International audienceThe mucus obstructing the airways of Cystic Fibrosis (CF) patients is a yield stress fluid. Linear and non-linear rheological analyses of CF sputa can provide relevant biophysical markers, which could be used for the management of this disease. Sputa were collected from CF patients either without any induction or following an aerosol treatment with the recombinant human DNAse (rhDNAse, Pulmozyme®). Several sample preparations were considered and multiple measurements were performed in order to assess both the repeatability and the robustness of the rheological measurements. The linear and non-linear rheological properties of all CF sputa were characterized. While no correlation between oscillatory shear linear viscoela...
AbstractBackgroundThere is conflicting evidence about the importance of airway mucins (MUC5AC and MU...
12noUse of Rheology and portable Low-Field NMR for the monitoring of lung functions in cystic fibros...
Background: Cystic fibrosis (CF) is characterized by a thick, sticky mucus responsible for both airw...
International audienceThe mucus obstructing the airways of Cystic Fibrosis (CF) patients is a yield ...
In cystic fibrosis (CF) patients airways mucus shows an increased viscoelasticity due to the concen...
In cystic fibrosis (CF) patients airways mucus shows an increased viscoelasticity due to the concent...
9noLung functionality assessment in cystic fibrosis (CF) patients is extremely relevant as most pati...
People with cystic fibrosis (CF) suffer from a sticky and thick sputum, which obstructs airways and ...
We evaluated test-retest reliability of sputum viscoelastic properties in clinically stable patients...
Background: As most cystic fibrosis (CF) patients progress to respiratory failure, lung functionalit...
14noCystic Fibrosis (CF), one of the most common lethal genetic diseases in people of Caucasian orig...
vised to measure the work of adhesion (WA) to a substrate of mucus, a viscoelastic gel, from the mea...
Cystic fibrosis (CF) is a disease characterized by the production of viscous mucoid secretions in mu...
Abstract Background Cystic fibrosis (CF) is a life-threatening multiorgan genetic disease, particula...
Sputum biomarkers hold promise as a direct measure of inflammation within the cystic fibrosis (CF) l...
AbstractBackgroundThere is conflicting evidence about the importance of airway mucins (MUC5AC and MU...
12noUse of Rheology and portable Low-Field NMR for the monitoring of lung functions in cystic fibros...
Background: Cystic fibrosis (CF) is characterized by a thick, sticky mucus responsible for both airw...
International audienceThe mucus obstructing the airways of Cystic Fibrosis (CF) patients is a yield ...
In cystic fibrosis (CF) patients airways mucus shows an increased viscoelasticity due to the concen...
In cystic fibrosis (CF) patients airways mucus shows an increased viscoelasticity due to the concent...
9noLung functionality assessment in cystic fibrosis (CF) patients is extremely relevant as most pati...
People with cystic fibrosis (CF) suffer from a sticky and thick sputum, which obstructs airways and ...
We evaluated test-retest reliability of sputum viscoelastic properties in clinically stable patients...
Background: As most cystic fibrosis (CF) patients progress to respiratory failure, lung functionalit...
14noCystic Fibrosis (CF), one of the most common lethal genetic diseases in people of Caucasian orig...
vised to measure the work of adhesion (WA) to a substrate of mucus, a viscoelastic gel, from the mea...
Cystic fibrosis (CF) is a disease characterized by the production of viscous mucoid secretions in mu...
Abstract Background Cystic fibrosis (CF) is a life-threatening multiorgan genetic disease, particula...
Sputum biomarkers hold promise as a direct measure of inflammation within the cystic fibrosis (CF) l...
AbstractBackgroundThere is conflicting evidence about the importance of airway mucins (MUC5AC and MU...
12noUse of Rheology and portable Low-Field NMR for the monitoring of lung functions in cystic fibros...
Background: Cystic fibrosis (CF) is characterized by a thick, sticky mucus responsible for both airw...