Objective To examine the distribution of early structural lung changes in clinically stable infants and young children with cystic fibrosis using chest computed tomography (CT)
Lung disease is the most frequent cause of morbidity and mortality in patients with cystic fibrosis ...
Children with cystic fibrosis (CF) routinely receive computed tomography (CT) scans in many centers ...
Objective: The aim of this study was to determine whether assessment of early CT scan-detected bronc...
In school-aged children with cystic fibrosis (CF) structural lung damage assessed using chest CT is ...
BACKGROUND: In school-aged children with cystic fibrosis (CF) structural lung damage assessed using ...
Cystic fibrosis is the most common lethal autosomal recessive disorder in the Caucasian population. ...
Rationale: The lung clearance index is a measure of ventilation distribution derived from the multip...
method We read with great interest the well written manuscript by Mott et al,1 which reported their ...
Thoracic computed tomography (CT) is the imaging reference method in the diagnosis, assessment and m...
International audienceRationale and Objectives: The progressive changes in lung morphology observed ...
textabstractFor effective clinical management of cystic fibrosis (CF) lung disease it is impor...
Background/Aims Morphological changes due to lung disease in patients with cystic fibrosis (CF) were...
Background: Infants with cystic fibrosis (CF) develop structural lung disease early in life, and vir...
Lung disease in cystic fibrosis (CF) starts early, with studies identifying abnormalities on chest c...
Cystic Fibrosis (CF) is the most common lethal genetic disorder in the Caucasian population, affecti...
Lung disease is the most frequent cause of morbidity and mortality in patients with cystic fibrosis ...
Children with cystic fibrosis (CF) routinely receive computed tomography (CT) scans in many centers ...
Objective: The aim of this study was to determine whether assessment of early CT scan-detected bronc...
In school-aged children with cystic fibrosis (CF) structural lung damage assessed using chest CT is ...
BACKGROUND: In school-aged children with cystic fibrosis (CF) structural lung damage assessed using ...
Cystic fibrosis is the most common lethal autosomal recessive disorder in the Caucasian population. ...
Rationale: The lung clearance index is a measure of ventilation distribution derived from the multip...
method We read with great interest the well written manuscript by Mott et al,1 which reported their ...
Thoracic computed tomography (CT) is the imaging reference method in the diagnosis, assessment and m...
International audienceRationale and Objectives: The progressive changes in lung morphology observed ...
textabstractFor effective clinical management of cystic fibrosis (CF) lung disease it is impor...
Background/Aims Morphological changes due to lung disease in patients with cystic fibrosis (CF) were...
Background: Infants with cystic fibrosis (CF) develop structural lung disease early in life, and vir...
Lung disease in cystic fibrosis (CF) starts early, with studies identifying abnormalities on chest c...
Cystic Fibrosis (CF) is the most common lethal genetic disorder in the Caucasian population, affecti...
Lung disease is the most frequent cause of morbidity and mortality in patients with cystic fibrosis ...
Children with cystic fibrosis (CF) routinely receive computed tomography (CT) scans in many centers ...
Objective: The aim of this study was to determine whether assessment of early CT scan-detected bronc...