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
Impact of other risk factors than age at diagnosis on outcome in cystic fibrosis patients Source: Eur Respir J 2006; 28: Suppl. 50, 715s Year: 2006
Accuracy of clinical diagnostic criteria in the diagnosis of idiopathic pulmonary fibrosis Source: Eur Respir J 2001; 18: Suppl. 33, 151s Year: 2001
Clinical and functional profile of patients with non-cystic fibrosis bronchiectasis according to the presence of chronic bronchial infection Source: International Congress 2019 – Phenotypes and endotypes of bronchiectasis Year: 2019
The role of imagistic and functional methods in severity evaluation in children with cystic fibrosis Source: Annual Congress 2007 - Cystic fibrosis: better diagnosis, improved progress, but long-term complications Year: 2007
The diagnosis of cystic fibrosis in adult COPD patients. A survey of 54 patients Source: Eur Respir J 2001; 18: Suppl. 33, 215s Year: 2001
Relationship between nutritional and clinical status in adult cystic fibrosis patients Source: Eur Respir J 2006; 28: Suppl. 50, 58s Year: 2006
Age at diagnosis and follow up, standards of care in cystic fibrosis patients: impact on outcomes Source: Eur Respir J 2007; 30: Suppl. 51, 386s Year: 2007
New radiological diagnostic criteria: impact on idiopathic pulmonary fibrosis diagnosis Source: Eur Respir J, 54 (5) 1900905; 10.1183/13993003.00905-2019 Year: 2019
The features of sarcoidosis in owerweight patients. Source: Virtual Congress 2021 – Moving forward in various aspects of sarcoidosis Year: 2021
Late presenting cystic fibrosis Source: Annual Congress 2005 - Cystic fibrosis: no longer just kids‘ stuff Year: 2005
Prognostic determinants in IPF patients with the histological features of usual interstitial pneumonia Source: Eur Respir J 2001; 18: Suppl. 33, 526s Year: 2001
Clinical features of pseudo-bartter syndrome in cystic fibrosis. Source: International Congress 2017 – Cystic fibrosis: clinical issues Year: 2017
Exacerbations in non cystic fibrosis bronchiectasis: clinical features and investigations Source: Annual Congress 2009 - Bacterial infections of upper and lower respiratory tract in childhood Year: 2009
An epidemiological study on the effect of age, sex and comorbidities on the clinical course of idiopathic pulmonary fibrosis Source: International Congress 2017 – Idiopathic pulmonary fibrosis: from the bench to the bedside Year: 2017
Clinical features and prognosis of Chinese sarcoidosis patients. Source: International Congress 2018 – Granulomatous disorders: heterogeneous diseases with variable management Year: 2018
Correlation of a progression of fibrotic changes in idiopathic pulmonary fibrosis 1 year after a diagnosis with initial functional and immunologic parameters Source: Eur Respir J 2004; 24: Suppl. 48, 667s Year: 2004
Analysis of the clinical and pathological features of 10 patients with pulmonary sclerosing hemangioma Source: Eur Respir J 2005; 26: Suppl. 49, 538s Year: 2005
Is age a predictor in prognosis of patients with idiopathic pulmonary fibrosis? Source: Annual Congress 2008 - Management of idiopathic pulmonary fibrosis: what can we learn from the pathophysiology? Year: 2008
Evaluation of disease knowledge in children with cystic fibrosis and their families Source: Annual Congress 2011 - Cystic fibrosis: clinical and laboratory studies Year: 2011