Rapid cystic fibrosis lung-function decline and in-vitro CFTR modulation

J Cyst Fibros. 2021 Sep;20(5):e69-e71. doi: 10.1016/j.jcf.2021.04.001. Epub 2021 May 3.
No abstract available

Publication types

  • Letter
  • Research Support, N.I.H., Extramural

MeSH terms

  • Adolescent
  • Biomarkers / analysis
  • Child
  • Chloride Channel Agonists / therapeutic use*
  • Cystic Fibrosis / drug therapy*
  • Cystic Fibrosis / genetics
  • Cystic Fibrosis / physiopathology*
  • Cystic Fibrosis Transmembrane Conductance Regulator / genetics
  • Disease Progression
  • Female
  • Humans
  • Male
  • Pilot Projects
  • Principal Component Analysis
  • Respiratory Function Tests
  • Young Adult

Substances

  • Biomarkers
  • Chloride Channel Agonists
  • Cystic Fibrosis Transmembrane Conductance Regulator