{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,10,4]],"date-time":"2025-10-04T17:46:10Z","timestamp":1759599970427,"version":"build-2065373602"},"reference-count":32,"publisher":"Elsevier BV","issue":"3","license":[{"start":{"date-parts":[[2009,4,1]],"date-time":"2009-04-01T00:00:00Z","timestamp":1238544000000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"},{"start":{"date-parts":[[2009,4,1]],"date-time":"2009-04-01T00:00:00Z","timestamp":1238544000000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/legal\/tdmrep-license"},{"start":{"date-parts":[[2009,4,1]],"date-time":"2009-04-01T00:00:00Z","timestamp":1238544000000},"content-version":"stm-asf","delay-in-days":0,"URL":"https:\/\/doi.org\/10.15223\/policy-017"},{"start":{"date-parts":[[2009,4,1]],"date-time":"2009-04-01T00:00:00Z","timestamp":1238544000000},"content-version":"stm-asf","delay-in-days":0,"URL":"https:\/\/doi.org\/10.15223\/policy-037"},{"start":{"date-parts":[[2009,4,1]],"date-time":"2009-04-01T00:00:00Z","timestamp":1238544000000},"content-version":"stm-asf","delay-in-days":0,"URL":"https:\/\/doi.org\/10.15223\/policy-012"},{"start":{"date-parts":[[2009,4,1]],"date-time":"2009-04-01T00:00:00Z","timestamp":1238544000000},"content-version":"stm-asf","delay-in-days":0,"URL":"https:\/\/doi.org\/10.15223\/policy-029"},{"start":{"date-parts":[[2009,4,1]],"date-time":"2009-04-01T00:00:00Z","timestamp":1238544000000},"content-version":"stm-asf","delay-in-days":0,"URL":"https:\/\/doi.org\/10.15223\/policy-004"}],"content-domain":{"domain":["clinicalkey.com","clinicalkey.com.au","clinicalkey.es","clinicalkey.fr","clinicalkey.jp","elsevier.com","sciencedirect.com"],"crossmark-restriction":true},"short-container-title":["Clinical Neurology and Neurosurgery"],"published-print":{"date-parts":[[2009,4]]},"DOI":"10.1016\/j.clineuro.2008.09.017","type":"journal-article","created":{"date-parts":[[2008,11,10]],"date-time":"2008-11-10T03:08:37Z","timestamp":1226286517000},"page":"282-291","update-policy":"https:\/\/doi.org\/10.1016\/elsevier_cm_policy","source":"Crossref","is-referenced-by-count":12,"title":["An unusually presenting case of sCJD\u2014The VV1 subtype"],"prefix":"10.1016","volume":"111","author":[{"given":"Kaloyan S.","family":"Tanev","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Mimi","family":"Yilma","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"78","reference":[{"issue":"April (4542)","key":"10.1016\/j.clineuro.2008.09.017_bib1","doi-asserted-by":"crossref","first-page":"136","DOI":"10.1126\/science.6801762","article-title":"Novel proteinaceous infectious particles cause scrapie","volume":"216","author":"Prusiner","year":"1982","journal-title":"Science"},{"key":"10.1016\/j.clineuro.2008.09.017_bib2","doi-asserted-by":"crossref","first-page":"13363","DOI":"10.1073\/pnas.95.23.13363","article-title":"Prions","volume":"95","author":"Prusiner","year":"1998","journal-title":"Proc Natl Acad Sci"},{"key":"10.1016\/j.clineuro.2008.09.017_bib3","doi-asserted-by":"crossref","first-page":"906","DOI":"10.1136\/jnnp.2004.048660","article-title":"Molecular neurology of prion disease","volume":"76","author":"Collinge","year":"2005","journal-title":"J Neurol Neurosurg Psychiatry"},{"key":"10.1016\/j.clineuro.2008.09.017_bib4","doi-asserted-by":"crossref","first-page":"224","DOI":"10.1002\/1531-8249(199908)46:2<224::AID-ANA12>3.0.CO;2-W","article-title":"Classification of