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Assessment of pulmonary structure–function relationships in young children and adolescents with cystic fibrosis by multivolume proton‐MRI and CT

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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… Click to show full 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 responses to therapy.

Keywords: cystic fibrosis; fibrosis; assessment pulmonary; function relationships; pulmonary structure; structure function

Journal Title: Journal of Magnetic Resonance Imaging
Year Published: 2018

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