Crossref Citations
This article has been cited by the following publications. This list is generated based on data provided by
Crossref.
2006.
Current awareness in geriatric psychiatry.
International Journal of Geriatric Psychiatry,
Vol. 21,
Issue. 5,
p.
500.
Whalen, Kimberly J.
and
Buchholz, Susan W.
2009.
The reliability, validity and feasibility of tools used to screen for caregiver burden: a systematic review.
JBI Library of Systematic Reviews,
Vol. 7,
Issue. 32,
p.
1373.
Whalen, Kimberly J.
and
Buchholz, Susan W.
2009.
The reliability, validity and feasibility of tools used to screen for caregiver burden: a systematic review.
JBI Database of Systematic Reviews and Implementation Reports,
Vol. 7,
Issue. 32,
p.
1373.
Schölzel-Dorenbos, Carla J.M.
Meeuwsen, Els J.
and
Olde Rikkert, Marcel G.M.
2010.
Integrating unmet needs into dementia health-related quality of life research and care: Introduction of the Hierarchy Model of Needs in Dementia.
Aging & Mental Health,
Vol. 14,
Issue. 1,
p.
113.
Shanley, Chris
Russell, Cherry
Middleton, Heather
and
Simpson-Young, Virginia
2011.
Living through end-stage dementia: The experiences and expressed needs of family carers.
Dementia,
Vol. 10,
Issue. 3,
p.
325.
Nunnemann, Sabine
Kurz, Alexander
Leucht, Stefan
and
Diehl-Schmid, Janine
2012.
Caregivers of patients with frontotemporal lobar degeneration: a review of burden, problems, needs, and interventions.
International Psychogeriatrics,
Vol. 24,
Issue. 9,
p.
1368.
Furniss, Kate Atkins
Loverseed, Annie
Lippold, Tessa
and
Dodd, Karen
2012.
The views of people who care for adults with Down’s syndrome and dementia: a service evaluation.
British Journal of Learning Disabilities,
Vol. 40,
Issue. 4,
p.
318.
Vaingankar, Janhavi Ajit
Subramaniam, Mythily
Picco, Louisa
Eng, Goi Khia
Shafie, Saleha
Sambasivam, Rajeswari
Zhang, Yun Jue
Sagayadevan, Vathsala
and
Chong, Siow Ann
2013.
Perceived unmet needs of informal caregivers of people with dementia in Singapore.
International Psychogeriatrics,
Vol. 25,
Issue. 10,
p.
1605.
Black, Betty S.
Johnston, Deirdre
Rabins, Peter V.
Morrison, Ann
Lyketsos, Constantine
and
Samus, Quincy M.
2013.
Unmet Needs of Community‐Residing Persons with Dementia and Their Informal Caregivers: Findings from the Maximizing Independence at Home Study.
Journal of the American Geriatrics Society,
Vol. 61,
Issue. 12,
p.
2087.
Martín-Carrasco, Manuel
Domínguez–Panchón, Ana Isabel
Muñoz-Hermoso, Paula
González-Fraile, Eduardo
and
Ballesteros-Rodríguez, Javier
2013.
Instrumentos para medir la sobrecarga en el cuidador informal del paciente con demencia.
Revista Española de Geriatría y Gerontología,
Vol. 48,
Issue. 6,
p.
276.
Gies, Cheryl
Pierce, Linda
Steiner, Victoria
van der Bijl, Joan
and
Salvador, Diane
2014.
Web-based Psychosocial Assessment for Caregivers of Persons with Dementia: A Feasibility Study.
Rehabilitation Nursing,
Vol. 39,
Issue. 2,
p.
102.
Schaller, Sandra
Marinova-Schmidt, Velislava
Gobin, Jasmin
Criegee-Rieck, Manfred
Griebel, Lena
Engel, Sabine
Stein, Veronika
Graessel, Elmar
and
Kolominsky-Rabas, Peter L
2015.
Tailored e-Health services for the dementia care setting: a pilot study of ‘eHealthMonitor’.
BMC Medical Informatics and Decision Making,
Vol. 15,
Issue. 1,
Lorgelly, Paula K.
Lorimer, Karen
Fenwick, Elisabeth A.L.
Briggs, Andrew H.
and
Anand, Paul
2015.
Operationalising the capability approach as an outcome measure in public health: The development of the OCAP-18.
Social Science & Medicine,
Vol. 142,
Issue. ,
p.
68.
Schaller, Sandra
Marinova-Schmidt, Velislava
Setzer, Manuela
Kondylakis, Haridimos
Griebel, Lena
Sedlmayr, Martin
Graessel, Elmar
Maler, Juan Manuel
Kirn, Stefan
and
Kolominsky-Rabas, Peter L
2016.
Usefulness of a Tailored eHealth Service for Informal Caregivers and Professionals in the Dementia Treatment and Care Setting: The eHealthMonitor Dementia Portal.
JMIR Research Protocols,
Vol. 5,
Issue. 2,
p.
e47.
Moyle, Wendy
Bramble, Marguerite
Bauer, Michael
Smyth, Wendy
and
Beattie, Elizabeth
2016.
‘They rush you and push you too much … and you can't really get any good response off them’: A qualitative examination of family involvement in care of people with dementia in acute care.
Australasian Journal on Ageing,
Vol. 35,
Issue. 2,
Mansfield, Elise
Boyes, Allison W
Bryant, Jamie
and
Sanson‐Fisher, Rob
2017.
Quantifying the unmet needs of caregivers of people with dementia: a critical review of the quality of measures.
International Journal of Geriatric Psychiatry,
Vol. 32,
Issue. 3,
p.
274.
Novais, T.
Dauphinot, V.
Krolak-Salmon, P.
and
Mouchoux, C.
2017.
How to explore the needs of informal caregivers of individuals with cognitive impairment in Alzheimer’s disease or related diseases? A systematic review of quantitative and qualitative studies.
BMC Geriatrics,
Vol. 17,
Issue. 1,
Sin, Jacqueline
Henderson, Claire
Spain, Debbie
Cornelius, Victoria
Chen, Tao
and
Gillard, Steve
2018.
eHealth interventions for family carers of people with long term illness: A promising approach?.
Clinical Psychology Review,
Vol. 60,
Issue. ,
p.
109.
Holden, Richard J.
Karanam, Yamini L.P.
Cavalcanti, Luiz Henrique
Parmar, Takshak
Kodthala, Prasanthi
Fowler, Nicole R.
and
Bateman, Daniel R.
2018.
Health information management practices in informal caregiving: An artifacts analysis and implications for IT design.
International Journal of Medical Informatics,
Vol. 120,
Issue. ,
p.
31.
Zwingmann, I.
Hoffmann, W.
Michalowsky, B.
Wucherer, D.
Eichler, T.
Teipel, S.
Dreier-Wolfgramm, A.
Kilimann, I.
and
Thyrian, J. R.
2018.
Offene Versorgungsbedarfe pflegender Angehöriger von Menschen mit Demenz.
Der Nervenarzt,
Vol. 89,
Issue. 5,
p.
495.