BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

499 related articles for article (PubMed ID: 17587358)

  • 1. Caregivers' perceptions about terminally ill family members' quality of life.
    Melin-Johansson C; Axelsson B; Danielson E
    Eur J Cancer Care (Engl); 2007 Jul; 16(4):338-45. PubMed ID: 17587358
    [TBL] [Abstract][Full Text] [Related]  

  • 2. The meaning of quality of life: narrations by patients with incurable cancer in palliative home care.
    Melin-Johansson C; Odling G; Axelsson B; Danielson E
    Palliat Support Care; 2008 Sep; 6(3):231-8. PubMed ID: 18662416
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Understanding the meaning of social well-being at the end of life.
    Prince-Paul M
    Oncol Nurs Forum; 2008 May; 35(3):365-71. PubMed ID: 18467287
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Adult oncology and chronically ill patients: comparison of depression, anxiety and caregivers' quality of life.
    Sherif T; Jehani T; Saadani M; Andejani AW
    East Mediterr Health J; 2001 May; 7(3):502-9. PubMed ID: 12690772
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Palliative family caregivers' accounts of health care experiences: the importance of "security".
    Funk LM; Allan DE; Stajduhar KI
    Palliat Support Care; 2009 Dec; 7(4):435-47. PubMed ID: 19939306
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Factors influencing family caregivers' ability to cope with providing end-of-life cancer care at home.
    Stajduhar KI; Martin WL; Barwich D; Fyles G
    Cancer Nurs; 2008; 31(1):77-85. PubMed ID: 18176135
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Caring for the terminally ill: experiences of Latvian family caregivers.
    Kalnins I
    Int Nurs Rev; 2006 Jun; 53(2):129-35. PubMed ID: 16650032
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Caring for family members with chronic physical illness: a critical review of caregiver literature.
    Lim JW; Zebrack B
    Health Qual Life Outcomes; 2004 Sep; 2():50. PubMed ID: 15377384
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Assessing informal caregivers' experiences: a qualitative and psychometric evaluation of the Caregiver Reaction Assessment Scale.
    Persson C; Wennman-Larsen A; Sundin K; Gustavsson P
    Eur J Cancer Care (Engl); 2008 Mar; 17(2):189-99. PubMed ID: 18302657
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Predictors of family caregivers' burden and quality of life when providing care for a family member with schizophrenia in the People's Republic of China.
    Li J; Lambert CE; Lambert VA
    Nurs Health Sci; 2007 Sep; 9(3):192-8. PubMed ID: 17688477
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Caregiving and its impact on families of the terminally ill.
    Brazil K; Bédard M; Willison K; Hode M
    Aging Ment Health; 2003 Sep; 7(5):376-82. PubMed ID: 12959807
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Patient awareness of prognosis, patient-family caregiver congruence on the preferred place of death, and caregiving burden of families contribute to the quality of life for terminally ill cancer patients in Taiwan.
    Tang ST; Liu TW; Tsai CM; Wang CH; Chang GC; Liu LN
    Psychooncology; 2008 Dec; 17(12):1202-9. PubMed ID: 18521969
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Psychometric testing of the Caregiver Quality of Life Index-Cancer on a Taiwanese family caregiver sample.
    Tang WR; Tang ST; Kao CY
    Cancer Nurs; 2009; 32(3):220-9. PubMed ID: 19295419
    [TBL] [Abstract][Full Text] [Related]  

  • 14. The meaning of the music: the role of music in palliative care music therapy as perceived by bereaved caregivers of advanced cancer patients.
    Magill L
    Am J Hosp Palliat Care; 2009; 26(1):33-9. PubMed ID: 19047488
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Discrepancy in the preferences of place of death between terminally ill cancer patients and their primary family caregivers in Taiwan.
    Tang ST; Liu TW; Lai MS; McCorkle R
    Soc Sci Med; 2005 Oct; 61(7):1560-6. PubMed ID: 16005787
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Caregiver bodywork: family members' experiences of caring for a person with motor neurone disease.
    Ray RA; Street AF
    J Adv Nurs; 2006 Oct; 56(1):35-43. PubMed ID: 16972916
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Dying with dementia: the views of family caregivers about quality of life.
    Russell C; Middleton H; Shanley C
    Australas J Ageing; 2008 Jun; 27(2):89-92. PubMed ID: 18713199
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Living with moderate or severe traumatic brain injury: the meaning of family members' experiences.
    Jumisko E; Lexell J; Söderberg S
    J Fam Nurs; 2007 Aug; 13(3):353-69. PubMed ID: 17641113
    [TBL] [Abstract][Full Text] [Related]  

  • 19. The association between meaning of caregiving, perceived social support and level of depression of Taiwanese caregivers of mentally ill patients.
    Yen WJ; Lundeen S
    Int J Psychiatr Nurs Res; 2006 Sep; 12(1):1378-92. PubMed ID: 17016900
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Congruence of knowledge, experiences, and preferences for disclosure of diagnosis and prognosis between terminally-ill cancer patients and their family caregivers in Taiwan.
    Tang ST; Liu TW; Lai MS; Liu LN; Chen CH; Koong SL
    Cancer Invest; 2006; 24(4):360-6. PubMed ID: 16777687
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 25.