Psychosocial Factors in Parkinson’s Disease

References 

1. Fitzsimmons B, Bunting L. Parkinson’s Disease: quality of life issues. J Neurosci Nurs. 1993;28(4):807–817
2. Backer JH. Stressors, social support, coping and health dysfunction in individuals with Parkinson’s disease. J Gerontological Nurs. 2000;26(11):6–16Nov
3. Calne SM. The psychological impact of late-stage Parkinson’s disease. J Neurosci Nurs. 2003;35:306–313
   • MEDLINE
   • CrossRef
4. Reese S. Issues in caring for the patient with young-onset Parkinson’s disease. Home Healthcare Consult. 1999;6(4):26–29
5. American Parkinson Disease Association National Young Onset Center, 2100 Pfingsten Road, Glenview, IL 60026.
6. Feldman RG, Mosbach P, Thomas C, et al. Psychosocial factors in the treatment of Parkinson’s disease: a contextual approach. In: The Comprehensive Management of Parkinson’s Disease. New York, NY: Demos Vermande Publications; 1995;Chapter 14
7. Habermann B. Day-to-day demands of Parkinson’s disease. Western J Nurs Res. 1996;18(4):397–413
8. Shulman LM, Taback RL, Rubenstein AA, et al. Non-recognition of depression and other non-motor symptoms in Parkinson’s disease. Parkinsonism Relat Disord. 2002;8(3):193–197
   • Abstract
   • Full Text
   • Full-Text PDF (166 KB)
   • CrossRef
9. Hutton T, Hutton T. Psychological issues. In: Young Parkinson’s Handbook. Staten Island, NY: American Parkinson Disease Association, Inc; 1995;p. 50–53
10. Blake-Krebs B, Herman L. In: When Parkinson’s Strikes Early. Alameda, CA: Hunter House, Inc; 2001;p. 8