(Q37404308)

20 August 2017

The impact on the family carer of motor neurone disease and intervention with noninvasive ventilation (English)

1 reference

20 August 2017

0 references

7

1 reference

20 August 2017

Wendy O Baird

2

0 references

Stephen J. Walters

object named as

Stephen J Walters

5

0 references

Pamela Shaw

object named as

Pamela J Shaw

9

0 references

Christopher McDermott

10

object named as

Christopher J McDermott

1 reference

20 August 2017

4

Stephen M Bianchi

1 reference

20 August 2017

3

Sue Thompson

1 reference

20 August 2017

6

Ellen Lee

1 reference

20 August 2017

Susan K Baxter

1

1 reference

20 August 2017

Alison Proctor

8

1 reference

20 August 2017

language of work or name

1 reference

16 November 2013

1 reference

20 August 2017

8

1 reference

Journal of Palliative Medicine

inferred from page(s)

published in

1 reference

20 August 2017

16

1 reference

20 August 2017

12

1 reference

20 August 2017

1602-1609

1 reference

Amyotrophic lateral sclerosis: a hormonal condition?

20 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3868397

Respiratory function of people with amyotrophic lateral sclerosis and caregiver distress level: a correlational study

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3868397

Social services homecare for people with motor neurone disease/amyotrophic lateral sclerosis: why are such services used or refused?

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3868397

How common is depression among ALS caregivers? A longitudinal study

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3868397

El Escorial revisited: revised criteria for the diagnosis of amyotrophic lateral sclerosis

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3868397

6 September 2017

Motor neurone disease.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3868397

The MOS 36-ltem Short-Form Health Survey (SF-36)

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3868397

The personal experience of partners of individuals with motor neuron disease

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3868397

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

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3868397

Differences in quality of life modalities give rise to needs of individual support in patients with ALS and their next of kin.

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3868397

Motor Neurone Disease family carers' experiences of caring, palliative care and bereavement: an exploratory qualitative study.

26 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3868397

Research priorities associated with family caregivers in palliative care: international perspectives

2 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3868397

The effect of noninvasive ventilation on ALS patients and their caregivers.

2 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3868397

Predictors of psychological distress in carers of people with amyotrophic lateral sclerosis: a longitudinal study

2 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3868397

Caregiver burden and patients' perception of being a burden in ALS.

2 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3868397

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

2 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3868397

Do SF-36 summary component scores accurately summarize subscale scores?

2 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3868397

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

2 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3868397

Support needs in the last year of life: patient and carer dilemmas

2 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3868397

Caregiver time use in ALS

3 December 2018

1 reference

12 December 2020

Validation of a Caregiver Strain Index

1 reference

12 December 2020

Burden of care in amyotrophic lateral sclerosis

1 reference

12 December 2020

A longitudinal study on quality of life and depression in ALS patient-caregiver couples

1 reference

12 December 2020

Identifiers

DOI

10.1089/JPM.2013.0211

1 reference

20 August 2017

1 reference

20 August 2017

PubMed publication ID

24236958

1 reference