Excessive active absorption of sodium is a unique abnormality of the airway epithelium in patients with cystic fibrosis. This defect is associated with thickened mucus and poor clearance of airway secretions and may contribute to the pulmonary disease in these patients. To study whether the inhibition of excessive absorption of sodium might affect the course of lung disease in cystic fibrosis, we performed a double-blind, crossover trial comparing aerosolized amiloride (5 mmol per liter; 3.5 ml four times daily), a sodium-channel blocker, with vehicle alone. Fourteen of the 18 adult patients initially enrolled in the study completed the one-year trial (25 weeks for each treatment). The mean (±SEM) loss of forced vital capacity (FVC) was red...
Aerosol administration of antipseudomonal antibiotics is commonly used in cystic fibrosis. However, ...
Background: Hypertonic saline (HS) is commonly prescribed for children with cystic fibrosis (CF) des...
Background: Impaired mucociliary clearance characterises lung disease in cystic fibrosis (CF).Hypert...
To the Editor: The April 26 issue of the Journal presented encouraging results by Knowles et al. reg...
Abstract Cystic fibrosis (CF) is a multisystem disorder, caused by mutations in the CF transmembrane...
BACKGROUND: Abnormal homeostasis of the volume of airway surface liquid in patients with cystic fibr...
A non-interventional prospective cohort study was conducted on adult patients with cystic fibrosis, ...
Cystic fibrosis is an autosomal recessive genetic disorder that severely affects the lungs as well a...
Background and Purpose Inhaled amiloride, a blocker of the epithelial sodium channel (ENaC), enhanc...
BACKGROUND:Among the many consequences of loss of CFTR protein function, a significant reduction of ...
Rationale: Increased airway Na+ absorption mediated by epithelial Na1 channels (ENaC) is a character...
Background: Our aim was to investigate the acute effect of inhaled NaCl 5% on spirometry indices in ...
Among the many consequences of loss of CFTR protein function, a significant reduction of the secreti...
Cystic fibrosis (CF) is a multisystem disorder with significantly shortened life expectancy. The maj...
The raised nasal transepithelial potential difference (PD) in cystic fibrosis (CF) reflects accelera...
Aerosol administration of antipseudomonal antibiotics is commonly used in cystic fibrosis. However, ...
Background: Hypertonic saline (HS) is commonly prescribed for children with cystic fibrosis (CF) des...
Background: Impaired mucociliary clearance characterises lung disease in cystic fibrosis (CF).Hypert...
To the Editor: The April 26 issue of the Journal presented encouraging results by Knowles et al. reg...
Abstract Cystic fibrosis (CF) is a multisystem disorder, caused by mutations in the CF transmembrane...
BACKGROUND: Abnormal homeostasis of the volume of airway surface liquid in patients with cystic fibr...
A non-interventional prospective cohort study was conducted on adult patients with cystic fibrosis, ...
Cystic fibrosis is an autosomal recessive genetic disorder that severely affects the lungs as well a...
Background and Purpose Inhaled amiloride, a blocker of the epithelial sodium channel (ENaC), enhanc...
BACKGROUND:Among the many consequences of loss of CFTR protein function, a significant reduction of ...
Rationale: Increased airway Na+ absorption mediated by epithelial Na1 channels (ENaC) is a character...
Background: Our aim was to investigate the acute effect of inhaled NaCl 5% on spirometry indices in ...
Among the many consequences of loss of CFTR protein function, a significant reduction of the secreti...
Cystic fibrosis (CF) is a multisystem disorder with significantly shortened life expectancy. The maj...
The raised nasal transepithelial potential difference (PD) in cystic fibrosis (CF) reflects accelera...
Aerosol administration of antipseudomonal antibiotics is commonly used in cystic fibrosis. However, ...
Background: Hypertonic saline (HS) is commonly prescribed for children with cystic fibrosis (CF) des...
Background: Impaired mucociliary clearance characterises lung disease in cystic fibrosis (CF).Hypert...