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Research Papers

An interpretative phenomenological analysis of delusions in people with Parkinson's disease

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Pages 1291-1299 | Accepted 01 Nov 2009, Published online: 20 Jan 2010

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Read on this site (3)

Jennifer A. Foley, Cliff Chen, Andrew Paget & Lisa Cipolotti. (2023) A Bayesian predictive processing account of Othello syndrome in Parkinson’s disease. Cognitive Neuropsychiatry 28:4, pages 269-284.
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Sarah Parry, Mike Lloyd & Jane Simpson. (2017) Experiences of therapeutic relationships on hospital wards, dissociation, and making connections. Journal of Trauma & Dissociation 18:4, pages 544-558.
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Jane Simpson, Helen McMillan, Ira Leroi & Craig D. Murray. (2015) Experiences of apathy in people with Parkinson’s disease: a qualitative exploration. Disability and Rehabilitation 37:7, pages 611-619.
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Articles from other publishers (13)

Krisna Patel, Alastair Cardno & Tom Isherwood. (2023) ‘ Like I said about culture. You don't talk about mental health ’ : An interpretative phenomenological analysis of the experience of first‐episode psychosis in South Asian individuals . Early Intervention in Psychiatry 17:8, pages 771-783.
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G PRAKASHA & Anthony KENNETH. (2022) COVID-19 sırasında 12. sınıf öğrencilerinin ruh sağlığı. Pamukkale University Journal of Education.
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Nicolò Zarotti, Maria Dale, Fiona J. R. Eccles & Jane Simpson. (2022) More than Just a Brain Disorder: A Five-Point Manifesto for Psychological Care for People with Huntington’s Disease. Journal of Personalized Medicine 12:1, pages 64.
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Nicolò Zarotti, Fiona J. R. Eccles, Jennifer A. Foley, Andrew Paget, Sarah Gunn, Iracema Leroi & Jane Simpson. (2020) Psychological interventions for people with Parkinson’s disease in the early 2020s: Where do we stand?. Psychology and Psychotherapy: Theory, Research and Practice 94:3, pages 760-797.
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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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Katarína Žiaková, Juraj Čáp, Michaela Miertová, Elena Gurková & Radka Kurucová. (2020) An interpretative phenomenological analysis of dignity in people with multiple sclerosis. Nursing Ethics 27:3, pages 686-700.
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Paul K Miller, Lisa Booth & Adam Spacey. (2017) Dementia and Clinical Interaction in Frontline Radiography: Mapping the Practical Experiences of Junior Clinicians in the UK. Dementia 18:3, pages 1010-1024.
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Müjde KOCA-ATABEY. (2016) Yeşilçam’da Körlüğün Temsili: Trajik, Tıbbi ve ZamansızThe Representations of Disability within Turkish Cinema (Yeşilçam): Tragic, Medical, and Ill Timed. AYNA Klinik Psikoloji Dergisi 3:1, pages 1-12.
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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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Shirley Lockeridge & Jane Simpson. (2012) The experience of caring for a partner with young onset dementia: How younger carers cope. Dementia 12:5, pages 635-651.
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Zoe C Nowell, Amanda Thornton & Jane Simpson. (2011) The subjective experience of personhood in dementia care settings. Dementia 12:4, pages 394-409.
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Malin Olsson, Lena Stafström & Siv Söderberg. (2013) Meanings of Fatigue for Women With Parkinson’s Disease. Qualitative Health Research 23:6, pages 741-748.
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Jane Simpson, Helen McMillan & Donna Reeve. (2013) Reformulating Psychological Difficulties in People with Parkinson’s Disease: The Potential of a Social Relational Approach to Disablism. Parkinson's Disease 2013, pages 1-8.
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