Should we monitor exhaled NO to assess the restoration of CFTR function in CF patients?

J Cyst Fibros. 2015 Nov;14(6):683-4. doi: 10.1016/S1569-1993(15)00247-7.
No abstract available

Publication types

  • Editorial
  • Comment

MeSH terms

  • Cystic Fibrosis Transmembrane Conductance Regulator / genetics*
  • Cystic Fibrosis*
  • Exhalation
  • Humans
  • Mutation

Substances

  • Cystic Fibrosis Transmembrane Conductance Regulator