논문KCI 등재
Familial Creutzfeldt-Jakob Disease with M232R Mutation Progressed Slowly like Alzheimer’s Disease
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참고문헌 (2)
- Choi BY, "Mutations at codons 178, 200-129, and 232 contributed to the inherited prion diseases in Korean patients", BMC Infect Dis, 9, pp.132~ (2009)
- Shiga Y, "Two different clinical phenotypes of Creutzfeldt-Jakob disease with a M232R substitution", J Neurol, 254, pp.1509~1517 (2007)
관련 논문AI추천
Creutzfeldt-Jakob Disease With Double Mutations at Codon 180 and Codon 232 of PRNPKee Duk Park, Seung-Ah Lee, Sumin Kim, Yong-Sun Kim대한신경과학회 · Journal of Clinical Neurology2025 · 제21권 제1호Familial Creutzfeldt–Jakob Disease with a PRNP Mutation at Codon 180 Presented with Visual Hallucinations and Illusions김성훈, 박정욱, 홍윤정, Byung Seok Kim, Dong Woo Ryu, Min Jae Seong, Si Baek Lee, Yongbang Kim대한치매학회 · Dementia and Neurocognitive Disorders(대한치매학회지)2019 · 제18권 제3호A Case of Creutzfeldt-Jakob Disease Presented as Rapid Progressive Parkinsonism이찬녕, Yoonah Park대한치매학회 · Dementia and Neurocognitive Disorders(대한치매학회지)2019 · 제18권 제4호유전 E200K변이 Creutzfeldt-Jakob병의 임상 특징김지영, 김현우, 이가현, 정대수, 조재욱대한신경과학회 · 대한신경과학회지2021 · 제39권 제3호Rapidly Progressive Parkinsonism and Dementia with No Insomnia due to the PRNP D178N Mutation김건우, 김미정, 박계원, 박관영, 이범희, 이승현, 이예나, 정선주, 최윤하, 황윤수대한신경과학회 · Journal of Clinical Neurology2021 · 제17권 제4호뇌경색 같은 첫 증상을 보인 Creutzfeldt-Jakob병김상진, 김여정, 노상우, 이석윤, 정혜영, 조규노대한신경과학회 · 대한신경과학회지2012 · 제30권 제4호
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