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Journal Abstract Search

2143 related items for PubMed ID: 18478489

  • 21. Status quo of palliative care in pediatric oncology-a nationwide survey in Germany.
    Friedrichsdorf SJ, Menke A, Brun S, Wamsler C, Zernikow B.
    J Pain Symptom Manage; 2005 Feb; 29(2):156-64. PubMed ID: 15733807
    [Abstract] [Full Text] [Related]

  • 22. Pain and symptom control in paediatric palliative care.
    Stevens MM, Dalla Pozza L, Cavalletto B, Cooper MG, Kilham HA.
    Cancer Surv; 1994 Feb; 21():211-31. PubMed ID: 8564995
    [Abstract] [Full Text] [Related]

  • 23. Home care for the dying child. A parent's perception.
    Collins JJ, Stevens MM, Cousens P.
    Aust Fam Physician; 1998 Jul; 27(7):610-4. PubMed ID: 9679382
    [Abstract] [Full Text] [Related]

  • 24. 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]

  • 25. Personal, social, and family adjustment in school-aged children with a cochlear implant.
    Nicholas JG, Geers AE.
    Ear Hear; 2003 Feb; 24(1 Suppl):69S-81S. PubMed ID: 12612482
    [Abstract] [Full Text] [Related]

  • 26. Quality of life following allogeneic stem cell transplantation, comparing parents' and children's perspective.
    Forinder U, Löf C, Winiarski J.
    Pediatr Transplant; 2006 Jun; 10(4):491-6. PubMed ID: 16712609
    [Abstract] [Full Text] [Related]

  • 27. Exploring parents' environmental needs at the time of a child's death in the pediatric intensive care unit.
    Meert KL, Briller SH, Schim SM, Thurston CS.
    Pediatr Crit Care Med; 2008 Nov; 9(6):623-8. PubMed ID: 18838930
    [Abstract] [Full Text] [Related]

  • 28. Parents' perceptions of the quality of pediatric and perinatal end-of-life care.
    Widger K, Picot C.
    Pediatr Nurs; 2008 Nov; 34(1):53-8. PubMed ID: 18361087
    [Abstract] [Full Text] [Related]

  • 29. Meeting the needs of parents around the time of diagnosis of disability among their children: evaluation of a novel program for information, support, and liaison by key workers.
    Rahi JS, Manaras I, Tuomainen H, Hundt GL.
    Pediatrics; 2004 Oct; 114(4):e477-82. PubMed ID: 15466074
    [Abstract] [Full Text] [Related]

  • 30. The supportive and palliative care needs of Australian families of children who die from cancer.
    Monterosso L, Kristjanson LJ, Phillips MB.
    Palliat Med; 2009 Sep; 23(6):526-36. PubMed ID: 19351793
    [Abstract] [Full Text] [Related]

  • 31. Sibling involvement at the end of life.
    Giovanola J.
    J Pediatr Oncol Nurs; 2005 Sep; 22(4):222-6. PubMed ID: 15994340
    [Abstract] [Full Text] [Related]

  • 32. Stop the pain! A nation-wide quality improvement programme in paediatric oncology pain control.
    Zernikow B, Hasan C, Hechler T, Huebner B, Gordon D, Michel E.
    Eur J Pain; 2008 Oct; 12(7):819-33. PubMed ID: 18222100
    [Abstract] [Full Text] [Related]

  • 33. [Palliative home care of children: an opinion survey of orphaned parents].
    Kuhlen M, Schlote A, Borkhardt A, Janßen G.
    Klin Padiatr; 2014 May; 226(3):182-7. PubMed ID: 24819389
    [Abstract] [Full Text] [Related]

  • 34. Posttraumatic stress disorder among parents of children on cancer treatment: a longitudinal study.
    Pöder U, Ljungman G, von Essen L.
    Psychooncology; 2008 May; 17(5):430-7. PubMed ID: 17847123
    [Abstract] [Full Text] [Related]

  • 35. [How to discuss death with children and families?].
    Seigneur É.
    Bull Cancer; 2011 May; 98(5):581-8. PubMed ID: 21636343
    [Abstract] [Full Text] [Related]

  • 36. Symptoms affecting children with malignancies during the last month of life: a nationwide follow-up.
    Jalmsell L, Kreicbergs U, Onelöv E, Steineck G, Henter JI.
    Pediatrics; 2006 Apr; 117(4):1314-20. PubMed ID: 16585329
    [Abstract] [Full Text] [Related]

  • 37. 'No control whatsoever': end-of-life care on a medical teaching unit from the perspective of family members.
    Workman S, Mann OE.
    QJM; 2007 Jul; 100(7):433-40. PubMed ID: 17566011
    [Abstract] [Full Text] [Related]

  • 38. Parent participation in paediatric rehabilitation treatment centres in the Netherlands: a parents' viewpoint.
    Siebes RC, Wijnroks L, Ketelaar M, van Schie PE, Gorter JW, Vermeer A.
    Child Care Health Dev; 2007 Mar; 33(2):196-205. PubMed ID: 17291324
    [Abstract] [Full Text] [Related]

  • 39. Knowledge and beliefs about end-of-life care and the effects of specialized palliative care: a population-based survey in Japan.
    Morita T, Miyashita M, Shibagaki M, Hirai K, Ashiya T, Ishihara T, Matsubara T, Miyoshi I, Nakaho T, Nakashima N, Onishi H, Ozawa T, Suenaga K, Tajima T, Akechi T, Uchitomi Y.
    J Pain Symptom Manage; 2006 Apr; 31(4):306-16. PubMed ID: 16632078
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  • 40. The experience of dying with dementia: a retrospective study.
    McCarthy M, Addington-Hall J, Altmann D.
    Int J Geriatr Psychiatry; 1997 Mar; 12(3):404-9. PubMed ID: 9152728
    [Abstract] [Full Text] [Related]

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