159 related articles for article (PubMed ID: 15463884)
1. Validation of the Dutch cystic fibrosis questionnaire (CFQ) in adolescents and adults.
Klijn PH; van Stel HF; Quittner AL; van der Net J; Doeleman W; van der Schans CP; van der Ent CK
J Cyst Fibros; 2004 Mar; 3(1):29-36. PubMed ID: 15463884
[TBL] [Abstract][Full Text] [Related]
2. Development and validation of The Cystic Fibrosis Questionnaire in the United States: a health-related quality-of-life measure for cystic fibrosis.
Quittner AL; Buu A; Messer MA; Modi AC; Watrous M
Chest; 2005 Oct; 128(4):2347-54. PubMed ID: 16236893
[TBL] [Abstract][Full Text] [Related]
3. Longitudinal trends in health-related quality of life in adults with cystic fibrosis.
Dill EJ; Dawson R; Sellers DE; Robinson WM; Sawicki GS
Chest; 2013 Sep; 144(3):981-989. PubMed ID: 23670667
[TBL] [Abstract][Full Text] [Related]
4. Quality of life in cystic fibrosis: the impact of gender, general health perceptions and disease severity.
Gee L; Abbott J; Conway SP; Etherington C; Webb AK
J Cyst Fibros; 2003 Dec; 2(4):206-13. PubMed ID: 15463875
[TBL] [Abstract][Full Text] [Related]
5. Development of the Cystic Fibrosis Questionnaire (CFQ) for assessing quality of life in pediatric and adult patients.
Henry B; Aussage P; Grosskopf C; Goehrs JM
Qual Life Res; 2003 Feb; 12(1):63-76. PubMed ID: 12625519
[TBL] [Abstract][Full Text] [Related]
6. Psychometric evaluation of the Swedish translation of the revised Cystic Fibrosis Questionnaire in adults.
Hochwälder J; Bergsten Brucefors A; Hjelte L
Ups J Med Sci; 2017 Mar; 122(1):61-66. PubMed ID: 27628957
[TBL] [Abstract][Full Text] [Related]
7. Validation of the Danish version of the revised cystic fibrosis quality of life questionnaire in adolescents and adults (CFQ-R14+).
Bregnballe V; Thastum M; Lund LD; Hansen CR; Preissler T; Schiøtz PO
J Cyst Fibros; 2008 Nov; 7(6):531-6. PubMed ID: 18694658
[TBL] [Abstract][Full Text] [Related]
8. Reliability and validity of the Cystic Fibrosis Questionnaire-Revised for children and parents in Turkey: cross-sectional study.
Yuksel H; Yilmaz O; Dogru D; Karadag B; Unal F; Quittner AL
Qual Life Res; 2013 Mar; 22(2):409-14. PubMed ID: 22492294
[TBL] [Abstract][Full Text] [Related]
9. A systematic review of factors associated with health-related quality of life in adolescents and adults with cystic fibrosis.
Habib AR; Manji J; Wilcox PG; Javer AR; Buxton JA; Quon BS
Ann Am Thorac Soc; 2015 Mar; 12(3):420-8. PubMed ID: 25642976
[TBL] [Abstract][Full Text] [Related]
10. Development of a disease specific health related quality of life measure for adults and adolescents with cystic fibrosis.
Gee L; Abbott J; Conway SP; Etherington C; Webb AK
Thorax; 2000 Nov; 55(11):946-54. PubMed ID: 11050265
[TBL] [Abstract][Full Text] [Related]
11. Erratum to: Psychometric evaluation of the Cystic Fibrosis Questionnaire-Revised in a national, US sample.
Quittner AL; Sawicki GS; McMullen A; Rasouliyan L; Pasta DJ; Yegin A; Konstan MW
Qual Life Res; 2012 Sep; 21(7):1279-90. PubMed ID: 22240933
[TBL] [Abstract][Full Text] [Related]
12. Health-related quality-of-life in children with cystic fibrosis aged 5-years and associations with health outcomes.
Cheney J; Vidmar S; Gailer N; Wainwright C; Douglas TA;
J Cyst Fibros; 2020 May; 19(3):483-491. PubMed ID: 32165156
[TBL] [Abstract][Full Text] [Related]
13. Psychometric evaluation of the Cystic Fibrosis Questionnaire-Revised in a national sample.
Quittner AL; Sawicki GS; McMullen A; Rasouliyan L; Pasta DJ; Yegin A; Konstan MW
Qual Life Res; 2012 Sep; 21(7):1267-78. PubMed ID: 21993695
[TBL] [Abstract][Full Text] [Related]
14. Validation of a disease-specific measure of health-related quality of life for children with cystic fibrosis.
Modi AC; Quittner AL
J Pediatr Psychol; 2003 Dec; 28(8):535-45. PubMed ID: 14602844
[TBL] [Abstract][Full Text] [Related]
15. How about your peers? Cystic fibrosis questionnaire data from healthy children and adolescents.
Tibosch MM; Sintnicolaas CJ; Peters JB; Merkus PJ; Yntema JB; Verhaak CM; Vercoulen JH
BMC Pediatr; 2011 Oct; 11():86. PubMed ID: 21989260
[TBL] [Abstract][Full Text] [Related]
16. The revised German Cystic Fibrosis Questionnaire: validation of a disease-specific health-related quality of life instrument.
Wenninger K; Aussage P; Wahn U; Staab D;
Qual Life Res; 2003 Feb; 12(1):77-85. PubMed ID: 12625520
[TBL] [Abstract][Full Text] [Related]
17. Reliability and validity of the adapted Dutch version of the revised Scoliosis Research Society 22-item questionnaire.
Schlösser TP; Stadhouder A; Schimmel JJ; Lehr AM; van der Heijden GJ; Castelein RM
Spine J; 2014 Aug; 14(8):1663-72. PubMed ID: 24360746
[TBL] [Abstract][Full Text] [Related]
18. Determination of the minimal clinically important difference scores for the Cystic Fibrosis Questionnaire-Revised respiratory symptom scale in two populations of patients with cystic fibrosis and chronic Pseudomonas aeruginosa airway infection.
Quittner AL; Modi AC; Wainwright C; Otto K; Kirihara J; Montgomery AB
Chest; 2009 Jun; 135(6):1610-1618. PubMed ID: 19447923
[TBL] [Abstract][Full Text] [Related]
19. Development and electronic validation of the revised Cystic Fibrosis Questionnaire (CFQ-R Teen/Adult): New tool for monitoring psychosocial health in CF.
Solé A; Olveira C; Pérez I; Hervás D; Valentine V; Baca Yepez AN; Olveira G; Quittner AL
J Cyst Fibros; 2018 Sep; 17(5):672-679. PubMed ID: 29157922
[TBL] [Abstract][Full Text] [Related]
20. Associations between illness perceptions and health-related quality of life in adults with cystic fibrosis.
Sawicki GS; Sellers DE; Robinson WM
J Psychosom Res; 2011 Feb; 70(2):161-7. PubMed ID: 21262419
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]