Background Newborn screening allows novel treatments for cystic fibrosis (CF) to be trialled in early childhood before irreversible lung injury occurs. As respiratory exacerbations are a potential trial outcome variable, we determined their rate, duration and clinical features in preschool children with CF; and whether they were associated with growth, lung structure and function at age 5 years
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)...
It is not known at what age lung function impairment may arise in children with cystic fibrosis (CF)...
BACKGROUND: Newborn screening allows novel treatments for cystic fibrosis (CF) to be trialled in ear...
Background Newborn screening allows novel treatments for cystic fibrosis (CF) to be trialled in earl...
Prospective evaluation of respiratory exacerbations in children with cystic fibrosis from newborn sc...
Prospective evaluation of respiratory exacerbations in children with cystic fibrosis from newborn sc...
Cystic fibrosis (CF) lung disease starts early in life and progresses even in the absence of clinica...
Cystic fibrosis (CF) lung disease starts early in life and progresses even in the absence of clinica...
Cystic fibrosis (CF) lung disease starts early in life and progresses even in the absence of clinica...
The onset of lung disease in cystic fibrosis (CF) begins early in life with respiratory infection, i...
The onset of lung disease in cystic fibrosis (CF) begins early in life with respiratory infection, i...
Cystic fibrosis (CF) lung disease commences early in the disease progression and is the most common ...
Most morbidity in cystic fibrosis (CF) is due to progressive pulmonary disease. Recently, small mole...
Purpose of review Most treatment of newborn screening-diagnosed cystic fibrosis is not evidence-base...
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)...
It is not known at what age lung function impairment may arise in children with cystic fibrosis (CF)...
BACKGROUND: Newborn screening allows novel treatments for cystic fibrosis (CF) to be trialled in ear...
Background Newborn screening allows novel treatments for cystic fibrosis (CF) to be trialled in earl...
Prospective evaluation of respiratory exacerbations in children with cystic fibrosis from newborn sc...
Prospective evaluation of respiratory exacerbations in children with cystic fibrosis from newborn sc...
Cystic fibrosis (CF) lung disease starts early in life and progresses even in the absence of clinica...
Cystic fibrosis (CF) lung disease starts early in life and progresses even in the absence of clinica...
Cystic fibrosis (CF) lung disease starts early in life and progresses even in the absence of clinica...
The onset of lung disease in cystic fibrosis (CF) begins early in life with respiratory infection, i...
The onset of lung disease in cystic fibrosis (CF) begins early in life with respiratory infection, i...
Cystic fibrosis (CF) lung disease commences early in the disease progression and is the most common ...
Most morbidity in cystic fibrosis (CF) is due to progressive pulmonary disease. Recently, small mole...
Purpose of review Most treatment of newborn screening-diagnosed cystic fibrosis is not evidence-base...
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)...
It is not known at what age lung function impairment may arise in children with cystic fibrosis (CF)...