논문KCI 등재
Familial Creutzfeldt–Jakob Disease with a PRNP Mutation at Codon 180 Presented with Visual Hallucinations and Illusions
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참고문헌 (7)
- Kovács GG, "Genetic prion disease: the EUROCJD experience", Hum Genet, 118, pp.166~174 (2005)
- Jin K, "Clinical features of Creutzfeldt-Jakob disease with V180I mutation", Neurology, 62, pp.502~505 (2004)
- 양태일, "Familial Creutzfeldt-Jakob Disease with V180I Mutation", Journal of Korean Medical Science, 25(7), pp.1097~1100 (2010), 대한의학회
- Baiardi S, "Revisiting the heidenhain variant of Creutzfeldt-Jakob disease: evidence for prion type variability influencing clinical course and laboratory findings", J Alzheimers Dis, 50, pp.465~476 (2016)
- 주재정, "우울증을 초기증상으로 발현한 가족성 크로이츠펠트-야콥병", Dementia and Neurocognitive Disorders(대한치매학회지), 11(2), pp.74~77 (2012), 대한치매학회
- Yeo MJ, "Familial Creutzfeldt-Jakob disease with a mutation at codon 180 presenting with an atypical phenotype", J Clin Neurosci, 20, pp.180~182 (2013)
- 김정연, "브로카실어증으로 발현한 가족성 V180I 변이Creutzfeldt-Jakob병", 대한신경과학회지, 36(4), pp.345~349 (2018), 대한신경과학회[DOI]
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 M232R Mutation Progressed Slowly like Alzheimer’s Disease배희원, 양영순, 이슬기대한치매학회 · Dementia and Neurocognitive Disorders(대한치매학회지)2017 · 제16권 제3호A Case of Creutzfeldt-Jakob Disease Presented as Rapid Progressive Parkinsonism이찬녕, Yoonah Park대한치매학회 · Dementia and Neurocognitive Disorders(대한치매학회지)2019 · 제18권 제4호Rapidly 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 제4호우울증을 초기증상으로 발현한 가족성 크로이츠펠트-야콥병강진호, 김두응, 양영순, 이선화, 조은경, 주재정, 하상원, 한정호대한치매학회 · Dementia and Neurocognitive Disorders(대한치매학회지)2012 · 제11권 제2호브로카실어증으로 발현한 가족성 V180I 변이Creutzfeldt-Jakob병김정연, 박경원, 이덕수대한신경과학회 · 대한신경과학회지2018 · 제36권 제4호
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