Tidal expiratory flow limitation and chronic dyspnoea in patients with cystic fibrosis Source: Eur Respir J 2002; 19: 492-498 Year: 2002
Does expiratory flow limitation predict chronic dyspnoea in adults with cystic fibrosis? Source: Eur Respir J 2006; 28: 96-101 Year: 2006
Positive expiratory pressure and lung function in cystic fibrosis patients Source: Annual Congress 2008 - Mucociliary clearance, novel techniques and assessments, in adult, paediatric and mechanically ventilated patients Year: 2008
Effect of baseline FVC on lung function decline with nintedanib in patients with IPF Source: International Congress 2015 – Treatment of IPF Year: 2015
Relationship between airflow limitation and lung volume in cystic fibrosis patients Source: Eur Respir J 2002; 20: Suppl. 38, 301s 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
Differences in FVC decline by extent of emphysema in patients with combined pulmonary fibrosis and emphysema (CPFE) syndrome Source: International Congress 2015 – New frontiers in the management of interstitial and orphan lung diseases Year: 2015
Forced inspiratory volume in one second (FIV1 ) in the assessment of reversibility of airway obstruction in patients with chronic obstructive pulmonary disease (COPD) and in relation to the severity Source: Eur Respir J 2002; 20: Suppl. 38, 300s Year: 2002
Effect of azithromycin on FEV1 and exacerbation frequency in adult non-cystic fibrosis bronchiectasis Source: Eur Respir J 2007; 30: Suppl. 51, 528s Year: 2007
Evaluation of functional capacity and pulmonary functions during acute pulmonary exacerbation in children with cystic fibrosis Source: Virtual Congress 2020 – Exercise tolerance and functional status across respiratory diseases Year: 2020
Lung clearance index in cystic fibrosis subjects treated for pulmonary exacerbations Source: Eur Respir J 2015; 46: 1055-1064 Year: 2015
Symptom duration and the lung clearance index in children with cystic fibrosis and pulmonary exacerbations Source: International Congress 2019 – Physiology of cystic fibrosis Year: 2019
Coexistent pulmonary emphysema delays the decrease in vital capacity in patients with idiopathic pulmonary fibrosis Source: Annual Congress 2008 - Miscellaneous aspects of interstitial lung disease Year: 2008
Revisiting FEV1 in cystic fibrosis Source: Eur Respir J 2001; 18: Suppl. 33, 127s Year: 2001
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
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
Forced vital capacity decreases rapidly in patients with idiopathic upper lobe-dominant pulmonary fibrosis Source: Annual Congress 2011 - Clinical perspectives in several interstitial diseases Year: 2011
The effect of pulmonary rehabilitation toward expiratory airflow limitation in patients with chronic obstructive pulmonary disease Source: Annual Congress 2011 - Challenges in rehabilitation: some old dilemmas revisited with some solutions? Year: 2011
Pulmonary function of infants with cystic fibrosis, with and without respiratory symptoms Source: Eur Respir J 2002; 20: Suppl. 38, 529s Year: 2002
The impact of idiopathic pulmonary fibrosis on the airway length per generation in the human lung Source: Virtual Congress 2021 – Translational and other aspects of idiopathic interstitial pneumonia Year: 2021