Source: Virtual Congress 2021 – Monitoring of lung disease and CFTR function in children with cystic fibrosis



Rating:

Share or cite this content

Citations should be made in the following way:
B. Frauchiger (Bern, Switzerland), K. Ramsey (Bern, Switzerland), J. Usemann (Zurich, Switzerland), E. Kieninger (Bern, Switzerland), C. Casaulta (Bern, Switzerland), S. Yammine (Bern, Switzerland), D. Sirtes (Bern, Switzerland), B. Spycher (Bern, Switzerland), A. Moeller (Zurich, Switzerland), P. Latzin (Bern, Switzerland). Natural Variability of Clinically Measured Lung Clearance Index in Children with Cystic Fibrosis. 2674

Member's Comments

No comment yet.

Related content which might interest you: Does physiotherapy affect Lung Clearance Index in Cystic Fibrosis patients ? Source: International Congress 2018 – Cystic fibrosis in paediatric patients: current research Year: 2018 Bacterial Contamination of Home Nebulizers in Children with Cystic Fibrosis and Clinical Implication on the Number of Pulmonary Exacerbations Source: International Congress 2019 – Infection and inflammation in cystic fibrosis Year: 2019 Effects of Telerehabilitation on Peripheral Muscle Function in Pediatric Cystic Fibrosis Patients During Covid-19 Pandemic Source: Virtual Congress 2021 – Physical activity, exercise training and (tele)rehabilitation in respiratory patients Year: 2021 Dynamic Balance, Exercise Capacity and Muscle Oxygenation in Children with Non Cystic Fibrosis Bronchiectasis Source: Virtual Congress 2020 – Tapas of respiratory physiotherapy Year: 2020 Diffuse Pulmonary Non-Amyloid Light-Chain Deposition Disease: Phenotypes and Outcome Source: Virtual Congress 2021 – Exploring the phenotypic heterogeneity across rare diffuse parenchymal lung diseases Year: 2021 Comparative Evaluation of Clinical, Spiro/Oscillometric and Tomographic Parameters As A Global Assessment of Children With Cystic Fibrosis Source: International Congress 2018 – Cystic fibrosis in paediatric patients: current research Year: 2018 Energy Expenditure and Muscle oxygenation at Glittre Activities of Daily Living Test in Cystic Fibrosis with and without Airway Obstruction Source: Virtual Congress 2020 – Exercise tolerance and functional status across respiratory diseases Year: 2020 Resistance Training Alone Improves Lung Inflammation and Respiratory Muscle Strenght but not Lung Function and Mechanics in Mid-Age Women Source: Virtual Congress 2020 – Novel insights into exercise training Year: 2020 Modes of Disease Progression in Different Forms of Interstitial Lung Disease with Usual Interstitial Pneumonia Histology in Patients with Idiopathic and Non-idiopathic Etiologies - A Single Center Experience Source: International Congress 2019 – Immune-mediated interstitial lung diseases: from bench to bedside Year: 2019 Physical Training Improves Lung Function and Mechanics and Pulmonary and Systemic Immune Response in Eutrophic Women Source: Virtual Congress 2020 – Novel insights into exercise training Year: 2020 Development Of A Machine Learning Combination With Deep Learning For Diagnosing Idiopathic Pulmonary Fibrosis In Chronic Interstitial Lung Disease Source: Virtual Congress 2020 – Predictive markers of progression in connective tissue disease-associated interstitial lung disease and hypersensitivity pneumonitis Year: 2020 Utility of Lung Ultrasound in Interstitial Lung Disease - A Paradigm Shift Source: Virtual Congress 2020 – Natural history and management of interstitial lung diseases of known cause Year: 2020 Impact of Emphysema Heterogeneity on Lung Function after Bronchoscopic Lung Volume Reduction Source: International Congress 2019 – Interventional pulmonology: re-sculpting the airway Year: 2019 Prognostic Factors in Patients with Idiopathic Pulmonary Fibrosis; Evaluation using Quantitative CT Analysis of Fibrosis and Emphysema Source: International Congress 2019 – Innovations in idiopathic pulmonary fibrosis Year: 2019 Clinical Correlates of Physical Activity in Idiopathic Pulmonary Fibrosis (IPF) Source: International Congress 2019 – Pulmonary rehabilitation for non-obstructive lung diseases Year: 2019 Molecular Markers of Telomere Dysfunction and Senescence are Common Findings in the Usual Interstitial Pneumonia Pattern of Lung Fibrosis Source: International Congress 2018 – Progress in basic and translational research on idiopathic interstitial pneumonias Year: 2018 Cystic Fibrosis Patients Eligible for Modulator Drugs: Data from Cystic Fibrosis Registry of Turkey Source: International Congress 2019 – Treatments, adherence and psychosocial aspects of cystic fibrosis Year: 2019 Gait Parameters and Functional Balance in Adults with Non-Cystic Fibrosis Bronchiectasis Source: International Congress 2019 – Exercise and physiotherapy in patients with asthma, cystic fibrosis, bronchiectasis and primary ciliary dyskinesia Year: 2019 Impact of Eosinophilia and Time on Lung Function Decline in Adult Asthma Source: International Congress 2018 – Clinical determinants and biomarkers of COPD Year: 2018 The Effects Of Respiratory Viruses on The Acute Pulmonary Exacerbations In Cystic Fibrosis Patients Source: International Congress 2019 – Insights into paediatric bronchology Year: 2019