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Afolasade Fakolade, Amy Latimer-Cheung, Trisha Parsons & Marcia Finlayson. (2019) A concerns report survey of physical activity support needs of people with moderate-to-severe MS disability and family caregivers. Disability and Rehabilitation 41:24, pages 2888-2899.
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Daniel R. du Plooy & Chrisma Pretorius. (2014) The caregiver experience: a South African perspective on caring for people with multiple sclerosis. Journal of Psychology in Africa 24:4, pages 361-369.
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Robert Buchanan, Dagmar Radin, Bonnie J. Chakravorty & Tuula Tyry. (2010) Perceptions of informal care givers: Health and support services provided to people with multiple sclerosis. Disability and Rehabilitation 32:6, pages 500-510.
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Marta Aymerich, Imma Guillamón & Albert J Jovell. (2009) Health-related quality of life assessment in people with multiple sclerosis and their family caregivers. A multicenter study in Catalonia (Southern Europe). Patient Preference and Adherence 3, pages 311-321.
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Robert J. Buchanan, Dagmar Radin, Bonnie J. Chakravorty & Tuula Tyry. (2009) Informal care giving to more disabled people with multiple sclerosis. Disability and Rehabilitation 31:15, pages 1244-1256.
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D. Sapountzi-Krepia, V. Raftopoulos, M. Sgantzos, A. Dimitriadou, I. Ntourou & G. Sapkas. (2006) Informal in-hospital care in a rehabilitation setting in Greece: An estimation of the nursing staff required for substituting this care. Disability and Rehabilitation 28:1, pages 3-11.
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Articles from other publishers (47)
Monica Cueli Arce, Miguel Santibañez, Carmen Sarabia, Paula Paras‐Bravo, Marta Gomez & Ana Rosa Alconero‐Camarero. (2022) Transcultural adaptation of the revised caregiving appraisal scale (RCAS) in the Spanish population. International Journal of Older People Nursing 18:1.
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María Cuerda-Ballester, Antonio Bustos, Maribel Arrollo-Calvillo, Belén Proaño, Amalia Correcher-Calap & Jose Enrique de la Rubia Ortí. (2022) Influence of sex on functional capacity, and muscle strength and fine motor skills of upper limbs in patients with multiple sclerosis. Revista Científica de la Sociedad de Enfermería Neurológica (English ed.).
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María Cuerda-Ballester, Antonio Bustos, Maribel Arrollo-Calvillo, Belén Proaño, Amalia Correcher-Calap & Jose Enrique de la Rubia Ortí. (2022) Influencia del sexo en la capacidad funcional, y fuerza muscular y motricidad fina de miembros superiores en pacientes con esclerosis múltiple. Revista Científica de la Sociedad Española de Enfermería Neurológica.
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Roshanth Rajachandrakumar & Marcia Finlayson. (2021) Multiple sclerosis caregiving: A systematic scoping review to map current state of knowledge. Health & Social Care in the Community 30:4.
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María Florencia Tartaglini, Carolina Feldberg, Paula Daniela Hermida, Silvina Lidia Heisecke, Carol Dillon, Silvia Deborah Ofman, Macarena Liliana Nuñez & Verónica Somale. (2020) Escala de sobrecarga del cuidador de Zarit: análisis de sus propiedades psicométricas en cuidadores familiares residentes en Buenos Aires, Argentina. Neurología Argentina 12:1, pages 27-35.
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Félix Bravo-González & Arturo Álvarez-Roldán. (2019) Esclerosis múltiple, pérdida de funcionalidad y género. Gaceta Sanitaria 33:2, pages 177-184.
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Joel Olayiwola Faronbi, Howard K. Butcher & Adenike Ayobola Olaogun. (2019) Burden and Coping Ability of Individuals Caring for Chronically Ill Older Adults in Nigeria: A Mixed Methods Study. Journal of Gerontological Nursing 45:1, pages 39-46.
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Joel Olayiwola Faronbi & Adenike Ayobola Olaogun. (2017) The influence of caregivers’ burden on the quality of life for caregivers of older adults with chronic illness in Nigeria. International Psychogeriatrics 29:7, pages 1085-1093.
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José Meca-Lallana, Mar Mendibe, Rocío Hernández-Clares, Ana Belén Caminero, Javier Mallada-Frechin, Pablo Dávila-Gonzalez, Moisés Garcés-Redondo, Montserrat Gómez, Jorge Millán-Pascual, Gerardo Soriano-Hernández & María del Campo Amigo-Jorrín. (2016) Predictors of burden and depression among caregivers of relapsing-remitting MS patients in Spain: MS Feeling study. Neurodegenerative Disease Management 6:4, pages 277-287.
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Gillian G. Leibach, Marilyn Stern, Adriana Aguayo Arelis, Miguel Angel Macias Islas & Brenda Viridiana Rábago Barajas. (2016) Mental Health and Health-Related Quality of Life in Multiple Sclerosis Caregivers in Mexico. International Journal of MS Care 18:1, pages 19-26.
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Tamara McKenzie, Mary Elizabeth Quig, Tuula Tyry, Ruth Ann Marrie, Gary Cutter, Edward Shearin, Kamau Johnson & James Simsarian. (2015) Care Partners and Multiple Sclerosis. International Journal of MS Care 17:6, pages 253-260.
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Andrés Labiano-Fontcuberta, Alex J. Mitchell, Sara Moreno-García & Julián Benito-León. (2015) Anxiety and depressive symptoms in caregivers of multiple sclerosis patients: The role of information processing speed impairment. Journal of the Neurological Sciences 349:1-2, pages 220-225.
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Andrés Labiano-Fontcuberta, Alex J Mitchell, Sara Moreno-García & Julián Benito-León. (2014) Cognitive impairment in patients with multiple sclerosis predicts worse caregiver’s health-related quality of life. Multiple Sclerosis Journal 20:13, pages 1769-1779.
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Jens Peter Reese, Gabriele Wienemann, Axel John, Alexandra Linnemann, Monika Balzer-Geldsetzer, Ulrich Otto Mueller, Christian Eienbröker, Björn Tackenberg & Richard Dodel. (2013) Preference-based Health status in a German outpatient cohort with multiple sclerosis. Health and Quality of Life Outcomes 11:1.
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Beatriz Pozuelo-Moyano, Juli?n Benito-Le?n, Alex J. Mitchell & Jes?s Hern?ndez-Gallego. (2013) A Systematic Review of Randomized, Double-Blind, Placebo-Controlled Trials Examining the Clinical Efficacy of Vitamin D in Multiple Sclerosis. Neuroepidemiology 40:3, pages 147-153.
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