{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,10,23]],"date-time":"2025-10-23T11:08:04Z","timestamp":1761217684071},"reference-count":15,"publisher":"Japanese Society of Internal Medicine","issue":"5","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Intern. Med."],"published-print":{"date-parts":[[2014]]},"DOI":"10.2169\/internalmedicine.53.0916","type":"journal-article","created":{"date-parts":[[2014,2,28]],"date-time":"2014-02-28T23:13:20Z","timestamp":1393629200000},"page":"483-487","source":"Crossref","is-referenced-by-count":5,"title":["Creutzfeldt-Jakob Disease with a Codon 210 Mutation: First Pathological Observation in a Japanese Patient"],"prefix":"10.2169","volume":"53","author":[{"given":"Yasutaka","family":"Tajima","sequence":"first","affiliation":[{"name":"Department of Neurology, Brain Science Center, Sapporo City General Hospital, Japan"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Chika","family":"Satoh","sequence":"additional","affiliation":[{"name":"Department of Neurology, Brain Science Center, Sapporo City General Hospital, Japan"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Yasunori","family":"Mito","sequence":"additional","affiliation":[{"name":"Department of Neurology, Brain Science Center, Sapporo City General Hospital, Japan"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Tetsuyuki","family":"Kitamoto","sequence":"additional","affiliation":[{"name":"Division of CJD Science and Technology, Graduate School of Medicine, Tohoku University, Japan"}],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"962","reference":[{"key":"1","doi-asserted-by":"crossref","unstructured":"1. Prusiner SB. Prions. Proc. Natl Acad Sci USA 95: 13363-13383, 1998.","DOI":"10.1073\/pnas.95.23.13363"},{"key":"2","doi-asserted-by":"crossref","unstructured":"2. Parchi P, Giese A, Capellari S, et al. Classification of sporadic Creutzfeldt-Jakob disease based on molecular and phenotypic analysis of 300 subjects. Ann Neurol 46: 224-233, 1999.","DOI":"10.1002\/1531-8249(199908)46:2<224::AID-ANA12>3.3.CO;2-N"},{"key":"3","doi-asserted-by":"crossref","unstructured":"3. Parchi P, Castellani R, Capellari S, et al. Molecular basis of phenotypic variability in sporadic Creutzfeldt-Jakob disease. Ann Neurol 39: 767-778, 1996.","DOI":"10.1002\/ana.410390613"},{"key":"4","unstructured":"4. Kovacs GG, Puopolo M, Ladogana A, et al. Genetic prion disease: the EUROCJD experience. Hum Genet 118: 166-174, 2005."},{"key":"5","doi-asserted-by":"crossref","unstructured":"5. Nozaki I, Hamaguchi T, Sanjo N, et al. Prospective 10-year surveillance of human prion diseases in Japan. Brain 133: 3043-3057, 2010.","DOI":"10.1093\/brain\/awq216"},{"key":"6","doi-asserted-by":"crossref","unstructured":"6. Furukawa H, Kitamoto T, Hashiguchi H, Tateishi J. A Japanese case of Creutzfeldt-Jakob disease with a point mutation in the prion protein gene at codon 210. J Neurol Sci 141: 120-122, 1996.","DOI":"10.1016\/0022-510X(96)00157-8"},{"key":"7","doi-asserted-by":"crossref","unstructured":"7. Shiga Y, Sato A, Satoh K, et al. Two different clinical phenotypes of Creutzfeldt-Jakob disease with a M232R substitution. J Neurol 254: 1509-1517, 2007.","DOI":"10.1007\/s00415-007-0540-9"},{"key":"8","unstructured":"8. Sato A, Goto H, Satoh H, et al. A case of Creutzfeldt-Jakob disease with a point mutation at codon 232: Correlation of MRI and neurological findings. Neurology 49: 1469-1470, 1997."},{"key":"9","doi-asserted-by":"crossref","unstructured":"9. Jin K, Shiga Y, Shibuya S, et al. Clinical features of Creutzfeldt-Jakob disease with V180I mutation. Neurology 62: 502-505, 2004.","DOI":"10.1212\/01.WNL.0000106954.54011.80"},{"key":"10","doi-asserted-by":"crossref","unstructured":"10. Shiga Y, Miyazawa K, Sato S, et al. Diffusion-weighted MRI abnormalities as an early diagnostic marker for Creutzfeldt-Jakob disease. Neurology 163: 443-449, 2004.","DOI":"10.1212\/01.WNL.0000134555.59460.5D"},{"key":"11","doi-asserted-by":"crossref","unstructured":"11. Mittal S, Farmer P, Kalina P, Kingsley PB, Halperin J. Correlation of diffusion-weighted magnetic resonance imaging with neuropathology in Creutzfeldt-Jakob disease. Arc Neurol 59: 128-134, 2002.","DOI":"10.1001\/archneur.59.1.128"},{"key":"12","unstructured":"12. Young GS, Geshiwind MD, Fishbein NJ, et al. Diffusion-weighted and fluid attenuated inversion recovery imaging in Creutzfeldt-Jakob disease: High sensitivity and specificity for diagnosis. Am J Neuroradiol 26: 1551-1562, 2005."},{"key":"13","doi-asserted-by":"crossref","unstructured":"13. Pocchiari M, Salvatore M, Cutruzzola F, et al. A new point mutation of the prion protein gene in Creutzfeldt-Jakob disease. Ann Neurol 34: 802-807, 1993.","DOI":"10.1002\/ana.410340608"},{"key":"14","doi-asserted-by":"crossref","unstructured":"14. Ripoll L, Laplanche JL, Salzmann M, et al. A new point mutation in the prion protein gene at codon 210 in Creutzfeldt-Jakob disease. Neurology 43: 1934-1938, 1993.","DOI":"10.1212\/WNL.43.10.1934"},{"key":"15","doi-asserted-by":"crossref","unstructured":"15. Mastrianni JA, Capellari S, Telling GC, et al. Inherited prion disease caused by the V201 mutation. Transmission to transgenic mice. Neurology 57: 2198-2205, 2001.","DOI":"10.1212\/WNL.57.12.2198"}],"container-title":["Internal Medicine"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/www.jstage.jst.go.jp\/article\/internalmedicine\/53\/5\/53_53.0916\/_pdf","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2021,5,19]],"date-time":"2021-05-19T17:50:09Z","timestamp":1621446609000},"score":1,"resource":{"primary":{"URL":"https:\/\/www.jstage.jst.go.jp\/article\/internalmedicine\/53\/5\/53_53.0916\/_article"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2014]]},"references-count":15,"journal-issue":{"issue":"5","published-print":{"date-parts":[[2014]]}},"URL":"https:\/\/doi.org\/10.2169\/internalmedicine.53.0916","relation":{},"ISSN":["0918-2918","1349-7235"],"issn-type":[{"value":"0918-2918","type":"print"},{"value":"1349-7235","type":"electronic"}],"subject":[],"published":{"date-parts":[[2014]]}}}