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Research Reports

Communication and Huntington's disease: qualitative interviews and focus groups with persons with Huntington's disease, family members, and carers

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Pages 381-393 | Received 11 Jan 2009, Accepted 09 Jun 2009, Published online: 09 Feb 2010

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Carey Wexler Sherman, Ravi Iyer, Victor Abler, Alexandria Antonelli & Noelle E. Carlozzi. (2020) Perceptions of the impact of chorea on health-related quality of life in Huntington disease (HD): A qualitative analysis of individuals across the HD spectrum, family members, and clinicians. Neuropsychological Rehabilitation 30:6, pages 1150-1168.
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Anna M. Carmichael, Muireann Irish, Yifat Glikmann-Johnston & Julie C. Stout. (2019) Discrete changes in the frequency and functions of autobiographical reminiscence in Huntington's disease. Memory 27:10, pages 1345-1351.
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Monique van Bruggen-Rufi, Annemieke Vink, Wilco Achterberg & Raymund Roos. (2018) Improving quality of life in patients with Huntington’s disease through music therapy: A qualitative explorative study using focus group discussions. Nordic Journal of Music Therapy 27:1, pages 44-66.
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Melinda S. Kavanaugh, Hyunjin Noh & Lixia Zhang. (2016) Caregiving Youth Knowledge and Perceptions of Parental End-of-Life Wishes in Huntington’s Disease. Journal of Social Work in End-of-Life & Palliative Care 12:4, pages 348-365.
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Lisa Hallberg, Elin Mellgren, Lena Hartelius & Ulrika Ferm. (2013) Talking Mats in a discussion group for people with Huntington’s disease. Disability and Rehabilitation: Assistive Technology 8:1, pages 67-76.
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Nick Miller, Jill Taylor, Chloe Howe & Jennifer Read. (2011) Living with foreign accent syndrome: Insider perspectives. Aphasiology 25:9, pages 1053-1068.
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