Artiklar och rapporter

Rapporter och sammanställningar av konferenser och utredningar utgivna av olika myndigheter och organisationer

Demensförbundet (2006). Anhörigboken : Demenssjukdomar, läkemedelsbehandling, hjälpmedel, lag och rätt, vård och omsorg, praktiska råd och tips. Stockholm: Demensförbundet.

Socialstyrelsen (2001). Hälsofrämjande stöd för anhöriga i Varbergs kommun. Stockholm: Socialstyrelsen.

Socialstyrelsen (2002). Finns kvar och ställer upp : Hur anhöriga kan bidra till återhämtning från allvarlig psykisk störning, hur de återhämtades och de anhörigas perspektiv (Anhörig 300). Stockholm: Socialstyrelsen.

Socialstyrelsen (2007). Rehabilitering för hemmaboende äldre personer. Stockholm: Socialstyrelsen.

Statens folkhälsoinstitut (2007). Healthy ageing: a challenge for Europe. Rapport 2006:29. Stockholm: National Instiute of Public Health.

Statens folkhälsoinstitut (2007). Äldres hälsa: en utmaning för Europa. Kortversion av Health Ageing-projektet huvudrapport 2007:02. Stockholm: Statens folkhälsoinstitut.

Artiklar och rapporter sorterat efter författare

Abetz, L., Rofail, D., Mertzanis, P., Heelis, R., Rosa, K., Tellefsen, C., et al. (2009). Alzheimer's disease treatment: assessing caregiver preferences for mode of treatment delivery. Advances In Therapy, 26(6), 627-644.

Ablitt, A., Jones, G., & Muers, J. (2010). Awareness of carer distress in people with dementia. International Journal of Geriatric Psychiatry, 25(12), 1246-1252.

Ablitt, A., Jones, G. V., & Muers, J. (2009). Living with dementia: a systematic review of the influence of relationship factors. Aging & Mental Health, 13(4), 497-511.

Alma, A. U., Lau, K., Sit, E., Cheung, G., Lai, M., Wong, S. K. I., et al. (2010). The Role of Self-Efficacy in the Alzheimer's Family Caregiver Stress Process: A Partial Mediator between Physical Health and Depressive Symptoms. Clinical Gerontologist, 33(4), 298-315.

Almberg, B., Grafström, M., & Krichbaum, K. (2000). The interplay of institution and family caregiving - relations between patient hassles, nursing home hassles and caregivers' burnout. International Journal of Geriatric Psychiatry, 15(10), 931-939.

Almberg, B., & Jansson, W. (2002). Att vara anhörig till en person med demenssjukdom. Socialmedicinsk Tidskrift (2), 139-145.

Almberg, B., & Jansson, W. (2002). Being a relative of a person with dementia. Socialmedicinsk Tidskrift, 79(2), 139-145

Almberg, B., & Jansson, W. (2003).  Fånga stunden : Att vara anhörigvårdare till en person med demenssjukdom. Psykisk hälsa (4), 309-319.

Almberg, B. E., Grafström, M., & Winblad, B. (2000). Caregivers of relatives with dementia: Experiences encompassing social support and bereavement. Aging & Mental Health, 4(1), 82-89.

Althén, A. (2008). Hemsjukvård i samverkan för äldre med komplexa vård- och omsorgsbehov. Linköping: Forsknings- och utvecklingsenheten för närsjukvården, Östergötland.

Amen, K. (2010). Caring for caregivers: what is proven to relieve caregiver strain and burden? American Nurse Today, 5(8), 2p.

Andersson, A., Levin, L. A., & Emtinger, B. G. (2002). The economic burden of informal care. International Journal  of Technological Assessment in Health Care, 18(1), 46-54.

Andersson, M. (2003). Att leva med en demenssjuk person : Anhörigas upplevelse av sina vardagliga aktiviteter. Unpublished D-uppsats. Luleå: Luleå Tekniska Universitet, Institutionen för Hälsovetenskap.

Andersson, M., Karlsson, E., & Brännström, B. (2001). Att leva med en demenssjuk person : Anhörigas behov av stöd och hjälp (Rapport från FoU-enheten i Piteå Älvdal ; 2001:2). Piteå: FoU-enheten i Piteå Älvdal.

Andren, S. (2006). Intervention for family members of persons with dementia. Nordisk Geriatrik, 9(3), 4-7.

Andrén, S. (2006). Family caregivers of persons with dementia : Experiences of burden, satisfaction and psychosocial intervention. Malmö: Institutionen för hälsa, vård och samhälle, Malmö Universitetssjukhus, Lunds Universitet.

Andrén, S. (2006). Investera i närstående. Tidningen Äldreomsorg (3), 38-42.

Andren, S., & Elmståhl, S. (2005). Family caregivers' subjective experiences of satisfaction in dementia care: Aspects of burden, subjective health and sense of coherence. Scandinavian Journal of  Caring Science, 19(2), 157-168.

Andrén, S., & Elmståhl, S. (2002). Former family carers' subjective experiences of burden: A comparison between group living and nursing home environments in one municipality in Sweden. Dementia, 1(2), 241-254.

Andrén, S., & Elmståhl, S. (2007). Relationships between income, subjective health and caregiver burden in caregivers of people with dementia in group living care: A cross-sectional community-based study. International Journal of Nursing Studies, 44(3), 435-446.

Andrén, S., Elmstahl, S. (2008). The relationship between caregiver burden, caregivers' perceived health and their sense of coherence in caring for elders with dementia. Journal of Clinical Nursing, 17(6), 790-799.

Annerstedt, L., Elmståhl, S., Ingvad, B., & Samuelsson, S. (2000). Family caregiving in dementia: An analysis of the caregiver's burden and the "Breaking-point" When home care becomes inadequate. Scandinavian Journal of Public Health, 28(1), 23-31.

Aremyr, G., Hallin, S., & Hesselstrand, J. (2005). Asta i inre och yttre balans : Att stödja en person med demens (Astaserien, 99-2713547-5). Stockholm: Liber.

Axelsson, R., Bihari Axelsson, S. (2007). Folkhälsa i samverkan mellan professioner, organisationer och samhällssektorer. Lund: Studentlitteratur.

Bakker, C., de Vugt, M. E., Vernooij-Dassen, M., van Vliet, D., Verhey, F. R. J., & Koopmans, R. T. C. (2010). Needs in early onset dementia: a qualitative case from the NeedYD study. American Journal of Alzheimer's Disease & Other Dementias, 25(8), 634-640.

