Patients’ self‐perceived burden, caregivers’ burden and quality of life for amyotrophic lateral sclerosis patients: a cross‐sectional study
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DOI: 10.1111/jocn.13667
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References listed on IDEAS
- McPherson, Christine J. & Wilson, Keith G. & Murray, Mary Ann, 2007. "Feeling like a burden: Exploring the perspectives of patients at the end of life," Social Science & Medicine, Elsevier, vol. 64(2), pages 417-427, January.
- Anneli G Olsson Ozanne & Susann Strang & Lennart I Persson, 2011. "Quality of life, anxiety and depression in ALS patients and their next of kin," Journal of Clinical Nursing, John Wiley & Sons, vol. 20(1‐2), pages 283-291, January.
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