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PUBMED FOR HANDHELDS

Journal Abstract Search


299 related items for PubMed ID: 21196101

  • 21. The impact of pediatric tracheotomy on parental caregiver burden and health status.
    Hartnick CJ, Bissell C, Parsons SK.
    Arch Otolaryngol Head Neck Surg; 2003 Oct; 129(10):1065-9. PubMed ID: 14568788
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  • 23. Parental reactions following the diagnosis of cerebral palsy in their young child.
    Rentinck I, Ketelaar M, Jongmans M, Lindeman E, Gorter JW.
    J Pediatr Psychol; 2009 Jul; 34(6):671-6. PubMed ID: 18845588
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  • 25. 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
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  • 26. Comparison of impact on mood, health, and daily living experiences of primary caregivers of walking and non-walking children with cerebral palsy and provided community services support.
    Svedberg LE, Englund E, Malker H, Stener-Victorin E.
    Eur J Paediatr Neurol; 2010 May; 14(3):239-46. PubMed ID: 19628416
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  • 27. A national profile of the health care experiences and family impact of autism spectrum disorder among children in the United States, 2005-2006.
    Kogan MD, Strickland BB, Blumberg SJ, Singh GK, Perrin JM, van Dyck PC.
    Pediatrics; 2008 Dec; 122(6):e1149-58. PubMed ID: 19047216
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  • 29. Are family-centred principles, functional goal setting and transition planning evident in therapy services for children with cerebral palsy?
    Darrah J, Wiart L, Magill-Evans J, Ray L, Andersen J.
    Child Care Health Dev; 2012 Jan; 38(1):41-7. PubMed ID: 21083684
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  • 30. 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; 2012 Jan; 66(2):21-48. PubMed ID: 16878426
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  • 31. Socioeconomic and psychological variables as risk and protective factors for parental well-being in families of children with intellectual disabilities.
    Olsson MB, Hwang CP.
    J Intellect Disabil Res; 2008 Dec; 52(12):1102-13. PubMed ID: 18507702
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  • 32. 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 Dec; 220(3):166-74. PubMed ID: 18478489
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  • 34. Transition experience of parents caring of children with epilepsy: a phenomenological study.
    Mu PF.
    Int J Nurs Stud; 2008 Apr; 45(4):543-51. PubMed ID: 17157850
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  • 35. [Candid, not monitored children run less risk of becoming delinquent].
    Stattin H.
    Lakartidningen; 2001 Jun 20; 98(25):3009-13. PubMed ID: 11462873
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  • 36. Quality of life and mental health among parents of children with cerebral palsy: the influence of self-efficacy and coping strategies.
    Guillamón N, Nieto R, Pousada M, Redolar D, Muñoz E, Hernández E, Boixadós M, Gómez-Zúñiga B.
    J Clin Nurs; 2013 Jun 20; 22(11-12):1579-90. PubMed ID: 23461414
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  • 37. Parents' views of their child's health and family function in paediatric inflammatory bowel disease.
    Lindfred H, Saalman R, Nilsson S, Lepp M.
    Acta Paediatr; 2010 Apr 20; 99(4):612-7. PubMed ID: 20055780
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