{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,3,17]],"date-time":"2026-03-17T01:00:23Z","timestamp":1773709223044,"version":"3.50.1"},"reference-count":12,"publisher":"Springer Science and Business Media LLC","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[2026,3,16]]},"DOI":"10.7759\/cureus.105342","type":"journal-article","created":{"date-parts":[[2026,3,16]],"date-time":"2026-03-16T23:57:22Z","timestamp":1773705442000},"source":"Crossref","is-referenced-by-count":0,"title":["When Thiamine Is Not the Answer: Sporadic Creutzfeldt-Jakob Disease Mimicking Wernicke\u2019s Encephalopathy"],"prefix":"10.7759","author":[{"given":"Carlos","family":"Fagundo","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Catherine","family":"Xu","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Reyleen","family":"Loreto","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Hazem","family":"Abugrara","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"297","reference":[{"key":"ref1","doi-asserted-by":"publisher","DOI":"10.3390\/neurolint16050079","article-title":"A systematic review of sporadic Creutzfeldt-Jakob disease: pathogenesis, diagnosis, and therapeutic attempts","volume":"16","author":"Jurcau MC","year":"2024","unstructured":"Jurcau MC, Jurcau A, Diaconu RG, Hogea VO, Nunkoo VS. A systematic review of sporadic Creutzfeldt-Jakob disease: pathogenesis, diagnosis, and therapeutic attempts. Neurol Int. 2024, 16:1039-65. 10.3390\/neurolint16050079","journal-title":"Neurol Int"},{"key":"ref2","doi-asserted-by":"publisher","DOI":"10.1016\/j.jns.2024.123293","article-title":"Creutzfeldt-Jakob disease: a comprehensive review of current understanding and research","volume":"467","author":"Noor H","year":"2024","unstructured":"Noor H, Baqai MH, Naveed H, et al.. Creutzfeldt-Jakob disease: a comprehensive review of current understanding and research. J Neurol Sci. 2024, 467:123293. 10.1016\/j.jns.2024.123293","journal-title":"J Neurol Sci"},{"key":"ref3","doi-asserted-by":"publisher","DOI":"10.1056\/NEJMra2119323","article-title":"Laboratory diagnosis of Creutzfeldt-Jakob disease","volume":"386","author":"Zerr I","year":"2022","unstructured":"Zerr I. Laboratory diagnosis of Creutzfeldt-Jakob disease. N Engl J Med. 2022, 386:1345-50. 10.1056\/NEJMra2119323","journal-title":"N Engl J Med"},{"key":"ref4","doi-asserted-by":"publisher","DOI":"10.1002\/ana.410350404","article-title":"Human prion diseases","volume":"35","author":"Prusiner SB","year":"1994","unstructured":"Prusiner SB, Hsiao KK. Human prion diseases. Ann Neurol. 1994, 35:385-95. 10.1002\/ana.410350404","journal-title":"Ann Neurol"},{"key":"ref5","doi-asserted-by":"publisher","DOI":"10.2478\/amb-2024-0032","article-title":"Sporadic Creutzfeldt-Jakob disease","volume":"51","author":"Zhelyazkova S","year":"2024","unstructured":"Zhelyazkova S, Nachev S, Kalev O, Tournev I. Sporadic Creutzfeldt-Jakob disease. Acta Medica Bulgarica. 2024, 51:36-40. 10.2478\/amb-2024-0032","journal-title":"Acta Medica Bulgarica"},{"key":"ref6","doi-asserted-by":"publisher","DOI":"10.1212\/WNL.0b013e31826d5fc3","article-title":"Evidence-based guideline: diagnostic accuracy of CSF 14-3-3 protein in sporadic Creutzfeldt-Jakob disease: report of the guideline development subcommittee of the American Academy of Neurology","volume":"79","author":"Muayqil T","year":"2012","unstructured":"Muayqil T, Gronseth G, Camicioli R. Evidence-based guideline: diagnostic accuracy of CSF 14-3-3 protein in sporadic Creutzfeldt-Jakob disease: report of the guideline development subcommittee of the American Academy of Neurology. Neurology. 