Impact of lung disease on respiratory impedance in young children with cystic fibrosis Source: Eur Respir J 2015; 46: 1672-1679 Year: 2015
Relationship between pulmonary functions and respiratory muscle strength in children with non cystic fibrosis bronchiectasis Source: Eur Respir J 2004; 24: Suppl. 48, 698s Year: 2004
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
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
Relationship between respiratory muscle strength and pulmonary function in children with cystic fibrosis Source: Eur Respir J 2006; 28: Suppl. 50, 730s Year: 2006
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
Increased respiratory resistance using forced oscillations in symptomatic young children with cystic fibrosis Source: Eur Respir J 2005; 26: Suppl. 49, 728s Year: 2005
Neural respiratory drive and disease severity in cystic fibrosis Source: Annual Congress 2009 - Cystic fibrosis: advances in clinical research Year: 2009
Does expiratory flow limitation predict chronic dyspnoea in adults with cystic fibrosis? Source: Eur Respir J 2006; 28: 96-101 Year: 2006
Pulmonary function of infants with cystic fibrosis, with and without respiratory symptoms Source: Eur Respir J 2002; 20: Suppl. 38, 529s Year: 2002
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
Relationship between chronic dyspnoea and indices of disease severity in idiopathic pulmonary fibrosis (IPF) Source: Eur Respir J 2001; 18: Suppl. 33, 150s Year: 2001
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
Hyperinflation in adult cystic fibrosis (CF) patients: Clinical and functional correlates Source: Annual Congress 2010 - Cystic fibrosis: clinical and laboratory studies Year: 2010
Short-term effects of physiotherapy on ventilation inhomogeneity in cystic fibrosis patients with moderate to severe lung disease Source: Annual Congress 2013 –Cystic fibrosis: physiotherapy, exercise and lung function in adults and children Year: 2013
Forced oscillation technique reflects lung disease in young children with cystic fibrosis Source: Eur Respir J 2007; 30: Suppl. 51, 33s Year: 2007
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
Noninvasive ventilation in cystic fibrosis patients with acute or chronic respiratory failure. Source: Eur Respir J 2002; 20: 790 Year: 2002
Structural lung disease, pulmonary infection and inflammation in infancy is associated with reduced spirometry at school-age in children with cystic fibrosis (CF) Source: Annual Congress 2013 –Cystic fibrosis: lung function and change of lung function in infants and children before and after treatment Year: 2013
Ventilation distribution is not influenced by structural lung disease in infants with cystic fibrosis (CF) diagnosed following newborn screening (NBS) Source: Annual Congress 2009 - Cystic fibrosis: disease progression and novel therapies Year: 2009