Citations (61)
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Zeliha Cengiz, Mensure Turan, Dilek Olmaz & Çiğdem Erce. (2021) Care Burden and Quality of Life in Family Caregivers of Palliative Care Patients. Journal of Social Work in End-of-Life & Palliative Care 17:1, pages 50-63.
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Esther V. Hobson, Wendy O. Baird, Rebecca Partridge, Cindy L. Cooper, Susan Mawson, Ann Quinn, Pamela J. Shaw, Theresa Walsh, Daniel Wolstenholme & Christopher J. Mcdermott. (2018) The TiM system: developing a novel telehealth service to improve access to specialist care in motor neurone disease using user-centered design. Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration 19:5-6, pages 351-361.
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Gisella Bruletti, Laura Comini, Simonetta Scalvini, Roberta Morini, Alberto Luisa, Mara Paneroni & Michele Vitacca. (2015) A two-year longitudinal study on strain and needs in caregivers of advanced ALS patients. Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration 16:3-4, pages 187-195.
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Kristen Qutub, David Lacomis, Stephen M. Albert & Eleanor Feingold. (2014) Life factors affecting depression and burden in amyotrophic lateral sclerosis caregivers. Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration 15:3-4, pages 292-297.
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Anne Hogden, David Greenfield, Peter Nugus & Matthew C Kiernan. (2013) What are the roles of carers in decision-making for amyotrophic lateral sclerosis multidisciplinary care?. Patient Preference and Adherence 7, pages 171-181.
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Jan R. Oyebode, Hayley-Jane Smith & Karen Morrison. (2013) The personal experience of partners of individuals with motor neuron disease. Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration 14:1, pages 39-43.
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Anne Hogden, David Greenfield, Peter Nugus & Matthew C Kiernan. (2012) Engaging in patient decision-making in multidisciplinary care for amyotrophic lateral sclerosis: the views of health professionals. Patient Preference and Adherence 6, pages 691-701.
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Mary R. O’Brien, Bridget Whitehead, Barbara A. Jack & J. Douglas Mitchell. (2012) 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. Disability and Rehabilitation 34:3, pages 247-256.
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Judith G. Rabkin, Steven M. Albert, Lewis P. Rowland & Hiroshi Mitsumoto. (2009) How common is depression among ALS caregivers? A longitudinal study. Amyotrophic Lateral Sclerosis 10:5-6, pages 448-455.
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Carmel Armon. (2006) Who cares for the carers?. Amyotrophic Lateral Sclerosis 7:3, pages 131-131.
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Articles from other publishers (42)
Birgitta Jakobsson Larsson, Karin Nordin & Ingela Nygren. (2023) Symptoms of anxiety and depression in patients with amyotrophic lateral sclerosis and their relatives during the disease trajectory. Journal of the Neurological Sciences 455, pages 122780.
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