Pulmonary MRI can now provide high‐resolution images that are sensitive to early disease
and specific to inflammation in cystic fibrosis (CF) lung disease. With specificity and function …

With fabrication technology reaching nanolevels, systems are becoming more prone to
manufacturing defects with higher susceptibility to soft errors. This paper is focused on …

Pulmonary MRI provides structural and quantitative functional images of the lungs without
ionizing radiation, but it has had limited clinical use due to low signal intensity from the lung …

Quantitative mapping of MR tissue parameters such as the spin‐lattice relaxation time (T1),
the spin‐spin relaxation time (T2), and the spin‐lattice relaxation in the rotating frame (T1ρ) …

Progressive lung disease in cystic fibrosis (CF) is the life-limiting factor of this autosomal
recessive genetic disorder. Increasing implementation of CF newborn screening allows for a …

Interstitial lung diseases (ILDs) are a heterogeneous group of conditions, with a wide and
complex variety of imaging features. Difficulty in monitoring, treating and exploring novel …

Thin-slices multi-detector computed tomography (MDCT) plays a key role in the differential
diagnosis of interstitial lung disease (ILD). However, thin-slices MDCT has a limited ability to …

Recent imaging studies using chest computed tomography (CT) in presymptomatic infants
and young children with cystic fibrosis (CF) diagnosed by newborn screening presented …

Purpose Monitoring of regional lung function in interventional COPD trials requires
alternative endpoints beyond global parameters such as FEV1. T1 relaxation times of the …

Purpose To correct for RF inhomogeneity for in vivo 129Xe ventilation MRI using flip‐angle
mapping enabled by randomized 3D radial acquisitions. To extend this RF‐depolarization …