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Journal Abstract Search

124 related items for PubMed ID: 23459927

  • 1.
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  • 2. Quality of life in patients with sickle cell disease in Jamaica: rural-urban differences.
    Asnani MR, Reid ME, Ali SB, Lipps G, Williams-Green P.
    Rural Remote Health; 2008; 8(2):890. PubMed ID: 18410222
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  • 4. The lived experiences of adolescents with sickle cell disease in Kingston, Jamaica.
    Forrester AB, Barton-Gooden A, Pitter C, Lindo JL.
    Int J Qual Stud Health Well-being; 2015; 10():28104. PubMed ID: 26341889
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  • 5. How sickle cell disease patients experience, understand and explain their pain: An Interpretative Phenomenological Analysis study.
    Coleman B, Ellis-Caird H, McGowan J, Benjamin MJ.
    Br J Health Psychol; 2016 Feb; 21(1):190-203. PubMed ID: 26333530
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  • 6. Sickle cell disease patients with and without extremely high hospital use: pain, opioids, and coping.
    Brown SE, Weisberg DF, Balf-Soran G, Sledge WH.
    J Pain Symptom Manage; 2015 Mar; 49(3):539-47. PubMed ID: 25057985
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  • 7. The lives of adults over 30 living with sickle cell disorder.
    Caird H, Camic PM, Thomas V.
    Br J Health Psychol; 2011 Sep; 16(3):542-58. PubMed ID: 21722275
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  • 9. Living with sickle cell disease and depression in Lagos, Nigeria: A mixed methods study.
    Ola BA, Yates SJ, Dyson SM.
    Soc Sci Med; 2016 Jul; 161():27-36. PubMed ID: 27239705
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  • 10. Coping with sickle cell anemia in Nigerian universities: the case of Obafemi Awolowo University, Ile-Ife, Nigeria.
    Okumdi MC, Victor AO.
    Soc Work Health Care; 2013 Jul; 52(6):578-98. PubMed ID: 23865973
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  • 11. 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 15; 55(1):129-33. PubMed ID: 20213846
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  • 12. Psychological distress and coping in sickle cell disease: comparison of British and Jamaican attitudes.
    Thomas VJ, Hambleton I, Serjeant G.
    Ethn Health; 2001 May 15; 6(2):129-36. PubMed ID: 11480961
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  • 13. Using photovoice to explore the unique life perspectives of youth with sickle cell disease: a pilot study.
    Stegenga K, Burks LM.
    J Pediatr Oncol Nurs; 2013 May 15; 30(5):269-74. PubMed ID: 23962960
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  • 14. 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 May 15; 31(6):678-690. PubMed ID: 27451007
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  • 15. Clinical and sociodemographic factors predict coping styles among adults with sickle cell disease.
    Jonassaint CR, Jonassaint JC, Stanton MV, De Castro LM, Royal CD.
    J Natl Med Assoc; 2010 Nov 15; 102(11):1045-9. PubMed ID: 21141293
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  • 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 Nov 15; 29(5):424-34. PubMed ID: 25771820
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  • 17. Psychological complications in sickle cell disease.
    Anie KA.
    Br J Haematol; 2005 Jun 15; 129(6):723-9. PubMed ID: 15952997
    [Abstract] [Full Text] [Related]

  • 18. Disclosure and sickle cell disorder: a mixed methods study of the young person with sickle cell at school.
    Dyson SM, Atkin K, Culley LA, Dyson SE, Evans H, Rowley DT.
    Soc Sci Med; 2010 Jun 15; 70(12):2036-2044. PubMed ID: 20385437
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  • 19. Mothers raising children with sickle cell disease at the intersection of race, gender, and illness stigma.
    Burnes DP, Antle BJ, Williams CC, Cook L.
    Health Soc Work; 2008 Aug 15; 33(3):211-20. PubMed ID: 18773796
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