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Similar articles for PubMed (Select 16401890)

1.

Determinants of the quality of life in Alzheimer's disease patients as assessed by the Japanese version of the Quality of Life-Alzheimer's disease scale.

Matsui T, Nakaaki S, Murata Y, Sato J, Shinagawa Y, Tatsumi H, Furukawa TA.

Dement Geriatr Cogn Disord. 2006;21(3):182-91. Epub 2006 Jan 9.

PMID:
16401890
2.

Neuropsychiatric symptoms predict change in quality of life of Alzheimer disease patients: a two-year follow-up study.

Tatsumi H, Nakaaki S, Torii K, Shinagawa Y, Watanabe N, Murata Y, Sato J, Mimura M, Furukawa TA.

Psychiatry Clin Neurosci. 2009 Jun;63(3):374-84. doi: 10.1111/j.1440-1819.2009.01955.x.

PMID:
19566770
3.

Validation of the Brazilian version of the quality of life scale for patients with Alzheimer's disease and their caregivers (QOL-AD).

Novelli MM, Nitrini R, Caramelli P.

Aging Ment Health. 2010 Jul;14(5):624-31. doi: 10.1080/13607861003588840.

PMID:
20480421
4.

Assessing quality of life in Taiwanese patients with Alzheimer's disease.

Fuh JL, Wang SJ.

Int J Geriatr Psychiatry. 2006 Feb;21(2):103-7.

PMID:
16416471
5.

Psychometric properties of the Spanish QoL-AD with institutionalized dementia patients and their family caregivers in Spain.

León-Salas B, Logsdon RG, Olazarán J, Martínez-Martín P, The Msu-Adru.

Aging Ment Health. 2011 Aug;15(6):775-83. doi: 10.1080/13607863.2011.562183. Epub 2011 May 24.

PMID:
21547751
6.

Behavioral disorders and caregivers' reaction in Taiwanese patients with Alzheimer's disease.

Fuh JL, Liu CK, Mega MS, Wang SJ, Cummings JL.

Int Psychogeriatr. 2001 Mar;13(1):121-8.

PMID:
11352329
7.

Reliability and validity of the Japanese version of the Agitated Behaviour in Dementia Scale in Alzheimer's disease: three dimensions of agitated behaviour in dementia.

Torii K, Nakaaki S, Banno K, Murata Y, Sato J, Tatsumi H, Yamanaka K, Narumoto J, Mimura M, Akechi T, Furukawa TA.

Psychogeriatrics. 2011 Dec;11(4):212-20. doi: 10.1111/j.1479-8301.2011.00371.x. Epub 2011 Oct 27.

PMID:
22151240
8.

[Caregiver burden in dementia: evaluation with a Japanese version of the Zarit caregiver burden interview].

Hirono N, Kobayashi H, Mori E.

No To Shinkei. 1998 Jun;50(6):561-7. Japanese.

PMID:
9656252
9.

Proxy-rated quality of life in Alzheimer's disease: a three-year longitudinal study.

Vogel A, Bhattacharya S, Waldorff FB, Waldemar G.

Int Psychogeriatr. 2012 Jan;24(1):82-9. doi: 10.1017/S1041610211001128. Epub 2011 Jun 28.

PMID:
21729415
10.

[Validation of the Quality of Life in Alzheimer's Disease (QOL-AD) scale in Mexican patients with Alzheimer, vascular and mixed-type dementia].

Rosas-Carrasco O, Torres-Arreola Ldel P, Guerra-Silla Mde G, Torres-Castro S, Gutierrez-Robledo LM.

Rev Neurol. 2010 Jul 16;51(2):72-80. Spanish.

11.

Assessing the impact of neuropsychiatric symptoms in Alzheimer's disease: the Neuropsychiatric Inventory Caregiver Distress Scale.

Kaufer DI, Cummings JL, Christine D, Bray T, Castellon S, Masterman D, MacMillan A, Ketchel P, DeKosky ST.

J Am Geriatr Soc. 1998 Feb;46(2):210-5.

PMID:
9475452
12.

Use of the QOL-AD for measuring quality of life in people with severe dementia--the LASER-AD study.

Hoe J, Katona C, Roch B, Livingston G.

Age Ageing. 2005 Mar;34(2):130-5.

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Caregivers' assessments of preference-based quality of life in Alzheimer's disease.

Karlawish JH, Zbrozek A, Kinosian B, Gregory A, Ferguson A, Low DV, Glick HA.

Alzheimers Dement. 2008 May;4(3):203-11. doi: 10.1016/j.jalz.2007.11.018. Epub 2008 Apr 24.

PMID:
18631969
17.

[Predictors of long-term institutionalization in patients with Alzheimer's disease: role of caregiver burden].

Hirono N, Tsukamoto N, Inoue M, Moriwaki Y, Mori E.

No To Shinkei. 2002 Sep;54(9):812-8. Japanese.

PMID:
12428367
18.

Whose quality of life is it anyway? The validity and reliability of the Quality of Life-Alzheimer's Disease (QoL-AD) scale.

Thorgrimsen L, Selwood A, Spector A, Royan L, de Madariaga Lopez M, Woods RT, Orrell M.

Alzheimer Dis Assoc Disord. 2003 Oct-Dec;17(4):201-8.

PMID:
14657783
19.

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
20.

Validation of the Icelandic version of the Neuropsychiatric Inventory with Caregiver Distress (NPI-D).

Davidsdottir SR, Snaedal J, Karlsdottir G, Atladottir I, Hannesdottir K.

Nord J Psychiatry. 2012 Feb;66(1):26-32. doi: 10.3109/08039488.2011.593100. Epub 2011 Jul 20.

PMID:
21770826
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