Family caregivers' views on coordination of care in Huntington's disease: a qualitative study.
about
Unmet needs for healthcare and social support services in patients with Huntington's disease: a cross-sectional population-based studyHealth-related quality of life and unmet healthcare needs in Huntington's disease.Evolving Motivations: Patients' and Caregivers' Perceptions About Seeking Myotonic Dystrophy (DM1) and Huntington's Disease Care.Filling the gaps and finding our way: family carers navigating the healthcare system to access physical health services for the people they care for.Informal caregivers' views on the division of responsibilities between themselves and professionals: A scoping review.
P2860
Family caregivers' views on coordination of care in Huntington's disease: a qualitative study.
description
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2015年の論文
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2015年論文
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2015年論文
@zh-hant
2015年論文
@zh-hk
2015年論文
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2015年論文
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2015年论文
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name
Family caregivers' views on co ...... disease: a qualitative study.
@en
type
label
Family caregivers' views on co ...... disease: a qualitative study.
@en
prefLabel
Family caregivers' views on co ...... disease: a qualitative study.
@en
P2860
P356
P1476
Family caregivers' views on co ...... s disease: a qualitative study
@en
P2093
Kirsti Malterud
Merete Røthing
P2860
P304
P356
10.1111/SCS.12212
P50
P577
2015-04-28T00:00:00Z