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Items: 1 to 20 of 218

1.

Social representation and practices related to dementia in Hai District of Tanzania.

Mushi D, Rongai A, Paddick SM, Dotchin C, Mtuya C, Walker R.

BMC Public Health. 2014 Mar 19;14:260. doi: 10.1186/1471-2458-14-260.

2.

[The role of family carers of people with dementia in the assessment of need on the example of the CarenapD study].

Riesner C.

Pflege. 2014 Aug;27(4):243-55. doi: 10.1024/1012-5302/a000374. German.

PMID:
25047953
3.

Unmet needs, quality of life and support networks of people with dementia living at home.

Miranda-Castillo C, Woods B, Galboda K, Oomman S, Olojugba C, Orrell M.

Health Qual Life Outcomes. 2010 Nov 12;8:132. doi: 10.1186/1477-7525-8-132.

4.

Unmet needs of community-residing persons with dementia and their informal caregivers: findings from the maximizing independence at home study.

Black BS, Johnston D, Rabins PV, Morrison A, Lyketsos C, Samus QM.

J Am Geriatr Soc. 2013 Dec;61(12):2087-95.

5.

The effect of coping on the burden in family carers of persons with dementia.

Bruvik FK, Ulstein ID, Ranhoff AH, Engedal K.

Aging Ment Health. 2013;17(8):973-8. doi: 10.1080/13607863.2013.790928. Epub 2013 Apr 24.

PMID:
23614391
6.

Knowledge exchange throughout the dementia care journey by Canadian rural community-based health care practitioners, persons with dementia, and their care partners: an interpretive descriptive study.

Forbes DA, Finkelstein S, Blake CM, Gibson M, Morgan DG, Markle-Reid M, Culum I, Thiessen E.

Rural Remote Health. 2012 Oct;12(4):2201. Epub 2012 Nov 26.

7.

EUROCARE: a cross-national study of co-resident spouse carers for people with Alzheimer's disease: I--Factors associated with carer burden.

Schneider J, Murray J, Banerjee S, Mann A.

Int J Geriatr Psychiatry. 1999 Aug;14(8):651-61.

PMID:
10489656
8.

A comparison of caregiver burden in older persons and persons with Parkinson's disease or dementia in sub-Saharan Africa.

Dotchin CL, Paddick SM, Longdon AR, Kisoli A, Gray WK, Dewhurst F, Chaote P, Dewhurst M, Walker RW.

Int Psychogeriatr. 2014 Apr;26(4):687-92. doi: 10.1017/S104161021300255X. Epub 2014 Feb 10.

PMID:
24507385
9.

Quality of life in dementia: the role of non-cognitive factors in the ratings of people with dementia and family caregivers.

Sousa MF, Santos RL, Arcoverde C, Simões P, Belfort T, Adler I, Leal C, Dourado MC.

Int Psychogeriatr. 2013 Jul;25(7):1097-105. doi: 10.1017/S1041610213000410. Epub 2013 Apr 8.

PMID:
23561627
10.

People with dementia living alone: what are their needs and what kind of support are they receiving?

Miranda-Castillo C, Woods B, Orrell M.

Int Psychogeriatr. 2010 Jun;22(4):607-17. doi: 10.1017/S104161021000013X. Epub 2010 Mar 10.

PMID:
20214844
11.

Desired characteristics and outcomes of community care services for persons with dementia: what is important according to clients, service providers and policy?

Low LF, White F, Jeon YH, Gresham M, Brodaty H.

Australas J Ageing. 2013 Jun;32(2):91-6. doi: 10.1111/j.1741-6612.2012.00625.x. Epub 2012 Aug 23.

PMID:
23773247
12.

Psychosocial impact of early onset dementia among caregivers.

Kimura NR, Maffioletti VL, Santos RL, Baptista MA, Dourado MC.

Trends Psychiatry Psychother. 2015 Dec;37(4):213-9. doi: 10.1590/2237-6089-2015-0038.

13.

A pilot study examining the awareness, attitude, and burden of informal caregivers of patients with dementia.

Qadir F, Gulzar W, Haqqani S, Khalid A.

Care Manag J. 2013;14(4):230-40.

PMID:
24579270
14.

Empowering older people with early dementia and family caregivers: a participatory action research study.

Nomura M, Makimoto K, Kato M, Shiba T, Matsuura C, Shigenobu K, Ishikawa T, Matsumoto N, Ikeda M.

Int J Nurs Stud. 2009 Apr;46(4):431-41. Epub 2007 Nov 5.

PMID:
17983619
15.

Correlates of objective and subjective measures of caregiver burden among dementia caregivers: influence of unmet patient and caregiver dementia-related care needs.

Hughes TB, Black BS, Albert M, Gitlin LN, Johnson DM, Lyketsos CG, Samus QM.

Int Psychogeriatr. 2014 Nov;26(11):1875-83. doi: 10.1017/S1041610214001240. Epub 2014 Aug 8.

16.

START (STrAtegies for RelaTives) study: a pragmatic randomised controlled trial to determine the clinical effectiveness and cost-effectiveness of a manual-based coping strategy programme in promoting the mental health of carers of people with dementia.

Livingston G, Barber J, Rapaport P, Knapp M, Griffin M, Romeo R, King D, Livingston D, Lewis-Holmes E, Mummery C, Walker Z, Hoe J, Cooper C.

Health Technol Assess. 2014 Oct;18(61):1-242. doi: 10.3310/hta18610.

17.

The impact of neuropsychiatric symptoms on caregiver distress and quality of life in persons with dementia in an Asian tertiary hospital memory clinic.

Khoo SA, Chen TY, Ang YH, Yap P.

Int Psychogeriatr. 2013 Dec;25(12):1991-9. doi: 10.1017/S1041610213001518.

PMID:
24230964
18.

Quality of life of community-residing persons with dementia based on self-rated and caregiver-rated measures.

Black BS, Johnston D, Morrison A, Rabins PV, Lyketsos CG, Samus QM.

Qual Life Res. 2012 Oct;21(8):1379-89. doi: 10.1007/s11136-011-0044-z. Epub 2011 Oct 26.

20.

The relationship between caregiver burden, caregivers' perceived health and their sense of coherence in caring for elders with dementia.

Andrén S, Elmståhl S.

J Clin Nurs. 2008 Mar;17(6):790-9. doi: 10.1111/j.1365-2702.2007.02066.x.

PMID:
18279282
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