Beck-Friis, B. (2000). Det blir lättare när det blir svårare : Råd till personal och anhöriga som vårdar demenshandikappade. Stockholm: Gothia.

Benzein, E., Hagberg, M., Saveman. B. (2008). 'Being appropriately unusual': a challenge for nurses in health-promoting conversations with families. Nursing Inquiry, 15(2), 106-115.

Benzein, E., Saveman, B. (2008). Health-promoting conversations about hope and suffering with couples in palliative care. International Journal of Palliative Nursing, 14(9), 439-445.

Bergs, D. (2002, Sep). "The hidden client"--women caring for husbands with COPD: Their experience of quality of life. Journal of Clinical Nursing, 11(5), 613-621.

Bergström, A. L., Eriksson, G., von Koch, L., & Tham, K. (2011). Combined life satisfaction of persons with stroke and their caregivers: associations with caregiver burden and the impact of stroke. Health And Quality Of Life Outcomes, 9, 1-1.

Bezkow, J. (2008). När himlen är nära ... Att samtala med äldre om liv, död och självmord. Psykisk hälsa, 49(3), 35-42.

Bilotta, C., Bergamaschini, L., Arienti, R., Spreafico, S., & Vergani, C. (2010). Caregiver burden as a short-term predictor of weight loss in older outpatients suffering from mild to moderate Alzheimer's disease: a three months follow-up study. Aging & Mental Health, 14(4), 481-488.

Borg, C., (2005). Livstillfredsställelse hos äldre, särskilt med nedsatt funktionsförmåga samt informella vårdare. I relation till hälsa, självkänsla, sociala och ekonomiska resurser i ett svenskt och europeiskt perspektiv. Thesis. Lund: Lunds universitet.

Borg, C., & Hallberg, I. R. (2006). Life satisfaction among informal caregivers in comparison with non-caregivers. Scandinavian Journal of Caring Science, 20(4), 427-438.

Boström, K., Ahlström, G., & Sunvisson, H. (2006). Being the next of kin of an adult person with muscular dystrophy. Clinical Nursing Research, 15(2), 86-104; discussion 105-106.

Brorsson, A. K. K. (2005). Att leva med en demenssjuk. Unpublished C-uppsats, Karlskrona: Blekinge Tekniska Högskola/HAL.

Brännström, B., Tibblin, Å., & Löwenborg, C. (2000). Counselling groups for spouses of elderly demented patients: A qualitative evaluation study. International Journal of Nursing Practice, 6(4), 183-191.

Brännström, M., Ekman, I., Boman, K., & Strandberg, G. (2007). Being a close relative of a person with severe, chronic heart failure in palliative advanced home care--a comfort but also a strain. Scandinavian Journal of Caring Science, 21(3), 338-344.

Buchanan, R., & Huang, C. (2011). Health-related quality of life among informal caregivers assisting people with multiple sclerosis. Disability & Rehabilitation, 33(2), 113-121.

Burman, U. (2006). I lust och nöd. Socialpolitik (4), 16-19.

Butterworth, P., Pymont, C., Rodgers, B., Windsor, T. D., & Anstey, K. J. (2010). Factors that explain the poorer mental health of caregivers: results from a community survey of older Australians. Australian & New Zealand Journal of Psychiatry, 44(7), 616-624.

Bäckstedt, A-M., Lundmark, L. & Svensson, K. (2007). Säkrare vård av äldre : När patienter möter fler rådgivare ; Läkemedelshantering och informationsöverföring mellan kommun och landsting. Linköping.

Cahill, E., Lewis, L. M., Barg, F. K., & Bogner, H. R. (2009). "You don't want to burden them": older adults' views on family involvement in care. Journal of Family Nursing, 15(3), 295-317.

Callan, J. A., & Howland, R. H. (2009). Caregivers of loved ones with Alzheimer's disease: nursing care for the caregivers. Journal of Psychosocial Nursing & Mental Health Services, 47(11), 13-14.

Campbell, J. (2009). A model of consequences of dementia caregivers' stress process: influence on behavioral symptoms of dementia and caregivers' behavior-related reactions. Research & Theory for Nursing Practice, 23(3), 181-202.

Carbonneau, H., Caron, C., & Desrosiers, J. (2010). Development of a conceptual framework of positive aspects of caregiving in dementia. Dementia (14713012), 9(3), 327-353.

Carretero, S., Garces, J., Rodenas, F., & Sanjose, V. (2009). The informal caregiver's burden of dependent people: theory and empirical review. Archives of Gerontology & Geriatrics, 49(1), 74-79.

Cederqvist, J. (2008). Recept för vården : om effektivitet i sjukvården och äldreomsorgen. Stockholm, SNS förlag.

Chang, H., Chiou, C., & Chen, N. (2010). Impact of mental health and caregiver burden on family caregivers' physical health. Archives of Gerontology & Geriatrics, 50(3), 267-271.

Chang, C. (2008). Unbiased Alzheimer´s caregiver health assessment. Gerontologist 48, 333-333.

Chappell, N. L., & Dujela, C. (2009). Caregiver -- Who Copes How? International Journal of Aging and Human Development, 69(3), 221-244.

Chappell, N. L. & Dujela, C. (2008). Caregiving - predicting at-risk status. Canadian Journal on Aging, 27(2), 169-180.

Charlesworth, G., Shepstone, L., Wilson, E., Thalany, M., Mugford, M. & Poland F. (2008). Does befriending by trained lay workers improve psychological well-being and quality of life for carers of people with dementia, and at what cost? A randomised controlled trial. Health Technology Assessment, 12(4), 48.

Chen, Y.-M., Hedrick, S. C., & Young, H. M. (2010). A pilot evaluation of the Family Caregiver Support Program. Evaluation and Program Planning, 33(2), 113-119.

Chung, E., McLarney, C. & Gillen, M. C. (2008). Social policy recommendations to alleviate stress among informal providers of elder care. International Journal of Sociology and Social Policy, 28(9-10), 340-350.

Clark, M. C., & Diamond, P. M. (2010). Depression in family caregivers of elders: a theoretical model of caregiver burden, sociotropy, and autonomy. Research in Nursing & Health, 33(1), 20-34.

Clark, S. M. & Ambrosia, T. F. (2008). Caring for caregivers: NPs' "hidden" patients. American Journal for Nurse Practitioners, 12(1), 10.

