{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,2,11]],"date-time":"2026-02-11T15:26:03Z","timestamp":1770823563273,"version":"3.50.1"},"reference-count":110,"publisher":"Elsevier BV","issue":"3","license":[{"start":{"date-parts":[[2000,5,1]],"date-time":"2000-05-01T00:00:00Z","timestamp":957139200000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Journal of Clinical Neuroscience"],"published-print":{"date-parts":[[2000,5]]},"DOI":"10.1054\/jocn.1999.0191","type":"journal-article","created":{"date-parts":[[2002,7,26]],"date-time":"2002-07-26T07:35:14Z","timestamp":1027668914000},"page":"195-202","source":"Crossref","is-referenced-by-count":30,"title":["Recent advances in the pre-mortem diagnosis of Creutzfeldt-Jakob disease"],"prefix":"10.1054","volume":"7","author":[{"given":"S","family":"Collins","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"A","family":"Boyd","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"A","family":"Fletcher","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"M.F","family":"Gonzales","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"C.A","family":"McLean","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"C.L","family":"Masters","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"78","reference":[{"key":"10.1054\/jocn.1999.0191_RF1","doi-asserted-by":"crossref","first-page":"638","DOI":"10.1016\/0959-4388(92)90032-G","article-title":"Natural and experimental prion diseases of humans and animals","volume":"2","author":"Prusiner","year":"1992","journal-title":"Curr Opin Neurobiol"},{"key":"10.1054\/jocn.1999.0191_RF2","doi-asserted-by":"crossref","first-page":"385","DOI":"10.1002\/ana.410350404","article-title":"Human prion diseases","volume":"35","author":"Prusiner","year":"1994","journal-title":"Ann Neurol"},{"key":"10.1054\/jocn.1999.0191_RF3","doi-asserted-by":"crossref","first-page":"913","DOI":"10.1001\/archneur.1996.00550090125018","article-title":"Diagnostic criteria for sporadic Creutzfeldt-Jakob disease","volume":"53","author":"Kretzschmar","year":"1996","journal-title":"Arch Neurol"},{"key":"10.1054\/jocn.1999.0191_RF4","doi-asserted-by":"crossref","first-page":"437","DOI":"10.1038\/38876","article-title":"Human BSE","volume":"389","author":"Almond","year":"1997","journal-title":"Nature"},{"key":"10.1054\/jocn.1999.0191_RF5","doi-asserted-by":"crossref","first-page":"921","DOI":"10.1016\/S0140-6736(96)91412-9","article-title":"A new variant of Creutzfeldt-Jakob disease","volume":"347","author":"Will","year":"1996","journal-title":"Lancet"},{"key":"10.1054\/jocn.1999.0191_RF6","doi-asserted-by":"crossref","first-page":"569","DOI":"10.1212\/WNL.48.3.569","article-title":"BSE and a new variant of Creutzfeldt-Jakob disease","volume":"48","author":"Epstein","year":"1997","journal-title":"Neurology"},{"key":"10.1054\/jocn.1999.0191_RF7","doi-asserted-by":"crossref","first-page":"598","DOI":"10.5694\/j.1326-5377.1996.tb122202.x","article-title":"Iatrogenic and zoonotic Creutzfeldt-Jakob disease: the Australian perspective","volume":"164","author":"Collins","year":"1996","journal-title":"Med J Aust"},{"key":"10.1054\/jocn.1999.0191_RF8","doi-asserted-by":"crossref","first-page":"763","DOI":"10.1002\/ana.410430611","article-title":"Descriptive epidemiology of Creutzfeldt-Jakob disease in six European countries, 1993\u20131995","volume":"43","author":"Will","year":"1998","journal-title":"Ann Neurol"},{"key":"10.1054\/jocn.1999.0191_RF9","doi-asserted-by":"crossref","first-page":"259","DOI":"10.1007\/s004390050204","article-title":"Genetic basis of Creutzfeldt-Jakob disease in the United Kingdom: a systematic analysis of