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 *

256 related articles for article (PubMed ID: 26122085)

  • 21. Addressing the cultural, spiritual and religious perspectives of palliative care.
    Nalayeh H
    Ann Palliat Med; 2018 Jan; 7(Suppl 1):AB016. PubMed ID: 29402110
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Can specially trained community care workers effectively support patients and their families in the home setting at the end of life?
    Poulos RG; Harkin D; Poulos CJ; Cole A; MacLeod R
    Health Soc Care Community; 2018 Mar; 26(2):e270-e279. PubMed ID: 29164739
    [TBL] [Abstract][Full Text] [Related]  

  • 23. "It doesn't exist…": negotiating palliative care from a culturally and linguistically diverse patient and caregiver perspective.
    Kirby E; Lwin Z; Kenny K; Broom A; Birman H; Good P
    BMC Palliat Care; 2018 Jul; 17(1):90. PubMed ID: 29966521
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Among neighbors: an ethnographic account of responsibilities in rural palliative care.
    Pesut B; Robinson CA; Bottorff JL
    Palliat Support Care; 2014 Apr; 12(2):127-38. PubMed ID: 23510757
    [TBL] [Abstract][Full Text] [Related]  

  • 25. A knowledge synthesis of culturally- and spiritually-sensitive end-of-life care: findings from a scoping review.
    Fang ML; Sixsmith J; Sinclair S; Horst G
    BMC Geriatr; 2016 May; 16():107. PubMed ID: 27193395
    [TBL] [Abstract][Full Text] [Related]  

  • 26. 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]  

  • 27. The needs of terminally ill cancer patients versus those of caregivers for information regarding prognosis and end-of-life issues.
    Clayton JM; Butow PN; Tattersall MH
    Cancer; 2005 May; 103(9):1957-64. PubMed ID: 15789363
    [TBL] [Abstract][Full Text] [Related]  

  • 28. 'I am part of the community but...' The changing context of rural living for persons with advanced cancer and their families.
    Duggleby WD; Penz K; Leipert BD; Wilson DM; Goodridge D; Williams A
    Rural Remote Health; 2011; 11(3):1733. PubMed ID: 21787109
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Evaluation of a Video-Based Seminar to Raise Health Care Professionals' Awareness of Culturally Sensitive End-of-Life Care.
    Cruz-Oliver DM; Malmstrom TK; Roegner M; Yeo G
    J Pain Symptom Manage; 2017 Oct; 54(4):546-554. PubMed ID: 28716618
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Socio-cultural contexts of end- of- life conversations and decisions: bereaved family cancer caregivers' retrospective co-constructions.
    Githaiga JN; Swartz L
    BMC Palliat Care; 2017 Aug; 16(1):40. PubMed ID: 28806952
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Part 2: Home-based family caregiving at the end of life: a comprehensive review of published qualitative research (1998-2008).
    Funk L; Stajduhar K; Toye C; Aoun S; Grande G; Todd C
    Palliat Med; 2010 Sep; 24(6):594-607. PubMed ID: 20576673
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Challenges in providing breast and cervical cancer screening services to Vietnamese Canadian women: the healthcare providers' perspective.
    Donnelly TT
    Nurs Inq; 2008 Jun; 15(2):158-68. PubMed ID: 18476858
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Gender and family caregiving at the end-of-life in the context of old age: A systematic review.
    Morgan T; Ann Williams L; Trussardi G; Gott M
    Palliat Med; 2016 Jul; 30(7):616-24. PubMed ID: 26814213
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Working with immigrant families raising a child with a disability: challenges and recommendations for healthcare and community service providers.
    Lindsay S; King G; Klassen AF; Esses V; Stachel M
    Disabil Rehabil; 2012; 34(23):2007-17. PubMed ID: 22455458
    [TBL] [Abstract][Full Text] [Related]  

  • 35. An Ecological Understanding of Caregiver Experiences in Palliative Care.
    Chandran D; Corbin JH; Shillam C
    J Soc Work End Life Palliat Care; 2016; 12(1-2):162-82. PubMed ID: 27143579
    [TBL] [Abstract][Full Text] [Related]  

  • 36. The preferences and perspectives of family caregivers towards place of care for their relatives at the end-of-life. A systematic review and thematic synthesis of the qualitative evidence.
    Woodman C; Baillie J; Sivell S
    BMJ Support Palliat Care; 2016 Dec; 6(4):418-429. PubMed ID: 25991565
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Supporting family caregivers at the end of life: "they don't know what they don't know".
    Rabow MW; Hauser JM; Adams J
    JAMA; 2004 Jan; 291(4):483-91. PubMed ID: 14747506
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Belgian general practitioners' perspectives on the use of palliative sedation in end-of-life home care: a qualitative study.
    Sercu M; Pype P; Christiaens T; Derese A; Deveugele M
    J Pain Symptom Manage; 2014 Jun; 47(6):1054-63. PubMed ID: 24095283
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Comparing the experiences of rural and urban family caregivers of the terminally ill.
    Brazil K; Kaasalainen S; Williams A; Rodriguez C
    Rural Remote Health; 2013; 13(1):2250. PubMed ID: 23294373
    [TBL] [Abstract][Full Text] [Related]  

  • 40. 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]  

    [Previous]   [Next]    [New Search]
    of 13.