Tímarit hjúkrunarfræðinga - 2019, Qupperneq 62
Theed, r., Eccles, f., og Simpson, j. (2017). Experiences of caring for a family member with Parkinson’s
disease: a meta-synthesis. Aging & Mental Health, 21(10), 1007–1016. doi: 10.1080/13607863.
2016.1247414
Thordardottir, B., nilsson, M. h., iwarsson, S., og haak, M. (2014). „You plan, but you never know“.
Participation among people with different levels of severity of Parkinson’s disease. Disability and Re-
habilitation, 36(26), 2216–2224.doi: 10.3109/09638288.2014.898807
Tod, a. M., kennedy, f., Stocks, a. j., McDonnell, a., ramaswamy, B., Wood, B., og Whitfield, M. (2016).
good-quality social care for people with Parkinson’s disease: a qualitative study. BMJ Open, 6(2),
1–10. doi: 10.1136/bmjopen-2014-006813
Tysnes, O. B., og Storstein, a. (2017). Epidemiology of Parkinson’s disease. Journal of Neural Transmis -
sion, 124(8), 901–905. doi: 10.1007/s00702-017-1686-y
Valcarenghi, r. V., alvarez, a. M., Santos, S. S. C., Siewert, j. S., nunes, S. f. L., og Tomasi, a.V. r. (2018).
The daily lives of people with Parkinson’s disease. Revista Brasileira de Enfermagem, 7(2), 272–279.
doi: 10.1590/0034-7167-2016-0577
Vernon, g. M. (2009). Parkinson disease and the nurse practitioner: Diagnostic and management chal-
lenges. The Journal for Nurse Practitioners, 5(3), 195–206. doi: 10.1016/j.nurpra.2008.12.007
marianne e. klinke, ólöf sólrún vilhjálmsdóttir, sara jane friðriksdóttir, jónína h. hafliðadóttir
62 tímarit hjúkrunarfræðinga • 3. tbl. 95. árg. 2019