Do causes influence clinical, functional and quality of life aspects on patients with bronchiectasis not associated with cystic fibrosis? Source: International Congress 2019 – Chronic cough, a1-antitrypsin deficiency and other conditions Year: 2019
Clinical characteristics and disease severity of adults with cystic fibrosis with at least one residual function mutation Source: International Congress 2018 – Cystic fibrosis in adults: current research Year: 2018
Comparison of clinical features in patients with cystic fibrosis according to the age at diagnosis Source: Annual Congress 2009 - Cystic fibrosis: advances in clinical research Year: 2009
Lung clearance index and functional MRI outcomes to assess lung disease in preschool children with cystic fibrosis Source: Virtual Congress 2020 – New frontiers in cystic fibrosis imaging and lung physiology Year: 2020
Correlation between radiologic and functional status in stable cystic fibrosis Source: Eur Respir J 2005; 26: Suppl. 49, 728s Year: 2005
Clinical and functional determinants of exercise limitation in adult patients with cystic fibrosis Source: Annual Congress 2012 - Limiting factors in exercise Year: 2012
Early renal involvement in children with cystic fibrosis. Source: International Congress 2018 – Cystic fibrosis in paediatric patients: current research Year: 2018
Late presenting cystic fibrosis Source: Annual Congress 2005 - Cystic fibrosis: no longer just kids‘ stuff Year: 2005
The use of non-invasive inflammatory markers to predict presence, severity and stability of cystic fibrosis lung disease Source: Eur Respir J 2006; 28: Suppl. 50, 327s Year: 2006
Association of lung function, chest radiographs and clinical features in infants with cystic fibrosis Source: Eur Respir J 2013; 42: 1545-1552 Year: 2013
Evaluation of disease knowledge in children with cystic fibrosis and their families Source: Annual Congress 2011 - Cystic fibrosis: clinical and laboratory studies Year: 2011
The impact of a network based approach on lung function and symptom duration at diagnosis in idiopathic pulmonary fibrosis Source: International Congress 2018 – News on the diagnosis of idiopathic interstitial pneumonia Year: 2018
Leveraging early markers of cystic fibrosis structural lung disease to improve outcomes Source: Eur Respir J, 55 (4) 2000105; 10.1183/13993003.00105-2020 Year: 2020
The role of lung ultrasonography in the assessment of idiopathic pulmonary fibrosis –correlation with HRCT finding Source: International Congress 2019 – Biomarkers of idiopathic interstitial pneumonia Year: 2019
Structural determinants of long-term functional outcomes in young children with cystic fibrosis Source: Eur Respir J, 55 (5) 1900748; 10.1183/13993003.00748-2019 Year: 2020
Polysomnograpgic findings in children with cystic fibrosis Source: Eur Respir J 2003; 22: Suppl. 45, 391s Year: 2003
Long-term outcomes and clinical worsening in cystic fibrosis patients with at least one residual function mutation Source: International Congress 2018 – Cystic fibrosis in adults: current research Year: 2018
Stratifying infants with cystic fibrosis for disease severity using intestinal organoid swelling as a biomarker of CFTR function Source: Eur Respir J, 52 (3) 1702529; 10.1183/13993003.02529-2017 Year: 2018
Impact of CFTR modulator use on outcomes in people with severe cystic fibrosis lung disease Source: Eur Respir Rev, 29 (155) 190112; 10.1183/16000617.0112-2019 Year: 2020