{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,8,15]],"date-time":"2025-08-15T00:06:31Z","timestamp":1755216391932,"version":"3.43.0"},"reference-count":6,"publisher":"Vilnius University Press","issue":"2","license":[{"start":{"date-parts":[[2022,7,25]],"date-time":"2022-07-25T00:00:00Z","timestamp":1658707200000},"content-version":"unspecified","delay-in-days":0,"URL":"https:\/\/creativecommons.org\/licenses\/by\/4.0"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["AML"],"abstract":"<jats:p>Creutzfeldt\u2013Jakob disease (CJD) is a rare, progressive, and fatal prion disease. Often the first sign of CJD is rapidly progressive dementia, leading to memory loss, personality changes, and hallucinations. Myoclonus typically occurs in 90% of cases, but often may not be an initial symptom. Other frequently occurring psychiatric symptoms include depression, anxiety, paranoia, obsessive-compulsive symptoms, and psychosis. Speech disorder, loss of balance and coordination may also accompany. We present a case of CJD with sudden onset of right hemiparesis.<\/jats:p>","DOI":"10.15388\/amed.2022.29.2.3","type":"journal-article","created":{"date-parts":[[2022,7,25]],"date-time":"2022-07-25T03:52:35Z","timestamp":1658721155000},"page":"306-310","source":"Crossref","is-referenced-by-count":0,"title":["Creutzfeldt\u2013Jakob Disease with Stroke-Like Symptoms: Case report"],"prefix":"10.15388","volume":"29","author":[{"given":"B\u00fcnyamin","family":"Tosuno\u011flu","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"S\u0131dd\u0131ka Sena","family":"Dilek","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"\u00dcmm\u00fchan\u0131","family":"Emektar","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Tahir Kurtulu\u015f","family":"Yolda\u015f","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"6097","published-online":{"date-parts":[[2022,7,25]]},"reference":[{"key":"ref0","doi-asserted-by":"publisher","unstructured":"Will RG ,Ward HJT. Clinical features of variant Creutzfeldt-Jakob disease.Curr Top Microbiol Immunol.2004;284:121-32.doi: 10.1007\/978-3-662-08441-0_5.","DOI":"10.1007\/978-3-662-08441-0_5"},{"key":"ref1","unstructured":"Ko KF, Lau WY, Cheng WK, Kwan MC,Yip LK. Creutzfeldt-Jakob disease with initial right hemiparesis masquerading as a stroke. Hong Kong Med J.2010 Dec;16(6):487-8."},{"key":"ref2","doi-asserted-by":"publisher","unstructured":"Okamoto K,Takato A,Yoshiaki I. A Case of Creutzfeldt-Jakob Disease with Stroke-Like Onset. J Stroke Cerebrovasc Dis. 2020 Jun;29(6):104788.","DOI":"10.1016\/j.jstrokecerebrovasdis.2020.104788"},{"key":"ref3","doi-asserted-by":"publisher","unstructured":"Lyytinen J, Sairanen T, Valanne L, Salmi T, Paetau A,Pekkonen E. Progressive Stroke-Like Symptoms in a Patient with Sporadic Creutzfeldt-Jakob Disease. Case Rep Neurol. 2010 Jan-Apr; 2(1): 12-18.","DOI":"10.1159\/000289177"},{"key":"ref4","doi-asserted-by":"publisher","first-page":"635","DOI":"10.1016\/S1474-4422(05)70192-7","article-title":"Prion diseases","volume":"4","author":"Johnson","year":"2005","unstructured":"Johnson RT. Prion diseases. Lancet Neurol. 2005;4:635-642.","journal-title":"Lancet Neurol"},{"key":"ref5","doi-asserted-by":"publisher","first-page":"1724","DOI":"10.1016\/S1388-2457(03)00109-3","article-title":"Lateralized and focal clinical, EEG, and FLAIR MRI abnormalities in Creutzfeldt-Jakob disease","volume":"114","author":"Cambier","year":"2003","unstructured":"Cambier DM, Kantarci K, Worrell GA, Westmoreland BF, Aksamit AJ. Lateralized and focal clinical, EEG, and FLAIR MRI abnormalities in Creutzfeldt-Jakob disease. Clin Neurophysiol. 2003;114:1724-1728.","journal-title":"Clin Neurophysiol"}],"container-title":["Acta medica Lituanica"],"original-title":[],"link":[{"URL":"https:\/\/www.journals.vu.lt\/AML\/article\/download\/25438\/27729","content-type":"application\/pdf","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/www.journals.vu.lt\/AML\/article\/download\/25438\/27730","content-type":"text\/html","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/www.journals.vu.lt\/AML\/article\/download\/25438\/27730","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/www.journals.vu.lt\/AML\/article\/download\/25438\/27729","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2025,8,4]],"date-time":"2025-08-04T09:56:53Z","timestamp":1754301413000},"score":1,"resource":{"primary":{"URL":"https:\/\/www.journals.vu.lt\/AML\/article\/view\/25438"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2022,7,25]]},"references-count":6,"journal-issue":{"issue":"2","published-online":{"date-parts":[[2022,7,25]]}},"URL":"https:\/\/doi.org\/10.15388\/amed.2022.29.2.3","relation":{},"ISSN":["2029-4174","1392-0138"],"issn-type":[{"type":"electronic","value":"2029-4174"},{"type":"print","value":"1392-0138"}],"subject":[],"published":{"date-parts":[[2022,7,25]]}}}