Difficulties in diagnosing tuberculosis in patients with cystic fibrosis Source: Eur Respir J 2004; 24: Suppl. 48, 615s Year: 2004
A borderline, or negative sweat test, leads to a diagnostic delay in hypertrypsinaemic cystic fibrosis (CF) infants with mild CFTR mutations Source: Eur Respir J 2001; 18: Suppl. 33, 124s Year: 2001
Characteristics of cystic fibrosis patients diagnosed after false negative cystic fibrosis newborn screening results Source: International Congress 2019 – Treatments, adherence and psychosocial aspects of cystic fibrosis Year: 2019
Late presenting cystic fibrosis Source: Annual Congress 2005 - Cystic fibrosis: no longer just kids‘ stuff Year: 2005
The clinical significance of oropharyngeal cultures in young children with cystic fibrosis Source: Eur Respir J, 51 (5) 1800238; 10.1183/13993003.00238-2018 Year: 2018
Nasal and sinus problems in cystic fibrosis patients Source: Eur Respir Monogr 2017; 76: 48-66 Year: 2017
Nasal potential difference measurements in patients with atypical cystic fibrosis Source: Eur Respir J 2001; 17: 1208-1215 Year: 2001
Nasal potential difference (NPD) in cystic fibrosis (CF) and non-CF patients with borderline sweat test Source: Eur Respir J 2001; 18: Suppl. 33, 215s Year: 2001
Using sputum proteomics to develop a test for reflux aspiration in cystic fibrosis patients Source: International Congress 2019 – Infection and inflammation in cystic fibrosis 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
Does this patient have cystic fibrosis? Source: International Congress 2017 – GR6 Paediatric Ground Round: an interactive session Year: 2017
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
Relations between the sinonasal development and the lung disease in cystic fibrosis patients Source: Eur Respir J 2005; 26: Suppl. 49, 103s Year: 2005
The diagnosis of cystic fibrosis by sweat test: the establishment of age specific reference intervals Source: Annual Congress 2007 - Cystic fibrosis lung disease: what do we measure? What do we know? Year: 2007
Identifying undiagnosed cystic fibrosis in adults with bronchiectasis Source: Eur Respir Monogr 2018; 81: 29-44 Year: 2018
Six minute test in children and adults with cystic fibrosis Source: Virtual Congress 2020 – Exploring exercise responses in respiratory diseases Year: 2020
Can step be a maximal test in children with cystic fibrosis? Source: Annual Congress 2009 - Paediatric lung function, imaging and methodology in health and disease Year: 2009
The treatment burden of cystic fibrosis: a day-to-day experience with treatment as someone with cystic fibrosis Source: Breathe, 17 (1) 210013; 10.1183/20734735.0013-2021 Year: 2021
Sputum glucose as a marker of disease severity in adult patients with cystic fibrosis Source: International Congress 2018 – Cystic fibrosis in adults: current research Year: 2018