Citations (60)
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Christopher Poppe, Insa Koné, Luzia Margarete Iseli, Kathi Schweikert, Bernice Simone Elger & Tenzin Wangmo. (2020) Differentiating needs of informal caregivers of individuals with ALS across the caregiving course: a systematic review. Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration 21:7-8, pages 519-541.
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Louise Sofia Madsen, Jørgen Jeppesen & Charlotte Handberg. (2019) “Understanding my ALS”. Experiences and reflections of persons with amyotrophic lateral sclerosis and relatives on participation in peer group rehabilitation. Disability and Rehabilitation 41:12, pages 1410-1418.
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Geraldine Foley & Geralyn Hynes. (2018) Decision-making among patients and their family in ALS care: a review. Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration 19:3-4, pages 173-193.
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Samar M Aoun, Lauren J Breen, Denise Howting, Robert Edis, David Oliver, Robert Henderson, Margaret O’Connor, Rodney Harris & Carol Birks. (2016) Receiving the news of a diagnosis of motor neuron disease: What does it take to make it better?. Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration 17:3-4, pages 168-178.
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Jane Grose, Jennifer Freeman & Jonathon Marsden. (2014) Service delivery for people with hereditary spastic paraparesis living in the South West of England. Disability and Rehabilitation 36:11, pages 907-913.
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