References
- Admi, H., & Shaham, B. (2007). Living with epilepsy: ordinary people coping with extraordinary situations. Qualitative Health Research, 17, 1178-1187. https://doi.org/10.1177/1049732307307548
- Austin, J. K., Dunn, D. W., Perkins, S. M., & Shen, J. (2006). Youth with epilepsy: development of a model of children's attitudes toward their condition. Children's Health Care, 35, 123-140. https://doi.org/10.1207/s15326888chc3502_2
- Beresford, B. A., & Sloper, P. (2003). Chronically ill adolescents' experiences of communicating with doctors: a qualitative study. Journal of Adolescent Health, 33, 172-179. https://doi.org/10.1016/S1054-139X(03)00047-8
- Buck, D., Smith, M., Appleton, R., Baker, G. A., & Jacoby, A.(2007). The development and validation of the Epilepsy and Learning Disabilities Quality of Life (ELDQOL) scale. Epilepsy & Behavior, 10, 38-43. https://doi.org/10.1016/j.yebeh.2006.10.010
- Dictionary.com. (2010). Online Etymology Dictionary. Retrieved November 03, 2010, from http://dictionary.reference.com/browse/epilepsy
- Doosandonga Editorial Board. (2007). Dong-A New Korean Dictionary. Seoul: Dong-A Publishing & Printing.
- Elliott, I. M., Lach, L., & Smith, M. L. (2005). I just want to be normal: a qualitative study exploring how children and adolescents view the impact of intractable epilepsy on their quality of life. Epilepsy & behavior, 7, 664-678. https://doi.org/10.1016/j.yebeh.2005.07.004
- Faircloth, C. A. (1998). Epilepsies, identities, and difference: horizons of meaning for individuals with an epilepsy. Qualitative Heath Research, 8, 602-617. https://doi.org/10.1177/104973239800800503
- Ismail, H., Wright, J., Rhodes, P., Small, N., & Jacoby, A. (2005). South Asians and epilepsy: exploring health experiences, needs and beliefs of communities in the north of England. Seizure, 14, 497-503. https://doi.org/10.1016/j.seizure.2005.08.006
- Jeong. Y. M. (2002). Destructive drive. Seoul: Munhakdongne Publishing Co.
- Kim, S E., Suh, H. A., Yum, M. S., You, S. J., Kim, D. S., Yoo, H. I., et al. (2006). Clinical factors affecting quality of life in children with epilepsy. Journal of the Korean Child Neurology Society, 14, 295-302.
- Kim, S. (2003). Dogfight. Seoul: Munhakdongne Publishing Co.
- Korean Neurological Association. (2007). Neurology, Seoul: Koonja Publishing Co.
- Kwon, J. Y. (2000). International Practical Chinese Characters by the Picture and Explanation. Seoul: Sujiseolim.
- Kyngäs, H. (2003). Patient education: perspective of adolescents with a chronic disease. Journal of Clinical Nursing, 12, 744-751. https://doi.org/10.1046/j.1365-2702.2003.00788.x
- Lee, G. H. (2004). Sorrow of novel. Seoul: Hyundae Munhak Co.
- Lee, K. W. (2005). Textbook of Neurology. Seoul: E Public.
- McCorry, D., Marson, T., & Jacoby, A. (2009). Understanding routine antiepileptic drug decisions: a qualitative analysis of patients' accounts of hospital consultations, Epilepsy & Behavior, 14, 210-214. https://doi.org/10.1016/j.yebeh.2008.10.010
- McEwan, M. J., Espie, C. A., Metcalfe, J., Brodie, M. J., & Wilson, M. T. (2004). Quality of life and psychosocial development in adolescents with epilepsy: A qualitative investigation using focus group methods. Seizure, 13, 15-31. https://doi.org/10.1016/S1059-1311(03)00080-3
- McNelis, A. M., Buelow, J., Myers, J., & Johnson, E. A. (2007). Concerns and needs of children with epilepsy and their parents. Clinical Nurse Specialist, 21, 195-202. https://doi.org/10.1097/01.NUR.0000280488.33884.1d
- Meadows, L. M., & Morse, J. M. (2001). Constructing evidence within the qualitative project. In J. M. Morse., J. M. Swansen., & A. J. Kuzel. (Eds.), The nature of qualitative evidence (pp. 187-200). Thousand Oaks, CA: Sage.
- Moon, S. M. (2005). Psychosocial adjustment process in adolescents with epilepsy. Journal of Korean Academy of Nursing, 35, 16-26.
- Morse, J. M., & Field, P. A. (1997). Qualitative research methods for health professionals. (K. R. Shin, Trans.). Seoul: Ewha Womans University Press. (Original Work published 1995)
- Park, M. J. (2010). Drug compliance of pediatric patients with epilepsy. Unpublished master's thesis. Gachon University of Medicine and Science, Incheon.
- Rafael, F., Houinato, D., Nubukpo, P., Dubreuil, C. M., Tran, D. S., Odermatt, P., et al. (2010). Sociocultural and psychological features of perceived stigma reported by people with epilepsy in Benin, Epilepsia, 51, 1061-1068. https://doi.org/10.1111/j.1528-1167.2009.02511.x
- Ridsdale, L., Kwan, I., & Morgan, M. (2003). How can a nurse intervention help people with newly diagnosed epilepsy? A qualitative study of patients' views. Seizure, 12, 69-73. https://doi.org/10.1016/S1059131102001784
- Unger, W. R., & Buelow, J. M. (2009). Hybrid concept analysis of self-management in adults newly diagnosed with epilepsy, Epilepsy & Behavior. 14, 89-95. https://doi.org/10.1016/j.yebeh.2008.09.002
- van Manen, M. (1997). Researching lived experience (2nd ed.). Cobourg Ontario: The Althouse Press.
- Webster's Ninth Collegiate Dictionary. (1988). Webster's Ninth Collegiate Dictionary. Springfield, MA: Merriam-Webster Inc.
- Yoo, J. H. (2003). Life, vacant or filled with something and shaking. Seoul: Hyundae Munhak Co.