sporadic Creutzfeldt\u2013Jacob disease based on molecular and phenotypic analysis of 300 subjects","volume":"46","author":"Parchi","year":"1999","journal-title":"Ann Neurol"},{"key":"10.1016\/j.clineuro.2008.09.017_bib5","doi-asserted-by":"crossref","first-page":"213","DOI":"10.1093\/bmb\/66.1.213","article-title":"Sporadic and familial CJD: classification and characterization","volume":"66","author":"Gambetti","year":"2003","journal-title":"Br Med Bull"},{"key":"10.1016\/j.clineuro.2008.09.017_bib6","doi-asserted-by":"crossref","first-page":"1350","DOI":"10.1093\/brain\/awm063","article-title":"Creutzfeldt\u2013Jakob disease in Germany: a prospective 12-year surveillance","volume":"130","author":"Heinemann","year":"2007","journal-title":"Brain"},{"issue":"August (14)","key":"10.1016\/j.clineuro.2008.09.017_bib7","doi-asserted-by":"crossref","first-page":"328","DOI":"10.1016\/j.vetmic.2007.04.002","article-title":"Molecular subtype-specific clinical diagnosis of prion diseases","volume":"123","author":"Heinemann","year":"2007","journal-title":"Vet Microbiol"},{"key":"10.1016\/j.clineuro.2008.09.017_bib8","doi-asserted-by":"crossref","first-page":"1544","DOI":"10.1212\/01.wnl.0000184674.32924.c9","article-title":"Sporadic Creutzfeldt\u2013Jakob disease: clinical and diagnostic characteristics of the rare VV1 type","volume":"65","author":"Meissner","year":"2005","journal-title":"Neurology"},{"key":"10.1016\/j.clineuro.2008.09.017_bib9","unstructured":"World Health Organization: report of a WHO consultation on global surveillance, diagnosis and therapy of human transmissible spongiform encephalopathies. Geneva, Switzerland: WHO. February 9\u201311, 1998. WHO\/EMC\/ZDI\/98.9."},{"key":"10.1016\/j.clineuro.2008.09.017_bib10","unstructured":"World Health Organization, Weekly epidemiological record 1998, 73, 361\u2013372."},{"issue":"April (4)","key":"10.1016\/j.clineuro.2008.09.017_bib11","first-page":"263","article-title":"The psychiatric manifestation of Creutzfeldt\u2013Jakob disease","volume":"13","author":"Yen","year":"1997","journal-title":"Kaohsiung J Med Sci"},{"key":"10.1016\/j.clineuro.2008.09.017_bib12","doi-asserted-by":"crossref","first-page":"33","DOI":"10.1136\/jnnp.71.1.33","article-title":"Patients with Alzheimer's disease and dementia with Lewy bodies mistaken for Creutzfeldt\u2013Jakob disease","volume":"71","author":"Tschampa","year":"2001","journal-title":"J Neurol Nerusurg Psychiatry"},{"issue":"162","key":"10.1016\/j.clineuro.2008.09.017_bib13","article-title":"Accuracy and reiability of periodic sharp wave complexes in Creutzfeldt\u2013Jakob disease","volume":"53","author":"Steinhoff","year":"1996","journal-title":"Arch Neurol"},{"key":"10.1016\/j.clineuro.2008.09.017_bib14","doi-asserted-by":"crossref","first-page":"811","DOI":"10.1212\/WNL.55.6.811","article-title":"Analysis of EEG and CSF 14-3-3 proteins as aids to the diagnosis of Creutzfeldt\u2013Jakob disease","volume":"26","author":"Zerr","year":"2000","journal-title":"Neurology"},{"key":"10.1016\/j.clineuro.2008.09.017_bib15","doi-asserted-by":"crossref","first-page":"436","DOI":"10.1212\/01.WNL.0000135153.96325.3B","article-title":"Sensitivity of 14-3-3 protein test varies in subtypes of sporadic Creutzfeldt\u2013Jacob disease","volume":"63","author":"Castellani","year":"2004","journal-title":"Neurology"},{"issue":"Suppl 3","key":"10.1016\/j.clineuro.2008.09.017_bib16","first-page":"A250","article-title":"The