The optimal strategy for monitoring cystic fibrosis (CF) lung disease in infancy remains unclear
BACKGROUND: In school-aged children with cystic fibrosis (CF) structural lung damage assessed using ...
Rationale: The lung clearance index is a measure of ventilation distribution derived from the multip...
Cystic fibrosis (CF) lung disease commences early in the disease progression and is the most common ...
Rationale: Better understanding of evolution of lung function in infants with cystic fibrosis (CF) a...
Background Cystic fibrosis (CF) lung disease starts in infancy and can be assessed for structural lu...
Rationale: Better understanding of evolution of lung function in infants with cystic fibrosis (CF) a...
Rationale: Pulmonary inflammation, infection, and structural lung disease occur early in life in chi...
Background: In school-aged children with cystic fibrosis (CF) structural lung damage assessed using ...
It is not known at what age lung function impairment may arise in children with cystic fibrosis (CF)...
It is not known at what age lung function impairment may arise in children with cystic fibrosis (CF)...
BACKGROUND: Accelerated lung function decline in individuals with cystic fibrosis (CF) starts in ado...
Structural and functional defects within the lungs of children with cystic fibrosis (CF) are detecta...
Cystic fibrosis is the most common lethal genetic disorder in the white population. Chronic inflamma...
BACKGROUND: In school-aged children with cystic fibrosis (CF) structural lung damage assessed using ...
With the advent of novel designer molecules for cystic fibrosis (CF) treatment, there is huge need f...
BACKGROUND: In school-aged children with cystic fibrosis (CF) structural lung damage assessed using ...
Rationale: The lung clearance index is a measure of ventilation distribution derived from the multip...
Cystic fibrosis (CF) lung disease commences early in the disease progression and is the most common ...
Rationale: Better understanding of evolution of lung function in infants with cystic fibrosis (CF) a...
Background Cystic fibrosis (CF) lung disease starts in infancy and can be assessed for structural lu...
Rationale: Better understanding of evolution of lung function in infants with cystic fibrosis (CF) a...
Rationale: Pulmonary inflammation, infection, and structural lung disease occur early in life in chi...
Background: In school-aged children with cystic fibrosis (CF) structural lung damage assessed using ...
It is not known at what age lung function impairment may arise in children with cystic fibrosis (CF)...
It is not known at what age lung function impairment may arise in children with cystic fibrosis (CF)...
BACKGROUND: Accelerated lung function decline in individuals with cystic fibrosis (CF) starts in ado...
Structural and functional defects within the lungs of children with cystic fibrosis (CF) are detecta...
Cystic fibrosis is the most common lethal genetic disorder in the white population. Chronic inflamma...
BACKGROUND: In school-aged children with cystic fibrosis (CF) structural lung damage assessed using ...
With the advent of novel designer molecules for cystic fibrosis (CF) treatment, there is huge need f...
BACKGROUND: In school-aged children with cystic fibrosis (CF) structural lung damage assessed using ...
Rationale: The lung clearance index is a measure of ventilation distribution derived from the multip...
Cystic fibrosis (CF) lung disease commences early in the disease progression and is the most common ...