How common is depression among ALS caregivers? A longitudinal study
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Amyotrophic Lateral Sclerosis: An update for 2013 Clinical Features, Pathophysiology, Management and Therapeutic TrialsInformal caregivers of clients with neurological conditions: profiles, patterns and risk factors for distress from a home care prevalence study.Family caregivers' accounts of caring for a family member with motor neurone disease in Norway: a qualitative study.Caregiving in ALS - a mixed methods approach to the study of BurdenMedical and supportive care among people with ALS in the months before death or tracheostomy.The impact on the family carer of motor neurone disease and intervention with noninvasive ventilation.From first symptoms to diagnosis of amyotrophic lateral sclerosis: perspectives of an Irish informal caregiver cohort-a thematic analysisA 10-year literature review of family caregiving for motor neurone disease: moving from caregiver burden studies to palliative care interventions.Caregiver burden in amyotrophic lateral sclerosis: A systematic review.An Investigation of Perspectives of Respite Admission Among People Living With Amyotrophic Lateral Sclerosis and the Hospitals That Support Them.Factors to consider for motor neurone disease carer intervention research: A narrative literature review.Ethical issues in the evaluation of adults with suspected genetic neuromuscular disorders.The personal experience of partners of individuals with motor neuron disease.The importance of an idiographic approach for the severe chronic disorders-the case of the amyotrophic lateral sclerosis patient.Patients' self-perceived burden, caregivers' burden and quality of life for amyotrophic lateral sclerosis patients: a cross-sectional study.Factor analysis of the Zarit Burden Interview in family caregivers of patients with amyotrophic lateral sclerosis.The family experience of living with a person with amyotrophic lateral sclerosis: a qualitative study.Depression and anxiety in amyotrophic lateral sclerosis: correlations between the distress of patients and caregivers.Life factors affecting depression and burden in amyotrophic lateral sclerosis caregivers.Quality of life of patients with amyotrophic lateral sclerosis.A brain-computer interface as input channel for a standard assistive technology software.The need for support services for family carers of people with motor neurone disease (MND): views of current and former family caregivers a qualitative study.Impact of patient suffering on caregiver well-being: the case of amyotrophic lateral sclerosis patients and their caregivers.
P2860
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P2860
How common is depression among ALS caregivers? A longitudinal study
description
2009 nî lūn-bûn
@nan
2009 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2009 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
2009年の論文
@ja
2009年論文
@yue
2009年論文
@zh-hant
2009年論文
@zh-hk
2009年論文
@zh-mo
2009年論文
@zh-tw
2009年论文
@wuu
name
How common is depression among ALS caregivers? A longitudinal study
@ast
How common is depression among ALS caregivers? A longitudinal study
@en
type
label
How common is depression among ALS caregivers? A longitudinal study
@ast
How common is depression among ALS caregivers? A longitudinal study
@en
prefLabel
How common is depression among ALS caregivers? A longitudinal study
@ast
How common is depression among ALS caregivers? A longitudinal study
@en
P2093
P2860
P1476
How common is depression among ALS caregivers? A longitudinal study
@en
P2093
Judith G Rabkin
Lewis P Rowland
Steven M Albert
P2860
P304
P356
10.3109/17482960802459889
P577
2009-10-01T00:00:00Z