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논문 기본 정보

자료유형
학술저널
저자정보
Kim Dayoung (Department of Neurology, Konkuk University Medical Center, Seoul, Republic of Korea) Kim Sooyoung (Department of Neurology, Chungnam National University Hospital, Daejeon, Republic of Korea) Seok Jin Myoung (Department of Neurology, Soonchunhyang University Hospital Cheonan, Soonchunhyang University College of Medicine, Cheonan, Korea) Shin Kyong Jin (Department of Neurology, Haeundae Paik Hospital, Inje University College of Medicine, Busan, Republic of Korea) Oh Eungseok (Department of Neurology, Chungnam National University Hospital, Daejeon, Republic of Korea) Jeon Mi Young (Department of Neurology, Neuroscience Center, Samsung Medical Center, Seoul, Korea) Park Joungkyu (Department of Neurology, Soonchunhyang University Cheonan Hospital, Soonchunhyang University College of Medicine, Cheonan, Republic of Korea) Chang Hee Jin (Department of Neurology, Chungnam National University Hospital, Daejeon, Republic of Korea) Youn Jinyoung (Department of Neurology, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea.) Oh Jeeyoung (Department of Neurology, Konkuk University Medical Center, Konkuk University School of Medicine, Seoul, Korea.) Sohn Eunhee (Department of Neurology, Chungnam National University Hospital, Chungnam National University College of Medicine, Daejeon, Korea.) Park Jinse (Department of Neurology, Haeundae Paik Hospital, Inje University College of Medicine, Busan, Republic of Korea) Cho Jin Whan (Department of Neurology, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea.) 김병준 (삼성서울병원)
저널정보
질병관리본부 Osong Public Health and Research Persptectives Osong Public Health and Research Perspectives Vol.15 No.2
발행연도
2024.4
수록면
174 - 181 (8page)
DOI
10.24171/j.phrp.2023.0353

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초록· 키워드

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Rare diseases are predominantly genetic or inherited, and patients with these conditions frequently exhibit neurological symptoms. Diagnosing and treating many rare diseases is a complex challenge, and their low prevalence complicates the performance of research, which in turn hinders the advancement of therapeutic options. One strategy to address this issue is the creation of national or international registries for rare diseases, which can help researchers monitor and investigate their natural progression. In the Republic of Korea, we established a registry across 5 centers that focuses on 3 rare diseases, all of which are characterized by gait disturbances resulting from motor system dysfunction. The registry will collect clinical information and human bioresources from patients with amyotrophic lateral sclerosis, spinocerebellar ataxia, and hereditary spastic paraplegia. These resources will be stored at ICreaT and the National Biobank of Korea. Once the registry is complete, the data will be made publicly available for further research. Through this registry, our research team is dedicated to identifying genetic variants that are specific to Korean patients, uncovering biomarkers that show a strong correlation with clinical symptoms, and leveraging this information for early diagnosis and the development of treatments.

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