ALS: Family caregiver needs and quality of life (Q40073457)

17 September 2017

title

ALS: Family caregiver needs and quality of life (English)

1 reference

amyotrophic lateral sclerosis

17 September 2017

main subject

1 reference

1 reference

Mary Tederous Williams

1

1 reference

17 September 2017

James P Donnelly

2

1 reference

17 September 2017

Tomas Holmlund

3

1 reference

17 September 2017

Michael Battaglia

4

1 reference

17 September 2017

publication date

1 October 2008

1 reference

Amyotrophic Lateral Sclerosis and Other Motor Neuron Disorders

17 September 2017

published in

1 reference

17 September 2017

volume

9

1 reference

17 September 2017

issue

5

1 reference

17 September 2017

page(s)

279-286

1 reference

Health-promoting self-care in family caregivers

17 September 2017

cites work

1 reference

https://api.crossref.org/works/10.1080%2F17482960801934148

Palliative care in amyotrophic lateral sclerosis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F17482960801934148

Palliative care in non-cancer patients and the neglected caregiver

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F17482960801934148

Effect of a multidisciplinary amyotrophic lateral sclerosis (ALS) clinic on ALS survival: a population based study, 1996-2000.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F17482960801934148

Multidisciplinary ALS care improves quality of life in patients with ALS.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F17482960801934148

Concept mapping: an introduction to structured conceptualization in health care

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F17482960801934148

Individual quality of life is not correlated with health-related quality of life or physical function in patients with amyotrophic lateral sclerosis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F17482960801934148

Impact of caregiving: listening to the voice of informal caregivers

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F17482960801934148

Patient page. Treatment and quality of life for people with ALS.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F17482960801934148

A study comparing patients with amyotrophic lateral sclerosis and their caregivers on measures of quality of life, depression, and their attitudes toward treatment options

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F17482960801934148

Resilience and distress among amyotrophic lateral sclerosis patients and caregivers

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F17482960801934148

Quality of life of caregivers

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F17482960801934148

Loss, trauma, and human resilience: have we underestimated the human capacity to thrive after extremely aversive events?

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F17482960801934148

A cross sectional study on determinants of quality of life in ALS.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F17482960801934148

The final month of life in patients with ALS.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F17482960801934148

Conflicts of interest: experiences of close relatives of patients suffering from amyotrophic lateral sclerosis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F17482960801934148

10.1080/17482960801934148

21 January 2018

Identifiers

DOI

1 reference

17 September 2017

1 reference