Conde-Sala, J. L., Garre-Olmo, J., Turró-Garriga, O., Vilalta-Franch, J., & López-Pousa, S. (2010). Differential features of burden between spouse and adult-child caregivers of patients with Alzheimer's disease: an exploratory comparative design. International Journal of Nursing Studies, 47(10), 1262-1273.

Conde-Sala, J. L., Garre-Olmo, J., Turro-Garriga, O., Vilalta-Franch, J., & Lopez-Pousa, S. (2010). Quality of life of patients with Alzheimer's disease: differential perceptions between spouse and adult child caregivers. Dementia & Geriatric Cognitive Disorders, 29(2), 97-108.

Cooper, C., Katona, C. & Orrell, M. (2008). Coping strategies, anxiety and depression in caregivers of people with Alzheimer's disease. International Journal of Geriatric Psychiatry, 23(9), 929-936.

Cotter, V. T. (2009). Hope in early-stage dementia: a concept analysis. Holistic Nursing Practice, 23(5), 297-301.

Culshaw, M. (2009). Assessing the impact of sleep disorders on people with dementia and their caregivers. Journal of Dementia Care, 17(5), 38-39.

Dalenstam Lindgren, B. (2004). Ökad livskvalitet hos anhörigvårdare som får stöd. Sjukgymnasten (3), 26-30.

Davidson, T., Krevers, B. & Levin, L. A. (2008). In pursuit of QALY weights for relatives: empirical estimates in relatives caring for older people. European Journal of Health Economics. 9(3), 285-292.

Davidson, T. & Levin, L-Å. (2008). Närståendes konsekvenser [Elektronisk resurs] : hur kan de inkluderas i den hälsoekonomiska analysen? Linköping: Institutionen för medicin och hälsa, Linköpings universitet, (CMT).

Dessner, E-l. & Leijon, S. (2007). I nöd och lust : Att vara närstående till en person med demenssjukdom. Unpublished C-uppsats, Malmö: Malmö Högskola.

DeVany, M., Alverson, D., D'Iorio, J. & Simmons, S. (2008). Employing telehealth to enhance overall quality of life and health for families. Telemedicine Journal and E- Health, 14(9),1003-1007.

Diwan, S., Hougham, G. W., & Sachs, G. A. (2009). Chronological patterns and issues precipitating grieving over the course of caregiving among family caregivers of persons with dementia. Clinical Gerontologist, 32(4), 358-370.

Dow, B., & Meyer, C. (2010). Caring and Retirement: Crossroads and Consequences. International Journal of Health Services, 40(4), 645-665.

Duggleby, W., Holtslander, L., Kylma, J., Duncan, V., Hammond, C., & Williams, A. (2010). Metasynthesis of the hope experience of family caregivers of persons with chronic illness. Qualitative Health Research, 20(2), 148-158.

Duggleby, W., Williams, A., Wright, K., & Bollinger, S. (2009). Renewing everyday hope: the hope experience of family caregivers of persons with dementia. Issues in Mental Health Nursing, 30(8), 514-521.

Duggleby, W., Wright, K., Williams, A., Degner, L., Cammer, A., & Holtslander, L. (2007). Developing a Living with Hope Program for caregivers of family members with advanced cancer. Journal of Palliative Care, 23(1), 24-31.

Ekström, H. (2009). The influence of fracture on activity, social participation and quality of life among older adults. Results from the population study Good Ageing in Skåne. Diss. Lund: Lunds Universitet.

Ekwall, A., Sivberg, B. & Hallberg, I. R. (2004). Dimensions of informal care and quality of life among elderly family caregivers. Scandinavian Journal of Caring Science, 18(3), 239-248.

Ekwall, A. K. & Hallberg, I. R. (2007). The association between caregiving satisfaction, difficulties and coping among older family caregivers. Journal of  Clinical Nursing, 16(5), 832-844.

Ekwall, A. K., Sivberg, B., & Hallberg, I. R. (2005, Jan). Loneliness as a predictor of quality of life among older caregivers. Journal of Advanced Nursing, 49(1), 23-32.

Ekwall, A. K., Sivberg, B., & Hallberg, I. R. (2007). Older caregivers' coping strategies and sense of coherence in relation to quality of life. Journal of Advanced Nursing, 57(6), 584-596.

Elliott, A. F., Burgio, L. D., & DeCoster, J. (2010). Enhancing caregiver health: findings from the Resources for Enhancing Alzheimer's Caregiver Health II intervention. Journal of the American Geriatrics Society, 58(1), 30-37.

Eloniemi-Sulkava, U., Notkola, I.-L., & Hentinen, M. (2001, October). Effects of supporting community-living demented patients and their caregivers - a randomized trial. Journal of the American Geriatric Society, 49(10), 1282-1287.

Epstein-Lubow, G., Gaudiano, B. A., Hinckley, M., Salloway, S., & Miller, I. W. (2010). Evidence for the validity of the American Medical Association's Caregiver Self-Assessment Questionnaire as a screening measure for depression. Journal of the American Geriatrics Society, 58(2), 387-388.

Erlingsson, C., Magnusson, L., & Hanson, E. (2010). Anhörigvårdares hälsa, kunskapsöversikt 2010:3. Kalmar: Nationellt kompetenscentrum Anhöriga.

Etkin, C. D., Prohaska, T. R., Connell, C. M., Edelman, P.& Hughes, S. L. (2008). Antecedents of Physical Activity Among Family Caregivers. The Journal of Applied Gerontology, 27(3), 350-367.

Etters, L., Goodall, D. & Harrison, B. E. (2008). Caregiver burden among dementia patient caregivers: A review of the literature. Journal of the American Academy of Nurse Practitioners. 20(8), 423-428.

Falk, C. & Hanell, K.  (2008). "Och vem är du?" sa han till mig : en existentiell förståelse av den anhöriges livsvärld vid samvaro med en demenssjuk förälder. Lund: Institutionen för psykologi, Lunds universitet.

Faul, A. C., Yankeelov, P. A., Rowan, N. L., Gillette, P., Nicholas, L. D., Borders, K. W., et al. (2009). Impact of geriatric assessment and self-management support on community-dwelling older adults with chronic illnesses... `. Journal of Gerontological Social Work, 52(3), 230-249.

Feinberg, L. F. (2008). Caregiver Assessment. American Journal of Nursing, 108(9), 38-39.

Ferm, M. (2008). När himlen är nära- : till samtalsledare som leder "När himlen är nära-grupper". Stockholm: SPES.

