International audienceBackground: Lung MRI with ultrashort echo times (UTE-MRI) enables high-resolution and radiation-free morphological imaging, however, its imaging quality is still lower than CT. Purpose: To assess the image quality and clinical applicability of synthetic CTs generated from lung UTE-MRI using Generative Adversarial Networks (GAN).Methods and Materials: This retrospective study included patients with Cystic Fibrosis (CF) who underwent both UTE-MRI and CT on the same day at six institutions between January 2018 and December 2022. The 2D GAN algorithm was trained using paired MR-to-CT slices and tested, along with an external dataset. Imaging quality was assessed quantitatively by measuring apparent contrast-to-noise-ratio...
PubMedID: 29976036Background/Aims: Morphological changes due to lung disease in patients with cystic...
To evaluate feasibility and diagnostic quality of ultra-short TR/TE two-dimensional (2D) steady stat...
Objective: Imaging represents an important noninvasive means to assess cystic fibrosis (CF) lung dis...
International audienceTo assess airway and lung parenchymal damage noninvasively in cystic fibrosis ...
International audienceBackground: Chest computed tomography (CT) remains the imaging standard for de...
OBJECTIVE To evaluate whether magnetic resonance imaging (MRI) is effective as computed tomograph...
PURPOSE: The most important components of CF lung disease are bronchiectasis (BE) and trapped air (T...
Objectives We hypothesized that non-contrast-enhanced PETRA (pointwise encoding time reduction with ...
Pulmonary MRI can now provide high-resolution images that are sensitive to early disease and specifi...
To explore the feasibility of diffusion-weighted imaging (DWI) to assess inflammatory lung changes i...
AIM To evaluate different magnetic resonance imaging (MRI) sequences for diagnosis of pulmonary m...
Computed Tomography (CT) is the gold standard to assess bronchiectasis and trapped air in cystic fib...
International audienceIn clinical practice, the modality of choice for lung diagnosis is usually com...
AIM: To evaluate image quality acquired at lung imaging using magnetic resonance imaging (MRI) seque...
Introduction: Chest computed tomography (CT) examinations are performed routinely in some cystic fib...
PubMedID: 29976036Background/Aims: Morphological changes due to lung disease in patients with cystic...
To evaluate feasibility and diagnostic quality of ultra-short TR/TE two-dimensional (2D) steady stat...
Objective: Imaging represents an important noninvasive means to assess cystic fibrosis (CF) lung dis...
International audienceTo assess airway and lung parenchymal damage noninvasively in cystic fibrosis ...
International audienceBackground: Chest computed tomography (CT) remains the imaging standard for de...
OBJECTIVE To evaluate whether magnetic resonance imaging (MRI) is effective as computed tomograph...
PURPOSE: The most important components of CF lung disease are bronchiectasis (BE) and trapped air (T...
Objectives We hypothesized that non-contrast-enhanced PETRA (pointwise encoding time reduction with ...
Pulmonary MRI can now provide high-resolution images that are sensitive to early disease and specifi...
To explore the feasibility of diffusion-weighted imaging (DWI) to assess inflammatory lung changes i...
AIM To evaluate different magnetic resonance imaging (MRI) sequences for diagnosis of pulmonary m...
Computed Tomography (CT) is the gold standard to assess bronchiectasis and trapped air in cystic fib...
International audienceIn clinical practice, the modality of choice for lung diagnosis is usually com...
AIM: To evaluate image quality acquired at lung imaging using magnetic resonance imaging (MRI) seque...
Introduction: Chest computed tomography (CT) examinations are performed routinely in some cystic fib...
PubMedID: 29976036Background/Aims: Morphological changes due to lung disease in patients with cystic...
To evaluate feasibility and diagnostic quality of ultra-short TR/TE two-dimensional (2D) steady stat...
Objective: Imaging represents an important noninvasive means to assess cystic fibrosis (CF) lung dis...