Longitudinal assessment of lung function from infancy to childhood in patients with cystic fibrosis
Author:
Publisher
Wiley
Subject
Pulmonary and Respiratory Medicine,Pediatrics, Perinatology and Child Health
Reference37 articles.
1. Early detection of lung disease and its association with the nutritional status, genetic background and life events in patients with cystic fibrosis;Kraemer;Respiration,2000
2. Airway Function in infants newly diagnosed with cystic fibrosis;Ranganathan;Lancet,2001
3. Reduced lung function in cystic fibrosis: a primary or secondary phenotype?;Davis;Am J Respir Crit Care Med,2008
4. Genetic modifiers of lung disease in cystic fibrosis;Drumm;N Engl J Med,2005
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3. Progress in Model Systems of Cystic Fibrosis Mucosal Inflammation to Understand Aberrant Neutrophil Activity;Frontiers in Immunology;2020-04-07
4. Raised-Volume Forced Expiratory Flow-Volume Curve in Healthy Taiwanese Infants;Scientific Reports;2017-07-24
5. Early pulmonary disease manifestations in cystic fibrosis mice;Journal of Cystic Fibrosis;2016-11
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