These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
202 related articles for article (PubMed ID: 23881472)
1. Psychosocial burden of sickle cell disease on parents with an affected child in Cameroon. Wonkam A; Mba CZ; Mbanya D; Ngogang J; Ramesar R; Angwafo FF J Genet Couns; 2014 Apr; 23(2):192-201. PubMed ID: 23881472 [TBL] [Abstract][Full Text] [Related]
2. Psychosocial stressors of sickle cell disease on adult patients in Cameroon. Wonkam A; Mba CZ; Mbanya D; Ngogang J; Ramesar R; Angwafo FF J Genet Couns; 2014 Dec; 23(6):948-56. PubMed ID: 24557660 [TBL] [Abstract][Full Text] [Related]
3. Would you terminate a pregnancy affected by sickle cell disease? Analysis of views of patients in Cameroon. Wonkam A; de Vries J; Royal CD; Ramesar R; Angwafo FF J Med Ethics; 2014 Sep; 40(9):615-20. PubMed ID: 23918815 [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. 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]
6. A call for policy action in sub-Saharan Africa to rethink diagnostics for pregnancy affected by sickle cell disease: differential views of medical doctors, parents and adult patients predict value conflicts in Cameroon. Wonkam A; Hurst S OMICS; 2014 Jul; 18(7):472-80. PubMed ID: 24754796 [TBL] [Abstract][Full Text] [Related]
7. Coping and coping assistance among children with sickle cell disease and their parents. Hildenbrand AK; Barakat LP; Alderfer MA; Marsac ML J Pediatr Hematol Oncol; 2015 Jan; 37(1):25-34. PubMed ID: 24327131 [TBL] [Abstract][Full Text] [Related]
8. Acceptability of prenatal diagnosis by a sample of parents of sickle cell anemia patients in Cameroon (sub-Saharan Africa). Wonkam A; Njamnshi AK; Mbanya D; Ngogang J; Zameyo C; Angwafo FF J Genet Couns; 2011 Oct; 20(5):476-85. PubMed ID: 21604069 [TBL] [Abstract][Full Text] [Related]
9. Adherence to hydroxyurea, health-related quality of life domains, and patients' perceptions of sickle cell disease and hydroxyurea: a cross-sectional study in adolescents and young adults. Badawy SM; Thompson AA; Lai JS; Penedo FJ; Rychlik K; Liem RI Health Qual Life Outcomes; 2017 Jul; 15(1):136. PubMed ID: 28679417 [TBL] [Abstract][Full Text] [Related]
10. The impact of the oral condition of children with sickle cell disease on family quality of life. Fernandes ML; Kawachi I; Corrêa-Faria P; Paiva SM; Pordeus IA Braz Oral Res; 2016; 30():. PubMed ID: 26910017 [TBL] [Abstract][Full Text] [Related]
11. Impact of sickle cell disease on patients' daily lives, symptoms reported, and disease management strategies: Results from the international Sickle Cell World Assessment Survey (SWAY). Osunkwo I; Andemariam B; Minniti CP; Inusa BPD; El Rassi F; Francis-Gibson B; Nero A; Trimnell C; Abboud MR; Arlet JB; Colombatti R; de Montalembert M; Jain S; Jastaniah W; Nur E; Pita M; DeBonnett L; Ramscar N; Bailey T; Rajkovic-Hooley O; James J Am J Hematol; 2021 Apr; 96(4):404-417. PubMed ID: 33264445 [TBL] [Abstract][Full Text] [Related]
12. Paternal Stress and Child Outcomes in Youth with Sickle Cell Disease. Moody KL J Pediatr Psychol; 2021 Sep; 46(9):1140-1147. PubMed ID: 34051095 [TBL] [Abstract][Full Text] [Related]
13. Socio-demographic characteristics and psychosocial consequences of sickle cell disease: the case of patients in a public hospital in Ghana. Adzika VA; Glozah FN; Ayim-Aboagye D; Ahorlu CS J Health Popul Nutr; 2017 Jan; 36(1):4. PubMed ID: 28143586 [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. Psychosocial and mental profile of children with sickle cell disease and their caregivers. Ebeid FSE; Mokhtar GM; Zaky EA; Abdelmageed RI; Elkamel NM; Ali HGA Pediatr Hematol Oncol; 2024; 41(1):15-29. PubMed ID: 37773584 [TBL] [Abstract][Full Text] [Related]
16. The mediating effects of family functioning on psychosocial outcomes in healthy siblings of children with sickle cell disease. Gold JI; Treadwell M; Weissman L; Vichinsky E Pediatr Blood Cancer; 2011 Dec; 57(6):1055-61. PubMed ID: 21360652 [TBL] [Abstract][Full Text] [Related]
17. Psychosocial impact of sickle cell disease on mothers of affected children seen at University of Ilorin Teaching Hospital, Ilorin, Nigeria. Tunde-Ayinmode MF East Afr Med J; 2007 Sep; 84(9):410-9. PubMed ID: 18074959 [TBL] [Abstract][Full Text] [Related]
18. Quality of Life of Latino and Non-Latino Youth With Sickle Cell Disease as Reported by Parents and Youth. Osborne JC; Green NS; Smaldone AM Hisp Health Care Int; 2020 Dec; 18(4):224-231. PubMed ID: 32124643 [TBL] [Abstract][Full Text] [Related]
19. Parental attitudes toward research participation in pediatric sickle cell disease. Liem RI; Cole AH; Pelligra SA; Mason M; Thompson AA Pediatr Blood Cancer; 2010 Jul; 55(1):129-33. PubMed ID: 20213846 [TBL] [Abstract][Full Text] [Related]
20. Predictors of health-related quality of life in a large cohort of adult patients living with sickle cell disease in France: the DREPAtient study. Yaya I; Pourageaud A; Derbez B; Odièvre MH; Oudin Doglioni D; Podevin M; Thomas G; Yombo-Kokule L; Godart C; Lepetit M; Cassubie-Mercier T; Galacteros F; Chassany O; Front Public Health; 2024; 12():1374805. PubMed ID: 38832226 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]