International audienceRationale and Objectives: The progressive changes in lung morphology observed in cystic fibrosis (CF) can potentially affect the statistical distribution of computed tomography (CT) density values. This study aimed to characterize the lung CT density distributions by quantifying indices of the kurtosis and skewness of the lung density distribution and to compare these indices to radiologic scores and lung function parameters in children and young adults with CF. Materials and Methods: CT scans and lung function of 26 patients with CF were retrospectively examined. The Bhalla radiologic scoring was performed separately, in random order, by two expert radiologists, blinded to the patient's identity, age, clinical status,...
Cystic fibrosis is the most common lethal autosomal recessive disorder in the Caucasian population. ...
Background: The dawn of precision medicine and CFTR modulators require more detailed assessment of l...
textabstractFor effective clinical management of cystic fibrosis (CF) lung disease it is impor...
International audienceRationale and Objectives: The progressive changes in lung morphology observed ...
Background: A study was undertaken to compare the ability of computed tomographic (CT) scores and pu...
Background: To reduce the mortality and morbidity rates of cystic fibrosis (CF) patients, and to hav...
Background/Aims Morphological changes due to lung disease in patients with cystic fibrosis (CF) were...
Background: Computed tomography (CT) of the lungs is the gold standard for assessing the extent of s...
Running title: CT worsens faster than lung function in children and adults with CF What this paper a...
OBJECTIVE. The objective of our study was to assess the accuracy of one of the most used scoring sys...
To explore the feasibility of diffusion-weighted imaging (DWI) to assess inflammatory lung changes i...
OBJECTIVE To evaluate whether magnetic resonance imaging (MRI) is effective as computed tomograph...
BACKGROUND: High-resolution CT (HRCT) scanning plays an important role in the diagnosis of diffuse c...
Rationale: The lung clearance index is a measure of ventilation distribution derived from the multip...
BACKGROUND: Structural lung changes seen on computed tomography (CT) scans in Cystic Fibrosis (CF) a...
Cystic fibrosis is the most common lethal autosomal recessive disorder in the Caucasian population. ...
Background: The dawn of precision medicine and CFTR modulators require more detailed assessment of l...
textabstractFor effective clinical management of cystic fibrosis (CF) lung disease it is impor...
International audienceRationale and Objectives: The progressive changes in lung morphology observed ...
Background: A study was undertaken to compare the ability of computed tomographic (CT) scores and pu...
Background: To reduce the mortality and morbidity rates of cystic fibrosis (CF) patients, and to hav...
Background/Aims Morphological changes due to lung disease in patients with cystic fibrosis (CF) were...
Background: Computed tomography (CT) of the lungs is the gold standard for assessing the extent of s...
Running title: CT worsens faster than lung function in children and adults with CF What this paper a...
OBJECTIVE. The objective of our study was to assess the accuracy of one of the most used scoring sys...
To explore the feasibility of diffusion-weighted imaging (DWI) to assess inflammatory lung changes i...
OBJECTIVE To evaluate whether magnetic resonance imaging (MRI) is effective as computed tomograph...
BACKGROUND: High-resolution CT (HRCT) scanning plays an important role in the diagnosis of diffuse c...
Rationale: The lung clearance index is a measure of ventilation distribution derived from the multip...
BACKGROUND: Structural lung changes seen on computed tomography (CT) scans in Cystic Fibrosis (CF) a...
Cystic fibrosis is the most common lethal autosomal recessive disorder in the Caucasian population. ...
Background: The dawn of precision medicine and CFTR modulators require more detailed assessment of l...
textabstractFor effective clinical management of cystic fibrosis (CF) lung disease it is impor...