9noLung functionality assessment in cystic fibrosis (CF) patients is extremely relevant as most patients succumb to respiratory failure. Inflammatory markers (IMs) and respiratory functional tests, i.e. forced expiratory volume in the first second (FEV1), are used to test pulmonary functions/inflammation and to guide therapy. However, FEV1 has suboptimal reproducibility, and IMs detection is costly. Thus, aim of this work is to use rheology to assess lung functionality/inflammation recurring to the characterization CF patients sputum. Despite some known problems connected with the rheological characterization of inhomogeneous biological fluids, we found that there is a statistical linear correlation among the sputum elastic properties (G’ ...
11noThe increase of long surviving cystic fibrosis (CF) patients needs great effort for the assessme...
Cystic fibrosis (CF) lung disease is characterized by chronic airway inflammation and recurrent infe...
Background: Cystic fibrosis (CF) is characterized by a thick, sticky mucus responsible for both airw...
12noBackground: As most cystic fibrosis (CF) patients progress to respiratory failure, lung function...
We evaluated test-retest reliability of sputum viscoelastic properties in clinically stable patients...
People with cystic fibrosis (CF) suffer from a sticky and thick sputum, which obstructs airways and ...
The mucus obstructing the airways of Cystic Fibrosis (CF) patients is a yield stress fluid. Linear a...
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...
Background: Prior microrheologic assessments of selected, microlitre plugs of cystic fibrosis (CF) s...
12noUse of Rheology and portable Low-Field NMR for the monitoring of lung functions in cystic fibros...
15noTo develop a novel approach to monitor lung ventilation/inflammation in cystic fibrosis (CF) pat...
14noCystic Fibrosis (CF), one of the most common lethal genetic diseases in people of Caucasian orig...
Abstract Background Cystic fibrosis (CF) is a life-threatening multiorgan genetic disease, particula...
Cystic fibrosis (CF) is a disease characterized by the production of viscous mucoid secretions in mu...
11noThe increase of long surviving cystic fibrosis (CF) patients needs great effort for the assessme...
Cystic fibrosis (CF) lung disease is characterized by chronic airway inflammation and recurrent infe...
Background: Cystic fibrosis (CF) is characterized by a thick, sticky mucus responsible for both airw...
12noBackground: As most cystic fibrosis (CF) patients progress to respiratory failure, lung function...
We evaluated test-retest reliability of sputum viscoelastic properties in clinically stable patients...
People with cystic fibrosis (CF) suffer from a sticky and thick sputum, which obstructs airways and ...
The mucus obstructing the airways of Cystic Fibrosis (CF) patients is a yield stress fluid. Linear a...
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...
Background: Prior microrheologic assessments of selected, microlitre plugs of cystic fibrosis (CF) s...
12noUse of Rheology and portable Low-Field NMR for the monitoring of lung functions in cystic fibros...
15noTo develop a novel approach to monitor lung ventilation/inflammation in cystic fibrosis (CF) pat...
14noCystic Fibrosis (CF), one of the most common lethal genetic diseases in people of Caucasian orig...
Abstract Background Cystic fibrosis (CF) is a life-threatening multiorgan genetic disease, particula...
Cystic fibrosis (CF) is a disease characterized by the production of viscous mucoid secretions in mu...
11noThe increase of long surviving cystic fibrosis (CF) patients needs great effort for the assessme...
Cystic fibrosis (CF) lung disease is characterized by chronic airway inflammation and recurrent infe...
Background: Cystic fibrosis (CF) is characterized by a thick, sticky mucus responsible for both airw...