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Social capital components and social support of persons with multiple sclerosis: a systematic review of the literature from 2000 to 2018

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Pages 3437-3449 | Received 07 Dec 2017, Accepted 14 Mar 2019, Published online: 18 Apr 2019

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Maja Liković & Marko Buljevac. (2023) ‶You look really good, I don’t know why you came here″: persons with multiple sclerosis´ perspectives on social support. Home Health Care Services Quarterly 42:3, pages 243-264.
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Daniel Ståhl, Ylva Bjereld & Anna Dunér. (2022) Disabled in Society - A Scoping Review on Persons Living with Multiple Sclerosis and Disability. Journal of Multidisciplinary Healthcare 15, pages 375-390.
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Vladimira Timkova, Pavol Mikula, Marcela Linkova, Jarmila Szilasiova & Iveta Nagyova. (2021) Sexual functioning in patients with multiple sclerosis and its association with social support and self-esteem. Psychology, Health & Medicine 26:8, pages 980-990.
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Articles from other publishers (11)

Camilla Ihlebæk, Hilde Katralen, Emma C. A. Nordbø & Anni Skipstein. (2023) The role of social capital for wellbeing in people with long-term illness and disease. Nordic Journal of Wellbeing and Sustainable Welfare Development 2:2, pages 53-67.
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Hannah R. Cohen & Roee Holtzer. (2023) The association between perceived social support and cognition in older adults with and without multiple sclerosis. Multiple Sclerosis and Related Disorders 78, pages 104913.
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Sofie Olsgaard Bergien, Volkert Dirk Siersma, Maria Kristiansen & Lasse Skovgaard. (2023) Social relations and leisure activities as predictors of wellbeing among older adults with multiple sclerosis: A cross-sectional survey study in Denmark. Multiple Sclerosis and Related Disorders 77, pages 104878.
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Lynda Feenaughty. (2023) Social Network Characteristics and Correlations With Cognitive, Psychosocial, and Speech Function and Communication Participation for Adults With Multiple Sclerosis: A Pilot Study. Journal of Speech, Language, and Hearing Research 66:1, pages 163-177.
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Ruth Dobson, Dylan R. Rice, Marie D’hooghe, Rachel Horne, Yvonne Learmonth, Farrah J. Mateen, Claudia H. Marck, Saúl Reyes, Mitzi Joi Williams, Gavin Giovannoni & Helen L. Ford. (2022) Social determinants of health in multiple sclerosis. Nature Reviews Neurology 18:12, pages 723-734.
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Yael Goverover, Michelle H. Chen, Amanda Botticello, Gerald T. Voelbel, Grace Kim, John DeLuca & Helen M. Genova. (2022) Relationships between changes in daily occupations and health-related quality of life in persons with multiple sclerosis during the COVID-19 pandemic. Multiple Sclerosis and Related Disorders 57, pages 103339.
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Lindsay Welch, Euan Sadler, Anthony Austin & Anne Rogers. (2021) Social network participation towards enactment of self‐care in people with chronic obstructive pulmonary disease: A qualitative meta‐ethnography. Health Expectations 24:6, pages 1995-2012.
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Seada A Kassie, Jannat Alia & Lynda Hyland. (2021) Biopsychosocial implications of living with multiple sclerosis: a qualitative study using interpretative phenomenological analysis. BMJ Open 11:8, pages e049041.
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Valeria Donisi, Alberto Gajofatto, Maria Angela Mazzi, Francesca Gobbin, Isolde Martina Busch, Annamaria Ghellere, Alina Klonova, Doriana Rudi, Francesca Vitali, Federico Schena, Lidia Del Piccolo & Michela Rimondini. (2021) A Bio-Psycho-Social Co-created Intervention for Young Adults With Multiple Sclerosis (ESPRIMO): Rationale and Study Protocol for a Feasibility Study. Frontiers in Psychology 12.
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Berenice Anabel Silva, Esteban Alberto Miglietta & Carina Cintia Ferrari. (2020) Training the brain: could it improve multiple sclerosis treatment?. Reviews in the Neurosciences 31:7, pages 779-792.
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Saúl Reyes, Sebastian Suarez, Kimberley Allen‐Philbey, Alison Thomson & Gavin Giovannoni. (2020) The impact of social capital on patients with multiple sclerosis. Acta Neurologica Scandinavica 142:1, pages 58-65.
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