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Journal Abstract Search


348 related items for PubMed ID: 25115050

  • 1. Differences in quality of life between pediatric sickle cell patients who used hydroxyurea and those who did not.
    Nwenyi E, Leafman J, Mathieson K, Ezeobah N.
    Int J Health Care Qual Assur; 2014; 27(6):468-81. PubMed ID: 25115050
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  • 2. Daily home opioid use in adults with sickle cell disease: The PiSCES project.
    Smith WR, McClish DK, Dahman BA, Levenson JL, Aisiku IP, de A Citero V, Bovbjerg VE, Roberts JD, Penberthy LT, Roseff SD.
    J Opioid Manag; 2015; 11(3):243-53. PubMed ID: 25985809
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  • 3. Hydroxyurea for children with sickle cell disease.
    Heeney MM, Ware RE.
    Pediatr Clin North Am; 2008 Apr; 55(2):483-501, x. PubMed ID: 18381097
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  • 4. 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 05; 15(1):136. PubMed ID: 28679417
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  • 5. Barriers to the use of hydroxyurea in the management of sickle cell disease in Nigeria.
    Adeyemo TA, Diaku-Akinwunmi IN, Ojewunmi OO, Bolarinwa AB, Adekile AD.
    Hemoglobin; 2019 May 05; 43(3):188-192. PubMed ID: 31462098
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  • 7. A pilot study of electronic directly observed therapy to improve hydroxyurea adherence in pediatric patients with sickle-cell disease.
    Creary SE, Gladwin MT, Byrne M, Hildesheim M, Krishnamurti L.
    Pediatr Blood Cancer; 2014 Jun 05; 61(6):1068-73. PubMed ID: 24436121
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  • 8. The role of hydroxyurea in the management of sickle cell disease.
    Davies SC, Gilmore A.
    Blood Rev; 2003 Jun 05; 17(2):99-109. PubMed ID: 12642122
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  • 9. Hydroxyurea therapy in adult Nigerian sickle cell disease: a monocentric survey on pattern of use, clinical effects and patient's compliance.
    Adewoyin AS, Oghuvwu OS, Awodu OA.
    Afr Health Sci; 2017 Mar 05; 17(1):255-261. PubMed ID: 29026400
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  • 11. Hydroxyurea in sickle cell disease patients from Eastern Saudi Arabia.
    Al-Jam'a AH, Al-Dabbous IA.
    Saudi Med J; 2002 Mar 05; 23(3):277-81. PubMed ID: 11938415
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  • 13. Hydroxyurea therapy: improving the lives of patients with sickle cell disease.
    Anderson N.
    Pediatr Nurs; 2006 Mar 05; 32(6):541-3. PubMed ID: 17256291
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  • 14. [From Hemoglobin SS to SF: interest of hydroxyurea in the management of sickle cell disease in two Congolese children and review of the literature].
    Nkashama GM, Wakamb GK, Mulangu AM, Nkashama GM, Kupa BK, Numbi OL.
    Pan Afr Med J; 2015 Mar 05; 21():124. PubMed ID: 26327961
    [Abstract] [Full Text] [Related]

  • 15. Hydroxyurea therapy in sickle cell anemia patients aids to maintain oral fungal colonization balance.
    Salvia AC, Figueiredo MS, Braga JA, Pereira DF, Brighenti FL, Koga-Ito CY.
    J Oral Pathol Med; 2013 Aug 05; 42(7):570-5. PubMed ID: 23278631
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  • 17. Barriers to hydroxyurea adherence and health-related quality of life in adolescents and young adults with sickle cell disease.
    Badawy SM, Thompson AA, Penedo FJ, Lai JS, Rychlik K, Liem RI.
    Eur J Haematol; 2017 Jun 05; 98(6):608-614. PubMed ID: 28306171
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  • 18. Differences in health-related quality of life in children with sickle cell disease receiving hydroxyurea.
    Thornburg CD, Calatroni A, Panepinto JA.
    J Pediatr Hematol Oncol; 2011 May 05; 33(4):251-4. PubMed ID: 21516020
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