Ferm M, Beskow J. (2008). Att våga vara nära. Tidningen Äldreomsorg. 2008, (6), 48-51.

Fitzpatrick, K. E., & Vacha-Haase, T. (2010). Marital satisfaction and resilience in caregivers of spouses with dementia. Clinical Gerontologist, 33(3), 165-180.

Forsberg, E. & Eriksson, M. (2008). Hälsokonsekvensbedömning : ur ett äldreperspektiv. Karlskrona: Länsstyrelsen Blekinge län.

Fortinsky, R. H., Kulldorff, M., Kleppinger, A., & Kenyon-Pesce, L. (2009). Dementia care consultation for family caregivers: Collaborative model linking an Alzheimer's association chapter with primary care physicians. Aging & Mental Health, 162-170.

Fowler, C., & Fisher, C. L. (2009). Attitudes toward decision making and aging, and preparation for future care needs. Health Communication, 24(7), 619-630.

Franzen-Dahlin, A., Laska, A. C, Larson, J., Wredling, R., Billing, E. & Murray, V. (2008). Predictors of life situation among significant others of depressed or aphasic stroke patients. Journal of Clinical Nursing, 17(12), 1574-1580.

Freeman, S., Kurosawa, H., Ebihara, S., & Kohzuki, M. (2010). Caregiving burden for the oldest old: a population based study of centenarian caregivers in Northern Japan. Archives of Gerontology & Geriatrics, 50(3), 282-291.

Friberg, J. (2004). I nöd och lust : Informella anhörigvårdares vardag. Unpublished C-uppsats. Linköping: Linköpings Universitet.

Garces, J., Carretero, S., Rodenas, F., & Aleman, C. (2010). A review of programs to alleviate the burden of informal caregivers of dependent persons. Archives of Gerontology & Geriatrics, 50(3), 254-259.

Garcia-Willix, D., & Sferrazza, P. (2010). Research and nursing theory on family caregiving. Home Healthcare Nurse, 28(5), 264-269.

Gaugler, J. E., Mittelman, M. S., Hepburn, K., & Newcomer, R. (2009). Predictors of Change in Caregiver Burden and Depressive Symptoms Following Nursing Home Admission. Psychology and Aging, 24(2), 385-396.

Gelmini, G., Morabito, B., & Braidi, G. (2009). Educational and formative training reduce stress in the caregivers of demented patients. Archives of Gerontology & Geriatrics, 49, 119-124.

Georges, J. M. (2010). A contextually based theory of caregiver suffering. Communicating Nursing Research, 43, 375-375.

Giesbrecht, M., Crooks, V. A., & Williams, A. (2010). Perspectives from the frontlines: palliative care providers' expectations of Canada's compassionate care benefit programme. Health & Social Care in the Community, 18(6), 643-652.

Gitlin, L. N., Winter, L., Dennis, M. P., Hodgson, N., & Hauck, W. W. (2010). A biobehavioral home-based intervention and the well-being of patients with dementia and their caregivers: the COPE randomized trial. JAMA: Journal of the American Medical Association, 304(9), 983-991.

Gitlin, L. N., Winter, L., Earland, T. V., Herge, E. A., Chernett, N. L., Piersol, C. V., et al. (2009). The Tailored Activity Program to Reduce Behavioral Symptoms in Individuals With Dementia: Feasibility, Acceptability, and Replication Potential. The Gerontologist, 49(3), 428-439.

Gitlin, L. N., Jacobs, M., & Earland, T. V. (2010). Translation of a Dementia Caregiver Intervention for Delivery in Homecare as a Reimbursable Medicare Service: Outcomes and Lessons Learned. The Gerontologist, 50(6), 847-854.

Greenwood, N., Mackenzie, A., Cloud, G., & Wilson, N. (2010). Loss of autonomy, control and independence when caring: a qualitative study of informal carers of stroke survivors in the first three months after discharge. Disability & Rehabilitation, 32(2), 125-133.

Gregory, N., Collins-Atkins, C., Macpherson, R., Ford, S., & Palmer, A. (2006, Apr 25-May 1). Identifying the needs of carers in mental health services. Nursing Times, 102(17), 32-35.

Grimby, A., Johansson, A. K., Sundh, V. & Grimby, G. (2008). Walking habits of elderly widows. American Journal of Hospice & Palliative Medicine, 25(2), 81-87.

Gulwadi, G. B. (2009). Restorative home environments for family caregivers. Journal of Aging Studies, 23(3), 197-204.

Gustafson, M., & Rautio, U. (2002). Att vara anhörigvårdare till en person med demenssjukdom : En litteraturstudie. Luleå: Luleå Tekniska Universitet, Institutionen för Hälsovetenskap.

Gustavsson, A., Jönsson, L., McShane, R., Boada, M., Wimo, A., & Zbrozek, A. S. (2010). Willingness-to-pay for reductions in care need: estimating the value of informal care in Alzheimer's disease. International Journal of Geriatric Psychiatry, 25(6), 622-632.

Healing the caregiver: six steps to help you stay healthy while caring for a loved one. (2010). Johns Hopkins Medical Letter: Health After 50, 22(4), 3-3.

Haynes, P., Hill, M., & Banks, L. (2010). Older People's Family Contacts and Long-term Care Expenditure in OECD Countries: A Comparative Approach Using Qualitative Comparative Analysis. Social Policy and Administration, 44(1), 67-84

Heimroth, C. & Johansson, B. (2009). Närståendes upplevelse av hopp när en person drabbas av sjukdom [Elektronisk resurs]. Luleå: Luleå tekniska universitet/Hälsovetenskap/Omvårdnad.

Hellström, Y., Andersson, M., & Hallberg, I. R. (2004, Nov). Quality of life among older people in Sweden receiving help from informal and/or formal helpers at home or in special accommodation. Health and Social Care in the Community, 12(6), 504-516.

Hellström, Y., & Hallberg, I. R. (2001, Mar). Perspectives of elderly people receiving home help on health, care and quality of life. Health and Social Care in the Community, 9(2), 61-71.

Herlitz C. & Dahlberg L. (1999). Causes of strain affecting relatives of Swedish oldest elderly: A population-based study. Scandinavian Journal of Caring Science, 13(2), 109-115.

Hilton, J. M., Kopera-Frye, K. & Krave, A. (2009). Successful Aging From the Perspective of Family Caregivers. The Family Journal: Counseling and Therapy for Couples and Families, 17(1), 39-50.

