These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

563 related items for PubMed ID: 19628416

  • 1.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 2. Family pediatrics: report of the Task Force on the Family.
    Schor EL, American Academy of Pediatrics Task Force on the Family.
    Pediatrics; 2003 Jun; 111(6 Pt 2):1541-71. PubMed ID: 12777595
    [Abstract] [Full Text] [Related]

  • 3. 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
    [Abstract] [Full Text] [Related]

  • 4. Health care utilization and needs after pediatric traumatic brain injury.
    Slomine BS, McCarthy ML, Ding R, MacKenzie EJ, Jaffe KM, Aitken ME, Durbin DR, Christensen JR, Dorsch AM, Paidas CN, CHAT Study Group.
    Pediatrics; 2006 Apr; 117(4):e663-74. PubMed ID: 16533894
    [Abstract] [Full Text] [Related]

  • 5.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 6.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 7. Health status of caregivers of children with cerebral palsy.
    Byrne MB, Hurley DA, Daly L, Cunningham CG.
    Child Care Health Dev; 2010 Sep; 36(5):696-702. PubMed ID: 20074250
    [Abstract] [Full Text] [Related]

  • 8. Determinants of child-parent agreement in quality-of-life reports: a European study of children with cerebral palsy.
    White-Koning M, Arnaud C, Dickinson HO, Thyen U, Beckung E, Fauconnier J, McManus V, Michelsen SI, Parkes J, Parkinson K, Schirripa G, Colver A.
    Pediatrics; 2007 Oct; 120(4):e804-14. PubMed ID: 17908738
    [Abstract] [Full Text] [Related]

  • 9. 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 Oct; 220(3):166-74. PubMed ID: 18478489
    [Abstract] [Full Text] [Related]

  • 10. A profile of children with disabilities receiving SSI: highlights from the National Survey of SSI Children and Families.
    Rupp K, Davies PS, Newcomb C, Iams H, Becker C, Mulpuru S, Ressler S, Romig K, Miller B.
    Soc Secur Bull; 2008 Oct; 66(2):21-48. PubMed ID: 16878426
    [Abstract] [Full Text] [Related]

  • 11. Family needs of parents of children and youth with cerebral palsy.
    Palisano RJ, Almarsi N, Chiarello LA, Orlin MN, Bagley A, Maggs J.
    Child Care Health Dev; 2010 Jan; 36(1):85-92. PubMed ID: 19961501
    [Abstract] [Full Text] [Related]

  • 12. To what extent do children with cerebral palsy participate in everyday life situations?
    Parkes J, McCullough N, Madden A.
    Health Soc Care Community; 2010 May; 18(3):304-15. PubMed ID: 20201974
    [Abstract] [Full Text] [Related]

  • 13. Development of a condition-specific measure of quality of life for children with cerebral palsy: empirical thematic data reported by parents and children.
    Waters E, Maher E, Salmon L, Reddihough D, Boyd R.
    Child Care Health Dev; 2005 Mar; 31(2):127-35. PubMed ID: 15715691
    [Abstract] [Full Text] [Related]

  • 14. The health and well-being of caregivers of children with cerebral palsy.
    Raina P, O'Donnell M, Rosenbaum P, Brehaut J, Walter SD, Russell D, Swinton M, Zhu B, Wood E.
    Pediatrics; 2005 Jun; 115(6):e626-36. PubMed ID: 15930188
    [Abstract] [Full Text] [Related]

  • 15. Parents with first time major depression: perceptions of social support for themselves and their children.
    Skärsäter I.
    Scand J Caring Sci; 2006 Sep; 20(3):308-14. PubMed ID: 16922985
    [Abstract] [Full Text] [Related]

  • 16. The health of children with cerebral palsy and stress in their parents.
    Parkes J, McCullough N, Madden A, McCahey E.
    J Adv Nurs; 2009 Nov; 65(11):2311-23. PubMed ID: 19737327
    [Abstract] [Full Text] [Related]

  • 17. The health of family caregivers of older impaired persons in Lebanon: an interview survey.
    Séoud J, Nehmé C, Atallah R, Zablit C, Yérétzian J, Lévesque L, Giroux F, Ducharme F.
    Int J Nurs Stud; 2007 Feb; 44(2):259-72. PubMed ID: 16730728
    [Abstract] [Full Text] [Related]

  • 18. 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; 93(2):119-25. PubMed ID: 17932123
    [Abstract] [Full Text] [Related]

  • 19. Pain among children and adolescents: restrictions in daily living and triggering factors.
    Roth-Isigkeit A, Thyen U, Stöven H, Schwarzenberger J, Schmucker P.
    Pediatrics; 2005 Feb; 115(2):e152-62. PubMed ID: 15687423
    [Abstract] [Full Text] [Related]

  • 20. 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]

    Page: [Next] [New Search]
    of 29.