cerebrospinal fluid 14-3-3 assay's diagnostic utility among clinically suspected Creutzfeldt\u2013Jakob disease patients: the NIH experience","volume":"58","author":"Kenney","year":"2002","journal-title":"Neurol"},{"key":"10.1016\/j.clineuro.2008.09.017_bib17","doi-asserted-by":"crossref","first-page":"25","DOI":"10.1186\/1471-2377-6-25","article-title":"Impact of the clinical context on the 14-3-3 test for the diagnosis of sporadic CJD","volume":"6","author":"Cuadrado-Corrales","year":"2006","journal-title":"BMC Neurol"},{"key":"10.1016\/j.clineuro.2008.09.017_bib18","doi-asserted-by":"crossref","first-page":"813","DOI":"10.1001\/archneur.60.6.813","article-title":"Challenging the clinical utility of the 14-3-3 protein for the diagnosis of sporadic Creutzfeldt\u2013Jakob disease","volume":"60","author":"Geschwind","year":"2003","journal-title":"Arch Neurol"},{"key":"10.1016\/j.clineuro.2008.09.017_bib19","doi-asserted-by":"crossref","first-page":"32","DOI":"10.1002\/ana.410430109","article-title":"Detection of 14-3-3 protein in the cerebrospinal fluid supports the diagnosis of Creutzfeldt\u2013Jakob disease","volume":"43","author":"Zerr","year":"1998","journal-title":"Ann Neurol"},{"key":"10.1016\/j.clineuro.2008.09.017_bib20","doi-asserted-by":"crossref","first-page":"1396","DOI":"10.1212\/WNL.55.9.1396","article-title":"Misleading results with the 14-3-3 assay for the diagnosis of Creutzfeldt\u2013Jakob disease","volume":"55","author":"Chapman","year":"2000","journal-title":"Neurology"},{"key":"10.1016\/j.clineuro.2008.09.017_bib21","doi-asserted-by":"crossref","first-page":"216","DOI":"10.1159\/000008054","article-title":"The 14-3-3 protein detectable in the cerevrospinal fluid of patients with prion-unrelated neurological diseases is expressed constitutively in neurons and glial cells in culture","volume":"41","author":"Satoh","year":"1999","journal-title":"Eur Neurol"},{"key":"10.1016\/j.clineuro.2008.09.017_bib22","doi-asserted-by":"crossref","first-page":"726","DOI":"10.1053\/crad.2001.0771","article-title":"MRI of Creutzfeldt\u2013Jacob disease: imaging features and recommended MRI protocol","volume":"56","author":"Collie","year":"2001","journal-title":"Clin Radiol"},{"key":"10.1016\/j.clineuro.2008.09.017_bib23","doi-asserted-by":"crossref","first-page":"1751","DOI":"10.1001\/archneur.57.12.1751","article-title":"Magnetic resonance imaging in the clinical diagnosis of Creutzfeldt\u2013Jakob disease","volume":"57","author":"Schr\u00f6ter","year":"2000","journal-title":"Arch Neurol"},{"issue":"June (6)","key":"10.1016\/j.clineuro.2008.09.017_bib24","doi-asserted-by":"crossref","first-page":"699","DOI":"10.1007\/s00415-002-0695-3","article-title":"Positron emission tomography with [(18)F]FDG in the diagnosis of Creutzfeldt\u2013Jakob disease (CJD)","volume":"249","author":"Henkel","year":"2002","journal-title":"J Neurol"},{"issue":"3","key":"10.1016\/j.clineuro.2008.09.017_bib25","doi-asserted-by":"crossref","first-page":"158","DOI":"10.1159\/000076350","article-title":"results of quinacrine administration to patients with Creutzfeldt\u2013Jakob disease","volume":"17","author":"Nakajima","year":"2004","journal-title":"Dement. Geriatr. Cogn. Disorders"},{"issue":"July (7)","key":"10.1016\/j.clineuro.2008.09.017_bib26","first-page":"403","article-title":"Quinacrine administration to a patient with Creutzfeldt\u2013Jakob disease who