Citations (41)
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Marina Yamamoto, Keiko Tsukasaki & Kaoru Kyota. (2023) Relationship Between Resilience Factors and Caregiving Status of Families of Patients with Amyotrophic Lateral Sclerosis (ALS) in Japan. Journal of Community Health Nursing 0:0, pages 1-13.
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Anna Maksymowicz-Śliwińska, Dorothée Lulé, Krzysztof NieporĘcki, Katarzyna Ciećwierska, Albert C. Ludolph & Magdalena Kuźma-Kozakiewicz. (2023) The quality of life and depression in primary caregivers of patients with amyotrophic lateral sclerosis is affected by patient-related and culture-specific conditions. Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration 24:3-4, pages 317-326.
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Jashelle Caga, Margaret C. Zoing, David Foxe, Eleanor Ramsey, Mirelle D’Mello, Eneida Mioshi, Rebekah M. Ahmed, Matthew C. Kiernan & Olivier Piguet. (2021) Problem-focused coping underlying lower caregiver burden in ALS-FTD: implications for caregiver intervention. Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration 22:5-6, pages 434-441.
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Samar M. Aoun, Paul A. Cafarella, Bruce Rumbold, Geoff Thomas, Anne Hogden, Leanne Jiang, Sonia Gregory & David W. Kissane. (2021) Who cares for the bereaved? A national survey of family caregivers of people with motor neurone disease. Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration 22:1-2, pages 12-22.
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Samar M Aoun, David W Kissane, Paul A. Cafarella, Bruce Rumbold, Anne Hogden, Leanne Jiang & Natasha Bear. (2020) Grief, depression, and anxiety in bereaved caregivers of people with motor neurone disease: a population-based national study. Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration 21:7-8, pages 593-605.
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Juyeon Oh & Jung A. Kim. (2018) Factor analysis of the Zarit Burden Interview in family caregivers of patients with amyotrophic lateral sclerosis. Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration 19:1-2, pages 50-56.
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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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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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Francesco Tramonti, Paolo Bongioanni, Carolina Di Bernardo, Sara Davitti & Bruno Rossi. (2012) Quality of life of patients with amyotrophic lateral sclerosis. Psychology, Health & Medicine 17:5, pages 621-628.
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Kathrin Boerner & StevenE. Mock. (2012) Impact of patient suffering on caregiver well-being: The case of amyotrophic lateral sclerosis patients and their caregivers. Psychology, Health & Medicine 17:4, pages 457-466.
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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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Articles from other publishers (30)
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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Paolo Bongioanni, Gian Domenico Borasio, David J Oliver, Andrea Romagnoli, Karl P Kapitza, Katie Sidle & Francesco Tramonti. (2023) Methods for informing people with amyotrophic lateral sclerosis/motor neuron disease of their diagnosis. Cochrane Database of Systematic Reviews 2023:2.
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Miriam Galvin, Bernie Corr, Caoifa Madden, Iain Mays, Regina McQuillan, Virpi Timonen, Anthony Staines & Orla Hardiman. (2016) Caregiving in ALS – a mixed methods approach to the study of Burden. BMC Palliative Care 15:1.
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