To explore the feasibility of diffusion-weighted imaging (DWI) to assess inflammatory lung changes in patients with Cystic Fibrosis (CF) CF patients referred for their annual check-up had spirometry, chest-CT and MRI on the same day. MRI was performed in a 1.5 T scanner with BLADE and EPI-DWI sequences (b = 0-600 s/mm(2)). End-inspiratory and end-expiratory scans were acquired in multi-row scanners. DWI was scored with an established semi-quantitative scoring system. DWI score was correlated to CT sub-scores for bronchiectasis (CF-CTBE), mucus (CF-CTmucus), total score (CF-CTtotal-score), FEV1, and BMI. T-test was used to assess differences between patients with and without DWI-hotspots. Thirty-three CF patients were enrolled (mean 21 years...
Cystic fibrosis is the most common lethal autosomal recessive disorder in the Caucasian population. ...
AIM To evaluate different magnetic resonance imaging (MRI) sequences for diagnosis of pulmonary m...
Lung function tests are commonly used to monitor lung disease in cystic fibrosis (CF). While practic...
To explore the feasibility of diffusion-weighted imaging (DWI) to assess inflammatory lung changes i...
The aim was to investigate whether diffusion-weighted magnetic resonance imaging (DWI) detects and m...
International audienceTo assess airway and lung parenchymal damage noninvasively in cystic fibrosis ...
Monitoring of pulmonary physiology is fundamental to the clinical management of patients with Cystic...
OBJECTIVE To evaluate whether magnetic resonance imaging (MRI) is effective as computed tomograph...
Pulmonary MRI can now provide high-resolution images that are sensitive to early disease and specifi...
Objectives We hypothesized that non-contrast-enhanced PETRA (pointwise encoding time reduction with ...
Background: MRI has been suggested as a radiation-free imaging modality to investigate early structu...
Background: MRI has been suggested as a radiation-free imaging modality to investigate early structu...
Background: The dawn of precision medicine and CFTR modulators require more detailed assessment of l...
To evaluate feasibility and diagnostic quality of ultra-short TR/TE two-dimensional (2D) steady stat...
OBJECTIVES To demonstrate, in patients with cystic fibrosis (CF), the correlation between three-dim...
Cystic fibrosis is the most common lethal autosomal recessive disorder in the Caucasian population. ...
AIM To evaluate different magnetic resonance imaging (MRI) sequences for diagnosis of pulmonary m...
Lung function tests are commonly used to monitor lung disease in cystic fibrosis (CF). While practic...
To explore the feasibility of diffusion-weighted imaging (DWI) to assess inflammatory lung changes i...
The aim was to investigate whether diffusion-weighted magnetic resonance imaging (DWI) detects and m...
International audienceTo assess airway and lung parenchymal damage noninvasively in cystic fibrosis ...
Monitoring of pulmonary physiology is fundamental to the clinical management of patients with Cystic...
OBJECTIVE To evaluate whether magnetic resonance imaging (MRI) is effective as computed tomograph...
Pulmonary MRI can now provide high-resolution images that are sensitive to early disease and specifi...
Objectives We hypothesized that non-contrast-enhanced PETRA (pointwise encoding time reduction with ...
Background: MRI has been suggested as a radiation-free imaging modality to investigate early structu...
Background: MRI has been suggested as a radiation-free imaging modality to investigate early structu...
Background: The dawn of precision medicine and CFTR modulators require more detailed assessment of l...
To evaluate feasibility and diagnostic quality of ultra-short TR/TE two-dimensional (2D) steady stat...
OBJECTIVES To demonstrate, in patients with cystic fibrosis (CF), the correlation between three-dim...
Cystic fibrosis is the most common lethal autosomal recessive disorder in the Caucasian population. ...
AIM To evaluate different magnetic resonance imaging (MRI) sequences for diagnosis of pulmonary m...
Lung function tests are commonly used to monitor lung disease in cystic fibrosis (CF). While practic...