received a cadaveric dura mater graft\u2014an EEG evaluation","volume":"43","author":"Kobayashi","year":"2003","journal-title":"Clin Neurol"},{"issue":"July (2\u20133)","key":"10.1016\/j.clineuro.2008.09.017_bib27","doi-asserted-by":"crossref","first-page":"193","DOI":"10.1016\/S0047-6374(00)00112-3","article-title":"Novel approaches in diagnosis and therapy of Creutzfeldt\u2013Jakob disease","volume":"116","author":"Muller","year":"2000","journal-title":"Mech Ageing Dev"},{"key":"10.1016\/j.clineuro.2008.09.017_bib28","first-page":"603","article-title":"Research groups fail to reach agreement on protocol for treatment trials for CJD","volume":"March (328)","author":"Dyer","year":"2004","journal-title":"BMJ"},{"key":"10.1016\/j.clineuro.2008.09.017_bib29","first-page":"326","article-title":"Family finds hospital willing to give experimental CJD treatment","volume":"8","author":"Dyer","year":"2003","journal-title":"BMJ"},{"key":"10.1016\/j.clineuro.2008.09.017_bib30","doi-asserted-by":"crossref","first-page":"714","DOI":"10.1212\/01.WNL.0000113764.35026.EF","article-title":"Efficacy of flupirtine on cognitive function in patients with CJD","volume":"62","author":"Otto","year":"2004","journal-title":"Neurology"},{"issue":"September (Pt 9)","key":"10.1016\/j.clineuro.2008.09.017_bib31","doi-asserted-by":"crossref","first-page":"2278","DOI":"10.1093\/brain\/awl159","article-title":"Determinants of diagnostic investigation sensitivities across the clinical spectrum of sporadic Creutzfeldt\u2013Jakob disease","volume":"129","author":"Collins","year":"2006","journal-title":"Brain"},{"issue":"November (5)","key":"10.1016\/j.clineuro.2008.09.017_bib32","doi-asserted-by":"crossref","first-page":"671","DOI":"10.1136\/jnnp.67.5.671","article-title":"Type 1 protease resistant prion protein and valine homozygosity at codon 129 of PRNP identify a subtype of sporadic Creutzfeldt\u2013Jakob disease","volume":"67","author":"Worrall","year":"1999","journal-title":"J Neurol Neurosurg Psychiatry"}],"container-title":["Clinical Neurology and Neurosurgery"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S030384670800320X?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S030384670800320X?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2025,10,4]],"date-time":"2025-10-04T14:26:28Z","timestamp":1759587988000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S030384670800320X"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2009,4]]},"references-count":32,"journal-issue":{"issue":"3","published-print":{"date-parts":[[2009,4]]}},"alternative-id":["S030384670800320X"],"URL":"https:\/\/doi.org\/10.1016\/j.clineuro.2008.09.017","relation":{},"ISSN":["0303-8467"],"issn-type":[{"type":"print","value":"0303-8467"}],"subject":[],"published":{"date-parts":[[2009,4]]},"assertion":[{"value":"Elsevier","name":"publisher","label":"This article is maintained by"},{"value":"An unusually presenting case of sCJD\u2014The VV1 subtype","name":"articletitle","label":"Article Title"},{"value":"Clinical Neurology and Neurosurgery","name":"journaltitle","label":"Journal Title"},{"value":"https:\/\/doi.org\/10.1016\/j.clineuro.2008.09.017","name":"articlelink","label":"CrossRef DOI link to publisher maintained version"},{"value":"article","name":"content_type","label":"Content Type"},{"value":"Copyright \u00a9 2008 Elsevier B.V. All rights reserved.","name":"copyright","label":"Copyright"}]}}