References
- Article 2 of the Rare Disease Control Act(2020.09.12.), https://www.law.go.kr/LSW/eng/engLsSc.do?menuId=2§ion=lawNm&query=RARE+DISEASE+MANAGEMENT+ACT&x=27&y=25#liBgcolor1)
- Muenzer, J. (2004). The mucopolysaccharidoses: a heterogeneous group of disorders with variable pediatric presentations. Journal of Pediatrics, 144(5Suppl), S27-34. DOI: 10.1016/j.jpeds.2004.01.052
- Khan S. A. et al. (2017). Epidemiology of mucopolysaccharidoses. Molecular Genetics and Metabolism, 121(3), 227-240. DOI: 10.1016/j.ymgme.2017.05.016
- Wang R. Y. et al. (2009). Treatment reduces or stabilizes brain imaging abnormalities in patients with MPS I and II. Molecular Genetics and Metabolism, 98(4), 406-411. DOI: 10.1016/j.ymgme.2009.07.015
- Y. B. Sohn. (2014). Long-term therapeutic effects of mucopolysaccharidoses and efforts to overcome limitations. Journal of Genetic and Metabolism in Korea, 14(1), 29-36.
- Buraczewska, M., O'Leary, D., Walsh, O., Monavari, A. & Crushell, E. (2013). Parental experience of enzyme replacement therapy for Hunter syndrome. Irish Medical Journal, 106(4), 120-122.
- Bitencourt, F. H., Vieira, T. A., Steiner, C. E., Neto, J. C., Boy, R. & Schwartz, IVD. (2015). Medical Costs Related to Enzyme Replacement Therapy for Mucopolysaccharidosis Types I, II, and VI in Brazil: A Multicenter Study. Value Health Reg 8, 99-106. DOI: 10.1016/j.vhri.2015.08.002
- Ministry of Health and Welfare. (2018). Increase the scope of rare diseases and increase support such as medical expenses "First announcement of a total of 927 designated list of rare diseases subject to state management". [Internet].2018 September[ cited 2018 September 17].Available from:http://www.mohw.go.kr/react/al/sal0301vw.jsp?PAR_MENU_ID=04&MENU_ID=0403&page=1&CONT_SEQ=346076
- Y. B. Sohn., S. Y. Cho, J. E. Lee, Y. H. Kwun, R. Huh & D. K. Jin. (2015). Safety and efficacy of enzyme replacement therapy with idursulfase beta in children aged younger than 6 years with Hunter syndrome. Molecular Genetics and Metabolism, 114(2), 156-160. DOI: 10.1016/j.ymgme.2014.08.009
- Franco, J. et al. (2017). Mucopolysaccharidosis type I, II and VI and response to enzyme replacement therapy: Results from a single-center case series study. Intractable Rare Dis Res, 6(3), 183-190. DOI: 10.5582/irdr.2017.01036
- Gomes, D. F., Gallo, L. G., Leite, B. F., Silva, R. B. & da Silva, E. N. (2019). Clinical effectiveness of enzyme replacement therapy with galsulfase in mucopolysaccharidosis type VI treatment: Systematic review. Journal of Inherited Metabolic Disease, 42(1), 66-76. DOI: 10.1002/jimd.12028
- S. Y. Kang. (2012). Life experiences of mothers in parenting children with Hunter's syndrome. Journal of Korean Academy of Nursing, 42(5), 609-621. DOI: 10.4040/jkan.2012.42.5.609
- H. S. Park & K. B. Kim. (2013). The Experience of Parents of Children with Mucopolysaccharidosis. The Academy of Qualitative Research, 14(1), 1-12. https://doi.org/10.22284/qr.2013.14.1.1
- Somanadhan, S. & Larkin, P. J. (2016). Parents' experiences of living with, and caring for children, adolescents and young adults with Mucopolysaccharidosis (MPS). Orphanet Journal of Rare Diseases, 11(1), 138. https://doi.org/10.1186/s13023-016-0521-0
- Guba, E. G. & Lincoln, Y. S. (1994). Competing paradigms in qualitative research. Handbook of qualitative research. Thousand Oaks: Sage Publications, 105-117.
- Elo, S. & Kyngas, H. (2008). The qualitative content analysis process. Journal of Advanced Nursing, 62(1), 107-115. DOI: 10.1111/j.1365-2648.2007.04569.x
- Chinn, Peggy L. (Peggy Lois), Kramer & Maeona K. (1999). Theory and nursing : integrated knowledge development (5th ed). St. Louis: Mosby.
- S. H. Choi, J. H. Jung & S. W. Jung. (2016). Concept and procedures of qualitative content analysis. Journal of Qualitative Inquiry, 2(1), 127-155.
- Robson, C. (1993). Real world research: A resource for social scientists and practitioner-researchers. Oxford: Blackwell.
- Muenzer, J., Gucsavas-Calikoglu, M., McCandless, S. E., Schuetz, T. J. & Kimura, A. (2007). A phase I/II clinical trial of enzyme replacement therapy in mucopolysaccharidosis II (Hunter syndrome). Molecular genetics and metabolism, 90(3), 329-337. DOI: 10.1016/j.ymgme.2006.09.001
- Laraway, S., Mercer, J., Jameson, E., Ashworth, J., Hensman, P. & Jones, S. A. (2016). Outcomes of Long-Term Treatment with Laronidase in Patients with Mucopolysaccharidosis Type I. Journal of Pediatrics, 178, 219-226.e211. DOI: 10.1016/j.jpeds.2016.08.033
- A. R. Yang, J. S. Kim, S. Y. Cho & D. K. Jin. (2017). A Review of Recent Research in Treatment Approaches of Mucopolysaccharidosis (MPS). Journal of mucopolysaccharidosis and rare disease, 3(2), 37-40. https://doi.org/10.19125/JMRD.2017.3.2.37
- D. K. Jin. (2011). Enzyme replacement therapy. Journal of The Korean Society of Inherited Metabolic disease, 11(1), 27-32.
- Harmatz, P., Hendriksz, C. J., Lampe, C., McGill, J. J. & Parini, R. (2017). Leao-Teles E, et al. The effect of galsulfase enzyme replacement therapy on the growth of patients with mucopolysaccharidosis VI (Maroteaux-Lamy syndrome). Molecular Genetics and Metabolism, 122(1-2), 107-112. DOI: 10.1016/j.ymgme.2017.03.008
- G. S. Lee. (2018). A Study on the Anxiety Experience of Disabled Person with Progressive Rare Disease. Korean Journal of Social Welfare, 70(2), 247-273. https://doi.org/10.20970/kasw.2018.70.2.010
- Ministry of Health and Welfare. (2017). Preparation of a roadmap for systematic diagnosis, treatment and management of rare diseases. [Internet].[2017 December 29].Available from:http://www.mohw.go.kr/react/al/sal0301vw.jsp?PAR_MENU_ID=04&MENU_ID=0403&CONT_SEQ=343355
- K. S. Lee & Y. C. Min. (2008). Psychological Adjusting Process to Diseases in People with Chronic Illnesses. Journal of the Psychiatric Nursing Society, 17(2), 151-160.
- The Economist Intelligence Unit Limited. (2020). Suffering in silence: Assessing rare disease awareness and management in Asia-Pacific, https://eiuperspectives.economist.com/sufferingsilence-rare-disease-asia-pacific