Tímarit hjúkrunarfræðinga - 2019, Page 61

Tímarit hjúkrunarfræðinga - 2019, Page 61
Heimildir atkins, S., Lewin, S., Smith, h., Engel, M., fretheim, a., og Volmink, j. (2008). Conducting a meta- ethnography of qualitative literature: Lessons learnt. BMC Medical Research Methodology, 8(21), 1–10. doi: 10.1186/1471-2288-8-21 DeMaagd, g., og Philip, a. (2015). Parkinson’s disease and its management. Part 1: Disease entity, risk factors, pathophysiology, clinical presentation, and diagnosis. Pharmacy and Therapeutics, 40(8), 504–510, 532. Sótt á https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4517533/ giles, S., og Miyasaki, j. (2009). Palliative stage Parkinson’s disease: Patient and family experiences of health-care services. Palliative Medicine, 23(2), 120–125. doi: 10.1177/0269216308100773 haahr, a., kirkevold, M., hall, E. O. C., og Østergaard, k. (2010). Living with advanced Parkinson’s dis- ease: a constant struggle with unpredictability. Journal of Advanced nursing, 67(2), 408–417. doi: 10.1111/j.1365-2648.2010.05459.x habermann, B., og Shin, j. Y. (2017). 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