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Journal Abstract Search

665 related items for PubMed ID: 17968039

  • 1. Professional carers' experiences of providing a pediatric palliative care service in Ireland.
    Clarke J, Quin S.
    Qual Health Res; 2007 Nov; 17(9):1219-31. PubMed ID: 17968039
    [Abstract] [Full Text] [Related]

  • 2. Exploring the role of partnership in the home care of children with special health needs: qualitative findings from two service evaluations.
    McIntosh J, Runciman P.
    Int J Nurs Stud; 2008 May; 45(5):714-26. PubMed ID: 17307182
    [Abstract] [Full Text] [Related]

  • 3. Providing care and sharing expertise: reflections of nurse-specialists in palliative home care.
    Arnaert A, Wainwright M.
    Palliat Support Care; 2009 Sep; 7(3):357-64. PubMed ID: 19788778
    [Abstract] [Full Text] [Related]

  • 4. The experiences of Chinese family members of terminally ill patients - a qualitative study.
    Wong MS, Chan SW.
    J Clin Nurs; 2007 Dec; 16(12):2357-64. PubMed ID: 18036125
    [Abstract] [Full Text] [Related]

  • 5. Supportive and palliative care needs of families of children with life-threatening illnesses in Western Australia: evidence to guide the development of a palliative care service.
    Monterosso L, Kristjanson LJ, Aoun S, Phillips MB.
    Palliat Med; 2007 Dec; 21(8):689-96. PubMed ID: 18073255
    [Abstract] [Full Text] [Related]

  • 6. Parental decision making in pediatric cancer end-of-life care: using focus group methodology as a prephase to seek participant design input.
    Tomlinson D, Capra M, Gammon J, Volpe J, Barrera M, Hinds PS, Bouffet E, Geenberg ML, Baruchel S, Llewellyn-Thomas HA, Sung L.
    Eur J Oncol Nurs; 2006 Jul; 10(3):198-206. PubMed ID: 16384746
    [Abstract] [Full Text] [Related]

  • 7. General practitioners' experiences of the psychological aspects in the care of a dying patient.
    Kelly B, Varghese FT, Burnett P, Turner J, Robertson M, Kelly P, Mitchell G, Treston P.
    Palliat Support Care; 2008 Jun; 6(2):125-31. PubMed ID: 18501047
    [Abstract] [Full Text] [Related]

  • 8. An exploration of best practice in multi-agency working and the experiences of families of children with complex health needs. What works well and what needs to be done to improve practice for the future?
    Carter B, Cummings J, Cooper L.
    J Clin Nurs; 2007 Mar; 16(3):527-39. PubMed ID: 17335529
    [Abstract] [Full Text] [Related]

  • 9. Searching for "the dying point:" providers' experiences with palliative care in pediatric acute care.
    Docherty SL, Miles MS, Brandon D.
    Pediatr Nurs; 2007 Mar; 33(4):335-41. PubMed ID: 17907734
    [Abstract] [Full Text] [Related]

  • 10. Maintaining the continuity of care in community children's nursing caseloads in a service for children with life-limiting, life-threatening or chronic health conditions: a qualitative analysis.
    Pontin D, Lewis M.
    J Clin Nurs; 2009 Apr; 18(8):1199-206. PubMed ID: 19320788
    [Abstract] [Full Text] [Related]

  • 11. Professionals' views on the roles and needs of family carers of adults with cerebral palsy and complex communication needs in hospital.
    Hemsley B, Balandin S, Togher L.
    J Intellect Dev Disabil; 2008 Jun; 33(2):127-36. PubMed ID: 18569400
    [Abstract] [Full Text] [Related]

  • 12. Caring for dying children: assessing the needs of the pediatric palliative care nurse.
    Morgan D.
    Pediatr Nurs; 2009 Jun; 35(2):86-90. PubMed ID: 19472671
    [Abstract] [Full Text] [Related]

  • 13. Planning with parents for seriously ill children: preliminary results on the development of the parental engagement scale.
    Kearney JA, Byrne MW.
    Palliat Support Care; 2011 Dec; 9(4):367-76. PubMed ID: 22104412
    [Abstract] [Full Text] [Related]

  • 14. Striving for independence: experiences and needs of service users with life limiting conditions.
    Cotterell P.
    J Adv Nurs; 2008 Jun; 62(6):665-73. PubMed ID: 18503650
    [Abstract] [Full Text] [Related]

  • 15. Supportive and palliative care needs of families of children who die from cancer: an Australian study.
    Monterosso L, Kristjanson LJ.
    Palliat Med; 2008 Jan; 22(1):59-69. PubMed ID: 18216078
    [Abstract] [Full Text] [Related]

  • 16. Assessing palliative care needs: views of patients, informal carers and healthcare professionals.
    McIlfatrick S.
    J Adv Nurs; 2007 Jan; 57(1):77-86. PubMed ID: 17184376
    [Abstract] [Full Text] [Related]

  • 17. '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
    [Abstract] [Full Text] [Related]

  • 18. The psychosocial impact on parents of tube feeding their child.
    Hazel R.
    Paediatr Nurs; 2006 May; 18(4):19-22. PubMed ID: 16719037
    [Abstract] [Full Text] [Related]

  • 19. Disabled children's services: how do we measure family-centred care?
    Pickering D, Busse M.
    J Child Health Care; 2010 Jun; 14(2):200-7. PubMed ID: 20418352
    [Abstract] [Full Text] [Related]

  • 20. Improving the quality of end-of-life care in the pediatric intensive care unit: parents' priorities and recommendations.
    Meyer EC, Ritholz MD, Burns JP, Truog RD.
    Pediatrics; 2006 Mar; 117(3):649-57. PubMed ID: 16510643
    [Abstract] [Full Text] [Related]

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