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

Frontiers Review: Quality of Life in Children with Non-cystic Fibrosis Bronchiectasis

PDF) The development and validation of the Bronchiectasis Health Questionnaire

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

PDF) 387 Validation of the Spanish version of the Leicester Cough Questionnaire in children with cystic fibrosis

PDF) Translation And Linguistic Validation Of A Disease Specific Quality Of Life Measure For Cystic Fibrosis

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

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

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

Full article: Development and preliminary validation of the challenges of living with cystic fibrosis (CLCF) questionnaire: a 46-item measure of treatment burden for parent/carers of children with CF

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

Full article: A Partial Picture, Without a Frame: Measuring Quality of Life in Cystic Fibrosis Caregivers

PDF) Cystic Fibrosis Questionnaire Reference Data in a healthy, Dutch population 6–20 yrs

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

PDF) Health related quality of life in adult Primary Ciliary Dyskinesia patients in Cyprus: development and validation of the Greek version of the QOL-PCD questionnaire

Quality of life and healthcare utilisation in cystic fibrosis: a multicentre study