Hjort, A., & Långström, A. (2006). Anhörigas vardag : En kvalitativ studie om att ge omsorg till en närstående. Unpublished C-uppsats. Karlstad: Karlstad Universitet.

Hjorth, Aronsson, C. (2008). Asta 90: "Nu ska jag sluta besöka pensionärer!" Individ, samhälle, åldrande - några bilder Svensk idrottsforskning, 17(3), 18-21.

Holland, J. M., Currier, J. M. & Gallagher-Thompson, D. (2009). Outcomes From the Resources for Enhancing Alzheimer's Caregiver Health (REACH) Program for Bereaved Caregivers. Psychology and Aging, 24(1), 190-202.

Hulter Åsberg, K., & Johansson, L. (2002). Två år med stroke ur ett anhörigperspektiv. Socialmedicinsk Tidskrift (2), 146-152.

Iecovich, E. (2008). Caregiving Burden, Community Services, and Quality of Life of Primary Caregivers of Frail Elderly Persons. The Journal of Applied Gerontology, 27(3), 309-330.

Janicki, M. P., Zendell, A., & DeHaven, K. (2010). Coping with dementia and older families of adults with Down syndrome. Dementia (14713012), 9(3), 391-407.

Jansson, W., Nordberg, G., & Grafström, M. (2001). Patterns of elderly spousal caregiving in dementia care: An observational study. Journal of Advanced Nursing, 34(6), 804-812.

Jeppsson-Grassman, E. (2008). Att åldras med funktionshinder. 1 ed. Lund: Studentlitteratur.

Johansson, A. (2006). Närståendes upplevelse av hur relationen förändras när närstående drabbas av demens. Unpublished C-uppsats. Luleå: Luleå Tekniska Universitet. Hälsovetenskap/Omvårdnad.

Johansson, L. (2000). Risk for early death among overloaded family caregivers. Nordisk Geriatrik (4), 32-33.

Johansson, L. (2008). Anhörigstödets grundpelare : Ett framgångsrikt anhörigstöd står på några viktiga grundpelare ; en av dessa är att stödet tillför något positivt till både den anhörige och den demenssjuke ; det menar docent Lennarth Johansson ; tema: Demens - en lägesrapport. Äldre i centrum (1), 22-23.

Johansson Olsson, E., Dehlin, O., & Wahlfrid, C. (2005). Quality of life among family caregivers of stroke patients. Svensk Rehabilitering, 7(3), 30-33.

Jonsson, A. (2006). Stöd till närstående lättar deras börda : Månadens forskare. Vårdfacket (8), 55-56.

Jonsson, A., & Rönnberg, M. (2004). Upplevelsen av att vårda sin make/maka med demenssjukdom i hemmet. Unpublished C-uppsats. Luleå: Luleå Tekniska Universitet, Hälsovetenskap. Omvårdnad.

Jonsson, A. C., Lindgren, I., Hallström, B., Norrving, B., & Lindgren, A. (2005, Apr). Determinants of quality of life in stroke survivors and their informal caregivers. Stroke, 36(4), 803-808.

Jonsson, L., Eriksdotter Jonhagen, M., Kilander, L., Soininen, H., Hallikainen, M., Waldemar, G., et al. (2006, May). Determinants of costs of care for patients with Alzheimer's disease. International Journal of Geriatric Psychiatry, 21(5), 449-459.

Judge, K. S., Menne, H. L., & Whitlatch, C. J. (2010). Stress Process Model for Individuals With Dementia. The Gerontologist, 50(3), 294-302.

Jutkowitz, E., Gitlin, L. N., & Pizzi, L. T. (2010). Evaluating Willingness-to-Pay Thresholds for Dementia Caregiving Interventions: Application to the Tailored Activity Program. Value in Health, 13(6), 720-725.

Jönsson, A., Lindgren, I., Hallström, B., Norrving, B., & Lindgren, A. (2005). Determinants of quality of life in stroke survivors and their informal caregivers. Stroke (00392499), 36(4), 803-808.

Karlsson, S., Edberg, A.-K., Westergren, A., & Hallberg, I. R. (2008, Mars). Functional ability and health complaints among older people with a combination of public and informal care vs. Public care only. Scandinavian Journal of Caring Science, 22(1), 136-148.

Kartalova-O'Doherty, Y., & Doherty, D. T. (2009). Satisfied carers of persons with enduring mental illness: who and why? International Journal of Social Psychiatry, 55(3), 257-271.

Khalsa, D. S. (2010). Mindfulness Effects on Caregiver Stress: Should We Expect More? Journal of Alternative & Complementary Medicine, 16(10), 1025-1026.

Kim, Y. & Schulz, R. (2008). Family caregivers' strains: comparative analysis of cancer caregiving with dementia, diabetes, and frail elderly caregiving. Journal of Aging and Health, 20(5), 483-503.

Klavzar, L. (2005). Att finna mening : Hur fyra anhörigvårdare finner mening i sina livssituationer. Unpublished C-uppsats. Stockholm: Stockholms Universitet. Institutionen för socialt arbete - Socialhögskolan.

Koerner, S. S., Shirai, Y., & Kenyon, D. B. (2010). Sociocontextual circumstances in daily stress reactivity among caregivers for elder relatives. Journals of Gerontology Series B: Psychological Sciences & Social Sciences, 65B(5), 561-572.

Kristensson Ekwall, A. (2004). Informal caregiving in old age : Content, coping, difficulties and satisfaction. Lund: Lunds Universitet. 

Kuuppelomaki, M., Sasaki, A., Yamada, K., Asakawa, N., & Shimanouchi, S. (2004, Sep). Coping strategies of family carers for older relatives in Finland. Journal of Clinical Nursing, 13(6), 697-706. 

Kuuppelomäki, M., Sasaki, A., Yamada, K., Asakawa, N., & Shimanouchi, S. (2004, Jul). Family carers for older relatives: Sources of satisfaction and related factors in Finland. Internation Journal of Nursing Studies, 41(5), 497-505.

Källtorp, O., & Uggla, C. (2003). Att vara anhörigvårdare : Fokusgrupper samtalar om dilemman, känslor och behov (X-fokus forskningsrapport , 1651-2146 ; 2003:1). Gävle: Kommunförbundet Gävleborg.

Lampinen, Å. (2007). Upplevelsen av sorg hos närstående till personer med demens : en litteraturstudie. [Elektronisk resurs]. Luleå: Luleå tekniska universitet/Hälsovetenskap/Omvårdnad.

