Hoping to Live a “Normal” Life Whilst Living with Unpredictable Health and Fear of Death: Impact of Cystic Fibrosis on Young Adults
Author:
Publisher
Wiley
Subject
Genetics(clinical)
Link
http://link.springer.com/content/pdf/10.1007/s10897-012-9555-1
Reference27 articles.
1. Anderson, D. L., Flume, P. A., & Hardy, K. K. (2001). Psychological functioning of adults with cystic fibrosis. Chest, 119, 1079–1084.
2. Arnett, J. J. (2000). Emerging adulthood. A theory of development from the late teens through the twenties. The American Psychologist, 55, 469–480.
3. Badlan, K. (2006). Young people living with cystic fibrosis: an insight into their subjective experience. Health & Social Care in the Community, 14, 264–270.
4. Berger, J. M., Patterson, J. M., Goetz, D., & Milla, C. (2007). Gender differences in young adults’ perceptions of living with cystic fibrosis during the transition to adulthood: a qualitative investigation. Families, Systems & Health, 25, 190–203.
5. Burden, C., Ion, R., Chung, Y., Henry, A., Downey, D. G., & Trinder, J. (2012). Current pregnancy outcomes in women with cystic fibrosis. European Journal of Obstetrics, Gynecology, and Reproductive Biology. doi: 10.1016/j.ejogrb.2012.06.013 .
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