Citations (29)
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Gina Wieringa, Maria Dale & Fiona J. R. Eccles. (2022) Adjusting to living with Parkinson’s disease; a meta-ethnography of qualitative research. Disability and Rehabilitation 44:23, pages 6949-6968.
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Alison Rowsell, Ann Ashburn, Carolyn Fitton, Victoria A. Goodwin, Sophia Hulbert, Sarah E. Lamb, Emma McIntosh, Alice Nieuwboer, Ruth Pickering, Lynn Rochester, Kim Chivers-Seymour & Claire Ballinger. (2022) Participant expectations and experiences of a tailored physiotherapy intervention for people with Parkinson’s and a history of falls. Disability and Rehabilitation 44:5, pages 727-735.
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Supreet Kaur Bhasin & Ishita U. Bharadwaj. (2021) Perceptions and meanings of living with Parkinson’s disease: an account of caregivers lived experiences. International Journal of Qualitative Studies on Health and Well-being 16:1.
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Joyce S. Sabari, Diego Ortiz, Katie Pallatto, Joanna Yagerman, Sofya Glazman & Ivan Bodis-Wollner. (2015) Activity engagement and health quality of life in people with Parkinson’s disease. Disability and Rehabilitation 37:16, pages 1411-1415.
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Radka Ghorbani Saeedian, Iveta Nagyova, Martina Krokavcova, Matej Skorvanek, Jaroslav Rosenberger, Zuzana Gdovinova, Johan W. Groothoff & Jitse P. van Dijk. (2014) The role of social support in anxiety and depression among Parkinson’s disease patients. Disability and Rehabilitation 36:24, pages 2044-2049.
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Linda Dauwerse, Annette Hendrikx, Karen Schipper, Chris Struiksma & Tineke A. Abma. (2014) Quality-of-life of patients with Parkinson’s disease. Brain Injury 28:10, pages 1342-1352.
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Gerda Drutyte, Maria João Forjaz, Carmen Rodriguez-Blazquez, Pablo Martinez-Martin & Kieran C. Breen. (2014) What impacts on the stress symptoms of Parkinson’s carers? Results from the Parkinson’s UK Members’ Survey. Disability and Rehabilitation 36:3, pages 199-204.
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Articles from other publishers (20)
Deborah Hersh, Shi Jing Kong & Jessica Smith. (2023)
It's quite good fun
: A qualitative study of a singing/songwriting programme for people with Parkinson's disease and their spouses
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Angelika D. Geerlings, Willanka M. Kapelle, Charlotte J. Sederel, Emma Tenison, Hilde Wijngaards-Berenbroek, Marjan J. Meinders, Marten Munneke, Yoav Ben-Shlomo, Bastiaan R. Bloem & Sirwan K. L. Darweesh. (2023) Caregiver burden in Parkinson’s disease: a mixed-methods study. BMC Medicine 21:1.
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Inbal Bar-On, Gili Mayo & Shelly Levy-Tzedek. (2023) Socially Assistive Robots for Parkinson's Disease: Needs, Attitudes and Specific Applications as Identified by Healthcare Professionals. ACM Transactions on Human-Robot Interaction 12:1, pages 1-25.
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Hyun-Se Choi & Seung-Hyun Cho. (2022) Effects of Multimodal Rehabilitation on the Activities of Daily Living, Quality of Life, and Burden of Care for Patients with Parkinson’s Disease: A Randomized Control Study. Healthcare 10:10, pages 1888.
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Emilie Constant, Elodie Brugallé, Emilie Wawrziczny, Céline Sokolowski, Charlotte Manceau, Bérengère Flinois, Guillaume Baille, Defebvre Luc, Kathy Dujardin & Pascal Antoine. (2022) Relationship Dynamics of Couples Facing Advanced-Stage Parkinson’s Disease: A Dyadic Interpretative Phenomenological Analysis. Frontiers in Psychology 12.
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Qian Yue Tan, Natalie J. Cox, Stephen E.R. Lim, Laura Coutts, Simon D.S. Fraser, Helen C. Roberts & Kinda Ibrahim. (2021) The Experiences of Treatment Burden in People with Parkinson’s Disease and Their Caregivers: A Systematic Review of Qualitative Studies. Journal of Parkinson's Disease 11:4, pages 1597-1617.
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Caroline J. Deutsch, Noelle Robertson & Janis M. Miyasaki. (2021) Psychological Impact of Parkinson Disease Delusions on Spouse Caregivers: A Qualitative Study. Brain Sciences 11:7, pages 871.
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Nena Kruithof, Marjan Johanna Traa, Maria Karabatzakis, Suzanne Polinder, Jolanda de Vries & Mariska Adriana Cornelia de Jongh. (2018) Perceived Changes in Quality of Life in Trauma Patients: A Focus Group Study. Journal of Trauma Nursing 25:3, pages 177-186.
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I. Guimaraes, R. Cardoso, S. Pinto & J.J. Ferreira. (2017) The Psychometric Properties of the Voice Handicap Index in People With Parkinson's Disease. Journal of Voice 31:2, pages 258.e13-258.e18.
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Xiao-Jing Tu, Wen-Juh Hwang, Shih-Pin Hsu & Hui-Ing Ma. (2017) Responsiveness of the short-form health survey and the Parkinson’s disease questionnaire in patients with Parkinson’s disease. Health and Quality of Life Outcomes 15:1.
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Danice B. Greer, Melinda Hermanns & Cheryl M. Cooper. (2015) Making Lemonade Out of Life’s Lemons: A View Into the World of Aging With Parkinson’s Disease. Journal of Psychosocial Nursing and Mental Health Services 53:7, pages 20-23.
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Radka Ghorbani Saeedian, Iveta Nagyova, Daniel Klein, Matej Skorvanek, Jaroslav Rosenberger, Zuzana Gdovinova, Johan W Groothoff & Jitse P van Dijk. (2014) Self-rated health mediates the association between functional status and health-related quality of life in Parkinson's disease. Journal of Clinical Nursing 23:13-14, pages 1970-1977.
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Ramona Lucas-Carrasco, Brenda L. Den Oudsten, Erhan Eser & Michael J. Power. (2014) Using the Satisfaction with Life Scale in People with Parkinson’s Disease: A Validation Study in Different European Countries. The Scientific World Journal 2014, pages 1-7.
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Andrew Soundy, Brendon Stubbs & Carolyn Roskell. (2014) The Experience of Parkinson’s Disease: A Systematic Review and Meta-Ethnography. The Scientific World Journal 2014, pages 1-19.
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Ingrid H Sturkenboom, Maud J Graff, George F Borm, Yvonne Veenhuizen, Bastiaan R Bloem, Marten Munneke & Maria W Nijhuis-van der Sanden. (2012) The impact of occupational therapy in Parkinson’s disease: a randomized controlled feasibility study. Clinical Rehabilitation 27:2, pages 99-112.
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Anita Palepu, Anita M Hubley, Lara B Russell, Anne M Gadermann & Mary Chinni. (2012) Quality of life themes in Canadian adults and street youth who are homeless or hard-to-house: A multi-site focus group study. Health and Quality of Life Outcomes 10:1, pages 93.
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