Larson, J. (2005). Life situation after stroke : The spouses' perspective. Huddinge: Karolinska Institutet.

Larson, J., Franzen-Dahlin, A., Billing, E., Murray, V., & Wredling, R. (2005, Nov). Spouse's life situation after partner's stroke event: Psychometric testing of a questionnaire. Journal of Advanced Nursing, 52(3), 300-306.

Larsson, L. (2005). "Ensamhet i tvåsamheten" : Anhörigas erfarenheter av att vårda personer med demenssjukdom i hemmet (Meddelande från Blekinge FoU-enhet, 1400-7959 ; 2005:1). Karlshamn: Blekinge Forsknings- och Utvecklingsenhet.

Lee, M. (2009). A Path Analysis on Elder Abuse by Family Caregivers: Applying the ABCX Model. Journal of Family Violence, 24(1), 1-9.

Lin, C C, Lin, P. Y, Lu, P. K, Hsieh, G. Y, Lee, W. L. & Lee, R. G. (2008). A healthcare integration system for disease assessment and safety monitoring of dementia patients. IEEE Transactions on Information Technology in Biomedicine,12(5), 579-586.

Lindhardt, T., Bolmsjö, I. A., & Hallberg, I. R. (2006). Standing guard -- being a relative to a hospitalised, elderly person. Journal of Aging Studies, 20(2), 133-149.

Lokk ,J. (2008). Caregiver strain in Parkinson's disease and the impact of disease duration. European Journal of Physical and Rehabilitation Medicine, 44(1), 39-45.

Losada, A., Márquez-González, M., Peñacoba, C., & Romero-Moreno, R. (2010). Development and validation of the caregiver guilt questionnaire. International Psychogeriatrics, 22(4), 650-660.

Losada, A., Perez-Penaranda, A., Rodriguez-Sanchez, E., Gomez-Marcos, M. A., Ballesteros-Rios, C., Ramos-Carrera, I. R., et al. (2010). Leisure and distress in caregivers for elderly patients. Archives of Gerontology & Geriatrics, 50(3), 347-350.

Losada, A., Marquez-Gonzalez, M., Knight, B. G., Yanguas, J., Sayegh, P., & Romero-Moreno, R. (2010). Psychosocial factors and caregivers' distress: effects of familism and dysfunctional thoughts. Aging & Mental Health, 14(2), 193-202.

Luchetti, L., Uhunmwangho, E., Dordoni, G., Lorido, A., Barbieri, S., Bolognesi, A. G., et al. (2009). The subjective feeling of burden in caregivers of elderly with dementia: how to intervene? Archives of Gerontology & Geriatrics, 49, 153-161.

Lundenmark ,T. (2008). Viktigare med aktivitetsstöd än mätning av funktionsförmåga. Arbetsterapeuten, (4), 13-14.

Lundgren, E., & Sjöblom, J. (2005). Anhörigvårdares upplevelse av sitt vardagliga arbete. Unpublished C-uppsats. Kristianstad: Högskolan Kristianstad.

Lundh, U. (2004). Att vara äldre och vårdare. In: Att vara äldre : "- man har ju sina krämpor", (Eds:  Blomqvist, K., Edberg, A. K). (145-156). Lund: Studentlitteratur.

Lundqvist, M. (2006). Att vårda en anhörig med demens. Örebro: Bokverksta'n.

Lyons, K. S., Stewart, B. J., Archbold, P. G., & Carter, J. H. (2009). Optimism, pessimism, mutuality, and gender: Predicting 10-year role strain in Parkinson's disease spouses. Gerontologist, 49(3), 378-387.

MacKenzie, C. S., Wiprzycka, U. J., Hasher, L. & Goldstein, D. (2008). Seeing the glass half full: Optimistic expressive writing improves mental health among chronically stressed caregivers. British Journal of Health Psychology, 13(1), 73-76.

Malmberg, B., & Sundström, G. (2004). Äldres levnadsförhållanden 1988-2002 : Hälsa, funktionsförmåga och vård- och omsorgsmönster. Stockholm: Socialstyrelsen.

Mannion, E. (2008). Alzheimer's disease: the psychological and physical effects of the caregiver's role - Part 1. Nursing Older People, 20(4), 27-32.

Martinez-Martin, P., Arroyo, S., Rojo-Abuin, J. M., Rodriguez-Blazquez,  C., Frades, B., Cuesta, J. D., et al. (2008). Burden, perceived health status, and mood among caregivers of Parkinson's disease patients. Movement Disorders, 23(12), 1673-1680.

Martire, L. M., Schulz, R., Reynolds, C. F., III, Karp, J. F., Gildengers, A. G., & Whyte, E. M. (2010). Treatment of late-life depression alleviates caregiver burden. Journal of the American Geriatrics Society, 58(1), 23-29.

Mausbach, B. T., Patterson, T. L. & Grant, I. (2008). Is depression in Alzheimer's caregivers really due to activity restriction? A preliminary mediational test of the Activity Restriction Model. Journal of Behavior Therapy and Experimental Psychiatry, 39(4), 459-466.

McKee, K. J., Philp, I., & Lamura, G. (2003, January). The cope index - a first stage assessment of negative impact, positive value and quality of support of caregiving in informal carers of older people. Aging & Mental Health, 7(1), 39-52.

Mellor, D., Russo, S., McCabe, M. R., Davison, T. E. & George, K. (2008). Depression training program for caregivers of elderly care recipients - Implementation and qualitative evaluation. Journal of Gerontological Nursing, 34(9), 8-15.

Modin, S., & Furhoff, A. K. (2004, Aug). The medical care of patients with primary care home nursing is complex and influenced by non-medical factors: A comprehensive retrospective study from a suburban area in Sweden. BMC Health Services Research, 4(1), 22.

Molyneux, G. J., McCarthy, G. M., McEniff ,S., Cryan, M.& Conroy ,R. M. (2008). Prevalence and predictors of carer burden and depression in carers of patients referred to an old age psychiatric service. International Psychogeriatrics, 20(6), 1193-1202.

Montoro-Rodriguez, J., Kosloski, K., Kercher, K. & Montgomery, R. J. V. (2009). The Impact of Social Embarrassment on Caregiving Distress in a Multicultural Sample of Caregivers. The Journal of Applied Gerontology, 28(2), 195-217.

