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Patients experiences of maintaining mental well-being and hope within motor neuron disease: a thematic synthesis.How common is depression among ALS caregivers? A longitudinal studyCaregiver burden in amyotrophic lateral sclerosis is more dependent on patients' behavioral changes than physical disability: a comparative study.Management of motor neurone diseasePromoting excellence in end-of-life care in ALS.A Review: carers, MND and service provision.Psychological health in patients with amyotrophic lateral sclerosis.Carer quality of life and experiences of health services: a cross-sectional survey across three neurological conditions.Psychological wellbeing and quality of life in amyotrophic lateral sclerosis: a review.Depression and disease progression in amyotrophic lateral sclerosis: A comprehensive meta-regression analysis.Caregiver burden in amyotrophic lateral sclerosis: A systematic review.Economic Studies in Motor Neurone Disease: A Systematic Methodological Review.Multidimensional apathy in ALS: validation of the Dimensional Apathy Scale.Cognitive-behavioral changes in amyotrophic lateral sclerosis: Screening prevalence and impact on patients and caregivers.Impact of disease, cognitive and behavioural factors on caregiver outcome in amyotrophic lateral sclerosis.An eye-tracking assistive device improves the quality of life for ALS patients and reduces the caregivers' burden.Quality of life of patients with amyotrophic lateral sclerosis.The impact of perceived lack of support provided by health and social care services to caregivers of people with motor neuron disease.Processing and memory for emotional and neutral material in amyotrophic lateral sclerosis.Neurobehavioral symptoms in ALS are negatively related to caregivers' burden and quality of life.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.Marital relationships in amyotrophic lateral sclerosis.Prevalence of depression in a 12-month consecutive sample of patients with ALS.Caregiver bodywork: family members' experiences of caring for a person with motor neurone disease.A two-year longitudinal study on strain and needs in caregivers of advanced ALS patients.Determining the burden of the family caregivers of people with neuromuscular diseases who use a wheelchair.Living with motor neurone disease: lives, experiences of services and suggestions for change
P2860
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P2860
description
1998 nî lūn-bûn
@nan
1998年の論文
@ja
1998年学术文章
@wuu
1998年学术文章
@zh-cn
1998年学术文章
@zh-hans
1998年学术文章
@zh-my
1998年学术文章
@zh-sg
1998年學術文章
@yue
1998年學術文章
@zh
1998年學術文章
@zh-hant
name
The psychological impact of MND on patients and carers.
@en
type
label
The psychological impact of MND on patients and carers.
@en
prefLabel
The psychological impact of MND on patients and carers.
@en
P2093
P1476
The psychological impact of MND on patients and carers.
@en
P2093
Goldstein LH
P304
P356
10.1016/S0022-510X(98)00209-3
P478
160 Suppl 1
P577
1998-10-01T00:00:00Z