predisposting mutations and allelic variation in the PRNP gene","volume":"98","author":"Windl","year":"1996","journal-title":"Hum Genet"},{"key":"10.1054\/jocn.1999.0191_RF10","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 Creutzffeldt-Jakob disease based on molecular and phenotypic analysis of 300 subjects","volume":"46","author":"Parchi","year":"1999","journal-title":"Ann Neurol"},{"key":"10.1054\/jocn.1999.0191_RF11","doi-asserted-by":"crossref","first-page":"10962","DOI":"10.1073\/pnas.90.23.10962","article-title":"Conversion of \u03b1-helices into \u03b2-sheets features in the formation of the scrapie prion proteins","volume":"90","author":"Pan","year":"1993","journal-title":"Proc Natl Acad Sci"},{"key":"10.1054\/jocn.1999.0191_RF12","doi-asserted-by":"crossref","first-page":"11604","DOI":"10.1074\/jbc.272.17.11604","article-title":"Identification of intermediate steps in the formation of a mutant prion protein to a scrapie-like form in cultured cells","volume":"272","author":"Daude","year":"1997","journal-title":"J Biol Chem"},{"key":"10.1054\/jocn.1999.0191_RF13","doi-asserted-by":"crossref","first-page":"1339","DOI":"10.1016\/0092-8674(93)90360-3","article-title":"Mice devoid of PrP are resistant to scrapie","volume":"73","author":"B\u00fceler","year":"1993","journal-title":"Cell"},{"key":"10.1054\/jocn.1999.0191_RF14","doi-asserted-by":"crossref","first-page":"295","DOI":"10.1038\/370295a0","article-title":"Prion protein is necessary for normal synaptic function","volume":"370","author":"Collinge","year":"1994","journal-title":"Nature"},{"key":"10.1054\/jocn.1999.0191_RF15","doi-asserted-by":"crossref","first-page":"639","DOI":"10.1038\/380639a0","article-title":"Altered circadian activity rhythms and sleep in mice devoid of prion protein","volume":"380","author":"Tobler","year":"1996","journal-title":"Nature"},{"key":"10.1054\/jocn.1999.0191_RF16","doi-asserted-by":"crossref","first-page":"528","DOI":"10.1038\/380528a0","article-title":"Loss of cerebellar Purkinje cells in aged mice homozygous for a disrupted PrP gene","volume":"380","author":"Sakaguchi","year":"1996","journal-title":"Nature"},{"key":"10.1054\/jocn.1999.0191_RF17","doi-asserted-by":"crossref","first-page":"684","DOI":"10.1038\/37733","article-title":"The cellular prion protein binds copper in vivo","volume":"390","author":"Brown","year":"1997","journal-title":"Nature"},{"key":"10.1054\/jocn.1999.0191_RF18","doi-asserted-by":"crossref","first-page":"7185","DOI":"10.1021\/bi972827k","article-title":"Prion protein selectively binds copper(II) ions","volume":"37","author":"St\u00f6ckel","year":"1998","journal-title":"Biochemistry"},{"key":"10.1054\/jocn.1999.0191_RF19","doi-asserted-by":"crossref","first-page":"1686","DOI":"10.1046\/j.1471-4159.1998.70041686.x","article-title":"Effects of copper on survival of prion protein knockout neurons and glia","volume":"70","author":"Brown","year":"1998","journal-title":"J Neurochem"},{"key":"10.1054\/jocn.1999.0191_RF20","doi-asserted-by":"crossref","first-page":"104","DOI":"10.1006\/exnr.1997.6505","article-title":"Prion protein-deficient cells show altered response to oxidative stress due to decreased SOD-1 activity","volume":"147","author":"Brown","year":"1997","journal-title":"Exp Neurol"},{"key":"10.1054\/jocn.1999.0191_RF21","doi-asserted-by":"crossref","first-page":"423","DOI":"10.1042\/bj3340423","article-title":"Prion protein expression and superoxide dismutase activity","volume":"334","author":"Brown","year":"1998","journal-title":"Biochem J"},{"key":"10.1054\/jocn.1999.0191_RF22","doi-asserted-by":"crossref","first-page":"335","DOI":"10.1016\/S0165-0173(97)00045-3","article-title":"Neurodegenerative