Abdullah, T. and Brown, T. L. (2011). Mental illness stigma and ethno-cultural beliefs, values, and norms: an integrative review. Clinical Psychology Review, 31, 934–948.
Aiken, L. S. and West, S. G. (1991). Multiple Regression: Testing and Interpreting Interactions. Newbury Park, London: Sage.
Basri, M., Subramaniam, P., Ghazali, S. E. and Singh, D. K. (2017). A review of knowledge and attitudes towards dementia among college students. Journal of Clinical and Diagnostic Research, 11, LEO1–LEO7.
Brodsky, J., Bentur, N., Laron, M. and Ben-Israel, S. (2013). Addressing Alzheimer’s and Other Types of Dementia: Israeli National Strategy. Jerusalem, Israel: Myers-JDC-Brookdale Institute and Ministry of Health.
Cahill, S., Werner, P. and Bobesky, A. (2015). A systematic review of the public’s knowledge and understanding of Alzheimer’s disease and dementia. Alzheimer’s Disease and Other Related Diseases, 29, 255–275. doi: 10.1097/WAD.0000000000000102
Celdran, M., Villar, F. and Triado, C. (2014). Thinking about my grandparent: how dementia influences adolescent grandchildren’s perceptions of their grandparents. Journal of Aging Studies, 29, 1–8. doi: 10.1016/j.aging.2013.12.004
Chow, S. et al. (2018). National dementia strategies: what should Canada learn?. Canadian Geriatrics Journal, 21, 173–209.
Corrigan, P., Markowitz, F. E., Watson, A., Rowan, D. and Kubiak, M. A. (2003). An attribution model of public discrimination towards persons with mental illness. Journal of Health and Social Behavior, 44, 162–179.
Dawson, J. F. (2014). Moderation in management research: what, why, when and how. Journal of Business and Psychology, 29, 1–19.
Eccleston, C. E., Lea, E. J., McInerney, F., Crisp, E., Marlow, A. and Robinson, A. L. (2015). An investigation of nursing students’ knowledge of dementia: a questionnaire study. Nurse Education Today, 35, 800–805.
Fiest, K. M. et al. (2016). The prevalence and incidence of dementia due to Alzheimer’s disease: a systematic review and meta-analysis. Canadian Journal of Neurological Sciences, 43, S51–S82.
Gal, J. (2010). Is there an extended family of Mediterranean welfare states?. Journal of European Social Policy, 20, 283–300.
Gilmartin-Thomas, J. F. M., McNeil, J., Powell, A., Malone, D. T. and Larson, I. C. (2018). Qualitative evaluation of how a virtual dementia experience impacts medical and pharmacy students’ self-reported knowledge and attitudes towards people with dementia. Dementia, 1–16. doi: 10.1177/1471301218770270.
Goncalves Ferreira, R., Brandao, M. P. and Fonseca Cardoso, M. (2018). An update of the profile of older adults with dementia in Europe: findings from SHARE. Aging and Mental Health. doi: org/10.1080/13607863.2018.1531385.
Hampton, N. Z. and Xiao, F. (2007). Attitudes toward people with developmental disabilities in Chinese and American students: the role of cultural values, contact, and knowledges. Journal of Rehabilitation, 73, 23–32.
Hanssen, I. and Tran, P. T. M. (2018). The influence of individualistic and collectivistic morality on dementia care choices. Nursing Ethics, doi: 10.1177/0969733018791342.
Herrmann, L. K. et al. (2018). A systematic review of dementia-related stigma research: can we move the stigma dial?. The American Journal of Geriatric Psychiatry, 26, 316–331.
Hillman, A. and Latimer, J. (2017). Cultural representations of dementia. PlosMedicine, 14, e1002274. doi: 10.1371/journal.pmed.1002274
Hofstede, G. (1980). Culture’s Consequences: International Differences in Work-Related Values. Beverly Hills, CA: Sage.
Isobe, A., Izumi, M. and Akifusa, S. (2018). Relationship between resilience and self-rated health in dental hygiene students and registered dental hygienists. Journal of Dental Education, 82, 1343–1350.
Kemmelmeier, M. (2016). Cultural differences in survey responding: issues and insights in the study of response biases. International Journal of Psychology, 51, 439–444.
Kimzey, M., Mastel-Smith, B. and Alfred, D. (2016). The impact of educational experiences on nursing students’ knowledge and attitudes toward people with Alzheimer’s disease: a mixed method study. Nurse Education Today, 46, 57–63.
Konerding, U. et al. (2018). Investigating burden of informal caregivers in England, Finland and Greece: an analysis with the short form of the Burden Scale for Family Caregivers (BSFC-s). Aging and Mental Health, 22, 280–287.