Muliira, J. K., & Musil, C. M. (2010). Relationship Between Methods of Coping, Social Support and Receipt of Preventive Care Procedures by Primary Grandmother Caregivers. Journal of Community Health, 35(5), 479-486.

Mårtensson, J., Dracup, K., & Fridlund, B. (2001, Sep-Oct). Decisive situations influencing spouses' support of patients with heart failure: A critical incident technique analysis. Heart & Lung, 30(5), 341-350.

Nilsson, E. (2004). Socialt stöd och livstillfredsställelse bland äldre kvinnor med funktionshinder. Unpublished D-uppsats, Stockholm: Stockholms Universitet.

Netto, N. R., Jenny, G. Y. N., & Philip, Y. L. K. (2009). Growing and gaining through caring for a loved one with dementia. Dementia, 8(2), 245-261.

Nichols, L. O., Martindale-Adams, J., Greene, W. A., Burns, R., Graney, M. J., & Lummus, A. (2009). Dementia caregivers' most pressing concerns. Clinical Gerontologist, 32(1), 1-14.

Okamoto, K., & Harasawa, Y. (2009). Predictor of increase in caregiver burden for disabled elderly at home. Archives of Gerontology & Geriatrics, 49(1), 129-131.

Oken, B. S., Fonareva, I., Haas, M., Wahbeh, H., Lane, J. B., Zajdel, D., et al. (2010). Pilot Controlled Trial of Mindfulness Meditation and Education for Dementia Caregivers. Journal of Alternative & Complementary Medicine, 16(10), 1031-1038.

O'Reilly, D., Connolly, S., Rosato, M., Patterson, C. (2008). Is caring associated with an increased risk of mortality? A longitudinal study. Social Science & Medicine, 67(8), 1282-1290.

Ornstein, K., Smith, K. L., & Boal, J. (2009). Understanding and improving the burden and unmet needs of informal caregivers of homebound patients enrolled in a home-based primary care program. Journal of Applied Gerontology, 28(4), 482-503.

O'Shaughnessy, M. O., Lee, K., & Lintern, T. (2010). Changes in the couple relationship in dementia care: spouse carers' experiences. Dementia (14713012), 9(2), 237-258.

Ott, C. H., Kelber, S. T., & Blaylock, M. (2010). "Easing the way" for spouse caregivers of individuals with dementia: a pilot feasibility study of a grief intervention. Research in Gerontological Nursing, 3(2), 89-99.

Peacock, S., Forbes, D., Markle-Reid, M., Hawranik, P., Morgan, D., Jansen, L., et al. (2010). The positive aspects of the caregiving journey with dementia: using a strengths-based perspective to reveal opportunities. Journal of Applied Gerontology, 29(5), 640-659.

Peldan, K. (2005). Att kalla det vårdare då…det vet jag inte… : En studie om anhöriga, äldres individuella upplevelse av att vårda sin partner. Unpublished C-uppsats, Stockholms Universitet, Institutionen för socialt arbete - Socialhögskolan.

Perrin, P. B., Johnston, A., Vogel, B., Heesacker, M., Vega-Trujillo, M., Anderson, J., et al. (2010). A culturally sensitive transition assistance program for stroke caregivers: examining caregiver mental health and stroke rehabilitation. Journal of Rehabilitation Research & Development, 47(7), 605-615.

Phillips, A. C., Gallagher, S., Hunt, K., Der, G., & Carroll, D. (2009). Symptoms of depression in non-routine caregivers: the role of caregiver strain and burden. British Journal of Clinical Psychology, 48(Part 4), 335-346.

Pruchno, R. A., Cartwright, F. P., & Wilson-Genderson, M. (2009). Effects of marital closeness on the transition from caregiving to widowhood. Aging & Mental Health, 808-817.

Ron, P. (2008). Offspring Caring for Their Elderly Parents: The Effect of Social Support and Gender-Role Orientation on These Caregivers' Well-Being. Illness, Crisis & Loss, 16(3), 183-201.

Ron, P. (2009). Daughters as Caregivers of Aging Parents: The Shattering Myth. Journal of Gerontological Social Work, 52(2), 135-153.

Ronning, R. (2002, December). In defence of care - the importance of care as a positive concept. Quality in Ageing, 3(4), 34-43.

Rosness, T. A., Ulstein, I., & Engedal, K. (2009). Stress affects carers before patient's first visit to a memory clinic. International Journal of Geriatric Psychiatry, 24(10), 1143-1150.

Rowe, M. A., Kairalla, J. A., & McCrae, C. S. (2010). Sleep in Dementia Caregivers and the Effect of a Nighttime Monitoring System. Journal of Nursing Scholarship, 42(3), 338-347.

Rudenstam, C. (2004). Love - motivation behind home care. Omvårdnadsmagasinet, 2(4), 34-38.

Rudenstam, C. (2006). The important support - to give and receive. Omvårdnadsmagasinet, 4(4), 8-11.

Russell, R. (2008). Their Story, My Story: Health of Older Men as Caregivers. Generations, 32(1), 62-67.

Rydberg, I. & Stenborg, A. (2008). Vuxna barns erfarenheter som anhörigvårdare till en förälder med demenssjukdom [C-uppsats]. Kalmar: Högskolan i Kalmar.

Rönnberg, A. J. M. (2004). Upplevelsen av att vårda sin make/maka med demenssjukdom i hemmet. Unpublished C-uppsats, Luleå: Luleå Tekniska Universitet, Hälsovetenskap/Omvårdnad.

Sand, A.-B. M. (2004). Kärleken prövas när livspartnern blir vårdare : Tema : Kärlekens låga. Äldre i centrum (3), 18-19.

Sayegh, P., & Knight, B. G. (2011). The effects of familism and cultural justification on the mental and physical health of family caregivers. The Journals Of Gerontology. Series B, Psychological Sciences And Social Sciences, 66(1), 3-14.

Schoenmakers, B., Buntinx, F., & DeLepeleire, J. (2010). Supporting the dementia family caregiver: the effect of home care intervention on general well-being. Aging & Mental Health, 14(1), 44-56.

Schulz, R., Monin, J. K., Czaja, S. J., Lingler, J. H., Beach, S. R., Martire, L. M., et al. (2010). Measuring the experience and perception of suffering. The Gerontologist, 50(6), 774-784.

Sjöberg, M. (2001). Men hur mår du själv? : Om stöd till dem som vårdar anhöriga (Sköndalsinstitutets metodbokserie, 1650-4933 ; 2). Stockholm: Sköndalsinstitutet.

