Minimal structural lung disease in early life represents significant pathology.

[1]  P. Sly,et al.  BAL inflammatory markers can predict pulmonary exacerbations in children with cystic fibrosis. , 2020, Chest.

[2]  H. Tiddens,et al.  Structural determinants of long-term functional outcomes in young children with cystic fibrosis , 2020, European Respiratory Journal.

[3]  P. Sly,et al.  The cumulative effect of inflammation and infection on structural lung disease in early cystic fibrosis , 2019, European Respiratory Journal.

[4]  L. Garratt,et al.  Elastase Exocytosis by Airway Neutrophils Is Associated with Early Lung Damage in Children with Cystic Fibrosis , 2019, American journal of respiratory and critical care medicine.

[5]  Dean P. Jones,et al.  Myeloperoxidase oxidation of methionine associates with early cystic fibrosis lung disease , 2018, European Respiratory Journal.

[6]  Hans-Ulrich Kauczor,et al.  Comparison of Lung Clearance Index and Magnetic Resonance Imaging for Assessment of Lung Disease in Children with Cystic Fibrosis , 2016, American journal of respiratory and critical care medicine.

[7]  S. Stick,et al.  Lung Clearance Index and Structural Lung Disease on Computed Tomography in Early Cystic Fibrosis. , 2015, American journal of respiratory and critical care medicine.

[8]  A. Wade,et al.  New reference ranges for interpreting forced expiratory manoeuvres in infants and implications for clinical interpretation: a multicentre collaboration , 2015, Thorax.

[9]  Peter D Sly,et al.  Distribution of early structural lung changes due to cystic fibrosis detected with chest computed tomography. , 2013, The Journal of pediatrics.

[10]  Peter D Sly,et al.  Risk factors for bronchiectasis in children with cystic fibrosis. , 2013, The New England journal of medicine.

[11]  P. Sly,et al.  Progression of early structural lung disease in young children with cystic fibrosis assessed using CT , 2011, Thorax.

[12]  P. Sly,et al.  Air Trapping on Chest CT Is Associated with Worse Ventilation Distribution in Infants with Cystic Fibrosis Diagnosed following Newborn Screening , 2011, PloS one.

[13]  J. Carlin,et al.  Effect of bronchoalveolar lavage-directed therapy on Pseudomonas aeruginosa infection and structural lung injury in children with cystic fibrosis: a randomized trial. , 2011, JAMA.

[14]  S. Stanojevic,et al.  Lung Clearance Index and HRCT are complementary markers of lung abnormalities in young children with CF , 2011, Thorax.

[15]  P. Sly,et al.  Lung disease at diagnosis in infants with cystic fibrosis detected by newborn screening. , 2009, American journal of respiratory and critical care medicine.

[16]  H. Tiddens,et al.  Multiple-breath inert gas washout and spirometry versus structural lung disease in cystic fibrosis , 2007, Thorax.

[17]  R. Castile,et al.  Comparison of quiet breathing and controlled ventilation in the high-resolution CT assessment of airway disease in infants with cystic fibrosis , 2005, Pediatric Radiology.

[18]  P. Molina,et al.  High-resolution computed tomography in young patients with cystic fibrosis: distribution of abnormalities and correlation with pulmonary function tests. , 2004, The Journal of pediatrics.

[19]  I. Masters,et al.  Application of chest high‐resolution computer tomography in young children with cystic fibrosis , 2001, Pediatric pulmonology.

[20]  Christina J. Herold,et al.  Cystic fibrosis: CT assessment of lung involvement in children and adults. , 1999, Radiology.

[21]  R. Stiglbauer,et al.  High Resolution CT in Children with Cystic Fibrosis , 1992, Acta radiologica.

[22]  M. Rosenfeld,et al.  Cystic Fibrosis: A Multi-Organ System Approach , 2020 .

[23]  O. M. Arıyürek,et al.  High resolution CT in children with cystic fibrosis: correlation with pulmonary functions and radiographic scores. , 2001, European journal of radiology.

[24]  M. Candusso,et al.  Cystic Fibrosis in Children: HRCT Findings and Distribution of Disease , 1996, Journal of thoracic imaging.