2021
DOI: 10.1002/ppul.24929
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The remaining barriers to normalcy in CF: Advances in assessment of CF lung disease

Abstract: Despite early diagnosis of cystic fibrosis (CF) through newborn screening, a substantial proportion of infants and young children with CF still demonstrate physiologic and structural evidence of lung disease progression, such as obstructive airway disease and bronchiectasis. The growing availability of highly effective CF transmembrane conductance regulatory modulator therapy to the vast majority of people with CF has led to the potential to alter the natural history of CF lung disease, but to assess the full … Show more

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References 69 publications
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