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PurposeTo evaluate cystic fibrosis (CF) subjects over 4 years using 3He magnetic resonance imaging (MRI), pulmonary function tests, and track hospitalization and physician visits.
Materials and MethodsFive CF adults provided written informed consent to an approved protocol and underwent MRI, spirometry, and plethysmography at baseline, 7 days, and 4 ± 1 years later. 3He MRI ventilation defect percent...
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