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 *

140 related articles for article (PubMed ID: 34485910)

  • 1. Traumatised, angry, abandoned but some empowered: a national survey of experiences of family caregivers bereaved by motor neurone disease.
    Aoun SM; Noonan K; Thomas G; Rumbold B
    Palliat Care Soc Pract; 2021; 15():26323524211038584. PubMed ID: 34485910
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Who cares for the bereaved? A national survey of family caregivers of people with motor neurone disease.
    Aoun SM; Cafarella PA; Rumbold B; Thomas G; Hogden A; Jiang L; Gregory S; Kissane DW
    Amyotroph Lateral Scler Frontotemporal Degener; 2021 Feb; 22(1-2):12-22. PubMed ID: 32909457
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Grief, depression, and anxiety in bereaved caregivers of people with motor neurone disease: a population-based national study.
    Aoun SM; Kissane DW; Cafarella PA; Rumbold B; Hogden A; Jiang L; Bear N
    Amyotroph Lateral Scler Frontotemporal Degener; 2020 Nov; 21(7-8):593-605. PubMed ID: 32668960
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Why and how the work of Motor Neurone Disease Associations matters before and during bereavement: a consumer perspective.
    Aoun SM; Cafarella PA; Hogden A; Thomas G; Jiang L; Edis R
    Palliat Care Soc Pract; 2021; 15():26323524211009537. PubMed ID: 34104885
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Experiences of burden, needs, rewards and resilience in family caregivers of people living with Motor Neurone Disease/Amyotrophic Lateral Sclerosis: A secondary thematic analysis of qualitative interviews.
    Weisser FB; Bristowe K; Jackson D
    Palliat Med; 2015 Sep; 29(8):737-45. PubMed ID: 25762578
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Building Community Capacity in Bereavement Support.
    Breen LJ; Aoun SM; Rumbold B; McNamara B; Howting DA; Mancini V
    Am J Hosp Palliat Care; 2017 Apr; 34(3):275-281. PubMed ID: 26566928
    [TBL] [Abstract][Full Text] [Related]  

  • 7. "It still haunts me whether we did the right thing": a qualitative analysis of free text survey data on the bereavement experiences and support needs of family caregivers.
    Harrop E; Morgan F; Byrne A; Nelson A
    BMC Palliat Care; 2016 Nov; 15(1):92. PubMed ID: 27825330
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. The journey with dementia from the perspective of bereaved family caregivers: a qualitative descriptive study.
    Peacock SC; Hammond-Collins K; Forbes DA
    BMC Nurs; 2014; 13(1):42. PubMed ID: 25435810
    [TBL] [Abstract][Full Text] [Related]  

  • 10. What sources of bereavement support are perceived helpful by bereaved people and why? Empirical evidence for the compassionate communities approach.
    Aoun SM; Breen LJ; White I; Rumbold B; Kellehear A
    Palliat Med; 2018 Sep; 32(8):1378-1388. PubMed ID: 29754514
    [TBL] [Abstract][Full Text] [Related]  

  • 11. The experiences of, and need for, palliative care for people with motor neurone disease and their informal caregivers: A qualitative systematic review.
    Flemming K; Turner V; Bolsher S; Hulme B; McHugh E; Watt I
    Palliat Med; 2020 Jun; 34(6):708-730. PubMed ID: 32286157
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. Family Caregivers' Experiences with Dying and Bereavement of Individuals with Motor Neuron Disease in India.
    Warrier MG; Thomas PT; Sadasivan A; Balasubramaniam B; Vengalil S; Nashi S; Preethish-Kumar V; Polavarapu K; Mahajan NP; Chevula PCR; Nalini A
    J Soc Work End Life Palliat Care; 2019; 15(2-3):111-125. PubMed ID: 31373263
    [TBL] [Abstract][Full Text] [Related]  

  • 14. The use of digital legacies with people affected by motor neurone disease for continuing bonds: An interpretative phenomenological analysis study.
    Clabburn O; Knighting K; Jack BA; O'Brien MR
    Palliat Med; 2019 Jul; 33(7):812-822. PubMed ID: 31023181
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Non-finite loss and emotional labour: family caregivers' experiences of living with motor neurone disease.
    Ray RA; Street AF
    J Clin Nurs; 2007 Mar; 16(3A):35-43. PubMed ID: 17518867
    [TBL] [Abstract][Full Text] [Related]  

  • 16. "How Long Can I Carry On?" The Need for Palliative Care in Parkinson's Disease: A Qualitative Study from the Perspective of Bereaved Family Caregivers.
    Lennaerts-Kats H; Ebenau A; Steppe M; van der Steen JT; Meinders MJ; Vissers K; Munneke M; Groot M; Bloem BR
    J Parkinsons Dis; 2020; 10(4):1631-1642. PubMed ID: 32651330
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Bereaved Caregivers to Patients With High-Grade Glioma: A Qualitative Explorative Study.
    Piil K; Jarden M
    J Neurosci Nurs; 2018 Apr; 50(2):94-99. PubMed ID: 29401154
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Identifying and addressing the support needs of family caregivers of people with motor neurone disease using the Carer Support Needs Assessment Tool.
    Aoun SM; Deas K; Kristjanson LJ; Kissane DW
    Palliat Support Care; 2017 Feb; 15(1):32-43. PubMed ID: 27173737
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Health profiles of spouse caregivers: The role of active coping and the risk for developing prolonged grief symptoms.
    Miller LM; Utz RL; Supiano K; Lund D; Caserta MS
    Soc Sci Med; 2020 Dec; 266():113455. PubMed ID: 33126099
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Qualitative exploration of emotional and social changes from diagnosis to bereavement for spousal caregivers of persons with dementia.
    Gibson K; Peacock S; Bayly M
    BMJ Open; 2019 Sep; 9(9):e031423. PubMed ID: 31551389
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.