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Journal Abstract Search

2143 related items for PubMed ID: 18478489

  • 1. Parents' perspective on symptoms, quality of life, characteristics of death and end-of-life decisions for children dying from cancer.
    Hechler T, Blankenburg M, Friedrichsdorf SJ, Garske D, Hübner B, Menke A, Wamsler C, Wolfe J, Zernikow B.
    Klin Padiatr; 2008; 220(3):166-74. PubMed ID: 18478489
    [Abstract] [Full Text] [Related]

  • 2. Symptoms in the palliative phase of children with cancer.
    Theunissen JM, Hoogerbrugge PM, van Achterberg T, Prins JB, Vernooij-Dassen MJ, van den Ende CH.
    Pediatr Blood Cancer; 2007 Aug; 49(2):160-5. PubMed ID: 16972239
    [Abstract] [Full Text] [Related]

  • 3. Parental perspectives on suffering and quality of life at end-of-life in children with advanced heart disease: an exploratory study*.
    Blume ED, Balkin EM, Aiyagari R, Ziniel S, Beke DM, Thiagarajan R, Taylor L, Kulik T, Pituch K, Wolfe J.
    Pediatr Crit Care Med; 2014 May; 15(4):336-42. PubMed ID: 24583501
    [Abstract] [Full Text] [Related]

  • 4. Quality of care at the end of life in children with cancer.
    Heath JA, Clarke NE, McCarthy M, Donath SM, Anderson VA, Wolfe J.
    J Paediatr Child Health; 2009 Nov; 45(11):656-9. PubMed ID: 19903251
    [Abstract] [Full Text] [Related]

  • 5. Symptoms and suffering at the end of life in children with cancer.
    Wolfe J, Grier HE, Klar N, Levin SB, Ellenbogen JM, Salem-Schatz S, Emanuel EJ, Weeks JC.
    N Engl J Med; 2000 Feb 03; 342(5):326-33. PubMed ID: 10655532
    [Abstract] [Full Text] [Related]

  • 6. Agreement between children with cancer and their parents in reporting the child's health-related quality of life during a stay at the hospital and at home.
    Speyer E, Herbinet A, Vuillemin A, Chastagner P, Briançon S.
    Child Care Health Dev; 2009 Jul 03; 35(4):489-95. PubMed ID: 19638023
    [Abstract] [Full Text] [Related]

  • 7. Anxiety is contagious-symptoms of anxiety in the terminally ill child affect long-term psychological well-being in bereaved parents.
    Jalmsell L, Kreicbergs U, Onelöv E, Steineck G, Henter JI.
    Pediatr Blood Cancer; 2010 May 03; 54(5):751-7. PubMed ID: 20135696
    [Abstract] [Full Text] [Related]

  • 8. Fathers and the well-child visit.
    Garfield CF, Isacco A.
    Pediatrics; 2006 Apr 03; 117(4):e637-45. PubMed ID: 16585280
    [Abstract] [Full Text] [Related]

  • 9. Place of death of adolescents and young adults with cancer: first study in a French population.
    Montel S, Laurence V, Copel L, Pacquement H, Flahault C.
    Palliat Support Care; 2009 Mar 03; 7(1):27-35. PubMed ID: 19619372
    [Abstract] [Full Text] [Related]

  • 10. [Home care services and the role of "caregivers"].
    Massimo L.
    Minerva Pediatr; 2001 Jun 03; 53(3):161-9. PubMed ID: 11455302
    [Abstract] [Full Text] [Related]

  • 11. Bereaved parents' perspectives on pediatric palliative care.
    Robert R, Zhukovsky DS, Mauricio R, Gilmore K, Morrison S, Palos GR.
    J Soc Work End Life Palliat Care; 2012 Jun 03; 8(4):316-38. PubMed ID: 23194168
    [Abstract] [Full Text] [Related]

  • 12. A comparison study of parental adaptation following a child's death at home or in the hospital.
    Lauer ME, Mulhern RK, Wallskog JM, Camitta BM.
    Pediatrics; 1983 Jan 03; 71(1):107-12. PubMed ID: 6848957
    [Abstract] [Full Text] [Related]

  • 13. Being a parent of a child with cancer throughout the end-of-life course.
    Kars MC, Grypdonck MH, van Delden JJ.
    Oncol Nurs Forum; 2011 Jul 03; 38(4):E260-71. PubMed ID: 21708521
    [Abstract] [Full Text] [Related]

  • 14. Care-related distress: a nationwide study of parents who lost their child to cancer.
    Kreicbergs U, Valdimarsdóttir U, Onelöv E, Björk O, Steineck G, Henter JI.
    J Clin Oncol; 2005 Dec 20; 23(36):9162-71. PubMed ID: 16172455
    [Abstract] [Full Text] [Related]

  • 15. Parent and physician perspectives on quality of care at the end of life in children with cancer.
    Mack JW, Hilden JM, Watterson J, Moore C, Turner B, Grier HE, Weeks JC, Wolfe J.
    J Clin Oncol; 2005 Dec 20; 23(36):9155-61. PubMed ID: 16172457
    [Abstract] [Full Text] [Related]

  • 16. Care of a child dying of cancer: the role of the palliative care team in pediatric oncology.
    Postovsky S, Ben Arush MW.
    Pediatr Hematol Oncol; 2004 Dec 20; 21(1):67-76. PubMed ID: 14660308
    [Abstract] [Full Text] [Related]

  • 17. Parents' assessment of quality of care and grief following a child's death.
    Seecharan GA, Andresen EM, Norris K, Toce SS.
    Arch Pediatr Adolesc Med; 2004 Jun 20; 158(6):515-20. PubMed ID: 15184212
    [Abstract] [Full Text] [Related]

  • 18. 'A bed in the middle of nowhere': parents' meanings of place of death for adults with cystic fibrosis.
    Lowton K.
    Soc Sci Med; 2009 Oct 20; 69(7):1056-62. PubMed ID: 19692159
    [Abstract] [Full Text] [Related]

  • 19. Different priorities: a comparison of parents' and health professionals' perceptions of quality of life in quadriplegic cerebral palsy.
    Morrow AM, Quine S, Loughlin EV, Craig JC.
    Arch Dis Child; 2008 Feb 20; 93(2):119-25. PubMed ID: 17932123
    [Abstract] [Full Text] [Related]

  • 20. Children dying from cancer: parents' perspectives on symptoms, quality of life, characteristics of death, and end-of-life decisions.
    von Lützau P, Otto M, Hechler T, Metzing S, Wolfe J, Zernikow B.
    J Palliat Care; 2012 Feb 20; 28(4):274-81. PubMed ID: 23413763
    [Abstract] [Full Text] [Related]

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