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.
157 related articles for article (PubMed ID: 32868699)
21. Longitudinal predictors of caregiver burden in amyotrophic lateral sclerosis: a population-based cohort of patient-caregiver dyads. Burke T; Hardiman O; Pinto-Grau M; Lonergan K; Heverin M; Tobin K; Staines A; Galvin M; Pender N J Neurol; 2018 Apr; 265(4):793-808. PubMed ID: 29396678 [TBL] [Abstract][Full Text] [Related]
22. Information Needs and Preferences of Family Caregivers of Patients With Amyotrophic Lateral Sclerosis. J Neurosci Nurs; 2020 Oct; 52(5):E9-E10. PubMed ID: 32890100 [No Abstract] [Full Text] [Related]
23. Burden and preparedness of care partners of people living with amyotrophic lateral sclerosis at home in Korea: A care partner survey. Lee SY; Yoo SH; Cho B; Kim KH; Jang MS; Shin J; Hwang I; Choi SJ; Sung JJ; Kim MS Muscle Nerve; 2024 Sep; 70(3):306-315. PubMed ID: 38760965 [TBL] [Abstract][Full Text] [Related]
24. A two-year longitudinal study on strain and needs in caregivers of advanced ALS patients. Bruletti G; Comini L; Scalvini S; Morini R; Luisa A; Paneroni M; Vitacca M Amyotroph Lateral Scler Frontotemporal Degener; 2015 Jun; 16(3-4):187-95. PubMed ID: 25428808 [TBL] [Abstract][Full Text] [Related]
25. ALS: Family caregiver needs and quality of life. Williams MT; Donnelly JP; Holmlund T; Battaglia M Amyotroph Lateral Scler; 2008 Oct; 9(5):279-86. PubMed ID: 18608102 [TBL] [Abstract][Full Text] [Related]
26. Health-Related Internet Use by Informal Caregivers of Children and Adolescents: An Integrative Literature Review. Park E; Kim H; Steinhoff A J Med Internet Res; 2016 Mar; 18(3):e57. PubMed ID: 26940750 [TBL] [Abstract][Full Text] [Related]
27. Caregiving in ALS - a mixed methods approach to the study of Burden. Galvin M; Corr B; Madden C; Mays I; McQuillan R; Timonen V; Staines A; Hardiman O BMC Palliat Care; 2016 Sep; 15(1):81. PubMed ID: 27596749 [TBL] [Abstract][Full Text] [Related]
28. Impact of patient suffering on caregiver well-being: the case of amyotrophic lateral sclerosis patients and their caregivers. Boerner K; Mock SE Psychol Health Med; 2012; 17(4):457-66. PubMed ID: 22117117 [TBL] [Abstract][Full Text] [Related]
29. Comparing perspectives of family caregivers and healthcare professionals regarding caregiver burden in dementia care: results of a mixed methods study in a rural setting. Krutter S; Schaffler-Schaden D; Essl-Maurer R; Wurm L; Seymer A; Kriechmayr C; Mann E; Osterbrink J; Flamm M Age Ageing; 2020 Feb; 49(2):199-207. PubMed ID: 31875879 [TBL] [Abstract][Full Text] [Related]
30. The burden of apathy for caregivers of patients with amyotrophic lateral sclerosis. Caga J; Hsieh S; Highton-Williamson E; Zoing MC; Ramsey E; Devenney E; Ahmed RM; Hogden A; Kiernan MC Amyotroph Lateral Scler Frontotemporal Degener; 2018 Nov; 19(7-8):599-605. PubMed ID: 30369270 [TBL] [Abstract][Full Text] [Related]
31. Unmet supportive care needs mediate the relationship between functional status and quality of life in patients with amyotrophic lateral sclerosis. Oh J; Kim SH; Kim JA Palliat Support Care; 2019 Dec; 17(6):650-654. PubMed ID: 31104645 [TBL] [Abstract][Full Text] [Related]
32. Bereavement and Support Experiences of Informal Caregivers of Persons with Amyotrophic Lateral Sclerosis: A Qualitative Study. Poppe C; Iseli LM; Verwey M; Wangmo T J Soc Work End Life Palliat Care; 2022; 18(1):63-79. PubMed ID: 34605373 [TBL] [Abstract][Full Text] [Related]
33. Burden, depression, and anxiety in caregivers of people with amyotrophic lateral sclerosis. Pagnini F; Rossi G; Lunetta C; Banfi P; Castelnuovo G; Corbo M; Molinari E Psychol Health Med; 2010 Dec; 15(6):685-93. PubMed ID: 21154021 [TBL] [Abstract][Full Text] [Related]
34. Supportive care needs of patients with amyotrophic lateral sclerosis/motor neuron disease and their caregivers: A scoping review. Oh J; Kim JA J Clin Nurs; 2017 Dec; 26(23-24):4129-4152. PubMed ID: 28681543 [TBL] [Abstract][Full Text] [Related]
35. The amyotrophic lateral sclerosis supportive care needs assessment instrument: Development and psychometric evaluation. Oh J; Oh SI; Kim JA Palliat Support Care; 2018 Dec; 16(6):692-697. PubMed ID: 29375038 [TBL] [Abstract][Full Text] [Related]
36. Need and value of case management in multidisciplinary ALS care: A qualitative study on the perspectives of patients, spousal caregivers and professionals. Bakker M; Creemers H; Schipper K; Beelen A; Grupstra H; Nollet F; Abma T Amyotroph Lateral Scler Frontotemporal Degener; 2015 Jun; 16(3-4):180-6. PubMed ID: 25611162 [TBL] [Abstract][Full Text] [Related]
37. The Palliative Care Information Needs of Patients with Amyotrophic Lateral Sclerosis and their Informal Caregivers: A Scoping Review. Gillespie J; Przybylak-Brouillard A; Watt CL J Pain Symptom Manage; 2021 Oct; 62(4):848-862. PubMed ID: 33757892 [TBL] [Abstract][Full Text] [Related]
38. What do people affected by amyotrophic lateral sclerosis want from health communications? Evidence from the ALS Talk Project. Genuis SK; Luth W; Bubela T; Johnston WS Muscle Nerve; 2023 Sep; 68(3):286-295. PubMed ID: 37462337 [TBL] [Abstract][Full Text] [Related]
39. Caregiver experience, health-related quality of life and life satisfaction among informal caregivers to patients with amyotrophic lateral sclerosis: A cross-sectional study. Sandstedt P; Littorin S; Cröde Widsell G; Johansson S; Gottberg K; Ytterberg C; Olsson M; Widén Holmqvist L; Kierkegaard M J Clin Nurs; 2018 Dec; 27(23-24):4321-4330. PubMed ID: 29964322 [TBL] [Abstract][Full Text] [Related]
40. Discrete choice experiment for eliciting preference for health services for patients with ALS and their informal caregivers. Tobin K; Maguire S; Corr B; Normand C; Hardiman O; Galvin M BMC Health Serv Res; 2021 Mar; 21(1):213. PubMed ID: 33750360 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]