Challenges for the effective management of interstitial lung diseases (ILDs) include
difficulties with the early detection of disease, accurate prognostication with baseline data …

Idiopathic pulmonary fibrosis (IPF) is a chronic fibrosing interstitial lung disease with a poor
prognosis. 68Ga-labeled FAP ligands exhibited highly promising results due to the crucial …

The purpose of this study was to evaluate oxygen‐enhanced pulmonary imaging at 0.55 T
with 3D stack‐of‐spirals ultrashort‐TE (UTE) acquisition. Oxygen‐enhanced pulmonary MRI …

Idiopathic pulmonary fibrosis (IPF) is a chronic, debilitating, fibrotic lung disease leading to
respiratory failure and ultimately to death. Being the prototype of interstitial lung diseases …

Pulmonary functional magnetic resonance imaging (PfMRI) provides a way to non-invasively
map and measure the spatial distribution of pulmonary ventilation, perfusion and gas …

Background Pulmonary imaging of chronic obstructive pulmonary disease (COPD) has
focused on CT or MRI measurements, but these have not been evaluated in combination …

Monitoring of pulmonary physiology is fundamental to the clinical management of patients
with Cystic Fibrosis. The current standard clinical practise uses spirometry to assess lung …

Idiopathic Pulmonary Fibrosis (IPF) is a chronic, progressive, debilitating disease of
unknown etiology and a median survival from diagnosis of 3-5 years. Despite extensive …

Objectives We propose a novel computational approach for the automated classification of
classic versus atypical usual interstitial pneumonia (UIP). Materials and Methods Thirty-three …

With advances in multidetector-row computed tomography (MDCT), it is now possible to
image the lung in 10 s or less and accurately extract the lungs, lobes, and airway tree to the …