Multivolume magnetic resonance imaging (1H-MRI) for the longitudinal assessment of cystic fibrosis (CF) lung disease: comparison with spirometry Source: Virtual Congress 2020 – New frontiers in cystic fibrosis imaging and lung physiology Year: 2020
Assessment of a new magnetic resonance imaging (MRI)-scoring- system for pulmonary changes in patients with cystic fibrosis (CF) – comparison with clinical parameters and high resolution computed tomography (HRCT) Source: Annual Congress 2006 - New modalities and application in imaging of the chest Year: 2006
Quantitative multivolume proton-magnetic resonance imaging in patients with cystic fibrosis lung disease: comparison with clinical indicators Source: Eur Respir J, 53 (5) 1702020; 10.1183/13993003.02020-2017 Year: 2019
Role of chest magnetic resonance imaging (MRI) in the assessment and follow up of patients with cystic fibrosis (CF) Source: Annual Congress 2010 - Infection, inflammation and destruction Year: 2010
Structure-function relationships in the lungs of cystic fibrosis (CF) patients using multi-volume high-resolution CT (HRCT) and proton MRI (1H-MRI) Source: International Congress 2016 – Lung function and imaging: new findings and new approaches Year: 2016
Evaluation of the peripheral airway microstructure in children with cystic fibrosis (CF) using 3 He magnetic resonance imaging Source: Annual Congress 2012 - Cystic fibrosis (adults and children): new therapies and detection of early lung disease Year: 2012
Comparison of ventilation heterogeneity (VH) measured with multiple breath washout (MBW) imaging to whole lung MBW LCI and FEV1 in asthma and cystic fibrosis (CF) Source: International Congress 2015 – Functional imaging approaches for evaluating alteration of lung, airways and respiratory muscles Year: 2015
Assessment of chest magnetic resonance imaging in non-cystic fibrosis chronic lung disease: comparison to high-resolution computed tomography and correlation with clinical and pulmonary function data Source: Annual Congress 2009 - Paediatric lung function, imaging and methodology in health and disease Year: 2009
Hyperpolarised 3He MRI versus HRCT in COPD and normal volunteers: PHIL trial Source: Eur Respir J 2009; 34: 1311-1321 Year: 2009
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
In adults with cystic fibrosis (CF), the high-resolution computed tomography (HRCT) predicts maximal exercise capacity Source: International Congress 2018 – Cystic fibrosis in adults: current research Year: 2018
Non-contrast-enhanced assessment of lung perfusion in CF patients during respiratory tract exacerbation using Fourier decomposition magnetic resonance imaging (FDMRI) Source: Virtual Congress 2020 – Advances in cystic fibrosis: from microbiome to MRI Year: 2020
Multivolume proton-magnetic resonance imaging (1H-MRI) in lung transplant recipients: comparison with low dose computed tomography (CT). Source: International Congress 2017 – Evaluating lung function, dyspnoea and related respiratory diseases Year: 2017
Comparison of 1H MRI and 3He MRI ventilation images in patients with cystic fibrosis and patients with lung cancer Source: International Congress 2018 – Evaluation of COPD and various diseases by different imaging modalities Year: 2018
CT scans from CF patients screened for lung transplant; the severe advanced lung disease (SALD) CT scoring system and correlation with survival Source: Annual Congress 2007 - Cystic fibrosis lung disease: from diagnosis to end-stage Year: 2007
Quantitative computed tomography (QCT) measured 5th generation airways, emphysema and airflow obstruction in chronic obstructive pulmonary disease (COPD) from a COPDMAP cohort Source: International Congress 2014 – COPD and PAH related imaging Year: 2014
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
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
Interstitial lung disease (ILD) in juvenile systemic sclerosis (JSS): correlation between high-resolution computed tomography (HRCT) and pulmonary function test (PFT) changes Source: Annual Congress 2008 - Miscellaneous respiratory infections Year: 2008