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A Case of Hypoglycemic Brain Injuries with Cortical Laminar Necrosis
이병완,진은선,황형식,유형준,정제훈 대한의학회 2010 Journal of Korean medical science Vol.25 No.6
We report a case of 68-yr-old male who died from brain injuries following an episode of prolonged hypoglycemia. While exploring controversies surrounding magnetic resonance imaging (MRI) findings indicating the bad prognosis in patients with hypoglycemia-induced brain injuries, we here discuss interesting diffusion-MRI of hypoglycemic brain injuries and their prognostic importance focusing on laminar necrosis of the cerebral cortex.
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홍성식,진형식 혜전대학 1997 論文集 Vol.15 No.-
지역 정보 신문의 인터넷 서비스 제공 즉 인터넷 전자신문화 하는데 있어서 필요한 정보 자원 입력, 관리, 서비스 제공 등 전 과정에서 화장 및 운용 하기에 편리하도록 전자신문을 설계하고 구현했다.
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안형진,진형식 한국장애인복지학회 2023 한국장애인복지학 Vol.62 No.62
The purpose of this study is to analyze the debate in the domestic disability community surrounding the personal budget system through frame analysis and, based on this, to suggest the roles of the public and private sectors in implementing a Korean personal budget system. This study demonstrated that the points of contention in the domestic disability community regarding the personal budget system are related to the self-direction of welfare services, the marketization and public nature of welfare services, and the person-centered practice of welfare services. To solve this problem, it is a public task to establish a service system that can flexibly yet rigorously identify the support needs of each disabled individual, and to flexibly identify the preferences and desires of disabled individuals, and to develop a support plan to support these, including the person and their family. Building capacity that can be established together with stakeholders and building a network that can advocate and support individuals with disabilities in the community were presented as tasks for the private sector.
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발달장애 국가책임제에 관한 발달장애인 부모의 인식 고찰
김성심(Sung-Sim Kim),전인선(In-Sun Jeon),진형식(Hyung-Sik Jin) 한국장애학회 2022 한국장애학 Vol.7 No.1
본 연구는 「발달장애 국가책임제」에 대한 요구가 높아지고 있는 가운데, 발달장애 부모들의 참여를 통해 발달장애 국가책임의 성격을 탐색해 보고자 하였다. 이를 위해 책임은 개인에게 있지만 국가가 주도해야 한다는 복지론, 책임성과 주도성 모두 개인에게 주어지는 윤리론, 책임은 국가에게 있지만 개인이 주도하는 권리중심론에 기초하여 발달장애 부모의 국가책임제에 대한 이해를 살펴보았다. 연구는 4명의 발달장애 부모의 참여로 인터뷰 방식으로 이루어졌고, 질적 연구방법의 자료분석법인 반복적 비교분석법으로 결과를 도출하였다. 연구결과 ‘안 되는 게 많은 아이’, ‘장애는 사회가 알아주지 않는 불편함’, ‘부모가 짊어지고 가야 되는 짐’, ‘국가책임제는 당연’, ‘발달장애인 당사자는 모르는 국가책임제’의 범주로 나타났다. 이는 발달장애의 특성상 가족의 돌봄이 큰 고통에 놓여있고, 무엇보다도 사회가 발달장애인을 배제함으로서 발달장애인과 가족의 고립이 가장 큰 어려움임을 알 수 있었다. 발달장애 부모들은 장애자녀를 부모가 짊어져야 할 ‘십자가’라고 하였으며, 장애자녀의 불안한 삶에 대한 부모의 걱정을 국가가 나눠 짊어지는 의미에서 국가책임제를 긍정적으로 인식하였다. 반면 발달장애 당사자는 국가책임제를 알지 못한다고 하여, 당사자 권리중심의 공적돌봄으로 인식되지 못하고 있음을 알 수 있었다. 이러한 연구결과에 기초하여 진정한 「발달장애 국가책임제」 실현을 위해서는 발달장애인의 시민권적 권리에 대한 인식개선이 필요하며, 발달장애인 당사자의 욕구와 자기결정권 실현을 위한 실천이 강조되어야 함을 제언하였다. This study attempted to explore the nature of state responsibility for developmental disabilities through the participation of parents with developmental disabilities amid the increasing demand for the ‘state responsibility system for developmental disabilities’. To this end, we looked at the understanding of the state responsibility system of parents with developmental disabilities based on the welfare theory that individuals are responsible, the ethics given to individuals, and the individual-led rights-centered theory. The study was conducted in an interview method with the participation of parents with developmental disabilities, and the results were derived using the iterative comparative analysis method, which is a data analysis method of qualitative research method. As a result of the study, the categories were “children with many things that cannot be done,” “disability is inconvenient that society does not recognize,” “the burden that parents should bear,” “the national responsibility system is natural,” and “the national responsibility system that those with developmental disabilities do not know.” Due to the nature of developmental disabilities, family care is in great pain, and above all, society excludes people with developmental disabilities, indicating that isolation of people with developmental disabilities and their families is the biggest difficulty. Parents with developmental disabilities called children with disabilities a “cross” that parents should bear, and positively recognized the national responsibility system in the sense that the state shared their parents’ concerns about the unstable life of children with disabilities. On the other hand, it was found that the parties with developmental disabilities were not aware of the state responsibility system, and were not recognized as public care centered on the rights of the parties. Based on these research results, it was suggested that in order to realize a true ‘state responsibility system for developmental disabilities’, awareness of the citizenship rights of people with developmental disabilities should be improved, and practice for realizing the needs and self-determination rights should be emphasized.
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