192 related articles for article (PubMed ID: 35390069)
1. 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]
2. 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]
3. Burden experienced by informal caregivers of children with sickle cell disease (SCD): a qualitative exploratory study at Tamale Teaching Hospital, Ghana.
Mumuni ND; Osman W; Alhassan BA; Alhassan A
BMJ Open; 2023 Apr; 13(4):e066311. PubMed ID: 37024250
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. Understanding caregiver burden with accessing sickle cell care in the Midwest and their perspective on telemedicine.
Jacob SA; Bouck J; Daas R; Jackson MD; LaMotte JE; Carroll AE
BMC Health Serv Res; 2023 May; 23(1):500. PubMed ID: 37198614
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. Psychosocial burden of sickle cell disease on caregivers in a Nigerian setting.
Ohaeri JU; Shokunbi WA
J Natl Med Assoc; 2002 Dec; 94(12):1058-70. PubMed ID: 12510705
[TBL] [Abstract][Full Text] [Related]
8. Knowledge and nutrition-related practices among caregivers of adolescents with sickle cell disease in the Greater Accra region of Ghana.
Ohemeng A; Nartey EB; Quaidoo E; Ansong RS; Asiedu MS
BMC Public Health; 2023 Mar; 23(1):434. PubMed ID: 36879231
[TBL] [Abstract][Full Text] [Related]
9. Caregiver experiences with accessing sickle cell care and the use of telemedicine.
Jacob SA; Daas R; Feliciano A; LaMotte JE; Carroll AE
BMC Health Serv Res; 2022 Feb; 22(1):239. PubMed ID: 35193570
[TBL] [Abstract][Full Text] [Related]
10. Sickle Cell Disease in Children: Knowledge and Home-Based Management Strategies among Caregivers at a Tertiary Facility in Northern Ghana.
Ajinkpang S; Anim-Boamah O; Bimpong KA; Kanton FJ; Pwavra JBP; Abdul-Mumin A
Biomed Res Int; 2022; 2022():3384813. PubMed ID: 35845932
[TBL] [Abstract][Full Text] [Related]
11. Effects of Experienced Discrimination in Pediatric Sickle Cell Disease: Caregiver and Provider Perspectives.
Blakey AO; Lavarin C; Brochier A; Amaro CM; Eilenberg JS; Kavanagh PL; Garg A; Drainoni ML; Long KA
J Racial Ethn Health Disparities; 2023 Dec; 10(6):3095-3106. PubMed ID: 36536165
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. Disease-modifying therapies for sickle cell disease: Decisional needs and supports among adolescents and young adults.
Ding K; Bear B; Sood E; Alderfer M; Crosby L; Hildenbrand AK
Pediatr Blood Cancer; 2024 Jul; 71(7):e30999. PubMed ID: 38622789
[TBL] [Abstract][Full Text] [Related]
14. Sickle cell disease in Grenada: Quality of life and barriers to care.
Grygiel A; Ikolo F; Stephen R; Bleasdille D; Robbins-Furman P; Nelson B; Sobering AK; Elsea SH
Mol Genet Genomic Med; 2021 Jan; 9(1):e1567. PubMed ID: 33332776
[TBL] [Abstract][Full Text] [Related]
15. Health literacy in adolescents with sickle cell disease: The influence of caregiver health literacy.
Caldwell EP
J Spec Pediatr Nurs; 2020 Apr; 25(2):e12284. PubMed ID: 31825171
[TBL] [Abstract][Full Text] [Related]
16. Challenges in Shifting Management Responsibility From Parents to Adolescents With Sickle Cell Disease.
Kayle M; Tanabe P; Shah NR; Baker-Ward L; Docherty SL
J Pediatr Nurs; 2016; 31(6):678-690. PubMed ID: 27451007
[TBL] [Abstract][Full Text] [Related]
17. Caregiving time in sickle cell disease: psychological effects in maternal caregivers.
Moskowitz JT; Butensky E; Harmatz P; Vichinsky E; Heyman MB; Acree M; Wrubel J; Wilson L; Folkman S
Pediatr Blood Cancer; 2007 Jan; 48(1):64-71. PubMed ID: 16622841
[TBL] [Abstract][Full Text] [Related]
18. Sickle-Cell Disease and Stroke: Quality of Life of Patients in a Chronic Transfusion Regimen from the Caregivers' Perspective.
Cerqueira MAF; Couto LMFMCB; Parente MPPD; Llerena JC
Pediatr Hematol Oncol; 2023; 40(7):607-616. PubMed ID: 36420998
[TBL] [Abstract][Full Text] [Related]
19. Experiences of Caring for Adolescents Living with HIV (ALHIV): A Qualitative Interview with Caregivers.
Kasande M; Natwijuka A; Katushabe Snr E; Tweheyo Otwine Snr A
HIV AIDS (Auckl); 2022; 14():577-589. PubMed ID: 36575691
[TBL] [Abstract][Full Text] [Related]
20. The experience of stroke survivors and caregivers during hospital-to-home transitional care: A qualitative longitudinal study.
Lin S; Wang C; Wang Q; Xie S; Tu Q; Zhang H; Peng M; Zhou J; Redfern J
Int J Nurs Stud; 2022 Jun; 130():104213. PubMed ID: 35378465
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]