status and conventional lung function measurements Source: Eur Respir J 2005; 26: Suppl. 49, 260s Year: 2005
Spirometric and plethysmographic measurements in healthy pre-school children and those with cystic fibrosis and chronic lung disease Source: Eur Respir J 2002; 20: Suppl. 38, 224s Year: 2002
Impact of lung disease on respiratory impedance in young children with cystic fibrosis Source: Eur Respir J 2015; 46: 1672-1679 Year: 2015
Sensitivity impulse oscillometry and spirometry for assessment degree of severity of bronchial asthma in preschool children Source: Eur Respir J 2006; 28: Suppl. 50, 477s Year: 2006
Longitudinal monitoring of cystic fibrosis lung disease in preschool children using forced oscillation technique Source: Annual Congress 2010 - Advances in lung function from infancy to adolescence Year: 2010
Nutritional status and pulmonary and respiratory muscle function in children and young people with cystic fibrosis Source: International Congress 2017 – Cystic fibrosis: treatments and monitoring Year: 2017
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
Pulmonary function of infants with cystic fibrosis, with and without respiratory symptoms Source: Eur Respir J 2002; 20: Suppl. 38, 529s Year: 2002
Assessment of pulmonary function by impulse oscillometry in young children with bronchopulmonary dysplasia Source: Annual Congress 2013 –Monitoring respiratory diseases: role of comorbidities and lung involvement Year: 2013
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
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
Changes in mechanical properties of respiratory system in children with cystic fibrosis during therapy of exacerbation Source: Eur Respir J 2005; 26: Suppl. 49, 612s Year: 2005
Lung function measurements in preschool children with bronchopulmonary displasia in the past by impulse oscillometry Source: Annual Congress 2010 - Innovations in the assessment of airway diseases Year: 2010
Comparison of HRCT lung abnormalities with exercise capacity among children and adolescents with cystic fibrosis Source: Annual Congress 2010 - Cystic fibrosis: lung disease and much more Year: 2010
Increased respiratory resistance using forced oscillations in symptomatic young children with cystic fibrosis Source: Eur Respir J 2005; 26: Suppl. 49, 728s Year: 2005
Lung function measurements in young children with respiratory diseases by impulse oscillometry Source: Eur Respir J 2005; 26: Suppl. 49, 394s Year: 2005
Early detection of pulmonary exacerbations in children with cystic fibrosis by electronic home monitoring of symptoms and lung function Source: International Congress 2016 – Cystic fibrosis: monitoring and management Year: 2016
Intra-breath oscillometry for assessing respiratory outcomes in preterm-born children Source: International Congress 2019 – Evaluation of breathing in children when they are asleep, healthy or ill Year: 2019
The relationships between hyperinflation during exercise and symptoms in adults with cystic fibrosis Source: Annual Congress 2012 - Limiting factors in exercise Year: 2012