Neutrophilic airway inflammation plays a role in early structural lung disease in cystic fibrosis (CF), but the mechanisms underlying this pathway are incompletely understood
Background: In adults with cystic fibrosis (CF), induced sputum (IS) is a minimally invasive alterna...
Progressive lung function decline and, ultimately, respiratory failure are the most common cause of ...
The early detection of inflammation and infection is important to prevent irreversible lung damage i...
Metabolomic evaluation of cystic fibrosis (CF) airway secretions could identify metabolites and meta...
Metabolite profiles of bronchoalveolar lavage fluid (BALF) from pediatric patients with cystic fibro...
Although destructive airway disease is evident in young children with cystic fibrosis (CF), little i...
Rationale: Cystic fibrosis (CF) lung disease progressively worsens from infancy to adulthood. Diseas...
Background. Cystic fibrosis (CF) is a genetic disease that results in chronic infections of the lung...
The most common cause of death in cystic fibrosis (CF) patients is progressive lung function decline...
Background: Airway inflammation in cystic fibrosis (CF) is exaggerated and characterized by neutroph...
Background: Cystic fibrosis (CF) is a hereditary disorder in which persistent unresolved inflammatio...
The cystic fibrosis (CF) lung microbiome has been studied in children and adults; however, little is...
Metabolomics could provide new insights into the pathophysiology of cystic fibrosis (CF) by identify...
BackgroundProteomics can reveal molecular pathways of disease and provide translational perspectives...
RATIONALE: The underlying defect in the cystic fibrosis (CF) airway leads to defective mucociliar...
Background: In adults with cystic fibrosis (CF), induced sputum (IS) is a minimally invasive alterna...
Progressive lung function decline and, ultimately, respiratory failure are the most common cause of ...
The early detection of inflammation and infection is important to prevent irreversible lung damage i...
Metabolomic evaluation of cystic fibrosis (CF) airway secretions could identify metabolites and meta...
Metabolite profiles of bronchoalveolar lavage fluid (BALF) from pediatric patients with cystic fibro...
Although destructive airway disease is evident in young children with cystic fibrosis (CF), little i...
Rationale: Cystic fibrosis (CF) lung disease progressively worsens from infancy to adulthood. Diseas...
Background. Cystic fibrosis (CF) is a genetic disease that results in chronic infections of the lung...
The most common cause of death in cystic fibrosis (CF) patients is progressive lung function decline...
Background: Airway inflammation in cystic fibrosis (CF) is exaggerated and characterized by neutroph...
Background: Cystic fibrosis (CF) is a hereditary disorder in which persistent unresolved inflammatio...
The cystic fibrosis (CF) lung microbiome has been studied in children and adults; however, little is...
Metabolomics could provide new insights into the pathophysiology of cystic fibrosis (CF) by identify...
BackgroundProteomics can reveal molecular pathways of disease and provide translational perspectives...
RATIONALE: The underlying defect in the cystic fibrosis (CF) airway leads to defective mucociliar...
Background: In adults with cystic fibrosis (CF), induced sputum (IS) is a minimally invasive alterna...
Progressive lung function decline and, ultimately, respiratory failure are the most common cause of ...
The early detection of inflammation and infection is important to prevent irreversible lung damage i...
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