disorders in humans: the role of glutathione in oxidative stress-mediated neuronal death","volume":"25","author":"Bains","year":"1997","journal-title":"Brain Res REv"},{"key":"10.1054\/jocn.1999.0191_RF23","doi-asserted-by":"crossref","first-page":"449","DOI":"10.1111\/j.1750-3639.1998.tb00167.x","article-title":"Role of microglia in neuronal cell death in prion disease","volume":"8","author":"Giese","year":"1998","journal-title":"Brain Pathol"},{"key":"10.1054\/jocn.1999.0191_RF24","doi-asserted-by":"crossref","first-page":"433","DOI":"10.1006\/exnr.1997.6424","article-title":"PrP deposition, microglial activation, and neuronal apoptosis in murine scrapie","volume":"144","author":"Williams","year":"1997","journal-title":"Exp Neurol"},{"key":"10.1054\/jocn.1999.0191_RF25","doi-asserted-by":"crossref","first-page":"531","DOI":"10.1111\/j.1750-3639.1998.tb00175.x","article-title":"Neuronal apoptosis in fatal familial insomnia","volume":"8","author":"Dorandeu","year":"1998","journal-title":"Brain Pathol"},{"key":"10.1054\/jocn.1999.0191_RF26","doi-asserted-by":"crossref","first-page":"345","DOI":"10.1038\/380345a0","article-title":"Role of microglia and host prion protein in neurotoxicity of a prion protein fragment","volume":"380","author":"Brown","year":"1996","journal-title":"Nature"},{"key":"10.1054\/jocn.1999.0191_RF27","doi-asserted-by":"crossref","first-page":"518","DOI":"10.1006\/exnr.1997.6559","article-title":"Effect of flupirtine on Bcl-2 and glutathione level in neuronal cells treated in vitro with the prion protein fragment (PrP106\u2013126)","volume":"147","author":"Perovic","year":"1997","journal-title":"Exp Neurol"},{"key":"10.1054\/jocn.1999.0191_RF28","doi-asserted-by":"crossref","first-page":"693","DOI":"10.1016\/S0140-6736(98)08138-0","article-title":"Surgical treatment and risk of sporadic Creutzfeldt-Jakob disease: a case-control study","volume":"353","author":"Collins","year":"1999","journal-title":"Lancet"},{"key":"10.1054\/jocn.1999.0191_RF29","doi-asserted-by":"crossref","first-page":"197","DOI":"10.1038\/385197a0","article-title":"Predicting the CJD epidemic in humans","volume":"385","author":"Cousens","year":"1997","journal-title":"Nature"},{"key":"10.1054\/jocn.1999.0191_RF30","doi-asserted-by":"crossref","first-page":"74","DOI":"10.1038\/36337","article-title":"Prion (PrPsc)-specific epitope defined by a monoclonal antibody","volume":"390","author":"Korth","year":"1997","journal-title":"Nature"},{"key":"10.1054\/jocn.1999.0191_RF31","doi-asserted-by":"crossref","first-page":"1056","DOI":"10.1212\/WNL.38.7.1056","article-title":"Creutzfeldt-Jakob disease without periodic sharp wave complexes: a clinical, electroencephalographic, and pathologic study","volume":"38","author":"Zochodne","year":"1988","journal-title":"Neurology"},{"key":"10.1054\/jocn.1999.0191_RF32","doi-asserted-by":"crossref","first-page":"323","DOI":"10.1016\/0013-4694(94)90048-5","article-title":"Reliability of EEG in the diagnosis of Creutzfeldt-Jakob disease","volume":"90","author":"Bortone","year":"1994","journal-title":"Electroencephalogr Clin Neurophysiol"},{"key":"10.1054\/jocn.1999.0191_RF33","doi-asserted-by":"crossref","first-page":"295","DOI":"10.1002\/ana.410160305","article-title":"Creutzfeldt-Jakob disease of long duration: clinicopathological characteristics, transmissibility, and differential diagnosis","volume":"16","author":"Brown","year":"1984","journal-title":"Ann Neurol"},{"key":"10.1054\/jocn.1999.0191_RF34","doi-asserted-by":"crossref","first-page":"597","DOI":"10.1002\/ana.410200507","article-title":"Creutzfeldt-Jakob disease: