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.
1146 related articles for article (PubMed ID: 15717908)
1. 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]
2. Experiences of living with motor neurone disease: a review of qualitative research. Sakellariou D; Boniface G; Brown P Disabil Rehabil; 2013 Oct; 35(21):1765-73. PubMed ID: 23336121 [TBL] [Abstract][Full Text] [Related]
3. 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]
4. Palliative care for patients with motor neurone disease and their bereaved carers: a qualitative study. Mc Veigh C; Donaghy C; Mc Laughlin B; Dick A; Kaur K; Mc Conville J; Watson M BMC Palliat Care; 2019 Apr; 18(1):39. PubMed ID: 31027498 [TBL] [Abstract][Full Text] [Related]
5. 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]
6. The impact of communication on healthcare involvement for people living with motor neurone disease and their carers: A longitudinal qualitative study. Paynter C; Mathers S; Gregory H; Vogel AP; Cruice M Int J Lang Commun Disord; 2022 Nov; 57(6):1318-1333. PubMed ID: 35860953 [TBL] [Abstract][Full Text] [Related]
7. 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]
8. Implementation and evaluation of an education program to guide palliative care for people with motor neurone disease. McConigley R; Aoun S; Kristjanson L; Colyer S; Deas K; O'Connor M; Harris R; Currow D; Yates P Palliat Med; 2012 Dec; 26(8):994-1000. PubMed ID: 22064045 [TBL] [Abstract][Full Text] [Related]
9. 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]
10. 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]
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. Access to palliative care for people with motor neurone disease in New Zealand. McKenna C; MacLeod R N Z Med J; 2005 Sep; 118(1222):U1667. PubMed ID: 16222359 [TBL] [Abstract][Full Text] [Related]
13. Health care professionals' views on psychological factors affecting nutritional behaviour in people with motor neuron disease: A thematic analysis. Zarotti N; Coates E; McGeachan A; Williams I; Beever D; Hackney G; Norman P; Stavroulakis T; White D; White S; Halliday V; McDermott C; Br J Health Psychol; 2019 Nov; 24(4):953-969. PubMed ID: 31449739 [TBL] [Abstract][Full Text] [Related]
14. 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]
15. Meeting the needs of parents around the time of diagnosis of disability among their children: evaluation of a novel program for information, support, and liaison by key workers. Rahi JS; Manaras I; Tuomainen H; Hundt GL Pediatrics; 2004 Oct; 114(4):e477-82. PubMed ID: 15466074 [TBL] [Abstract][Full Text] [Related]
16. 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]
17. Social services homecare for people with motor neurone disease/amyotrophic lateral sclerosis: why are such services used or refused? O'Brien MR; Whitehead B; Murphy PN; Mitchell JD; Jack BA Palliat Med; 2012 Mar; 26(2):123-31. PubMed ID: 21383059 [TBL] [Abstract][Full Text] [Related]
18. Health professionals' responses to multiple sclerosis and motor neurone disease. Carter H; McKenna C; MacLeod R; Green R Palliat Med; 1998 Sep; 12(5):383-94. PubMed ID: 9924601 [TBL] [Abstract][Full Text] [Related]
19. 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]
20. 'All in the same boat'? Patient and carer attitudes to peer support and social comparison in Motor Neurone Disease (MND). Locock L; Brown JB Soc Sci Med; 2010 Oct; 71(8):1498-505. PubMed ID: 20719422 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]