Reduced lung function in cystic fibrosis: a primary or secondary phenotype?

Am J Respir Crit Care Med. 2008 Jul 1;178(1):2-3. doi: 10.1164/rccm.200804-502ED.
No abstract available

Publication types

  • Comment
  • Editorial

MeSH terms

  • Child
  • Child, Preschool
  • Cystic Fibrosis / diagnosis
  • Cystic Fibrosis / microbiology
  • Cystic Fibrosis / physiopathology*
  • Forced Expiratory Volume
  • Humans
  • Infant
  • Maximal Midexpiratory Flow Rate
  • Pseudomonas Infections / complications
  • Respiratory Function Tests*