clinical analysis of a consecutive series of 230 neuropathologically verified cases","volume":"20","author":"Brown","year":"1986","journal-title":"Ann Neurol"},{"key":"10.1054\/jocn.1999.0191_RF35","doi-asserted-by":"crossref","first-page":"513","DOI":"10.1002\/ana.410350504","volume":"35","author":"Brown","year":"1994","journal-title":"Ann Neurol"},{"key":"10.1054\/jocn.1999.0191_RF36","doi-asserted-by":"crossref","first-page":"143","DOI":"10.1001\/archneur.1980.00500520041005","article-title":"Serial EEG findings in 27 cases of Creutzfeldt-Jakob disease","volume":"37","author":"Chiofalo","year":"1980","journal-title":"Arch Neurol"},{"key":"10.1054\/jocn.1999.0191_RF37","doi-asserted-by":"crossref","first-page":"428","DOI":"10.1001\/archneur.1972.00490110062006","article-title":"Creutzfeldt-Jakob disease: an electroencephalographic study","volume":"26","author":"Burger","year":"1972","journal-title":"Arch Neurol"},{"key":"10.1054\/jocn.1999.0191_RF38","doi-asserted-by":"crossref","first-page":"482","DOI":"10.1007\/BF00146403","article-title":"A retrospective study of Creutzfeldt-Jakob disease in Italy (1972\u20131986)","volume":"4","author":"Masullo","year":"1988","journal-title":"Eur J Epidemiol"},{"key":"10.1054\/jocn.1999.0191_RF39","doi-asserted-by":"crossref","first-page":"162","DOI":"10.1001\/archneur.1996.00550020074017","article-title":"Accuracy and reliability of periodic sharp wave complexes in Creutzfeldt-Jakob disease","volume":"53","author":"Steinhoff","year":"1996","journal-title":"Arch Neurol"},{"key":"10.1054\/jocn.1999.0191_RF40","doi-asserted-by":"crossref","first-page":"444","DOI":"10.1056\/NEJM199202133260704","article-title":"Fatal familial insomnia, a prion disease with a mutation at codon 178 of the prion protein gene","volume":"326","author":"Medori","year":"1992","journal-title":"N Engl J Med"},{"key":"10.1054\/jocn.1999.0191_RF41","doi-asserted-by":"crossref","first-page":"903","DOI":"10.1016\/S0140-6736(97)07472-2","article-title":"New variant Creutzfeldt-Jakob disease: neurological features and diagnostic tests","volume":"350","author":"Zeidler","year":"1997","journal-title":"Lancet"},{"key":"10.1054\/jocn.1999.0191_RF42","first-page":"653","article-title":"Electroencephalographic studies after cardiorespiratory resuscitation","volume":"55","author":"Pampiglione","year":"1962","journal-title":"Proc R Soc Med"},{"key":"10.1054\/jocn.1999.0191_RF43","doi-asserted-by":"crossref","first-page":"120","DOI":"10.1136\/jnnp.51.1.120","article-title":"A Creutzfeldt-Jakob like syndrome due to lithium toxicity","volume":"51","author":"Smith","year":"1988","journal-title":"J Neurol Neurosurg Pssychiatr"},{"key":"10.1054\/jocn.1999.0191_RF44","doi-asserted-by":"crossref","first-page":"582","DOI":"10.1016\/0013-4694(59)90059-8","article-title":"The EEG in necrotizing encephalitis","volume":"11","author":"Millar","year":"1959","journal-title":"Electroencephalogr Clin Neurophysiol"},{"key":"10.1054\/jocn.1999.0191_RF45","doi-asserted-by":"crossref","first-page":"368","DOI":"10.1002\/ana.410060415","article-title":"Clinical similarity of Alzheimer and Creutzfeldt-Jakob disease","volume":"6","author":"Watson","year":"1979","journal-title":"Ann Neurol"},{"key":"10.1054\/jocn.1999.0191_RF46","doi-asserted-by":"crossref","first-page":"341","DOI":"10.1002\/ana.410080323","article-title":"EEG characteristics in Creutzfeldt-Jakob disease","volume":"8","author":"Gloor","year":"1980","journal-title":"Ann Neurol"},{"key":"10.1054\/jocn.1999.0191_RF47","doi-asserted-by":"crossref","first-page":"611","DOI":"10.1212\/WNL.30.6.611","article-title":"Periodic lateralized epileptiform