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 *

138 related articles for article (PubMed ID: 31242093)

  • 1. Making her end of life her own: further reflections on supporting a loved one with motor neurone disease.
    Harris DA; Jack K; Wibberley C
    Int J Palliat Nurs; 2019 Jun; 25(6):284-292. PubMed ID: 31242093
    [TBL] [Abstract][Full Text] [Related]  

  • 2. The meaning of living with uncertainty for people with motor neurone disease.
    Harris DA; Jack K; Wibberley C
    J Clin Nurs; 2018 May; 27(9-10):2062-2071. PubMed ID: 29518277
    [TBL] [Abstract][Full Text] [Related]  

  • 3. The need to consider 'temporality' in person-centred care of people with motor neurone disease.
    Harris DA; Jack K; Wibberley C
    J Eval Clin Pract; 2023 Aug; 29(5):802-807. PubMed ID: 37357676
    [TBL] [Abstract][Full Text] [Related]  

  • 4. End of life decision making when home mechanical ventilation is used to sustain breathing in Motor Neurone Disease: patient and family perspectives.
    Wilson E; Palmer J; Armstrong A; Messer B; Presswood E; Faull C
    BMC Palliat Care; 2024 May; 23(1):115. PubMed ID: 38698397
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Lived-through past, experienced present, anticipated future: Understanding "existential loss" in the context of life-limiting illness.
    Harris DA
    Palliat Support Care; 2015 Dec; 13(6):1579-94. PubMed ID: 26063467
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Dying with motor neurone disease, what can we learn from family caregivers?
    Ray RA; Brown J; Street AF
    Health Expect; 2014 Aug; 17(4):466-76. PubMed ID: 22512686
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Australian family carer responses when a loved one receives a diagnosis of Motor Neurone Disease-"Our life has changed forever".
    O'Connor M; Aoun SM; Breen LJ
    Health Soc Care Community; 2018 May; 26(3):e415-e421. PubMed ID: 29359485
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Healthcare professionals' accounts of challenges in managing motor neurone disease in primary healthcare: a qualitative study.
    Lerum SV; Solbraekke KN; Frich JC
    Health Soc Care Community; 2017 Jul; 25(4):1355-1363. PubMed ID: 28226395
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Palliative care experiences of adult cancer patients from ethnocultural groups: a qualitative systematic review protocol.
    Busolo D; Woodgate R
    JBI Database System Rev Implement Rep; 2015 Jan; 13(1):99-111. PubMed ID: 26447011
    [TBL] [Abstract][Full Text] [Related]  

  • 10. The End-of-Life Experiences of People with Motor Neuron Disease: Family Carers' Perspectives.
    Bentley B; O'Connor M
    J Palliat Med; 2016 Aug; 19(8):857-62. PubMed ID: 27135175
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Patients' perspectives of multidisciplinary home-based e-Health service delivery for motor neurone disease.
    James N; Power E; Hogden A; Vucic S
    Disabil Rehabil Assist Technol; 2019 Oct; 14(7):737-743. PubMed ID: 30182780
    [No Abstract]   [Full Text] [Related]  

  • 12. Experiences of dying, death and bereavement in motor neurone disease: a qualitative study.
    Whitehead B; O'Brien MR; Jack BA; Mitchell D
    Palliat Med; 2012 Jun; 26(4):368-78. PubMed ID: 21712334
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Lived Experience of Spouses of Persons with Motor Neuron Disease: Preliminary Findings through Interpretative Phenomenological Analysis.
    Warrier MG; Sadasivan A; Polavarapu K; Kumar VP; Mahajan NP; Reddy CPC; Vengalil S; Nashi S; Nalini A; Thomas PT
    Indian J Palliat Care; 2020; 26(1):60-65. PubMed ID: 32132786
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. Living with motor neurone disease: lives, experiences of services and suggestions for change.
    Hughes RA; Sinha A; Higginson I; Down K; Leigh PN
    Health Soc Care Community; 2005 Jan; 13(1):64-74. PubMed ID: 15717908
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. Understanding psycho-social processes underpinning engagement with services in motor neurone disease: a qualitative study.
    Foley G; Timonen V; Hardiman O
    Palliat Med; 2014 Apr; 28(4):318-25. PubMed ID: 24637571
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Staying just one step ahead: providing care for patients with motor neurone disease.
    McConigley R; Kristjanson LJ; Aoun SM; Oldham L; Currow DC; O'Connor M; Holloway K
    BMJ Support Palliat Care; 2014 Mar; 4(1):38-42. PubMed ID: 24644769
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Exploring the transitional process from receiving a diagnosis to living with motor neurone disease.
    Mistry K; Simpson J
    Psychol Health; 2013; 28(8):939-53. PubMed ID: 23464923
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Feasibility, acceptability, and potential effectiveness of dignity therapy for people with motor neurone disease.
    Bentley B; O'Connor M; Kane R; Breen LJ
    PLoS One; 2014; 9(5):e96888. PubMed ID: 24816742
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.