PDF) Linguistic validation of cystic fibrosis quality of life questionnaires

The purpose of this study was to validate the Portuguese translations of four cystic fibrosis quality of life questionnaires (CFQ). The first three were developed for patients with cystic fibrosis aged from 6 to 11 years, from 12 to 13 years and 14

PDF] Quality of life assessment in patients with cystic fibrosis by means of the Cystic Fibrosis Questionnaire.

Development and electronic validation of the revised Cystic Fibrosis Questionnaire (CFQ-R Teen/Adult): New tool for monitoring psychosocial health in CF - ScienceDirect

PDF) Validation of the Dutch cystic fibrosis questionnaire (CFQ) in adolescents and adults

PDF) Common content between quality of life questionnaires for children with cystic fibrosis and the International Classification of Functionality, Disability and Health

Quality of Life: The Concept - David F. Cella, 1992

The World Health Organization Quality of Life instrument for people with intellectual and physical disabilities (WHOQOL-Dis): evidence of validity of the Brazilian version – topic of research paper in Psychology. Download scholarly

PDF) Development and validation of The Cystic Fibrosis Questionnaire in the United States: a health-related quality-of-life measure for cystic fibrosis

Parental Uncertainty About a Child's Health Scale (PUCHS): Development and Validation of a Novel Measure

(PDF) Linguistic validation of cystic fibrosis quality of life questionnaires

Jornal Brasileiro de Pneumologia - Quality of life assessment in patients with cystic fibrosis by means of the Cystic Fibrosis Questionnaire

Development and validation of a novel personalized electronic patient-reported outcome measure to assess quality of life (Q-LIFE): a prospective observational study in people with Cystic Fibrosis - eClinicalMedicine

Children, Free Full-Text

Quality of Life in Cystic Fibrosis - Janice Abbott, Kevin Webb, Mary Dodd, 1997

Cystic Fibrosis Disease Knowledge Questionnaire

Collaborative research protocol to define patient-reported experience measures of the cystic fibrosis care pathway in France: the ExPaParM study, Orphanet Journal of Rare Diseases