250 related articles for article (PubMed ID: 28877143)
1. Stigma and Pain in Adolescents Hospitalized for Sickle Cell Vasoocclusive Pain Episodes.
Martin SR; Cohen LL; Mougianis I; Griffin A; Sil S; Dampier C
Clin J Pain; 2018 May; 34(5):438-444. PubMed ID: 28877143
[TBL] [Abstract][Full Text] [Related]
2. Health related quality of life and perception of stigmatisation in adolescents living with sickle cell disease in Nigeria: A cross sectional study.
Adeyemo TA; Ojewunmi OO; Diaku-Akinwumi IN; Ayinde OC; Akanmu AS
Pediatr Blood Cancer; 2015 Jul; 62(7):1245-51. PubMed ID: 25810358
[TBL] [Abstract][Full Text] [Related]
3. Perceived Racial Bias and Health-Related Stigma Among Youth with Sickle Cell Disease.
Wakefield EO; Popp JM; Dale LP; Santanelli JP; Pantaleao A; Zempsky WT
J Dev Behav Pediatr; 2017; 38(2):129-134. PubMed ID: 28059954
[TBL] [Abstract][Full Text] [Related]
4. Caregiver Perspectives of Stigma Associated With Sickle Cell Disease in Adolescents.
Wesley KM; Zhao M; Carroll Y; Porter JS
J Pediatr Nurs; 2016; 31(1):55-63. PubMed ID: 26534838
[TBL] [Abstract][Full Text] [Related]
5. Widespread Pain Among Youth With Sickle Cell Disease Hospitalized With Vasoocclusive Pain: A Different Clinical Phenotype?
Zempsky WT; Wakefield EO; Santanelli JP; New T; Smith-Whitley K; Casella JF; Palermo TM
Clin J Pain; 2017 Apr; 33(4):335-339. PubMed ID: 27322398
[TBL] [Abstract][Full Text] [Related]
6. Gender differences in pain and healthcare utilization for adult sickle cell patients: The PiSCES Project.
McClish DK; Levenson JL; Penberthy LT; Roseff SD; Bovbjerg VE; Roberts JD; Aisiku IP; Smith WR
J Womens Health (Larchmt); 2006 Mar; 15(2):146-54. PubMed ID: 16536678
[TBL] [Abstract][Full Text] [Related]
7. Stigma of Sickle Cell Disease: A Systematic Review.
Bulgin D; Tanabe P; Jenerette C
Issues Ment Health Nurs; 2018 Aug; 39(8):675-686. PubMed ID: 29652215
[TBL] [Abstract][Full Text] [Related]
8. Descriptive analysis of sickle cell patients living in France: The PHEDRE cross-sectional study.
Gerardin M; Rousselet M; Couec ML; Masseau A; Guerlais M; Authier N; Deheul S; Roussin A; Micallef J; Djezzar S; ; Feuillet F; Jolliet P; Victorri-Vigneau C
PLoS One; 2021; 16(3):e0248649. PubMed ID: 33735176
[TBL] [Abstract][Full Text] [Related]
9. Sickle cell disease pain management in adolescents: a literature review.
Wilson BH; Nelson J
Pain Manag Nurs; 2015 Apr; 16(2):146-51. PubMed ID: 25175555
[TBL] [Abstract][Full Text] [Related]
10. Neuropathic pain is associated with poor health-related quality of life in adolescents with sickle cell disease: A preliminary report.
Román ME; Highland J; Retherford D; Pan AY; Panepinto JA; Brandow AM
Pediatr Blood Cancer; 2020 Dec; 67(12):e28698. PubMed ID: 33034107
[TBL] [Abstract][Full Text] [Related]
11. A review of the literature on the multiple dimensions of chronic pain in adults with sickle cell disease.
Taylor LE; Stotts NA; Humphreys J; Treadwell MJ; Miaskowski C
J Pain Symptom Manage; 2010 Sep; 40(3):416-35. PubMed ID: 20656451
[TBL] [Abstract][Full Text] [Related]
12. Mental health disorders influence admission rates for pain in children with sickle cell disease.
Myrvik MP; Burks LM; Hoffman RG; Dasgupta M; Panepinto JA
Pediatr Blood Cancer; 2013 Jul; 60(7):1211-4. PubMed ID: 23151972
[TBL] [Abstract][Full Text] [Related]
13. Psychosocial and pharmacological management of pain in pediatric sickle cell disease.
Hildenbrand AK; Nicholls EG; Daly BP; Marsac ML; Tarazi R; Deepti R
Postgrad Med; 2014 Mar; 126(2):123-33. PubMed ID: 24685976
[TBL] [Abstract][Full Text] [Related]
14. Executive Functioning Mediates the Relationship Between Pain Coping and Quality of Life in Youth With Sickle Cell Disease.
Ludwig NN; Sil S; Khowaja MK; Cohen LL; Dampier C
J Pediatr Psychol; 2018 Nov; 43(10):1160-1169. PubMed ID: 30053072
[TBL] [Abstract][Full Text] [Related]
15. Psychometrics of the Sickle Cell Disease Health-Related Stigma Scale-Short Form.
Jenerette C; O'Brien J; Jaja C; Carvalho ESS; Brewer C; Hickman RL
West J Nurs Res; 2023 May; 45(5):425-431. PubMed ID: 36495228
[TBL] [Abstract][Full Text] [Related]
16. How patients' self-disclosure about sickle cell pain episodes to significant others relates to living with sickle cell disease.
Derlega VJ; Janda LH; Miranda J; Chen IA; Goodman BM; Smith W
Pain Med; 2014 Sep; 15(9):1496-507. PubMed ID: 25159869
[TBL] [Abstract][Full Text] [Related]
17. Health related quality of life among adolescents with sickle cell disease in Saudi Arabia.
Amr MA; Amin TT; Al-Omair OA
Pan Afr Med J; 2011; 8():10. PubMed ID: 22121419
[TBL] [Abstract][Full Text] [Related]
18. Preliminary validity and reliability of the Sickle Cell Disease Health-Related Stigma Scale.
Jenerette C; Brewer CA; Crandell J; Ataga KI
Issues Ment Health Nurs; 2012 Jun; 33(6):363-9. PubMed ID: 22646200
[TBL] [Abstract][Full Text] [Related]
19. Caught between pity, explicit bias, and discrimination: a qualitative study on the impact of stigma on the quality of life of persons living with sickle cell disease in three African countries.
Munung NS; Treadwell M; Kamga KK; Dennis-Antwi J; Anie K; Bukini D; Makani J; Wonkam A
Qual Life Res; 2024 Feb; 33(2):423-432. PubMed ID: 37889387
[TBL] [Abstract][Full Text] [Related]
20. Quality of life among caregivers of sickle cell disease patients: a cross sectional study.
Madani BM; Al Raddadi R; Al Jaouni S; Omer M; Al Awa MI
Health Qual Life Outcomes; 2018 Sep; 16(1):176. PubMed ID: 30200992
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]