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Other Guidelines

Real-life acute lung function changes after lumacaftor/ivacaftor first administration in pediatric patients with cystic fibrosis

  • Read more about Real-life acute lung function changes after lumacaftor/ivacaftor first administration in pediatric patients with cystic fibrosis

Lower exhaled nitric oxide in infants with Cystic Fibrosis compared to healthy controls

  • Read more about Lower exhaled nitric oxide in infants with Cystic Fibrosis compared to healthy controls

Outcomes associated with antibiotic regimens for treatment of Mycobacterium abscessus in cystic fibrosis patients.

  • Read more about Outcomes associated with antibiotic regimens for treatment of Mycobacterium abscessus in cystic fibrosis patients.

Pharmacokinetics and safety of cavosonstat (N91115) in healthy and cystic fibrosis adults homozygous for F508DEL-CFTR

  • Read more about Pharmacokinetics and safety of cavosonstat (N91115) in healthy and cystic fibrosis adults homozygous for F508DEL-CFTR

Effectiveness of a stepwise Pseudomonas aeruginosa eradication protocol in children with cystic fibrosis

  • Read more about Effectiveness of a stepwise Pseudomonas aeruginosa eradication protocol in children with cystic fibrosis

Macronutrient Intake in Preschoolers with Cystic Fibrosis and the Relationship between Macronutrients and Growth

  • Read more about Macronutrient Intake in Preschoolers with Cystic Fibrosis and the Relationship between Macronutrients and Growth

Use of FEV1 in Cystic Fibrosis Epidemiologic Studies and Clinical Trials: A Statistical Perspective for the Clinical Researcher

  • Read more about Use of FEV1 in Cystic Fibrosis Epidemiologic Studies and Clinical Trials: A Statistical Perspective for the Clinical Researcher

Worsening anxiety and depression after initiation of lumacaftor/ivacaftor combination therapy in adolescent females with cystic fibrosis

  • Read more about Worsening anxiety and depression after initiation of lumacaftor/ivacaftor combination therapy in adolescent females with cystic fibrosis

Development and Validation of CF-Medication Beliefs Questionnaire: A mixed-methods approach

  • Read more about Development and Validation of CF-Medication Beliefs Questionnaire: A mixed-methods approach

What Keeps Children with Cystic Fibrosis awake at night?

  • Read more about What Keeps Children with Cystic Fibrosis awake at night?
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