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Pulmonary exacerbations

Blood Biomarkers to Predict Short-term Pulmonary Exacerbation Risk in Children and Adolescents with CF: A Pilot Study

  • Read more about Blood Biomarkers to Predict Short-term Pulmonary Exacerbation Risk in Children and Adolescents with CF: A Pilot Study

The use of antimicrobial susceptibility testing in pediatric cystic fibrosis pulmonary exacerbations

  • Read more about The use of antimicrobial susceptibility testing in pediatric cystic fibrosis pulmonary exacerbations

Lumacaftor/Ivacaftor reduces pulmonary exacerbations in patients irrespective of initial changes in FEV1.

  • Read more about Lumacaftor/Ivacaftor reduces pulmonary exacerbations in patients irrespective of initial changes in FEV1.

Correspondence between symptoms and preference-based health status measures in the STOP study.

  • Read more about Correspondence between symptoms and preference-based health status measures in the STOP study.

Pulmonary exacerbations and acute declines in lung function in patients with cystic fibrosis

  • Read more about Pulmonary exacerbations and acute declines in lung function in patients with cystic fibrosis

Recovery of lung function following a pulmonary exacerbation in patients with cystic fibrosis and the G551D-CFTR mutation treated with ivacaftor.

  • Read more about Recovery of lung function following a pulmonary exacerbation in patients with cystic fibrosis and the G551D-CFTR mutation treated with ivacaftor.

Standardized Treatment of Pulmonary exacerbations (STOP) study: Physician treatment practices and outcomes for individuals with cystic fibrosis with pulmonary exacerbations.

  • Read more about Standardized Treatment of Pulmonary exacerbations (STOP) study: Physician treatment practices and outcomes for individuals with cystic fibrosis with pulmonary exacerbations.

Association between glucose intolerance and bacterial colonisation in an adult population with cystic fibrosis, emergence of Stenotrophomonas maltophilia.

  • Read more about Association between glucose intolerance and bacterial colonisation in an adult population with cystic fibrosis, emergence of Stenotrophomonas maltophilia.
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