Assessment of pulmonary structure–function relationships in young children and adolescents with cystic fibrosis by multivolume proton‐MRI and CT
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DOI: 10.1002/jmri.25978
Abstract: Lung disease is the most frequent cause of morbidity and mortality in patients with cystic fibrosis (CF), and there is a shortage of sensitive biomarkers able to regionally monitor disease progression and to assess early… read more here.
Keywords: cystic fibrosis; fibrosis; assessment pulmonary; function relationships ... See more keywords