BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

456 related articles for article (PubMed ID: 22987493)

  • 21. What makes grief difficult? Perspectives from bereaved family caregivers and healthcare providers of advanced cancer patients.
    Stajduhar KI; Martin W; Cairns M
    Palliat Support Care; 2010 Sep; 8(3):277-89. PubMed ID: 20875171
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Signs of post-traumatic stress disorder in caregivers following an expected death: a qualitative study.
    Sanderson C; Lobb EA; Mowll J; Butow PN; McGowan N; Price MA
    Palliat Med; 2013 Jul; 27(7):625-31. PubMed ID: 23579259
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Bereavement support for family caregivers: The gap between guidelines and practice in palliative care.
    Aoun SM; Rumbold B; Howting D; Bolleter A; Breen LJ
    PLoS One; 2017; 12(10):e0184750. PubMed ID: 28977013
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Factors associated with positive consequences of serving as a family caregiver for a terminal cancer patient.
    Kang J; Shin DW; Choi JE; Sanjo M; Yoon SJ; Kim HK; Oh MS; Kwen HS; Choi HY; Yoon WH
    Psychooncology; 2013 Mar; 22(3):564-71. PubMed ID: 22275212
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Preparing family caregivers for death and bereavement. Insights from caregivers of terminally ill patients.
    Hebert RS; Schulz R; Copeland VC; Arnold RM
    J Pain Symptom Manage; 2009 Jan; 37(1):3-12. PubMed ID: 18538977
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Effectiveness of a specialized outpatient palliative care service as experienced by patients and caregivers.
    Groh G; Vyhnalek B; Feddersen B; Führer M; Borasio GD
    J Palliat Med; 2013 Aug; 16(8):848-56. PubMed ID: 23678854
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Post-mortal bereavement of family caregivers in Germany: a prospective interview-based investigation.
    Wiese CH; Morgenthal HC; Bartels UE; Vossen-Wellmann A; Graf BM; Hanekop GG
    Wien Klin Wochenschr; 2010 Jul; 122(13-14):384-9. PubMed ID: 20602281
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Motor Neurone Disease family carers' experiences of caring, palliative care and bereavement: an exploratory qualitative study.
    Aoun SM; Connors SL; Priddis L; Breen LJ; Colyer S
    Palliat Med; 2012 Sep; 26(6):842-50. PubMed ID: 21775409
    [TBL] [Abstract][Full Text] [Related]  

  • 29. A survey of bereaved family members to assess quality of care on a palliative care unit.
    Roza KA; Lee EJ; Meier DE; Goldstein NE
    J Palliat Med; 2015 Apr; 18(4):358-65. PubMed ID: 25793359
    [TBL] [Abstract][Full Text] [Related]  

  • 30. The spiritual meaning of pre-loss music therapy to bereaved caregivers of advanced cancer patients.
    Magill L
    Palliat Support Care; 2009 Mar; 7(1):97-108. PubMed ID: 19619379
    [TBL] [Abstract][Full Text] [Related]  

  • 31. End-of-life care research with bereaved informal caregivers--analysis of recruitment strategy and participation rate from a multi-centre validation study.
    Stiel S; Heckel M; Bussmann S; Weber M; Ostgathe C
    BMC Palliat Care; 2015 May; 14():21. PubMed ID: 25934560
    [TBL] [Abstract][Full Text] [Related]  

  • 32. [Experiences in bereavement care for caregivers].
    Kondo F; Hasegawa S; Mimuro A; Nakajima H; Toyoda Y; Uchida K; Felicia MW; Francine G
    Gan To Kagaku Ryoho; 2002 Dec; 29 Suppl 3():547-50. PubMed ID: 12536847
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Inner power, physical strength and existential well-being in daily life: relatives' experiences of receiving soft tissue massage in palliative home care.
    Cronfalk BS; Strang P; Ternestedt BM
    J Clin Nurs; 2009 Aug; 18(15):2225-33. PubMed ID: 19583654
    [TBL] [Abstract][Full Text] [Related]  

  • 34. 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]  

  • 35. Perceptual consistency of pain and quality of life between hospice cancer patients and family caregivers: a pilot study.
    Tu MS; Chiou CP
    Int J Clin Pract; 2007 Oct; 61(10):1686-91. PubMed ID: 17537189
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Distress and quality of life concerns of family caregivers of patients undergoing palliative surgery.
    Juarez G; Ferrell B; Uman G; Podnos Y; Wagman LD
    Cancer Nurs; 2008; 31(1):2-10. PubMed ID: 18176125
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Bereaved carers' accounts of the end of life and the role of care providers in a 'good death': A qualitative study.
    Holdsworth LM
    Palliat Med; 2015 Oct; 29(9):834-41. PubMed ID: 25944545
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Quality of life and mental health in caregivers of outpatients with advanced cancer.
    Wadhwa D; Burman D; Swami N; Rodin G; Lo C; Zimmermann C
    Psychooncology; 2013 Feb; 22(2):403-10. PubMed ID: 22135229
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Evaluating palliative care: bereaved family members' evaluations of patients' pain, anxiety and depression.
    McPherson CJ; Addington-Hall JM
    J Pain Symptom Manage; 2004 Aug; 28(2):104-14. PubMed ID: 15276191
    [TBL] [Abstract][Full Text] [Related]  

  • 40. A Nationwide Survey of Quality of End-of-Life Cancer Care in Designated Cancer Centers, Inpatient Palliative Care Units, and Home Hospices in Japan: The J-HOPE Study.
    Miyashita M; Morita T; Sato K; Tsuneto S; Shima Y
    J Pain Symptom Manage; 2015 Jul; 50(1):38-47.e3. PubMed ID: 25656327
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 23.