Skip to main content
Home

Search form

  • ABOUT US
    • ECFS Society Details
      • Society Information
      • Applications for Support
    • ECFS Membership
      • Membership Subscription
      • Membership Demographics
    • Other Information
      • Latest News
      • Job Opportunities
      • Grants and Programmes
      • Links
  • RESEARCH
    • ECFS Projects
      • ECFS Clinical Trials Network
      • ECFS Patient Registry
    • ECFS Working Groups
      • Diagnostic Network
      • Exercise
      • Neonatal Screening
      • Fungal Pathogens
      • Pulmonary Exacerbation
    • Special Projects
      • ECFS / CF Europe Post-Doctoral Research Fellowship
      • CFQ-R questionnaire and CF candidates for lung transplant
      • EU funded projects
      • MucoFong International Project
      • Complete CFTR gene mutation analysis in European patients with Cystic Fibrosis
    • Past Working Groups
      • Cystic Fibrosis Molecular and Cell Biology and Physiology Basic Science
      • ECFS Gene Modifier Working Group
      • ECFS Non Tuberculous Mycobacteria Working Group
  • CARE
    • ECFS Standards Of Care
    • ECFS Working Groups
      • Exercise
      • Diagnostic Network
      • Neonatal Screening
      • Mental Health
      • Fungal Pathogens
      • Pulmonary Exacerbation
      • Telehealth
    • Allied Health Professionals
      • ECFS Nursing Special interest Group
      • European CF Pharmacy Group
      • European Cystic Fibrosis Nutrition Group
      • European Psychosocial Special Interest Group
      • ECFS Physiotherapy Special Interest International Group
  • EDUCATION
  • CONFERENCES & EVENTS
    • European Cystic Fibrosis Conference
    • ECFS Basic Science Conference
    • Related events
    • Past ECFS conferences
  • PUBLICATIONS
    • About Publications
      • The Journal of Cystic Fibrosis
      • ECFS Newsletter
      • ECFS Book
      • ERS Monograph
    • Resources
      • Search All Resources
      • CF Research News
      • Consensus Reports
      • ECFS Guidelines
      • Free Access Articles
      • CF Literature
  • MEMBERSHIP
  • LOG IN

Other Guidelines

Improvements in lung function and height among cohorts of 6-year-olds with cystic fibrosis from 1994 to 2012

  • Read more about Improvements in lung function and height among cohorts of 6-year-olds with cystic fibrosis from 1994 to 2012

Nasal Potential Difference in suspected Cystic Fibrosis patients with 5T: A step towards better characterization of a CFTR variant with varying clinical consequences

  • Read more about Nasal Potential Difference in suspected Cystic Fibrosis patients with 5T: A step towards better characterization of a CFTR variant with varying clinical consequences

Multicenter Observational Study on Factors and Outcomes Associated with Various Methicillin-Resistant Staphylococcus aureus Types in Children with Cystic Fibrosis

  • Read more about Multicenter Observational Study on Factors and Outcomes Associated with Various Methicillin-Resistant Staphylococcus aureus Types in Children with Cystic Fibrosis

Clinical trial participants compared with nonparticipants in cystic fibrosis

  • Read more about Clinical trial participants compared with nonparticipants in cystic fibrosis

Use is Associated with Higher Hemoglobin Levels in Individuals with Cystic Fibrosis

  • Read more about Use is Associated with Higher Hemoglobin Levels in Individuals with Cystic Fibrosis

Chronic Azithromycin Use in Cystic Fibrosis and Concern for Treatment-Emergent Pathogens

  • Read more about Chronic Azithromycin Use in Cystic Fibrosis and Concern for Treatment-Emergent Pathogens

Air pollution exposure is associated with MRSA acquisition in young U.S. children with cystic fibrosis

  • Read more about Air pollution exposure is associated with MRSA acquisition in young U.S. children with cystic fibrosis

Seasonality of acquisition of respiratory bacterial pathogens in young children with cystic fibrosis.

  • Read more about Seasonality of acquisition of respiratory bacterial pathogens in young children with cystic fibrosis.

A critical review of definitions used to describe Pseudomonas aeruginosa microbiological status in patients with Cystic Fibrosis for application in clinical trials

  • Read more about A critical review of definitions used to describe Pseudomonas aeruginosa microbiological status in patients with Cystic Fibrosis for application in clinical trials

Incretin dysfunction and hyperglycemia in cystic fibrosis: role of acyl-ghrelin

  • Read more about Incretin dysfunction and hyperglycemia in cystic fibrosis: role of acyl-ghrelin
  • first
  • previous
  • …
  • 60
  • 61
  • 62
  • 63
  • 64
  • 65
  • 66
  • 67
  • 68
  • …
  • next
  • last
Terms & Conditions Privacy policy  Accessibility Sitemap Contact 
© EUROPEAN CYSTIC FIBROSIS SOCIETY 2025. All rights reserved. Website by VidaVia (link is external)
European Cystic Fibrosis Society (ECFS)