Dying with motor neurone disease, what can we learn from family caregivers?
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Factors to consider for motor neurone disease carer intervention research: A narrative literature review.Advance care planning in motor neuron disease: A qualitative study of caregiver perspectives.Experiences of burden, needs, rewards and resilience in family caregivers of people living with Motor Neurone Disease/Amyotrophic Lateral Sclerosis: A secondary thematic analysis of qualitative interviews.What are the roles of carers in decision-making for amyotrophic lateral sclerosis multidisciplinary care?The development of the UK National Institute of Health and Care Excellence evidence-based clinical guidelines on motor neurone disease.Choosing the place of death: Empowering motor neurone disease/amyotrophic lateral sclerosis patients in end-of-life care decision making.
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Dying with motor neurone disease, what can we learn from family caregivers?
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article científic
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article scientifique
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articolo scientifico
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artigo científico
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bilimsel makale
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scientific article published on 19 April 2012
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vedecký článok
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vetenskaplig artikel
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videnskabelig artikel
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vědecký článek
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name
Dying with motor neurone disease, what can we learn from family caregivers?
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Dying with motor neurone disease, what can we learn from family caregivers?
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type
label
Dying with motor neurone disease, what can we learn from family caregivers?
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Dying with motor neurone disease, what can we learn from family caregivers?
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Dying with motor neurone disease, what can we learn from family caregivers?
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Dying with motor neurone disease, what can we learn from family caregivers?
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P2860
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Dying with motor neurone disease, what can we learn from family caregivers?
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P2093
Janice Brown
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P304
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10.1111/J.1369-7625.2012.00773.X
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2012-04-19T00:00:00Z