Longitudinal development of the airway microbiota in infants with cystic fibrosis
Author:
Publisher
Springer Science and Business Media LLC
Subject
Multidisciplinary
Link
http://www.nature.com/articles/s41598-019-41597-0.pdf
Reference34 articles.
1. Stafler, P., Davies, J. C., Balfour-Lynn, I. M., Rosenthal, M. & Bush, A. Bronchoscopy in cystic fibrosis infants diagnosed by newborn screening. Pediatric pulmonology 46, 696–700, https://doi.org/10.1002/ppul.21434 (2011).
2. Byrnes, C. A. et al. Prospective evaluation of respiratory exacerbations in children with cystic fibrosis from newborn screening to 5 years of age. Thorax 68, 643–651, https://doi.org/10.1136/thoraxjnl-2012-202342 (2013).
3. Tunney, M. M. et al. Detection of anaerobic bacteria in high numbers in sputum from patients with cystic fibrosis. American journal of respiratory and critical care medicine 177, 995–1001, https://doi.org/10.1164/rccm.200708-1151OC (2008).
4. Rogers, G. B. et al. Bacterial activity in cystic fibrosis lung infections. Respiratory research 6, 49, https://doi.org/10.1186/1465-9921-6-49 (2005).
5. Filkins, L. M. et al. Prevalence of streptococci and increased polymicrobial diversity associated with cystic fibrosis patient stability. Journal of bacteriology 194, 4709–4717, https://doi.org/10.1128/JB.00566-12 (2012).
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