(Q36590291)

15 August 2017

1 reference

title

A Review: carers, MND and service provision (English)

1 reference

15 August 2017

2

Crispin Jenkinson

1 reference

15 August 2017

Carole Mockford

1

1 reference

15 August 2017

Raymond Fitzpatrick

series ordinal

3

1 reference

15 August 2017

publication date

1 September 2006

1 reference

Amyotrophic Lateral Sclerosis and Other Motor Neuron Disorders

15 August 2017

published in

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15 August 2017

volume

7

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15 August 2017

issue

3

1 reference

15 August 2017

page(s)

132-141

1 reference

Disparities in perceptions of distress and burden in ALS patients and family caregivers.

15 August 2017

cites work

1 reference

https://api.crossref.org/works/10.1080%2F14660820600601028

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%2F14660820600601028

Comparison of instruments addressing quality of life in patients with ALS and their caregivers.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F14660820600601028

Attitudes of patients with amyotrophic lateral sclerosis and their care givers toward assisted suicide

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F14660820600601028

The final month of life in patients with ALS.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F14660820600601028

Quality of life for ventilator-dependent ALS patients and their caregivers

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F14660820600601028

The psychological impact of MND on patients and carers

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F14660820600601028

Attributions, strain and depression in carers of partners with MND: a preliminary investigation

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F14660820600601028

The ALS Health Profile Study: quality of life of amyotrophic lateral sclerosis patients and carers in Europe.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F14660820600601028

Quality of life and psychosocial issues in ventilated patients with amyotrophic lateral sclerosis and their caregivers

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F14660820600601028

Lasting impact in families after death from ALS.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F14660820600601028

The ALS patient care database: goals, design, and early results. ALS C.A.R.E. Study Group

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F14660820600601028

Resilience and distress among amyotrophic lateral sclerosis patients and caregivers

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F14660820600601028

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%2F14660820600601028

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F14660820600601028

Service use and needs of people with motor neurone disease and their carers in Scotland.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F14660820600601028

Sexuality in patients with amyotrophic lateral sclerosis and their partners.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F14660820600601028

Breaking the news: A survey of ALS patients and their caregivers

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F14660820600601028

10.1080/14660820600601028

21 January 2018

Identifiers

DOI

1 reference

15 August 2017

1 reference