Association of lung function, chest radiographs and clinical features in infants with cystic fibrosis Source: Eur Respir J 2013; 42: 1545-1552 Year: 2013
Comparison of high resolution computerized tomography (HRCT) of the chest and pulmonary function testing in evaluating the effect of tobramycin solution for inhalation in cystic fibrosis (CF) patients Source: Eur Respir J 2004; 24: Suppl. 48, 387s Year: 2004
Automatic evaluation of interstitial lung disorders (ILDs) with helical CT. A comparison with pulmonary function tests (PFT) Source: Eur Respir J 2002; 20: Suppl. 38, 415s Year: 2002
Correlation of dyspnea scores with pulmonary function, high-resolution computed tomography (HRCT) and exercise capacity in patients with idiopathic pulmonary fibrosis (IPF) Source: Eur Respir J 2006; 28: Suppl. 50, 305s Year: 2006
Radiological and functional changes over 3 years in young children with cystic fibrosis Source: Eur Respir J 2007; 30: 279-285 Year: 2007
Chest radiograph, lung function tests and induced sputum in chronic obstructive pulmonary disease (COPD) Source: Eur Respir J 2001; 18: Suppl. 33, 210s Year: 2001
Quantitative HRCT score in idiopathic pulmonary fibrosis (IPF): correlation with pulmonary function tests (PFT) Source: Annual Congress 2008 - Management of idiopathic pulmonary fibrosis: what can we learn from the pathophysiology? Year: 2008
Early investigations of patients presenting with haemoptysis and normal chest radiograph (CXR) for lung cancer Source: Annual Congress 2007 - Diagnosis and prognosis in thoracic oncology Year: 2007
Changes in quantitative measures of airways on computed tomography (CT) in children with cystic fibrosis (CF) Source: Eur Respir J 2005; 26: Suppl. 49, 728s Year: 2005
Imaging of sarcoidosis of the airways and lung parenchyma and correlation with lung function}, Source: Eur Respir J 2012; 40: 750-765 Year: 2012
HRCT lung abnormalities are not a surrogate for exercise limitation in bronchiectasis Source: Eur Respir J 2004; 24 : 538-544 Year: 2004
The number of exacerbations in children and adolescents with cystic fibrosis (CF) can be predicted by computed tomography (CT) bronchiectasis (BE) score and quality of life scores Source: Annual Congress 2011 - Monitoring exacerbations of airway diseases Year: 2011
Magnetic-resonance-imaging (MRI) for assessment of regional therapy response in patients with cystic fibrosis (CF) Source: Annual Congress 2009 - Cystic fibrosis: understanding a complex disease Year: 2009
Correlations of chest radiographs, pulmonary function tests and high resolution computed tomography findings with small airway disease in asymptomatic smokers Source: Eur Respir J 2004; 24: Suppl. 48, 494s Year: 2004
Impact of standardised chest physiotherapy with high frequency chest wall oscillation on lung clearance index in sputum producing patients with cystic fibrosis Source: Annual Congress 2010 - Cystic fibrosis: lung disease and much more Year: 2010
Short term effects of chest physiotherapy in children with cystic fibrosis assessed by a new lung function test Source: Annual Congress 2012 - Cystic fibrosis (adults and children): new basic and clinical physiology research Year: 2012
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
Tracking of lung function obtained by whole-body plethysmography in infants and children with cystic fibrosis (CF) Source: Annual Congress 2011 - Advances in lung function testing from infancy to adulthood Year: 2011
Agreement between the lung clearance index and bronchiectasis detected via chest computed tomography in infants and children with cystic fibrosis (CF) Source: International Congress 2014 – Cystic fibrosis: basic science, physiology and clinical aspects Year: 2014