Diagnostic efficiency of sweat conductivity testing in cystic fibrosis Source: International Congress 2015 – Cystic fibrosis: physiology, biomarkers, microbiology and miscellaneous Year: 2015
Usefulness of impulse oscillometry, single breath diffusion and bodypletysmography for lung function assessment in patients with cystic fibrosis Source: Eur Respir J 2006; 28: Suppl. 50, 715s Year: 2006
Characterisation of leaks during multiple breath washout and their influence on test results Source: International Congress 2015 – Paediatric respiratory physiology Year: 2015
Clinical utility of measuring ventilation inhomogeneity: cystic fibrosis Source: International Congress 2014 – Clinical utility of multiple breath washout (MBW): why is assessing ventilation inhomogeneity important? Year: 2014
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
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
CFTR biomarkers: time for promotion to surrogate end-point Source: Eur Respir J 2013; 41: 203-216 Year: 2013
Volumetric capnography: a promising lung function test in cystic fibrosis? Source: Virtual Congress 2020 – Respiratory physiology and sleep: from neonates to adults Year: 2020
The assesment of aerosol solution lung deposition in cystic fibrosis patients Source: Eur Respir J 2004; 24: Suppl. 48, 584s Year: 2004
Impulse oscillometry in patients with cystic fibrosis: relationship to health status and conventional lung function measurements Source: Eur Respir J 2005; 26: Suppl. 49, 260s Year: 2005
Non-invasive estimation of intra-pulmonary gas exchange efficiency during incremental exercise in healthy adults and patients with interstitial pulmonary fibrosis Source: Eur Respir J 2003; 22: Suppl. 45, 407s Year: 2003
Functional chloride secretion, CFTR-sequencing and transcript analysis in patients with inconclusive results in sweat test and CFTR-mutation screening Source: Eur Respir J 2005; 26: Suppl. 49, 402s Year: 2005
Differences in regional pulmonary function between children with cystic fibrosis and healthy children determined by electrical impedance tomography Source: Annual Congress 2013 –Cystic fibrosis: physiotherapy, exercise and lung function in adults and children Year: 2013
Electrical impedance tomography as a clinical monitoring tool in patients with cystic fibrosis Source: Virtual Congress 2020 – Clinical monitoring and new therapies for cystic fibrosis Year: 2020
Monitoring of tobramycin levels in patients with cystic fibrosis by finger-prick sampling Source: Eur Respir J 2012; 39: 1537-1538 Year: 2012
Oscillatory resistances measurement is an useful and reliable test to assess bronchial obstruction and reversibility Source: Eur Respir J 2004; 24: Suppl. 48, 575s Year: 2004
Rapid and portable MBW measurements for clinical application of LCI in routine clinics Source: International Congress 2016 – Assessing lower airway inflammation with different tools Year: 2016
Evaluation of the effectiveness of cyclical and constant current on sweat volume and stimulation for cystic fibroses diagnoses Source: International Congress 2014 – Cystic fibrosis: clinical assessment and treatment Year: 2014
Ability of lung clearance index to track changes in a routine clinical CF setting Source: International Congress 2015 – Paediatric respiratory physiology Year: 2015
The effect of spirometry on multiple breath washout outcomes in children with cystic fibrosis Source: International Congress 2018 – Cystic fibrosis in paediatric patients: current research Year: 2018