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PUBMED FOR HANDHELDS

Journal Abstract Search

185 related items for PubMed ID: 20304331

  • 1. Caregiver's burden and quality of life in mitochondrial disease.
    Kim KR, Lee E, Namkoong K, Lee YM, Lee JS, Kim HD.
    Pediatr Neurol; 2010 Apr; 42(4):271-6. PubMed ID: 20304331
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  • 2. The impact of severe respiratory syncytial virus on the child, caregiver, and family during hospitalization and recovery.
    Leidy NK, Margolis MK, Marcin JP, Flynn JA, Frankel LR, Johnson S, Langkamp D, Simoes EA.
    Pediatrics; 2005 Jun; 115(6):1536-46. PubMed ID: 15930214
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  • 4. Caregiving time in sickle cell disease: psychological effects in maternal caregivers.
    Moskowitz JT, Butensky E, Harmatz P, Vichinsky E, Heyman MB, Acree M, Wrubel J, Wilson L, Folkman S.
    Pediatr Blood Cancer; 2007 Jan; 48(1):64-71. PubMed ID: 16622841
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  • 8. Burden, perceived health status, and mood among caregivers of Parkinson's disease patients.
    Martinez-Martin P, Arroyo S, Rojo-Abuin JM, Rodriguez-Blazquez C, Frades B, de Pedro Cuesta J, Longitudinal Parkinson's Disease Patient Study (Estudio longitudinal de pacientes con enfermedad de Parkinson-ELEP) Group.
    Mov Disord; 2008 Sep 15; 23(12):1673-80. PubMed ID: 18709684
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  • 9. Health-related quality of life in children and adolescents who have a diagnosis of attention-deficit/hyperactivity disorder.
    Klassen AF, Miller A, Fine S.
    Pediatrics; 2004 Nov 15; 114(5):e541-7. PubMed ID: 15520087
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  • 10. [Family caregivers and hereditary muscular disorders: association between burden, quality of life and mental health].
    Boyer F, Novella JL, Coulon JM, Delmer F, Morrone I, Lemoussu N, Bombart V, Calmus A, Cornu JY, Dulieu V, Etienne JC.
    Ann Readapt Med Phys; 2006 Feb 15; 49(1):16-22. PubMed ID: 16146663
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  • 11. Assessment of the quality of life of mothers of children with cerebral palsy (primary caregivers).
    Ones K, Yilmaz E, Cetinkaya B, Caglar N.
    Neurorehabil Neural Repair; 2005 Sep 15; 19(3):232-7. PubMed ID: 16093414
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  • 12. Parents of childhood X-linked adrenoleukodystrophy: high risk for depression and neurosis.
    Kuratsubo I, Suzuki Y, Shimozawa N, Kondo N.
    Brain Dev; 2008 Aug 15; 30(7):477-82. PubMed ID: 18430533
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  • 13. 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 15; 117(4):e663-74. PubMed ID: 16533894
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  • 14. Predictors of quality of life and caregiver burden among maternal and paternal caregivers of patients with eating disorders.
    Martín J, Padierna A, Aguirre U, González N, Muñoz P, Quintana JM.
    Psychiatry Res; 2013 Dec 30; 210(3):1107-15. PubMed ID: 23998363
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  • 15. [Caregiver burden in dementia: evaluation with a Japanese version of the Zarit caregiver burden interview].
    Hirono N, Kobayashi H, Mori E.
    No To Shinkei; 1998 Jun 30; 50(6):561-7. PubMed ID: 9656252
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  • 16. The effect of rheumatoid arthritis on the quality of life of primary caregivers.
    das Chagas Medeiros MM, Ferraz MB, Quaresma MR.
    J Rheumatol; 2000 Jan 30; 27(1):76-83. PubMed ID: 10648021
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  • 17. Burden and quality of life among caregivers of children and adolescents with meningomyelocele: measuring the relationship to anxiety and depression.
    Valença MP, de Menezes TA, Calado AA, de Aguiar Cavalcanti G.
    Spinal Cord; 2012 Jul 30; 50(7):553-7. PubMed ID: 22391686
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  • 18. Burden and perceived health status among caregivers of stroke patients.
    Carod-Artal FJ, Ferreira Coral L, Trizotto DS, Menezes Moreira C.
    Cerebrovasc Dis; 2009 Jul 30; 28(5):472-80. PubMed ID: 19752548
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  • 19. Anxiety and depression in children with epilepsy and their mothers.
    Baki O, Erdogan A, Kantarci O, Akisik G, Kayaalp L, Yalcinkaya C.
    Epilepsy Behav; 2004 Dec 30; 5(6):958-64. PubMed ID: 15582845
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  • 20. Burden and health-related quality of life of Spanish caregivers of persons with multiple sclerosis.
    Rivera-Navarro J, Benito-León J, Oreja-Guevara C, Pardo J, Dib WB, Orts E, Belló M, Caregiver Quality of Life in Multiple Sclerosis (CAREQOL-MS) Study Group.
    Mult Scler; 2009 Nov 30; 15(11):1347-55. PubMed ID: 19797453
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