Purpose: To estimate the effect of the number of computed tomography (CT) sections on trapped air (TA) assessment in patients with cystic fibrosis (CF) by using an established scoring system and a new quantitative scoring system and to compare CT and pulmonary function test (PFT) estimates of TA in a cross-sectional and longitudinal study. Materials and Methods: In this institutional review board-approved pilot study, 20 subjects aged 6-20 years (12 female and eight male; median age, 12.6 years) contributed two expiratory CT studies (three-section baseline CT, volumetric follow-up CT) and two PFT studies over 2 years after parental informed consent was obtained. From follow-up CT studies, seven sets were composed: Se
Cystic fibrosis (CF) is primarily characterised by bronchiectasis and trapped air on chest computed ...
OBJECTIVE: To evaluate lung disease progression using airway and artery (AA) dimensions on chest CT ...
Clinical trials for the treatment of cystic fibrosis (CF) lung disease are important to test and opt...
Purpose: To estimate the effect of the number of computed tomography (CT) sections on trapped air (T...
textabstractPurpose: To estimate the effect of the number of computed tomography (CT) sections on tr...
Introduction: Mosaic attenuation on expiratory chest computed tomography (CT) is common in early lif...
textabstractBackground: A study was undertaken to compare the ability of computed tomographic (CT) s...
BACKGROUND: Cystic fibrosis (CF) is a disease marked by airway inflammation and airflow obstruction,...
AbstractBackgroundThe quality of chest Computed Tomography (CT) images in children is dependent upon...
Purpose: To automatically derive the degree of air trapping in mild cystic fibrosis (CF) disease fro...
Purpose: To determine if fluorine 18 fluorodeoxyglucose (FDG) positron emission tomographic (PET)/co...
In school-aged children with cystic fibrosis (CF) structural lung damage assessed using chest CT is ...
PURPOSE: The most important components of CF lung disease are bronchiectasis (BE) and trapped air (T...
Running title: CT worsens faster than lung function in children and adults with CF What this paper a...
Objective: The aim of this study was to determine whether assessment of early CT scan-detected bronc...
Cystic fibrosis (CF) is primarily characterised by bronchiectasis and trapped air on chest computed ...
OBJECTIVE: To evaluate lung disease progression using airway and artery (AA) dimensions on chest CT ...
Clinical trials for the treatment of cystic fibrosis (CF) lung disease are important to test and opt...
Purpose: To estimate the effect of the number of computed tomography (CT) sections on trapped air (T...
textabstractPurpose: To estimate the effect of the number of computed tomography (CT) sections on tr...
Introduction: Mosaic attenuation on expiratory chest computed tomography (CT) is common in early lif...
textabstractBackground: A study was undertaken to compare the ability of computed tomographic (CT) s...
BACKGROUND: Cystic fibrosis (CF) is a disease marked by airway inflammation and airflow obstruction,...
AbstractBackgroundThe quality of chest Computed Tomography (CT) images in children is dependent upon...
Purpose: To automatically derive the degree of air trapping in mild cystic fibrosis (CF) disease fro...
Purpose: To determine if fluorine 18 fluorodeoxyglucose (FDG) positron emission tomographic (PET)/co...
In school-aged children with cystic fibrosis (CF) structural lung damage assessed using chest CT is ...
PURPOSE: The most important components of CF lung disease are bronchiectasis (BE) and trapped air (T...
Running title: CT worsens faster than lung function in children and adults with CF What this paper a...
Objective: The aim of this study was to determine whether assessment of early CT scan-detected bronc...
Cystic fibrosis (CF) is primarily characterised by bronchiectasis and trapped air on chest computed ...
OBJECTIVE: To evaluate lung disease progression using airway and artery (AA) dimensions on chest CT ...
Clinical trials for the treatment of cystic fibrosis (CF) lung disease are important to test and opt...