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Journal Abstract Search

270 related items for PubMed ID: 18754901

  • 1. Parent and professional reports of the quality of life of children with cerebral palsy and associated intellectual impairment.
    White-Koning M, Grandjean H, Colver A, Arnaud C.
    Dev Med Child Neurol; 2008 Aug; 50(8):618-24. PubMed ID: 18754901
    [Abstract] [Full Text] [Related]

  • 2. 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]

  • 3. Measuring the quality of life of children with cerebral palsy: comparing the conceptual differences and psychometric properties of three instruments.
    Davis E, Shelly A, Waters E, Davern M.
    Dev Med Child Neurol; 2010 Feb; 52(2):174-80. PubMed ID: 19549193
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  • 4. Parent-reported quality of life of children with cerebral palsy in Europe.
    Arnaud C, White-Koning M, Michelsen SI, Parkes J, Parkinson K, Thyen U, Beckung E, Dickinson HO, Fauconnier J, Marcelli M, McManus V, Colver A.
    Pediatrics; 2008 Jan; 121(1):54-64. PubMed ID: 18166557
    [Abstract] [Full Text] [Related]

  • 5. Parent proxy-reported quality of life for children with cerebral palsy: is it related to parental psychosocial distress?
    Davis E, Mackinnon A, Waters E.
    Child Care Health Dev; 2012 Jul; 38(4):553-60. PubMed ID: 21671983
    [Abstract] [Full Text] [Related]

  • 6. The relationship between quality of life and functioning for children with cerebral palsy.
    Shelly A, Davis E, Waters E, Mackinnon A, Reddihough D, Boyd R, Reid S, Graham HK.
    Dev Med Child Neurol; 2008 Mar; 50(3):199-203. PubMed ID: 18215191
    [Abstract] [Full Text] [Related]

  • 7. Quality of life of adolescents with cerebral palsy: perspectives of adolescents and parents.
    Davis E, Shelly A, Waters E, Mackinnon A, Reddihough D, Boyd R, Graham HK.
    Dev Med Child Neurol; 2009 Mar; 51(3):193-9. PubMed ID: 19191833
    [Abstract] [Full Text] [Related]

  • 8. Parenting style impacts on quality of life in children with cerebral palsy.
    Aran A, Shalev RS, Biran G, Gross-Tsur V.
    J Pediatr; 2007 Jul; 151(1):56-60, 60.e1. PubMed ID: 17586191
    [Abstract] [Full Text] [Related]

  • 9. Longitudinal use of the Child Health Questionnaire in childhood cerebral palsy.
    Vargus-Adams J.
    Dev Med Child Neurol; 2006 May; 48(5):343-7. PubMed ID: 16608541
    [Abstract] [Full Text] [Related]

  • 10. Parent quality of life in the context of pediatric inflammatory bowel disease.
    Greenley RN, Cunningham C.
    J Pediatr Psychol; 2009 Mar; 34(2):129-36. PubMed ID: 18577543
    [Abstract] [Full Text] [Related]

  • 11. Interpreting parental proxy reports of (health-related) quality of life for children with unilateral cochlear implants.
    Sach TH, Barton GR.
    Int J Pediatr Otorhinolaryngol; 2007 Mar; 71(3):435-45. PubMed ID: 17161471
    [Abstract] [Full Text] [Related]

  • 12. 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; 35(4):489-95. PubMed ID: 19638023
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  • 14. Quality of life in parents of children with cerebral palsy: is it influenced by the child's behaviour?
    Romeo DM, Cioni M, Distefano A, Battaglia LR, Costanzo L, Ricci D, De Sanctis R, Romeo MG, Mazzone D, Mercuri E.
    Neuropediatrics; 2010 Jun; 41(3):121-6. PubMed ID: 20859830
    [Abstract] [Full Text] [Related]

  • 15. Agreement between pediatric brain tumor patients and parent proxy reports regarding the Pediatric Functional Assessment of Cancer Therapy-Childhood Brain Tumor Survivors questionnaire, version 2.
    Yoo HJ, Ra YS, Park HJ, Lai JS, Cella D, Shin HY, Kim DS.
    Cancer; 2010 Aug 01; 116(15):3674-82. PubMed ID: 20564119
    [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 01; 65(11):2311-23. PubMed ID: 19737327
    [Abstract] [Full Text] [Related]

  • 17. Agreement between child self-report and parent proxy-report to evaluate quality of life in children with cancer.
    Chang PC, Yeh CH.
    Psychooncology; 2005 Feb 01; 14(2):125-34. PubMed ID: 15386781
    [Abstract] [Full Text] [Related]

  • 18. The GMFM, PEDI, and CP-QOL and perspectives on functioning from children with CP, parents, and medical professionals.
    Vargus-Adams JN, Martin LK, Maignan SH, Klein AC, Salisbury S.
    J Pediatr Rehabil Med; 2011 Feb 01; 4(1):3-12. PubMed ID: 21757805
    [Abstract] [Full Text] [Related]

  • 19. 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 01; 31(2):127-35. PubMed ID: 15715691
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