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Articles

Why are some people with neurological illness more resilient than others?

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Pages 17-34 | Received 11 May 2010, Accepted 13 Feb 2011, Published online: 03 Jun 2011

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Nicola Glennie, Fiona M. Harris & Emma F. France. (2023) Perceptions and experiences of control among people living with motor neurone disease: a systematic review and thematic synthesis. Disability and Rehabilitation 45:16, pages 2554-2566.
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Sílvia Fernanda Cal & Mittermayer B. Santiago. (2013) Resilience in systemic lupus erythematosus. Psychology, Health & Medicine 18:5, pages 558-563.
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Articles from other publishers (19)

Sabina Vatter & Iracema Leroi. (2022) Resilience in People with Lewy Body Disorders and Their Care Partners: Association with Mental Health, Relationship Satisfaction, and Care Burden. Brain Sciences 12:2, pages 148.
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Cathy Bulley, Gillian Baer, Dawn Mahal, Christina H Buckton, Stewart Donald, Keith Lugton, David Gillespie & Brendan McCormack. (2021) Supporting families and carers of people living with multiple sclerosis: a rapid realist review and realist evaluation. International Journal of Care and Caring 5:2, pages 263-282.
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Sierra Martin & Susan L. Kasser. (2021) The role of resilience: Physical activity continuation after falling in adults with multiple sclerosis. Disability and Health Journal 14:2, pages 101046.
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Noora Ovaska-Stafford, John Maltby & Maria Dale. (2021) Literature Review: Psychological Resilience Factors in People with Neurodegenerative Diseases. Archives of Clinical Neuropsychology 36:2, pages 283-306.
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Elizabeth J Halstead, Victoria M Leavitt, Damian Fiore & Kim T Mueser. (2020) A feasibility study of a manualized resilience-based telehealth program for persons with multiple sclerosis and their support partners. Multiple Sclerosis Journal - Experimental, Translational and Clinical 6:3, pages 205521732094125.
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Laia Briones-Buixassa, Raimon Milà, Francesc X Arrufat, Josep Mª Aragonès, Enric Bufill, Olivier Luminet & Rona Moss-Morris. (2017) A case-control study of psychosocial factors and their relationship to impairment and functionality in multiple sclerosis. Journal of Health Psychology 24:8, pages 1023-1032.
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David Morley, Sarah Dummett, Laura Kelly, Ray Fitzpatrick & Crispin Jenkinson. (2018) Predictors of activity and participation across neurodegenerative conditions: a comparison of people with motor neurone disease, multiple sclerosis and Parkinson’s disease. BMC Neurology 18:1.
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Zeng Jie Ye, Chao Hua Peng, Hao Wei Zhang, Mu Zi Liang, Jing Jing Zhao, Zhe Sun, Guang Yun Hu & Yuan Liang Yu. (2018) A biopsychosocial model of resilience for breast cancer: A preliminary study in mainland China. European Journal of Oncology Nursing 36, pages 95-102.
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Pauline Boland, William MM Levack, Sheena Hudson & Elliot Bell. (2018) A qualitative exploration of barriers and facilitators to coping experienced by couples when one has multiple sclerosis. International Journal of Therapy and Rehabilitation 25:5, pages 240-246.
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Hossein Ebrahimi, Hadi Hasankhani, Hossein Namdar, Esmail Khodadadi & Marjaneh Fooladi. (2017) Dealing with Chronic Illness: Experiences of Iranian Families of Persons with Multiple Sclerosis—A Qualitative Study. Multiple Sclerosis International 2017, pages 1-8.
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Andrea M Shamaskin-Garroway, Sarah K Lageman & Bruce Rybarczyk. (2016) The roles of resilience and nonmotor symptoms in adjustment to Parkinson’s disease. Journal of Health Psychology 21:12, pages 3004-3015.
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R. Lanzillo, A. Chiodi, A. Carotenuto, V. Magri, A. Napolitano, R. Liuzzi, T. Costabile, N. Rainone, M.F. Freda, P. Valerio & V. Brescia Morra. (2016) Quality of life and cognitive functions in early onset multiple sclerosis. European Journal of Paediatric Neurology 20:1, pages 158-163.
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Rebecca Black & Diana Dorstyn. (2013) A biopsychosocial model of resilience for multiple sclerosis. Journal of Health Psychology 20:11, pages 1434-1444.
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Merete Røthing, Kirsti Malterud & Jan C. Frich. (2014) Balancing needs as a family caregiver in H untington's disease: a qualitative interview study . Health & Social Care in the Community 23:5, pages 569-576.
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Andrew Soundy & Nicola Condon. (2015) Patients experiences of maintaining mental well-being and hope within motor neuron disease: a thematic synthesis. Frontiers in Psychology 6.
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Rosanne Scerri. (2015) Living with advanced-stage Huntington's disease: an exploration of the experiences of Maltese family caregivers. British Journal of Neuroscience Nursing 11:1, pages 20-27.
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Euan Sadler, Charles DA Wolfe & Christopher McKevitt. (2014) Lay and health care professional understandings of self-management: A systematic review and narrative synthesis. SAGE Open Medicine 2, pages 205031211454449.
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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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David Rintell & Richard Melito. (2013) “Her Illness Is a Project We Can Work on Together”. International Journal of MS Care 15:3, pages 130-136.
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