Measurement of quality of well being in a child and adolescent cystic fibrosis population

Med Care. 1994 Sep;32(9):965-72. doi: 10.1097/00005650-199409000-00007.
No abstract available

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Activities of Daily Living
  • Adolescent
  • Age Factors
  • Child
  • Cystic Fibrosis / classification
  • Cystic Fibrosis / diagnosis
  • Cystic Fibrosis / physiopathology*
  • Cystic Fibrosis / psychology*
  • Evaluation Studies as Topic
  • Female
  • Forced Expiratory Flow Rates
  • Forced Expiratory Volume
  • Health Status Indicators*
  • Humans
  • Male
  • Quality of Life*
  • Regression Analysis
  • Reproducibility of Results
  • Severity of Illness Index
  • Surveys and Questionnaires / standards*
  • United States
  • Urban Population
  • Vital Capacity