Quality of life, anxiety and depression in ALS patients and their next of kin
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Abstract
Suggested Citation
DOI: 10.1111/j.1365-2702.2010.03509.x
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Citations
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Cited by:
- Petter Sandstedt & Susanne Littorin & Gunilla Cröde Widsell & Sverker Johansson & Kristina Gottberg & Charlotte Ytterberg & Mariann Olsson & Lotta Widén Holmqvist & Marie Kierkegaard, 2018. "Caregiver experience, health‐related quality of life and life satisfaction among informal caregivers to patients with amyotrophic lateral sclerosis: A cross‐sectional study," Journal of Clinical Nursing, John Wiley & Sons, vol. 27(23-24), pages 4321-4330, December.
- Benjamin Ilse & Tino Prell & Mario Walther & Viktor Hartung & Susanne Penzlin & Florian Tietz & Otto-Wilhelm Witte & Bernhard Strauss & Julian Grosskreutz, 2015. "Relationships Between Disease Severity, Social Support and Health-Related Quality of Life in Patients with Amyotrophic Lateral Sclerosis," Social Indicators Research: An International and Interdisciplinary Journal for Quality-of-Life Measurement, Springer, vol. 120(3), pages 871-882, February.
- Dan Geng & RuWei Ou & XiaoHui Miao & LiHong Zhao & QianQian Wei & XuePing Chen & Yan Liang & HuiFang Shang & Rong Yang, 2017. "Patients’ self‐perceived burden, caregivers’ burden and quality of life for amyotrophic lateral sclerosis patients: a cross‐sectional study," Journal of Clinical Nursing, John Wiley & Sons, vol. 26(19-20), pages 3188-3199, October.
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