Well-Being of Family Caregivers of Persons with Late-Stage Huntington's Disease: Lessons in Stress and Coping-Reference-Cited by-同舟云学术

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Well-Being of Family Caregivers of Persons with Late-Stage Huntington's Disease: Lessons in Stress and Coping

Published:2009-05-08 Issue:3 Volume:24 Page:239-248
ISSN:1041-0236
Container-title:Health Communication
language:en
Short-container-title:Health Communication

Author:

Roscoe Lori A.,Corsentino Elizabeth,Watkins Shirley,McCall Marcia,Sanchez-Ramos Juan

Publisher

Informa UK Limited

Subject

Communication,Health(social science)

Link

http://www.tandfonline.com/doi/pdf/10.1080/10410230902804133

Reference53 articles.

1. High incidence rate and absent family histories in one quarter of patients newly diagnosed with Huntington disease in British Columbia

2. Measures of Subjective Well-Being

Cited by 46 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. The meaning of apathy in Huntington's disease: A qualitative study of caregiver perspectives;Neuropsychological Rehabilitation;2024-08-05

2. Reducing the burden of caregivers in Huntington's by using an online interventional neuropsychological approach: a pilot study;Dementia & Neuropsychologia;2024

3. The Impact of Rapidly Progressing Neurodegenerative Disorders on Caregivers;Journal of Hospice & Palliative Nursing;2023-12-22

4. Caregiver burden for adults with epilepsy in Malaysian families: A qualitative study;Epilepsy & Behavior;2023-10

5. Facilitators and barriers in caring for a person with Huntington’s disease: input for a remote support program;Aging & Mental Health;2023-07-06

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