Spjuth, E. & Sundström, Å. (2008). Ett rikt och meningsfullt liv. Solna: Fortbildning AB.

Soldato, M., Liperoti, R., Landi, F., Carpenter, I. G., Bernabei, R., & Onder, G. (2008, Feb). Patient depression and caregiver attitudes: Results from the aged in home care study. Journal of Affective Disorders, 106(1-2), 107-115.

Stajduhar, K., Funk, L., Jakobsson, E., & Öhlén, J. (2010). A critical analysis of health promotion and ‘empowerment’ in the context of palliative family care-giving. Nursing Inquiry, 17(3), 221-230.

Stenwall, E. (2009). Ett ögonblick i sänder [Elektronisk resurs] : mötet vid akut förvirringstillstånd, äldre patienters, närståendes och professionella vårdares perspektiv [Diss.]. Stockholm: Karolinska institutet.

Stenwall, E., Jönhagen, M. E., Sandberg, S. & Fagerberg, I. (2008). The older patient's experience of encountering professional carers and close relatives during an acute confusional state: an interview study. International Journal of Nursing Studies, 45(11), 1577-1585.

Stenwall, E., Sandberg, J., Jönhagen, M. E. & Fagerberg, I. (2008). Relatives' experiences of encountering the older person with acute confusional state: experiencing unfamiliarity in a familiar person. International Journal of Older People Nursing, 3(4), 243-251.

Stokes, G. (2010). Explaining about... Day-to-day living with dementia. Working with Older People: Community Care Policy & Practice, 14(1), 5-7.

Sussman, T., & Regehr, C. (2009). The influence of community-based services on the burden of spouses caring for their partners with dementia. Health & Social Work, 34(1), 29-39.

Svensson, M. N. R. (2005). Anhörigvårdarens situation. Unpublished C-uppsats, Kristianstad: Kristianstad Universitet, Institutionen för Hälsovetenskaper.

Söderhielm Blid, S. (2007). Hälsosamtal och förebyggande hembesök : en lägesrapport. Stockholm: Stiftelsen Stockholms läns äldrecentrum.

Takai, M., Takahashi, M., Iwamitsu, Y., Ando, N., Okazaki, S., Nakajima, K., et al. (2009). The experience of burnout among home caregivers of patients with dementia: relations to depression and quality of life. Archives of Gerontology & Geriatrics, 49(1), e1-5.

te Boekhorst, S., Pot, A. M., Depla, M., Smit, D., de Lange, J. & Eefsting, J. (2008). Group living homes for older people with dementia: The effects on psychological distress of informal caregivers. Aging & Mental Health, 2(6), 761-768.

The legitimacy of rest: conditions for the relief of burden in advanced dementia care-giving. (2010). Journal of Advanced Nursing, 66(5), 988-998. 

Travis, S. S., McAuley, W. J., Dmochowski, J., Bernard, M. A., Kao, H. F., & Greene, R. (2007, Apr). Factors associated with medication hassles experienced by family caregivers of older adults. Patient Education and Counseling, 66(1), 51-57.

Törnkvist, L. & Wånell, S-E. (2008). Basal hemsjukvård för äldre personer med långvariga vårdbehov : hur kan vården förbättras? Stockholm: Stockholms läns landsting

Ulstein, I., Jacobsen, S., & Lille, K. A. (2005). Dementia in the family. Does knowledge have a significance for the experience of stress among. Demens, 9(2), 4-8.

Ulstein, I., Wyller, T. B., & Engedal, K. (2007, January). The relative stress scale, a useful instrument to identify various aspects of carer burden in dementia? International Journal of Geriatric Psychiatry, 22(1), 61-67.

Ulstein, I & Johannessen, A. (2008). Effekt av strukturert problemlösning i familier med demens. Demens & Alderspsykiatri, 12(2), 35-38.

Ulstein, I., Wyller, T. B. & Engedal, K. (2008). Correlates of intrusion and avoidance as stress response symptoms in family carers of patients suffering from dementia. International Journal of Geriatric Psychiatry, 23(10), 1051-1057.

Waldron-Perrine, B., Rapport, L. J., Ryan, K. A., & Harper, K. T. (2009). Predictors of life satisfaction among caregivers of individuals with multiple sclerosis. The Clinical Neuropsychologist, 23(3), 462-478.

Wilks, S. E. (2009). Support for Alzheimer's caregivers: psychometric evaluation of familial and friend support measures. Research on Social Work Practice, 19(6), 722-729.

Williams, V. P., Bishop-Fitzpatrick, L., Lane, J. D., Gwyther, L. P., Ballard, E. L., Vendittelli, A. P., et al. (2010). Video-based coping skills to reduce health risk and improve psychological and physical well-being in Alzheimer's disease family caregivers. Psychosomatic Medicine, 72(9), 897-904.

Wilson-Genderson, M., Pruchno, R. A., & Cartwright, F. P. (2009). Effects of caregiver burden and satisfaction on affect of older end-stage renal disease patients and their spouses. Psychology and Aging, 24(4), 955-967.

Wright, L. M., Watson, W. L., Bell, J. M., & Larsson-Wentz, K. (2002). Familjefokuserad omvårdnad : Föreställningar i samband med ohälsa och sjukdom. Lund: Studentlitteratur.

Ziegert, K., Fridlund, B., & Lidell, E. (2006, Jun). Health in everyday life among spouses of haemodialysis patients: A content analysis. Scandinavian Journal of  Caring Science, 20(2), 223-228.

Ziegert, K. (2010). Vård av anhörig : ett livsstilval med konsekvenser för hälsan Hälsa och livsstil : forskning och praktiska tillämpningar (pp. 289-305). Lund: Studentlitteratur.

Åberg, A. C., Sidenvall, B., Hepworth, M., O'Reilly, K., & Lithell, H. (2004, Jul). Continuity of the self in later life: Perceptions of informal caregivers. Qualitative Health Research, 14(6), 792-815.

Östman, M. (2000). Family burden and participation in care : A study of relatives to patients admitted to voluntary and compulsory psychiatric care. Lund: Lunds Universitet.

Östman, M. (2004, Oct). Family burden and participation in care: Differences between relatives of patients admitted to psychiatric care for the first time and relatives of re-admitted patients. Journal of Psychiatric and Mental Health Nursing, 11(5), 608-613.

Sidan uppdaterad den 29 oktober 2010Kommentera sidan