132 related articles for article (PubMed ID: 36463013)
1. Psycho-social challenges faced by caretakers of children and adolescents aged 0-19 years with sickle cell disease admitted in a tertiary hospital in Eastern Uganda.
Atoku AC; Nekaka R; Kagoya EK; Ssenyonga LVN; Iramiot JS; Tegu C
J Pediatr Nurs; 2023; 69():e21-e31. PubMed ID: 36463013
[TBL] [Abstract][Full Text] [Related]
2. Existence, triggers, and coping with chronic sorrow: a qualitative study of caretakers of children with sickle cell disease in a National Referral Hospital in Kampala, Uganda.
Olwit C; Mugaba M; Osingada CP; Nabirye RC
BMC Psychol; 2018 Oct; 6(1):50. PubMed ID: 30342559
[TBL] [Abstract][Full Text] [Related]
3. Caregivers' experience of seeking care for adolescents with sickle cell disease in a tertiary care hospital in Bahrain.
Al Saif K; Abdulla FM; Alrahim A; Abduljawad S; Matrook Z; Abdulla JJ; Bughamar F; Alasfoor F; Taqi R; Almarzooq A; Ahmed J
PLoS One; 2022; 17(4):e0266501. PubMed ID: 35390069
[TBL] [Abstract][Full Text] [Related]
4. Knowledge and attitude towards sickle cell anemia among care givers of paediatric sickle cell patients at a tertiary hospital in Eastern Uganda: a cross sectional study.
Namugerwa CH; Gavamukulya Y; Barugahare BJ
BMC Res Notes; 2023 Nov; 16(1):351. PubMed ID: 38012683
[TBL] [Abstract][Full Text] [Related]
5. Use of herbal medicine by caregivers in the management of children with sickle cell disease in Mulago National Referral Hospital - Uganda.
Lubega M; Osingada CP; Kasirye P
Pan Afr Med J; 2021; 39():163. PubMed ID: 34548892
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. Communication with children about sickle cell disease: A qualitative study of parent experience.
Middleton J; Calam R; Ulph F
Br J Health Psychol; 2018 Sep; 23(3):685-700. PubMed ID: 29885041
[TBL] [Abstract][Full Text] [Related]
8. Transfer as a component of the transition of adolescents with sickle cell disease to adult care: adolescent, adult, and parent perspectives.
Telfair J; Myers J; Drezner S
J Adolesc Health; 1994 Nov; 15(7):558-65. PubMed ID: 7857954
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. Knowledge, attitudes and beliefs of primary caretakers towards sickle cell anaemia in children.
Macharia WM; Shiroya A; Njeru EK
East Afr Med J; 1997 Jul; 74(7):416-9. PubMed ID: 9491171
[TBL] [Abstract][Full Text] [Related]
11. Health-related quality of life of adolescents with sickle cell disease in sub-Saharan Africa: a cross-sectional study.
Kambasu DM; Rujumba J; Lekuya HM; Munube D; Mupere E
BMC Hematol; 2019; 19():9. PubMed ID: 31114692
[TBL] [Abstract][Full Text] [Related]
12. Disease management, coping, and functional disability in pediatric sickle cell disease.
Oliver-Carpenter G; Barach I; Crosby LE; Valenzuela J; Mitchell MJ
J Natl Med Assoc; 2011 Feb; 103(2):131-7. PubMed ID: 21443065
[TBL] [Abstract][Full Text] [Related]
13. Psycho-social problems of adolescents with sickle-cell anaemia in Ekiti State, Nigeria.
Adegboyega LO
Afr Health Sci; 2021 Jun; 21(2):775-781. PubMed ID: 34795735
[TBL] [Abstract][Full Text] [Related]
14. Growing beyond sickle cell disease: A metasynthesis of children, adolescents, and young adult experiences living with sickle cell disease.
Coco M; Henderson WA; Park CL; Starkweather AR
Res Nurs Health; 2023 Jun; 46(3):299-312. PubMed ID: 37036038
[TBL] [Abstract][Full Text] [Related]
15. Caring for children with neurodevelopmental disability: Experiences from caretakers and health workers in rural eastern Uganda.
Namazzi G; Hanson C; Nalwadda C; Tetui M; Nampijja M; Waiswa P; Tumwine JK; Hildenwall H
PLoS One; 2020; 15(7):e0236488. PubMed ID: 32716925
[TBL] [Abstract][Full Text] [Related]
16. The Daily Experiences of Adolescents in Lebanon With Sickle Cell Disease.
Atoui M; Badr LK; Brand TD; Khoury R; Shahine R; Abboud M
J Pediatr Health Care; 2015; 29(5):424-34. PubMed ID: 25771820
[TBL] [Abstract][Full Text] [Related]
17. The stability of pain coping strategies in young children adolescents, and adults with sickle cell disease over an 18-month period.
Gil KM; Wilson JJ; Edens JL
Clin J Pain; 1997 Jun; 13(2):110-5. PubMed ID: 9186018
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. Family influences on coping processes in children and adolescents with sickle cell disease.
Kliewer W; Lewis H
J Pediatr Psychol; 1995 Aug; 20(4):511-25. PubMed ID: 7666291
[TBL] [Abstract][Full Text] [Related]
20. Broadening the scope of social support, coping skills and resilience among caretakers of children with disabilities in Uganda: a sequential explanatory mixed-methods study.
Namasaba M; Kazembe N; Seera G; Baguwemu AA
BMC Public Health; 2022 Apr; 22(1):690. PubMed ID: 35395786
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
