Potential difference test is valuable in the diagnosis of cystic fibrosis (CF) Source: Eur Respir J 2004; 24: Suppl. 48, 614s Year: 2004
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
Comparison of nanoduct versus macroduct sweat test for the diagnosis of cystic fibrosis in the newborn screening programme in Switzerland Source: Annual Congress 2012 - Cystic fibrosis (adults and children): new aspects of risk factors, treatments and diagnosis Year: 2012
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
Difficulty in diagnosis of patients who have cystic fibrosis like symptoms and borderline sweat test Source: Eur Respir J 2006; 28: Suppl. 50, 716s Year: 2006
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
Intestinal current measurement (ICM) as a new diagnostic test for cystic fibrosis (CF) Source: Annual Congress 2011 - Cystic fibrosis: New aspects of diagnosis, inflammation and detecting exacerbation Year: 2011
Inflammatory markers in cystic fibrosis patients with different values of pulmonary function tests Source: Eur Respir J 2002; 20: Suppl. 38, 528s Year: 2002
Six minute test in children and adults with cystic fibrosis Source: Virtual Congress 2020 – Exploring exercise responses in respiratory diseases Year: 2020
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
CFTR biomarkers: time for promotion to surrogate end-point Source: Eur Respir J 2013; 41: 203-216 Year: 2013
Atypical cystic fibrosis Source: ISSN=ISSN 1025-448x, ISBN=ISBN 1-904097-46-6, page=38 Year: 2006
How to make the diagnosis: the easy one, the difficult one Source: Annual Congress 2007 - PG4 - Paediatric respiratory medicine: cystic fibrosis – the basics Year: 2007
Is lung function diminished by 3 months of age in infants with cystic fibrosis (CF) diagnosed by newborn screening (NBS)? Source: Annual Congress 2010 - Functional assessment of paediatric lung disease Year: 2010
Inflammation, age and changing microbiology: the search for causation in the cystic fibrosis airways Source: Eur Respir J, 50 (5) 1701935; 10.1183/13993003.01935-2017 Year: 2017
Short and long term repeatability of N2 multiple breath washout indices in children with cystic fibrosis Source: Annual Congress 2013 –Clinical applications of respiratory physiology in children Year: 2013
The timed walk test as a measure of severity and survival in idiopathic pulmonary fibrosis Source: Eur Respir J 2005; 25: 96-103 Year: 2005
Which equations to estimate peak work rate from six minute walk test in patients with cystic fibrosis post lung transplantation? Source: Virtual Congress 2020 – Exercise tolerance and functional status across respiratory diseases Year: 2020
Newborn cystic fibrosis (CF) screening: influence of data transformation and density estimation on newborn recall Source: Eur Respir J 2007; 30: Suppl. 51, 30s Year: 2007
Evaluation of the pulmonary function of patients with cystic fibrosis aged 3-18 year old by using impulse oscillometry and spirometry Source: International Congress 2015 – Cystic fibrosis: microbiology, immunology and assessment Year: 2015