Rationale: Pulmonary inflammation, infection, and structural lung disease occur early in life in children with cystic fibrosis. Objectives: We hypothesized that the presence of these markers of cystic fibrosis lung disease in the first 2 years of life would be associated with reduced lung function in childhood
The purpose of this study was to examine the relationships between inflammation, infection and lung ...
© 2017 by the American Thoracic Society. Rationale: The lung clearance index is a measure of ventila...
Cystic fibrosis is the most common lethal genetic disorder in the white population. Chronic inflamma...
Rationale: Pulmonary inflammation, infection, and structural lung disease occur early in life in chi...
Rationale: Better understanding of evolution of lung function in infants with cystic fibrosis (CF) a...
Rationale: Better understanding of evolution of lung function in infants with cystic fibrosis (CF) a...
The past decade has seen significant advances in understanding of the pathogenesis and progression o...
BACKGROUND: We previously reported relatively normal pulmonary function (2 years of age) and compute...
The onset of lung disease in cystic fibrosis (CF) begins early in life with respiratory infection, i...
Lung disease in cystic fibrosis (CF) starts early, with studies identifying abnormalities on chest c...
Copyright © 2002 American Thoracic SocietyOur aim was to study the effect of lower airway infection ...
Rationale: Better understanding of evolution of lung function in infants with cystic fibrosis (CF) a...
Introduction: Pulmonary inflammation and infection are important clinical and prognostic markers of ...
BACKGROUND: Accelerated lung function decline in individuals with cystic fibrosis (CF) starts in ado...
© Copyright 2017 by the American Thoracic Society. The past decade has seen significant advances in ...
The purpose of this study was to examine the relationships between inflammation, infection and lung ...
© 2017 by the American Thoracic Society. Rationale: The lung clearance index is a measure of ventila...
Cystic fibrosis is the most common lethal genetic disorder in the white population. Chronic inflamma...
Rationale: Pulmonary inflammation, infection, and structural lung disease occur early in life in chi...
Rationale: Better understanding of evolution of lung function in infants with cystic fibrosis (CF) a...
Rationale: Better understanding of evolution of lung function in infants with cystic fibrosis (CF) a...
The past decade has seen significant advances in understanding of the pathogenesis and progression o...
BACKGROUND: We previously reported relatively normal pulmonary function (2 years of age) and compute...
The onset of lung disease in cystic fibrosis (CF) begins early in life with respiratory infection, i...
Lung disease in cystic fibrosis (CF) starts early, with studies identifying abnormalities on chest c...
Copyright © 2002 American Thoracic SocietyOur aim was to study the effect of lower airway infection ...
Rationale: Better understanding of evolution of lung function in infants with cystic fibrosis (CF) a...
Introduction: Pulmonary inflammation and infection are important clinical and prognostic markers of ...
BACKGROUND: Accelerated lung function decline in individuals with cystic fibrosis (CF) starts in ado...
© Copyright 2017 by the American Thoracic Society. The past decade has seen significant advances in ...
The purpose of this study was to examine the relationships between inflammation, infection and lung ...
© 2017 by the American Thoracic Society. Rationale: The lung clearance index is a measure of ventila...
Cystic fibrosis is the most common lethal genetic disorder in the white population. Chronic inflamma...