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Items: 1 to 20 of 180

1.

Social, psychological and existential well-being in patients with glioma and their caregivers: a qualitative study.

Cavers D, Hacking B, Erridge SE, Kendall M, Morris PG, Murray SA.

CMAJ. 2012 Apr 17;184(7):E373-82. doi: 10.1503/cmaj.111622. Epub 2012 Mar 19.

2.

The health and well-being of caregivers of children with cerebral palsy.

Raina P, O'Donnell M, Rosenbaum P, Brehaut J, Walter SD, Russell D, Swinton M, Zhu B, Wood E.

Pediatrics. 2005 Jun;115(6):e626-36.

PMID:
15930188
4.

Adjustment and support needs of glioma patients and their relatives: serial interviews.

Cavers D, Hacking B, Erridge SC, Morris PG, Kendall M, Murray SA.

Psychooncology. 2013 Jun;22(6):1299-305. doi: 10.1002/pon.3136. Epub 2012 Jul 30.

PMID:
22848038
5.

Inner power, physical strength and existential well-being in daily life: relatives' experiences of receiving soft tissue massage in palliative home care.

Cronfalk BS, Strang P, Ternestedt BM.

J Clin Nurs. 2009 Aug;18(15):2225-33. doi: 10.1111/j.1365-2702.2008.02517.x.

PMID:
19583654
6.

Unmet supportive care needs and interest in services among patients with a brain tumour and their carers.

Janda M, Steginga S, Dunn J, Langbecker D, Walker D, Eakin E.

Patient Educ Couns. 2008 May;71(2):251-8. doi: 10.1016/j.pec.2008.01.020. Epub 2008 Mar 7.

PMID:
18329220
7.

Caring for someone with high-grade glioma: a time of rapid change for caregivers.

McConigley R, Halkett G, Lobb E, Nowak A.

Palliat Med. 2010 Jul;24(5):473-9. doi: 10.1177/0269216309360118. Epub 2010 Feb 1.

PMID:
20123944
8.

Major stressors facing patients with amyotrophic lateral sclerosis (ALS): a survey to identify their concerns and to compare with those of their caregivers.

Trail M, Nelson N, Van JN, Appel SH, Lai EC.

Amyotroph Lateral Scler Other Motor Neuron Disord. 2004 Mar;5(1):40-5.

PMID:
15204023
9.

Needs and experiences of family caregivers during marrow transplantation.

Stetz KM, McDonald JC, Compton K.

Oncol Nurs Forum. 1996 Oct;23(9):1422-7.

PMID:
8899758
10.

Well-being in informal caregivers of survivors of acute respiratory distress syndrome.

Cameron JI, Herridge MS, Tansey CM, McAndrews MP, Cheung AM.

Crit Care Med. 2006 Jan;34(1):81-6.

PMID:
16374160
11.

How relatives of patients with head and neck cancer experience pain, disease progression and treatment: a qualitative interview study.

Schaller A, Liedberg GM, Larsson B.

Eur J Oncol Nurs. 2014 Aug;18(4):405-10. doi: 10.1016/j.ejon.2014.03.008. Epub 2014 Apr 13.

PMID:
24726013
12.

Support needs of patients with oral cancer and burden to their family caregivers.

Chen SC, Tsai MC, Liu CL, Yu WP, Liao CT, Chang JT.

Cancer Nurs. 2009 Nov-Dec;32(6):473-81. doi: 10.1097/NCC.0b013e3181b14e94.

PMID:
19816161
13.

Quality of life of family caregivers 5 years after a relative's cancer diagnosis: follow-up of the national quality of life survey for caregivers.

Kim Y, Spillers RL, Hall DL.

Psychooncology. 2012 Mar;21(3):273-81. doi: 10.1002/pon.1888. Epub 2010 Dec 20.

PMID:
22383269
14.

Longing for existential recognition: a qualitative study of everyday concerns for people with somatoform disorders.

Lind AB, Risoer MB, Nielsen K, Delmar C, Christensen MB, Lomborg K.

J Psychosom Res. 2014 Feb;76(2):99-104. doi: 10.1016/j.jpsychores.2013.11.005. Epub 2013 Nov 16.

PMID:
24439684
15.

The experience of the family caregivers' role: a qualitative study.

Lane P, McKenna H, Ryan A, Fleming P.

Res Theory Nurs Pract. 2003 Summer;17(2):137-51.

PMID:
12880218
17.

[A "I would like to give him my life": results of a psychological support intervention to caregivers of patients undergoing neuromotor rehabilitation].

Moroni L, Colangelo M, Gallì M, Bertolotti G.

G Ital Med Lav Ergon. 2007 Jul-Sep;29(3 Suppl B):B5-17. Italian.

PMID:
18575353
18.
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20.

Perceptual consistency of pain and quality of life between hospice cancer patients and family caregivers: a pilot study.

Tu MS, Chiou CP.

Int J Clin Pract. 2007 Oct;61(10):1686-91. Epub 2007 May 30.

PMID:
17537189
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