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Other Guidelines

Mini-guts help test responses to CFTR modulators in people with cystic fibrosis carrying F508del

  • Read more about Mini-guts help test responses to CFTR modulators in people with cystic fibrosis carrying F508del

Is ETI safe for the liver? A two-year study from Denmark offers reassuring results.

  • Read more about Is ETI safe for the liver? A two-year study from Denmark offers reassuring results.

Early access to the CFTR modulator treatment helps severely ill infant with Cystic Fibrosis

  • Read more about Early access to the CFTR modulator treatment helps severely ill infant with Cystic Fibrosis

Summary of an interactive meeting about treating babies with CF with modulators before birth

  • Read more about Summary of an interactive meeting about treating babies with CF with modulators before birth

Tracking the spread of Mycobacterium abscessus in a CF center: What bacterial genetics and patient data reveal and why it matters

  • Read more about Tracking the spread of Mycobacterium abscessus in a CF center: What bacterial genetics and patient data reveal and why it matters

CFAbd-Score.kid: a new, child-friendly version of the CFAbd-Score for tracking abdominal symptoms in children with cystic fibrosis

  • Read more about CFAbd-Score.kid: a new, child-friendly version of the CFAbd-Score for tracking abdominal symptoms in children with cystic fibrosis

How doctors decide to prescribe CFTR modulator therapies to their patients

  • Read more about How doctors decide to prescribe CFTR modulator therapies to their patients

Can we shorten test time for Lung Clearance Index (a lung function test used in CF)?

  • Read more about Can we shorten test time for Lung Clearance Index (a lung function test used in CF)?

Understanding Symptom Patterns in Adults with Cystic Fibrosis

  • Read more about Understanding Symptom Patterns in Adults with Cystic Fibrosis

The challenges of conducting large clinical studies in cystic fibrosis

  • Read more about The challenges of conducting large clinical studies in cystic fibrosis
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