Lamura, G. et al. (2008). Family carers’ experiences using support services in Europe: empirical evidence for the EUROFAMCARE study. The Gerontologist, 48, 752–771.
Lion, K.M. et al. (2019). Do people with dementia and mild cognitive impairments experience stigma? a cross-cultural investigation between Italy, Poland and the UK. Aging and Mental Health. doi: 10.1080/13607863.2019.1577799.
Mannarini, S., Bolfo, M., Rossi, A. and Balottin, L. (2018). Etiological beliefs, treatments, stigmatizing attitudes toward schizophrenia. What do Italians and Israelis think?. Frontiers in Psychology, 8, 2289–2897.
Matsushita, M., Pai, M., Jhou, C., Koyama, A. and Ikeda, M. (2016). Cross-cultural study of caregiver burden for Alzheimer’s disease in Japan and Taiwan: result for Dementia Research in Kumamoto and Tainan (DeReKat). International Psychogeriatrics, 28, 1125–1132.
Mitchell, G. et al. (2017). Evaluation of ‘Dementia Friends’ program for undergraduate nursing students: innovative practice. Dementia, 16, 1075–1080.
Mulvey, K. L., Hitti, A. and Killen, M. (2010). The development of stereotyping and exclusion. Wiley Interdisciplinary Reviews: Cognitive Science, 1, 597–606. doi: 10.1002/wcs.66.
Nguyen, T. and Li, X. (2018). Understanding public-stigma and self-stigma in the context of dementia: a systematic review of the global literature. Dementia, doi: 10.1177/147130128800122.
Papadopoulos, C., Foster, J. and Caldwell, K. (2013). ‘Individualism-collectivism’as an explanatory device for mental illness stigma. Community Mental Health Journal, 49, 270–280.
Papastylianou, D. and Lampridis, E. (2016). Social values priorities and orientation towards individualism and collectivism of Greek university students. Journal of Beliefs and Values, 37, 40–54.
Pouliasi, K. and Verkuyten, M. (2011). Self-evaluations, psychological well-being, and cultural context: the changing Greek society. Journal of Cross-Cultural Psychology, 42, 875–890.
Prince, M., Comas-Herrera, A., Knapp, M., Guerchet, M. and Karagiannidou, M. (2016). World Alzheimer Report 2016: Improving Healthcare for People Living With Dementia: Coverage, Quality and Costs Now and in the Future. London, UK: Alzheimer’s Disease International.
Rao, D., Angell, B., Lam, C. and Corrigan, P. (2008). Stigma in the workplace: employer attitudes about people with HIV in Beijing, Hong Kong, and Chicago. Social Science and Medicine, 67, 1541–1549.
Sakka, P. (2012). Current status regarding dementia in Greece – Towards the implementation of the Greek Dementia Strategy. Athens, Greece: National Observatory for Dementia, Athens Association of Alzheimer’s Disease and Related Disorders.
Scerri, A. and Scerri, C. (2013). Nursing students’ knowledge and attitudes towards dementia – a questionnaire survey. Nurse Education Today, 33, 962–968.
Shin, J.H., Seo, H., Kim, K., Kim, K. and Lee, Y. (2015). Knowledge about dementia in South Korean nursing students: a cross-sectional survey. BMC Nursing, 14, 67. doi: 10.1186/s12912-015-0116-4
Shinan-Altman, S. and Werner, P. (2019). Illness representations of dementia: a scoping review. Clinical Interventions in Aging, 14, 179–193.
Triandis, H. C. and Gelfand, M. J. (1998). Converging measurement of horizontal and vertical individualism and collectivism. Journal of Personality and Social Psychology, 74, 118–128.
Tsolaki, M., Paraskevi, S., Degleris, N. and Karamavrou, S. (2009). Attitudes and perceptions regarding Alzheimer’s disease in Greece. American Journal of Alzheimer’s Disease, 24, 21–26.
Werner, P. (2008). Discrimination towards a person with Alzheimer’s disease: examining the effects of being in a nursing home. Aging and Mental Health, 12, 786–794.
Werner, P. (2014). Stigma and Alzheimer’s disease: a systematic review of evidence, theory and methods. In Corrigan, P. (Ed.), The Stigma of Disease and Disability: Empirical Models and Implications for Change.Washington, DC: American Psychological Association.
Werner, P., Goldberg, S., Mandel, S. and Korczyn, A. (2013). Gender differences in lay persons’ beliefs and knowledge about Alzheimer’s disease: a national representative study of Israeli adults. Archives of Gerontology and Geriatrics, 56, 400–404. doi: 10.1016/j.archger.