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Upper airway microbiota development in infants with cystic fibrosis diagnosed by newborn screen.
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The nasal microbiota in infants with cystic fibrosis in the first year of life: a prospective cohort study.
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Development of the gut microbiota in early life: The impact of cystic fibrosis and antibiotic treatment.
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Development of the Nasopharyngeal Microbiota in Infants with Cystic Fibrosis.
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Association of Antibiotics, Airway Microbiome, and Inflammation in Infants with Cystic Fibrosis.
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Upper versus lower airway microbiome and metagenome in children with cystic fibrosis and their correlation with lung inflammation.
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Airway Microbiota in Bronchoalveolar Lavage Fluid from Clinically Well Infants with Cystic Fibrosis.
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The lower airway microbiota in early cystic fibrosis lung disease: a longitudinal analysis.
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Differences in the lower airway microbiota of infants with and without cystic fibrosis.
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Relationship between airway dysbiosis, inflammation and lung function in adults with cystic fibrosis.
J Cyst Fibros. 2021 Sep;20(5):754-760. doi: 10.1016/j.jcf.2020.12.022. Epub 2021 Jan 8.
2
The infant pharyngeal microbiomes: origin, impact and manipulation.
Curr Opin Infect Dis. 2020 Dec;33(6):548-555. doi: 10.1097/QCO.0000000000000691.
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Lung function and microbiota diversity in cystic fibrosis.
Microbiome. 2020 Apr 2;8(1):45. doi: 10.1186/s40168-020-00810-3.
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Fecal dysbiosis in infants with cystic fibrosis is associated with early linear growth failure.
Nat Med. 2020 Feb;26(2):215-221. doi: 10.1038/s41591-019-0714-x. Epub 2020 Jan 20.
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Longitudinal development of the airway microbiota in infants with cystic fibrosis.
Sci Rep. 2019 Mar 26;9(1):5143. doi: 10.1038/s41598-019-41597-0.
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Neonatal gut and respiratory microbiota: coordinated development through time and space.
Microbiome. 2018 Oct 26;6(1):193. doi: 10.1186/s40168-018-0566-5.
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On the Use of Diversity Measures in Longitudinal Sequencing Studies of Microbial Communities.
Front Microbiol. 2018 May 22;9:1037. doi: 10.3389/fmicb.2018.01037. eCollection 2018.
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Airway microbiota across age and disease spectrum in cystic fibrosis.
Eur Respir J. 2017 Nov 16;50(5). doi: 10.1183/13993003.00832-2017. Print 2017 Nov.

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