Abric, J.-C. (2003). Les représentations sociales: aspects théoriques. In Abric, J.-C., Pratiques sociales et représentations (pp. 11–36), Paris: PUF.
Angermeyer, M. C. and Matschinger, H. (1996). The effect of personal experience with mental illness on the attitude towards individuals suffering from mental disorders. Social Psychiatry and Psychiatric Epidemiology, 31, 321–326.
Berger, G., Bernhardt, T., Weimer, E., Peters, J., Kratzsch, T. and Frolich, L. (2005). Longitudinal study on the relationship between symptomatology of dementia and levels of subjective burden and depression among family caregivers in memory clinic patients. Journal of Geriatric Psychiatry and Neurolology, 18, 119–128.
Black, W. and Almeida, O. P. (2004). A systematic review of the association between the behavioral and psychological symptoms of dementia and burden of care. International Psychogeriatrics, 16, 295–315.
Bolognini, M., Bettschart, W., Zehnder-Gubler, M. and Rossier, L. (1989). The validity of the French version of the GHQ-28 and PSYDIS in a community sample of 20 year olds in Switzerland. European Archives of Psychiatry and Neurological Sciences, 238, 161–168.
Burgener, S. C. and Berger, B. (2008). Measuring perceived stigma in persons with progressive neurological disease. Dementia, 7, 31–53.
Chou, K. R., LaMontagne, L. L. and Hepworth, J. T. (1999). Burden experienced by caregivers of relatives with dementia in Taiwan. Nursing Research, 48, 206–214.
Cocco, E., Gatti, M., de Mendonca Lima, C. A. and Camus, V. (2003). A comparative study of stress and burnout among staff caregivers in nursing homes and acute geriatric wards. International Journal of Geriatric Psychiatry, 18, 78–85.
Coen, R. F., Swanwick, G. R., O'Boyle, C. A. and Coakley, D. (1997). Behaviour disturbance and other predictors of carer burden in Alzheimer's disease. International Journal of Geriatric Psychiatry, 12, 331–336.
Cossette, S., Levesque, L. and Laurin, L. (1995). Informal and formal support for caregivers of a demented relative: do gender and kinship make a difference? Research in Nursing and Health, 18, 437–451.
Coyne, A. C., Reichman, W. E. and Berbig, L. J. (1993). The relationship between dementia and elder abuse. American Journal of Psychiatry, 150, 643–646.
Croog, S. H., Sudilovsky, A., Burleson, J. A. and Baume, R. M. (2001). Vulnerability of husband and wife caregivers of Alzheimer disease patients to caregiving stressors. Alzheimer Disease and Associated Disorders, 15, 201–210.
Cummings, J. L., Mega, M., Gray, K., Rosenberg-Thompson, S., Carusi, D. A. and Gornbein, J. (1994). The Neuropsychiatric Inventory: comprehensive assessment of psychopathology in dementia. Neurology, 44, 2308–2314.
Donaldson, C. and Burns, A. (1999). Burden of Alzheimer's disease: helping the patient and caregiver. Journal of Geriatric Psychiatry and Neurolology, 12, 21–28.
Donaldson, C., Tarrier, N. and Burns, A. (1997). The impact of the symptoms of dementia on caregivers. British Journal of Psychiatry, 170, 62–68.
Donaldson, C., Tarrier, N. and Burns, A. (1998). Determinants of carer stress in Alzheimer's disease. International Journal of Geriatric Psychiatry, 13, 248–256.
Farran, C. J. (1997). Theoretical perspectives concerning positive aspects of caring for elderly persons with dementia: stress/adaptation and existentialism. Gerontologist, 37, 250–256.
Folstein, M. F., Folstein, S. E. and McHugh, P. R. (1975). “Mini-mental state”: a practical method for grading the cognitive state of patients for the clinician. Journal of Psychiatric Research, 12, 189–198.
Gallicchio, L., Siddiqi, N., Langenberg, P. and Baumgarten, M. (2002). Gender differences in burden and depression among informal caregivers of demented elders in the community. International Journal of Geriatric Psychiatry, 17, 154–163.
