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Louise Glover, Clare Dixon, Christopher Kobylecki & Fiona J. R. Eccles. (2023) Parkinson’s and the couple relationship: a qualitative meta-synthesis. Aging & Mental Health 0:0, pages 1-10.
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Yi-Wen Chen, Chu-Yun Huang, Jo-Hsin Chen, Chi-Lien Hsiao, Chien-Tai Hong, Chen-Yu Wu & Elizabeth H. Chang. (2022) Living with Parkinson’s disease: disease and medication experiences of patients and caregivers. International Journal of Qualitative Studies on Health and Well-being 17:1.
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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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Articles from other publishers (37)
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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Whitley W. Aamodt, Benzi M. Kluger, Miray Mirham, Anna Job, Samantha E. Lettenberger, Philip E. Mosley & Sandhya Seshadri. (2023) Caregiver Burden in Parkinson Disease: A Scoping Review of the Literature from 2017-2022. Journal of Geriatric Psychiatry and Neurology.
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Katy Gallop, Ngan Pham, Grant Maclaine, Emma Saunders, Bonnie Black & Sarah Acaster. (2023) Exploring the impact of caring for an individual with neurogenic orthostatic hypotension: a qualitative study. Neurodegenerative Disease Management 13:3, pages 191-201.
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Ian W. Garner, Craig D. Murray, Fiona J. R. Eccles, Nicolò Zarotti & Jane Simpson. (2023) “I Feel Like I Work Full-Time for Parkinson’s”: A Longitudinal Interpretative Phenomenological Analysis of the Experiences of Parkinson’s Informal Caregivers during COVID-19 in England. NeuroSci 4:2, pages 105-117.
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Ellen Gabrielsen Hjelle, Helle Rønn-Smidt, Anita Haahr, Silje Bjørnsen Haavaag, Dorthe Sørensen, Maria Victoria Navarta-Sánchez, Mari Carmen Portillo & Line Kildal Bragstad. (2023) Filling the gap in service provision. Partners as family carers to people with Parkinson's disease: A Scandinavian perspective. Chronic Illness, pages 174239532311744.
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Joy Read, Sarah Cable, Gergely Bartl, Charlotte Löfqvist, Susanne Iwarsson & Anette Schrag. (2023) The Lived Experience of Caregiving and Perception of Service Provision among Family-Caregivers of People with Late-Stage Parkinson’s: A Qualitative Study. Parkinson's Disease 2023, pages 1-12.
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Kantor Jiří. 2023. Speciální pedagogika osob s omezením pohyblivosti a koncept praxe založené na důkazech. Speciální pedagogika osob s omezením pohyblivosti a koncept praxe založené na důkazech.
Martyarini Budi Setyawati, John Parson, Bobbi Brennan Laing, Cecilia Wong-Cornall & Christantie Effendy. (2023) Positive Experience of Parkinson’s Disease Family Caregivers and why is this Significant in COVID Times?. Open Access Macedonian Journal of Medical Sciences 11:F, pages 20-30.
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Angelika D. Geerlings, Marjan J. Meinders, Bastiaan R. Bloem & Marjolein A. van der Marck. (2022) Using former carers’ expertise in peer support for carers of people with Parkinson’s Disease. npj Parkinson's Disease 8:1.
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Xiaohui Zhong, Priscilla P. Song, Zhe Wang & Honglin Chen. (2021) Resilience building among Chinese family caregivers of older people with Parkinson’s disease in Shanghai. Health & Social Care in the Community 30:5.
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Bethany Atkins, Debi Bhattacharya, Caroline Smith & Sion Scott. (2022) Barriers and enablers to switching from a solid to a liquid formulation of Parkinson’s medication: a theory-based mixed methods investigation. International Journal of Clinical Pharmacy 44:4, pages 1046-1056.
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Tamami Shiba, Miyae Yamakawa, Yoshimi Endo, Rie Konno & Satoshi Tanimukai. (2022) Experiences of families of people living with frontotemporal dementia: a qualitative systematic review. Psychogeriatrics 22:4, pages 530-543.
