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Journal Abstract Search

398 related items for PubMed ID: 15478136

  • 1. A qualitative study of the experience of caring for a person with bulimia nervosa. Part 2: Carers' needs and experiences of services and other support.
    Winn S, Perkins S, Murray J, Murphy R, Schmidt U.
    Int J Eat Disord; 2004 Nov; 36(3):269-79. PubMed ID: 15478136
    [Abstract] [Full Text] [Related]

  • 2. A qualitative study of the experience of caring for a person with bulimia nervosa. Part 1: The emotional impact of caring.
    Perkins S, Winn S, Murray J, Murphy R, Schmidt U.
    Int J Eat Disord; 2004 Nov; 36(3):256-68. PubMed ID: 15478131
    [Abstract] [Full Text] [Related]

  • 3. The needs of carers of patients with anorexia and bulimia nervosa.
    Graap H, Bleich S, Herbst F, Trostmann Y, Wancata J, de Zwaan M.
    Eur Eat Disord Rev; 2008 Jan; 16(1):21-9. PubMed ID: 18074327
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  • 4. Deliberate self-harm in children and adolescents: a qualitative study exploring the needs of parents and carers.
    Byrne S, Morgan S, Fitzpatrick C, Boylan C, Crowley S, Gahan H, Howley J, Staunton D, Guerin S.
    Clin Child Psychol Psychiatry; 2008 Oct; 13(4):493-504. PubMed ID: 18927136
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  • 8. Identifying the needs of carers in mental health services.
    Gregory N, Collins-Atkins C, Macpherson R, Ford S, Palmer A.
    Nurs Times; 2008 Oct; 102(17):32-5. PubMed ID: 16700232
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  • 10. The coping experiences of carers who live with someone who has schizophrenia.
    Huang XY, Sun FK, Yen WJ, Fu CM.
    J Clin Nurs; 2008 Mar; 17(6):817-26. PubMed ID: 18279285
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  • 11. Service users and carers' experiences of a psychosis service.
    McKenzie LH.
    J Psychiatr Ment Health Nurs; 2006 Dec; 13(6):636-40. PubMed ID: 17087665
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  • 12. Caring as worrying: the experience of spousal carers.
    Cheung J, Hocking P.
    J Adv Nurs; 2004 Sep; 47(5):475-82. PubMed ID: 15312110
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  • 13. A pilot study of how information and communication technology may contribute to health promotion among elderly spousal carers in Norway.
    Torp S, Hanson E, Hauge S, Ulstein I, Magnusson L.
    Health Soc Care Community; 2008 Jan; 16(1):75-85. PubMed ID: 18181817
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  • 14. Exploring supportive care for individuals affected by Huntington disease and their family caregivers in a community setting.
    Soltysiak B, Gardiner P, Skirton H.
    J Clin Nurs; 2008 Apr; 17(7B):226-34. PubMed ID: 18578798
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  • 15. Understanding how parents cope with living with someone with anorexia nervosa: modelling the factors that are associated with carer distress.
    Kyriacou O, Treasure J, Schmidt U.
    Int J Eat Disord; 2008 Apr; 41(3):233-42. PubMed ID: 18008326
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  • 16. 'It's the system working for the system': carers' experiences of learning disability services in Ireland.
    Power A.
    Health Soc Care Community; 2009 Feb; 17(1):92-8. PubMed ID: 18800982
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  • 17. Impact of eating disorders on family life: individual parents' stories.
    Hillege S, Beale B, McMaster R.
    J Clin Nurs; 2006 Aug; 15(8):1016-22. PubMed ID: 16879546
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  • 18. Daily living with distress and enrichment: the moral experience of families with ventilator-assisted children at home.
    Carnevale FA, Alexander E, Davis M, Rennick J, Troini R.
    Pediatrics; 2006 Jan; 117(1):e48-60. PubMed ID: 16396848
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  • 19. Family involvement in the care of a hospitalised child: a questionnaire survey of Mozambican family caregivers.
    Söderbäck M, Christensson K.
    Int J Nurs Stud; 2008 Dec; 45(12):1778-88. PubMed ID: 18657810
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  • 20. The need for support services for family carers of people with motor neurone disease (MND): views of current and former family caregivers a qualitative study.
    O'Brien MR, Whitehead B, Jack BA, Mitchell JD.
    Disabil Rehabil; 2012 Dec; 34(3):247-56. PubMed ID: 22087569
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