To evaluate feasibility and diagnostic quality of ultra-short TR/TE two-dimensional (2D) steady state free precession (SSFP) MRI for cystic fibrosis (CF) patients. We performed lung MRI at 1.5 Tesla in 20 CF-patients (6-17 years, 12 males). Axial, coronal, and sagittal sections were acquired in inspiration and expiration with maximum breath-hold time 10 s. MR and CT images were scored using a modified Brody scoring system to assess bronchiectasis, mucous plugging, atelectasis/consolidations, and air trapping. All images were scored by two experienced observers. A complete MR investigation took maximally 15 min. Maximal breath-holds were only 10 s and well tolerated. MRI identified major bronchiectasis, mucous plugging and atelectasis. End-e...
Background: MRI has been suggested as a radiation-free imaging modality to investigate early structu...
BACKGROUND: Because of its absence of ionising radiation and possibility for obtaining functional in...
Lung function tests are commonly used to monitor lung disease in cystic fibrosis (CF). While practic...
International audienceTo assess airway and lung parenchymal damage noninvasively in cystic fibrosis ...
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...
Monitoring of pulmonary physiology is fundamental to the clinical management of patients with Cystic...
AIM To evaluate different magnetic resonance imaging (MRI) sequences for diagnosis of pulmonary m...
Cystic fibrosis (CF) patients would benefit from a safe and effective tool to detect early-stage, re...
Cystic fibrosis (CF) patients would benefit from a safe and effective tool to detect early-stage, re...
To date, PROPELLER MRI, a breathing-motion-insensitive technique, has not been assessed for cystic f...
Background: Cystic fibrosis (CF) patients would benefit from a safe and effective tool to detect ear...
To explore the feasibility of diffusion-weighted imaging (DWI) to assess inflammatory lung changes i...
Background: MRI has been suggested as a radiation-free imaging modality to investigate early structu...
PURPOSE: The most important components of CF lung disease are bronchiectasis (BE) and trapped air (T...
Background: MRI has been suggested as a radiation-free imaging modality to investigate early structu...
BACKGROUND: Because of its absence of ionising radiation and possibility for obtaining functional in...
Lung function tests are commonly used to monitor lung disease in cystic fibrosis (CF). While practic...
International audienceTo assess airway and lung parenchymal damage noninvasively in cystic fibrosis ...
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...
Monitoring of pulmonary physiology is fundamental to the clinical management of patients with Cystic...
AIM To evaluate different magnetic resonance imaging (MRI) sequences for diagnosis of pulmonary m...
Cystic fibrosis (CF) patients would benefit from a safe and effective tool to detect early-stage, re...
Cystic fibrosis (CF) patients would benefit from a safe and effective tool to detect early-stage, re...
To date, PROPELLER MRI, a breathing-motion-insensitive technique, has not been assessed for cystic f...
Background: Cystic fibrosis (CF) patients would benefit from a safe and effective tool to detect ear...
To explore the feasibility of diffusion-weighted imaging (DWI) to assess inflammatory lung changes i...
Background: MRI has been suggested as a radiation-free imaging modality to investigate early structu...
PURPOSE: The most important components of CF lung disease are bronchiectasis (BE) and trapped air (T...
Background: MRI has been suggested as a radiation-free imaging modality to investigate early structu...
BACKGROUND: Because of its absence of ionising radiation and possibility for obtaining functional in...
Lung function tests are commonly used to monitor lung disease in cystic fibrosis (CF). While practic...