2012, 79:1499-506. 10.1212\/WNL.0b013e31826d5fc3","journal-title":"Neurology"},{"key":"ref7","doi-asserted-by":"publisher","DOI":"10.1001\/jamanetworkopen.2021.46319","article-title":"Validation of revised International Creutzfeldt-Jakob Disease Surveillance Network diagnostic criteria for sporadic Creutzfeldt-Jakob disease","volume":"5","author":"Watson N","year":"2022","unstructured":"Watson N, Hermann P, Ladogana A, et al.. Validation of revised International Creutzfeldt-Jakob Disease Surveillance Network diagnostic criteria for sporadic Creutzfeldt-Jakob disease. JAMA Netw Open. 2022, 5:e2146319. 10.1001\/jamanetworkopen.2021.46319","journal-title":"JAMA Netw Open"},{"key":"ref8","doi-asserted-by":"publisher","DOI":"10.1038\/s41572-021-00269-y","article-title":"Alzheimer disease","volume":"7","author":"Knopman DS","year":"2021","unstructured":"Knopman DS, Amieva H, Petersen RC, et al.. Alzheimer disease. Nat Rev Dis Primers. 2021, 7:33. 10.1038\/s41572-021-00269-y","journal-title":"Nat Rev Dis Primers"},{"key":"ref9","doi-asserted-by":"publisher","DOI":"10.1056\/NEJMcp0910236","article-title":"Clinical practice. Early Alzheimer's disease","volume":"362","author":"Mayeux R","year":"2010","unstructured":"Mayeux R. Clinical practice. Early Alzheimer's disease. N Engl J Med. 2010, 362:2194-201. 10.1056\/NEJMcp0910236","journal-title":"N Engl J Med"},{"key":"ref10","doi-asserted-by":"publisher","DOI":"10.1097\/00002093-198802030-00016","article-title":"Diffuse Lewy body disease","volume":"2","author":"Lennox G","year":"1988","unstructured":"Lennox G, Lowe J, Godwin-Austen R, Landon M, Mayer R. Diffuse Lewy body disease. Alzheimer Dis Assoc Disord. 1988, 2:167. 10.1097\/00002093-198802030-00016","journal-title":"Alzheimer Dis Assoc Disord"},{"key":"ref11","doi-asserted-by":"publisher","DOI":"10.1111\/pcn.13375","article-title":"Biological basis and psychiatric symptoms in frontotemporal dementia","volume":"76","author":"Mori K","year":"2022","unstructured":"Mori K, Ikeda M. Biological basis and psychiatric symptoms in frontotemporal dementia. Psychiatry Clin Neurosci. 2022, 76:351-60. 10.1111\/pcn.13375","journal-title":"Psychiatry Clin Neurosci"},{"key":"ref12","doi-asserted-by":"publisher","DOI":"10.1080\/14737175.2023.2246653","article-title":"The advances in the early and accurate diagnosis of Creutzfeldt-Jakob disease and other prion diseases: where are we today?","volume":"23","author":"Kishida H","year":"2023","unstructured":"Kishida H, Ueda N, Tanaka F. The advances in the early and accurate diagnosis of Creutzfeldt-Jakob disease and other prion diseases: where are we today?. Expert Rev Neurother. 2023, 23:803-17. 10.1080\/14737175.2023.2246653","journal-title":"Expert Rev Neurother"}],"container-title":["Cureus"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/www.cureus.com\/articles\/468985-when-thiamine-is-not-the-answer-sporadic-creutzfeldt-jakob-disease-mimicking-wernickes-encephalopathy","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2026,3,16]],"date-time":"2026-03-16T23:57:23Z","timestamp":1773705443000},"score":1,"resource":{"primary":{"URL":"https:\/\/www.cureus.com\/articles\/468985-when-thiamine-is-not-the-answer-sporadic-creutzfeldt-jakob-disease-mimicking-wernickes-encephalopathy"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2026,3,16]]},"references-count":12,"URL":"https:\/\/doi.org\/10.7759\/cureus.105342","relation":{},"ISSN":["2168-8184"],"issn-type":[{"value":"2168-8184","type":"print"}],"subject":[],"published":{"date-parts":[[2026,3,16]]}}}