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Dawn R. White & Patrick Albert Palmieri. (2022) Women Caring for Husbands Living with Parkinson’s Disease: A Phenomenological Study Protocol. Journal of Personalized Medicine 12:5, pages 659.
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Lisa Damron, Ece Bayram, Kevin McGehrin, Jane Reynolds, Robert Hess, David G. Coughlin & Irene Litvan. (2022)
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Dying: Access and Utilization in Patients with Movement Disorders
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Catharina Muente, Ann-Kristin Folkerts, Elke Kalbe, Franziska Thieken, Laura-Elisa Assmann, Maria Widritzki, Carsten Eggers, David Pedrosa & Marcel Wilhelm. (2022) Supporting Relatives Prior to Caregiver Burden—Preventive E-Mental Health Short Intervention for Family Members of Individuals with Parkinsonism in an Early Phase of the Disease: Protocol for a Feasibility Study. Brain Sciences 12:4, pages 442.
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Yolanda María Chacón Gámez, Florian Brugger & Nikola Biller-Andorno. (2021) Parkinson’s Disease and Deep Brain Stimulation Have an Impact on My Life: A Multimodal Study on the Experiences of Patients and Family Caregivers. International Journal of Environmental Research and Public Health 18:18, pages 9516.
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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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Monica Scharfenort, Jonathan Timpka, Thomas Sahlström, Tove Henriksen, Dag Nyholm & Per Odin. (2021) Close relationships in Parkinson´s disease patients with device‐aided therapy. Brain and Behavior 11:6.
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Melinda Hermanns, Beth Mastel-Smith, Rachel Donnell, Allison Quarles, Melissa Rodriguez & Tianjing Wang. (2021) Counterpunching to improve the health of people with Parkinson's disease. Journal of the American Association of Nurse Practitioners 33:12, pages 1230-1239.
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María Victoria Navarta‐Sánchez, Leire Ambrosio, Mari Carmen Portillo, Maria Eugenia Ursúa, Juana M. Senosiain & Mario Riverol. (2020) Evaluation of a psychoeducational intervention compared with education in people with Parkinson's disease and their informal caregivers: a quasi‐experimental study. Journal of Advanced Nursing 76:10, pages 2719-2732.
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Carmen M. Tyler, Richard S. Henry, Paul B. Perrin, Jack Watson, Teresita Villaseñor, Sarah K. Lageman, Erin R. Smith, Genoveva Rizo Curiel, Judith Avila, Miriam E. Jimenez Maldonado & Jose A. Soto-Escageda. (2020) Structural Equation Modeling of Parkinson’s Caregiver Social Support, Resilience, and Mental Health: A Strength-Based Perspective. Neurology Research International 2020, pages 1-8.
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Tara Rastgardani, Melissa J. Armstrong, Anna R. Gagliardi, Arthur Grabovsky & Connie Marras. (2020) Experience and Impact of OFF Periods in Parkinson’s Disease: A Survey of Physicians, Patients, and Carepartners. Journal of Parkinson's Disease 10:1, pages 315-324.
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Jennifer Martin, Meredith Butler, Anne Muldowney & Gabriel Aleksandrs. (2019) Carers of people from LGBTQ communities interactions with mental health service providers: Conflict and safety. International Journal of Mental Health Nursing 28:3, pages 766-775.
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Tara Rastgardani, Melissa J. Armstrong, Connie Marras & Anna R. Gagliardi. (2019) Improving patient‐centred care for persons with Parkinson's: Qualitative interviews with care partners about their engagement in discussions of “off” periods. Health Expectations 22:3, pages 555-564.
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Jennifer Martin, Meredith Butler, Anne Muldowney & Gabriel Aleksandrs. (2019) Impacts of regulatory processes on the experiences of carers of people in LGBTQ communities living with mental illness or experiencing a mental health crisis. Social Science & Medicine 230, pages 30-36.
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