Pulmonary symptoms in cystic fibrosis (CF) begin in early life with chronic lung infections and concomitant airway inflammation leading to progressive loss of lung function. Gradual pulmonary function decline is interspersed with periods of acute worsening of respiratory symptoms known as CF pulmonary exacerbations (CFPEs). Cumulatively, CFPEs are associated with more rapid disease progression. In this study multiple sputum samples were collected from adult CF patients over the course of CFPEs to better understand how changes in microbiota are associated with CFPE onset and management. Data were divided into five clinical periods: pre-CFPE baseline, CFPE, antibiotic treatment, recovery,and post-CFPE baseline. Samples were treated with prop...
AbstractBackgroundIntravenous antibiotics for pulmonary exacerbations (PEs) of cystic fibrosis (CF) ...
The lungs of patients with cystic fibrosis (CF) are colonised by a microbial community comprised of ...
<div><p>Cystic fibrosis (CF) is characterized by defective mucociliary clearance and chronic airway ...
© 2016 International Society for Microbial Ecology All rights reserved. Pulmonary symptoms in cystic...
© 2016 International Society for Microbial Ecology All rights reserved. Pulmonary symptoms in cystic...
Pulmonary symptoms in cystic fibrosis (CF) begin in early life with chronic lung infections and conc...
© 2016 International Society for Microbial Ecology All rights reserved. Pulmonary symptoms in cystic...
© 2016 International Society for Microbial Ecology All rights reserved. Pulmonary symptoms in cystic...
Pulmonary symptoms in cystic fibrosis (CF) begin in early life with chronic lung infections and conc...
Cystic fibrosis (CF) is characterized by defective mucociliary clearance and chronic airway infectio...
Cystic fibrosis (CF) is characterized by defective mucociliary clearance and chronic airway infectio...
This study was supported by the UK Natural Environment Research Council (NE/H019456/1) to CJvdG, by ...
Cystic fibrosis (CF) is caused by inherited mutations in the cystic fibrosis transmembrane conductan...
Cystic fibrosis (CF) is caused by inherited mutations in the cystic fibrosis transmembrane conductan...
The lungs of patients with cystic fibrosis (CF) are colonised by a microbial community comprised of ...
AbstractBackgroundIntravenous antibiotics for pulmonary exacerbations (PEs) of cystic fibrosis (CF) ...
The lungs of patients with cystic fibrosis (CF) are colonised by a microbial community comprised of ...
<div><p>Cystic fibrosis (CF) is characterized by defective mucociliary clearance and chronic airway ...
© 2016 International Society for Microbial Ecology All rights reserved. Pulmonary symptoms in cystic...
© 2016 International Society for Microbial Ecology All rights reserved. Pulmonary symptoms in cystic...
Pulmonary symptoms in cystic fibrosis (CF) begin in early life with chronic lung infections and conc...
© 2016 International Society for Microbial Ecology All rights reserved. Pulmonary symptoms in cystic...
© 2016 International Society for Microbial Ecology All rights reserved. Pulmonary symptoms in cystic...
Pulmonary symptoms in cystic fibrosis (CF) begin in early life with chronic lung infections and conc...
Cystic fibrosis (CF) is characterized by defective mucociliary clearance and chronic airway infectio...
Cystic fibrosis (CF) is characterized by defective mucociliary clearance and chronic airway infectio...
This study was supported by the UK Natural Environment Research Council (NE/H019456/1) to CJvdG, by ...
Cystic fibrosis (CF) is caused by inherited mutations in the cystic fibrosis transmembrane conductan...
Cystic fibrosis (CF) is caused by inherited mutations in the cystic fibrosis transmembrane conductan...
The lungs of patients with cystic fibrosis (CF) are colonised by a microbial community comprised of ...
AbstractBackgroundIntravenous antibiotics for pulmonary exacerbations (PEs) of cystic fibrosis (CF) ...
The lungs of patients with cystic fibrosis (CF) are colonised by a microbial community comprised of ...
<div><p>Cystic fibrosis (CF) is characterized by defective mucociliary clearance and chronic airway ...