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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

225 related articles for article (PubMed ID: 22081218)

  • 1. 'All the burden on all the carers': exploring quality of life with family caregivers of Huntington's disease patients.
    Aubeeluck AV; Buchanan H; Stupple EJ
    Qual Life Res; 2012 Oct; 21(8):1425-35. PubMed ID: 22081218
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Communication and Huntington's disease: qualitative interviews and focus groups with persons with Huntington's disease, family members, and carers.
    Hartelius L; Jonsson M; Rickeberg A; Laakso K
    Int J Lang Commun Disord; 2010; 45(3):381-93. PubMed ID: 20144006
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Further evidence of reliability and validity of the Huntington's disease quality of life battery for carers: Italian and French translations.
    Aubeeluck A; Dorey J; Squitieri F; Clay E; Stupple EJ; De Nicola A; Buchanan H; Martino T; Toumi M
    Qual Life Res; 2013 Jun; 22(5):1093-8. PubMed ID: 22821667
    [TBL] [Abstract][Full Text] [Related]  

  • 4. The Impact of Huntington Disease on Family Carers: a Literature Overview.
    Domaradzki J
    Psychiatr Pol; 2015; 49(5):931-44. PubMed ID: 26688844
    [TBL] [Abstract][Full Text] [Related]  

  • 5. The Huntington's disease quality of life battery for carers: reliability and validity.
    Aubeeluck A; Buchanan H
    Clin Genet; 2007 May; 71(5):434-45. PubMed ID: 17489849
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Exploring the Reliability and Validity of the Huntington's Disease Quality of Life Battery for Carers (HDQoL-C) within A Polish Population.
    Bartoszek A; Aubeeluck A; Stupple E; Bartoszek A; Kocka K; Ślusarska B
    Int J Environ Res Public Health; 2019 Jun; 16(13):. PubMed ID: 31262100
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A psychometric comparison of two carer quality of life questionnaires in Huntington's disease: implications for neurodegenerative disorders.
    Hagell P; Smith S
    J Huntingtons Dis; 2013; 2(3):315-22. PubMed ID: 25062679
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Caring for the carers: quality of life in Huntington's disease.
    Aubeeluck A
    Br J Nurs; 2005 Apr 28-May 11; 14(8):452-4. PubMed ID: 15924027
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Predictors of quality of life in carers for people with a progressive neurological illness: a longitudinal study.
    O'Connor EJ; McCabe MP
    Qual Life Res; 2011 Jun; 20(5):703-11. PubMed ID: 21127997
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Balancing needs as a family caregiver in Huntington's disease: a qualitative interview study.
    Røthing M; Malterud K; Frich JC
    Health Soc Care Community; 2015 Sep; 23(5):569-76. PubMed ID: 25471490
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Quality of Life on the Views of Older Family Carers of People with Dementia.
    Oliveira D; Vass C; Aubeeluck A
    Dementia (London); 2019 Apr; 18(3):990-1009. PubMed ID: 28358270
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Assessment of Caregiver Burden in Huntington's Disease.
    Yu M; Tan K; Koloms K; Bega D
    J Huntingtons Dis; 2019; 8(1):111-114. PubMed ID: 30594932
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Huntington's disease. Part 3: family aspects of HD.
    Aubeeluck A; Moskowitz CB
    Br J Nurs; 2008 Mar 13-26; 17(5):328-31. PubMed ID: 18414297
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Caring for a child with Juvenile Huntington's Disease: helpful and unhelpful support.
    Brewer HM; Smith JA; Eatough V; Stanley CA; Glendinning NW; Quarrell OW
    J Child Health Care; 2007 Mar; 11(1):40-52. PubMed ID: 17287223
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Avoidance as a strategy of (not) coping: qualitative interviews with carers of Huntington's Disease patients.
    Lowit A; van Teijlingen ER
    BMC Fam Pract; 2005 Sep; 6():38. PubMed ID: 16162290
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Perceptions of the impact of chorea on health-related quality of life in Huntington disease (HD): A qualitative analysis of individuals across the HD spectrum, family members, and clinicians.
    Sherman CW; Iyer R; Abler V; Antonelli A; Carlozzi NE
    Neuropsychol Rehabil; 2020 Jul; 30(6):1150-1168. PubMed ID: 30849283
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Quality of Life in Huntington's Disease: Critique and Recommendations for Measures Assessing Patient Health-Related Quality of Life and Caregiver Quality of Life.
    Mestre TA; Carlozzi NE; Ho AK; Burgunder JM; Walker F; Davis AM; Busse M; Quinn L; Rodrigues FB; Sampaio C; Goetz CG; Cubo E; Martinez-Martin P; Stebbins GT;
    Mov Disord; 2018 May; 33(5):742-749. PubMed ID: 29570848
    [TBL] [Abstract][Full Text] [Related]  

  • 18. The emotional experiences of family carers in Huntington disease.
    Williams JK; Skirton H; Paulsen JS; Tripp-Reimer T; Jarmon L; McGonigal Kenney M; Birrer E; Hennig BL; Honeyford J
    J Adv Nurs; 2009 Apr; 65(4):789-98. PubMed ID: 19228233
    [TBL] [Abstract][Full Text] [Related]  

  • 19. The experience of the family caregivers' role: a qualitative study.
    Lane P; McKenna H; Ryan A; Fleming P
    Res Theory Nurs Pract; 2003; 17(2):137-51. PubMed ID: 12880218
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Variances in family carers' quality of life based on selected relationship and caregiving indicators: A quantitative secondary analysis.
    Naef R; Hediger H; Imhof L; Mahrer-Imhof R
    Int J Older People Nurs; 2017 Jun; 12(2):. PubMed ID: 27863032
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.