Citations (58)
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Gogem Topcu, Heather Buchanan, Aimee Aubeeluck & Gülcan Garip. (2016) Caregiving in multiple sclerosis and quality of life: A meta-synthesis of qualitative research. Psychology & Health 31:6, pages 693-710.
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Kenneth
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Kenneth I. Pakenham. (2008) The nature of sense making in caregiving for persons with multiple sclerosis. Disability and Rehabilitation 30:17, pages 1263-1273.
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KellyA. Ryan, LisaJ. Rapport, TanyaE. Sherman, RobinA. Hanks, Robert Lisak & Omar Khan. (2007)
Predictors of Subjective Well-being among Individuals with Multiple Sclerosis. The Clinical Neuropsychologist 21:2, pages 239-262.
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J. Mccausland & K.I. Pakenham. (2003) Investigation of the benefits of HIV/AIDS caregiving and relations among caregiving adjustment, benefit finding, and stress and coping variables. AIDS Care 15:6, pages 853-869.
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Xingchao Wang & Wenyuan Wang. (2023) Perceived Economic Stress and Adolescents’ Bullying Victimization: The Roles of Self-Esteem and Student-Student Relationships. The Journal of Early Adolescence, pages 027243162311745.
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Yuka Iwata (Shindo) & Etsuko Tadaka. (2022) Effectiveness of web-based intervention for life-change adaptation in family caregivers of community-dwelling individuals with acquired brain injury: A cluster-randomized controlled trial. PLOS ONE 17:8, pages e0273278.
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Man-Man Peng, Zhiying Ma, She-Ying Chen, Wei Luo, Shi-Hui Hu, Xin Yang, Bo Liu, Cecilia Lai-Wan Chan & Mao-Sheng Ran. (2022) Predictors of family caregiving burden of persons with schizophrenia with and without transition of primary caregivers from 1994 to 2015 in rural China. BJPsych Open 8:3.
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Man-Man Peng, Jianli Xing, Xinfeng Tang, Qinglu Wu, Dannuo Wei & Mao-Sheng Ran. (2022) Disease-Related Risk Factors for Caregiver Burden among Family Caregivers of Persons with Schizophrenia: A Systematic Review and Meta-Analysis. International Journal of Environmental Research and Public Health 19:3, pages 1862.
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Cheng Hui-Lin & Gan Ting. (2022) The experiences, perceptions, and support needs among family caregivers of patients with advanced cancer and eating problems: An integrative review. Palliative Medicine 36:2, pages 219-236.
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Gogem Topcu, Heather Buchanan, Aimee Aubeeluck & Hatice Ülsever. (2020) Informal carers’ experiences of caring for someone with Multiple Sclerosis: A photovoice investigation. British Journal of Health Psychology 26:2, pages 360-384.
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Kristin Corey Magan, Mary K. McCurry, Kristen A. Sethares, Meg Bourbonniere, Salimah H. Meghani & Karen B. Hirschman. (2020) The Post-caregiving Health Model. Advances in Nursing Science 43:4, pages 292-305.
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Kenneth Ian Pakenham & Stephen Cox. (2018) Effects of Benefit Finding, Social Support and Caregiving on Youth Adjustment in a Parental Illness Context. Journal of Child and Family Studies 27:8, pages 2491-2506.
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Kate Greenwell, William K. Gray, Anna van Wersch, Paul van Schaik & Richard Walker. (2015) Predictors of the psychosocial impact of being a carer of people living with Parkinson's disease: A systematic review. Parkinsonism & Related Disorders 21:1, pages 1-11.
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