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 *

205 related articles for article (PubMed ID: 15924027)

  • 21. Informal carers of mentally infirm elderly in Lancashire.
    Mafullul YM
    East Afr Med J; 2002 Jun; 79(6):284-90. PubMed ID: 12638818
    [TBL] [Abstract][Full Text] [Related]  

  • 22. '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]  

  • 23. Nurse's assessment of caregiver burden.
    Nguyen M
    Medsurg Nurs; 2009; 18(3):147-51; quiz 152. PubMed ID: 19591360
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Family carers for older relatives: sources of satisfaction and related factors in Finland.
    Kuuppelomäki M; Sasaki A; Yamada K; Asakawa N; Shimanouchi S
    Int J Nurs Stud; 2004 Jul; 41(5):497-505. PubMed ID: 15120978
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Caring for a person with dementia: exploring relationships between perceived burden, depression, coping and well-being.
    McConaghy R; Caltabiano ML
    Nurs Health Sci; 2005 Jun; 7(2):81-91. PubMed ID: 15877684
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Dementia carer education and patient behaviour disturbance.
    Coen RF; O'Boyle CA; Coakley D; Lawlor BA
    Int J Geriatr Psychiatry; 1999 Apr; 14(4):302-6. PubMed ID: 10340192
    [TBL] [Abstract][Full Text] [Related]  

  • 27. The need for support services for family carers of people with motor neurone disease (MND): views of current and former family caregivers a qualitative study.
    O'Brien MR; Whitehead B; Jack BA; Mitchell JD
    Disabil Rehabil; 2012; 34(3):247-56. PubMed ID: 22087569
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Living with Huntington's disease: need for supportive care.
    Dawson S; Kristjanson LJ; Toye CM; Flett P
    Nurs Health Sci; 2004 Jun; 6(2):123-30. PubMed ID: 15130098
    [TBL] [Abstract][Full Text] [Related]  

  • 29. An exploratory study of GP awareness of carer emotional needs in Western Australia.
    Bulsara CE; Fynn N
    BMC Fam Pract; 2006 May; 7():33. PubMed ID: 16719930
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Which carers of family members at the end of life need more support from health services and why?
    McNamara B; Rosenwax L
    Soc Sci Med; 2010 Apr; 70(7):1035-41. PubMed ID: 20116158
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Health-related quality of life in Huntington's disease: a comparison of two generic instruments, SF-36 and SIP.
    Ho AK; Robbins AO; Walters SJ; Kaptoge S; Sahakian BJ; Barker RA
    Mov Disord; 2004 Nov; 19(11):1341-8. PubMed ID: 15389986
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Using research to develop care for patients with Huntington's disease.
    Skirton H; Glendinning N
    Br J Nurs; 1997 Jan 23-Feb 12; 6(2):83-90. PubMed ID: 9116444
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Alzheimer's disease in real life--the dementia carer's survey.
    Georges J; Jansen S; Jackson J; Meyrieux A; Sadowska A; Selmes M
    Int J Geriatr Psychiatry; 2008 May; 23(5):546-51. PubMed ID: 18232054
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Huntington's disease--falling through the net.
    Shakespeare J; Anderson J
    Health Trends; 1993; 25(1):19-23. PubMed ID: 10125696
    [TBL] [Abstract][Full Text] [Related]  

  • 35. 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]  

  • 36. Caregiver burden among dementia patient caregivers: a review of the literature.
    Etters L; Goodall D; Harrison BE
    J Am Acad Nurse Pract; 2008 Aug; 20(8):423-8. PubMed ID: 18786017
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Caring for the caregiver.
    Tamayo GJ; Broxson A; Munsell M; Cohen MZ
    Oncol Nurs Forum; 2010 Jan; 37(1):E50-7. PubMed ID: 20044332
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Meaningful and Measurable Health Domains in Huntington's Disease: Large-Scale Validation of the Huntington's Disease Health-Related Quality of Life Questionnaire Across Severity Stages.
    Ho AK; Horton MC; Landwehrmeyer GB; Burgunder JM; Tennant A;
    Value Health; 2019 Jun; 22(6):712-720. PubMed ID: 31198189
    [TBL] [Abstract][Full Text] [Related]  

  • 39. The pressures felt by informal carers of people with dementia.
    Armstrong M
    Nurs Stand; 2001 Jan 10-16; 15(17):47-53; quiz 54-5. PubMed ID: 12211851
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Validation of the first quality-of-life measurement for patients with Huntington's disease: the Huntington Quality of Life Instrument.
    Clay E; De Nicola A; Dorey J; Squitieri F; Aballéa S; Martino T; Tedroff J; Zielonka D; Auquier P; Verny C; Toumi M
    Int Clin Psychopharmacol; 2012 Jul; 27(4):208-14. PubMed ID: 22508443
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 11.