“A monster that lives in our lives”: experiences of caregivers of people with motor neuron disease and identifying avenues for support: Table 1-Reference-Cited by-同舟云学术

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“A monster that lives in our lives”: experiences of caregivers of people with motor neuron disease and identifying avenues for support: Table 1

Published:2016-04-28 Issue: Volume: Page:bmjspcare-2015-001057
ISSN:2045-435X
Container-title:BMJ Supportive & Palliative Care
language:en
Short-container-title:BMJ Support Palliat Care

Author:

Anderson Nicole Hennessy,Gluyas Cathy,Mathers Susan,Hudson Peter,Ugalde Anna

Publisher

BMJ

Subject

Medical–Surgical Nursing,Oncology (nursing),General Medicine,Medicine (miscellaneous)

Reference25 articles.

1. The epidemiology of ALS: a conspiracy of genes, environment and time

2. Changes in cognition and behaviour in amyotrophic lateral sclerosis: nature of impairment and implications for assessment

3. Caregiver burden in amyotrophic lateral sclerosis is more dependent on patients’ behavioral changes than physical disability: a comparative study

4. Home care of patients with amyotrophic lateral sclerosis (ALS);J Neurol Sci,1997

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1. Caregivers of ALS Patients: Their Experiences and Needs;Neuroethics;2023-11-09

2. Psychologisch geleitete Gruppentreffen für Angehörige von ALS-Patient*innen;Fortschritte der Neurologie · Psychiatrie;2023-11-06

3. Nurses’ challenges when supporting the family of patients with ALS in specialized palliative home care: A qualitative study;International Journal of Qualitative Studies on Health and Well-being;2023-07-25

4. Needs of persons living with ALS at home and their family caregivers: A scoping review;Muscle & Nerve;2023-05-29

5. Covid-19 threat and coping: application of protection motivation theory to the pandemic experiences of people affected by amyotrophic lateral sclerosis;BMC Neurology;2022-04-12

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