Goldberg, D. P. and Hillier, V. F. (1979). A scaled version of the General Health Questionnaire. Psychological Medicine, 9, 139–145.
Graham, N. et al. . (2003). Reducing stigma and discrimination against older people with mental disorders: a technical consensus statement. International Journal of Geriatric Psychiatry, 18, 670–678.
Heok, K. E. and Li, T. S. (1997). Stress of caregivers of dementia patients in the Singapore Chinese family. International Journal of Geriatric Psychiatry, 12, 466–469.
Hodgson, P. H., Wood, V. A. and Langton-Hewer, R. (1996). Identification of stroke carers ‛at risk': a preliminary study of the predictors of carers' psychological well-being at one year post stroke. Clinical Rehabilitation, 10, 337–346.
Israël, L. (1996). Évaluation de l'autonomie, les activités instrumentales de la vie quotidienne (IADL). In Guelfi, J.D. (ed.), L'évaluation clinique standardisée en psychiatrie, vol. 2 (pp. 477–480). Paris: Éd. Méd Pierre Fabre.
Kaufer, D. I. et al. . (1998). Assessing the impact of neuropsychiatric symptoms in Alzheimer's disease: the Neuropsychiatric Inventory Caregiver Distress Scale. Journal of the American Geriatrics Society, 46, 210–215.
Lawton, M. P. and Brody, E. M. (1969). Assessment of older people: self-maintaining and instrumental activities of daily living. Gerontologist, 9, 179–186.
McKhann, G., Drachman, D., Folstein, M., Katzman, R., Price, D. and Stadlan, E. M. (1984). Clinical diagnosis of Alzheimer's disease: report of the NINCDS-ADRDA Work Group under the auspices of Department of Health and Human Services Task Force on Alzheimer's Disease. Neurology, 34, 939–944.
Mui, A. C. (1995). Caring for frail elderly parents: a comparison of adult sons and daughters. Gerontologist, 35, 86–93.
Ngatcha-Ribert, L. (2004). [Alzheimer's disease and society: an analysis of its social representation]. Psychologie and Neuropsychiatrie du Vieillissement, 2, 49–66.
Noonan, A. E. and Tennstedt, S. L. (1997). Meaning in caregiving and its contribution to caregiver well-being. Gerontologist, 37, 785–794.
Pearlin, L. I., Mullan, J. T., Semple, S. J. and Skaff, M. M. (1990). Caregiving and the stress process: an overview of concepts and their measures. Gerontologist, 30, 583–594.
Purk, J. K. and Richardson, R. A. (1994). Older adult stroke patients and their spousal caregivers. Family and Society, 75, 608–615.
Sartorius, N. and Schulze, H. (2005). Reducing the Stigma of Mental Illness: A Report from a Global Programme of the World Psychiatric Association. Cambridge: Cambridge University Press.
Seligman, M. (1975). Helplessness: On Development, Depression and Death. San Francisco: Freeman.
Steeman, E., Abraham, I. and Godderis, J. (1997). Risk profiles for institutionalization in a cohort of elderly people with dementia or depression. Archives of Psychiatric Nursing, 11, 293–303.
Taylor, S. M. and Dear, M. J. (1981). Scaling community attitudes toward the mentally ill. Schizophrenia Bulletin, 7, 225–240.
Thomas, P. et al. . (2006). Dementia patients' caregivers' quality of life: the PIXEL study. International Journal of Geriatric Psychiatry, 21, 50–56.
Werner, P. (2006). Lay perceptions regarding the competence of persons with Alzheimer's disease. International Journal of Geriatric Psychiatry, 21, 674–680.
Werner, P. and Davidson, M. (2004). Emotional reactions of lay persons to someone with Alzheimer's disease. International Journal of Geriatric Psychiatry, 19, 391–397.
Yaffe, K. et al. . (2002). Patient and caregiver characteristics and nursing home placement in patients with dementia. JAMA, 287, 2090–2097.
Zarit, S. H., Orr, N. K. and Zarit, J. M. (1985). Understanding the stress of caregivers: planning an intervention. In Zarit, S.H., Orr, N.K. and Zarit, J.M., The Hidden Victims of Alzheimer's Disease: Families under Stress. New York: New York University Press.