complexes (PLEDs) in Creutzfeldt-Jakob disease","volume":"30","author":"Au","year":"1980","journal-title":"Neurology"},{"key":"10.1054\/jocn.1999.0191_RF48","doi-asserted-by":"crossref","first-page":"1609","DOI":"10.1016\/S0140-6736(95)90118-3","article-title":"Cerebrospinal fluid concentration of neuron-specific enolase in diagnosis of Creutzfeldt-Jakob disease","volume":"345","author":"Zerr","year":"1995","journal-title":"Lancet"},{"key":"10.1054\/jocn.1999.0191_RF49","doi-asserted-by":"crossref","first-page":"279","DOI":"10.1056\/NEJM198607313150502","article-title":"Abnormal proteins in the cerebrospinal fluid of patients with Creutzfeldt-Jakob disease","volume":"315","author":"Harrington","year":"1986","journal-title":"N Engl J Med"},{"key":"10.1054\/jocn.1999.0191_RF50","doi-asserted-by":"crossref","first-page":"37","DOI":"10.1016\/0009-8981(92)90103-W","article-title":"High levels of nervous system-specific proteins in cerebrospinal fluid in patients with early stage Creutzfeldt-Jakob disease","volume":"211","author":"Jimi","year":"1992","journal-title":"Clinica Chimica Acta"},{"key":"10.1054\/jocn.1999.0191_RF51","first-page":"10 40","article-title":"14\u20133\u20133 protein, neuron-specific enolase, and S-100 protein in cerebrospinal fluid of patients with Creutzfeldt-Jakob disease","author":"Beaudry","year":"1999","journal-title":"Dement Geriatr Cogn Disord"},{"key":"10.1054\/jocn.1999.0191_RF52","doi-asserted-by":"crossref","first-page":"566","DOI":"10.1007\/s004150050145","article-title":"S-100 protein concentration in the cerebrospinal fluid of patients with Creutzfeldt-Jakob disease","volume":"244","author":"Otto","year":"1997","journal-title":"J Neurol"},{"key":"10.1054\/jocn.1999.0191_RF53","doi-asserted-by":"crossref","first-page":"210","DOI":"10.1016\/S0304-3940(97)00215-2","article-title":"Elevated levels of tau-protein in cerebrospinal fluid of patients with Creutzfeldt-Jakob disease","volume":"225","author":"Otto","year":"1997","journal-title":"Neurosci Lett"},{"key":"10.1054\/jocn.1999.0191_RF54","doi-asserted-by":"crossref","first-page":"924","DOI":"10.1056\/NEJM199609263351303","article-title":"Creutzfeldt-Jakob disease. The 14\u20133\u20133 brain protein in cerebrospinal fluid as a marker for transmissible spongiform encephalopathies","volume":"335","author":"Hsich","year":"1996","journal-title":"N Engl J Med"},{"key":"10.1054\/jocn.1999.0191_RF55","article-title":"The 14\u20133\u20133 brain protein and transmissible spongiform encephalopathy","volume":"336","author":"Zerr","year":"1997","journal-title":"N Engl J Med"},{"key":"10.1054\/jocn.1999.0191_RF56","doi-asserted-by":"crossref","first-page":"32","DOI":"10.1002\/ana.410430109","article-title":"Detection of 14\u20133\u20133 protein in the cerebrospinal fluid supports the diagnosis of Creutzfeldt-Jakob disease","volume":"43","author":"Zerr","year":"1998","journal-title":"Ann Neurol"},{"key":"10.1054\/jocn.1999.0191_RF57","doi-asserted-by":"crossref","first-page":"47","DOI":"10.1016\/0304-3940(92)90854-Z","article-title":"Marked increase in cerebrospinal fluid ubiquitin in Creutzfeldt-Jakob disease","volume":"139","author":"Manaka","year":"1992","journal-title":"Neurosci Lett"},{"key":"10.1054\/jocn.1999.0191_RF58","doi-asserted-by":"crossref","first-page":"216","DOI":"10.1159\/000008054","article-title":"The 14\u20133\u20133 protein detectable in the cerebrospinal 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":"10.1054\/jocn.1999.0191_RF59","doi-asserted-by":"crossref","first-page":"95","DOI":"10.1016\/S0960-9822(95)00022-4","article-title":"14\u20133\u20133 proteins: hot numbers in signal transduction","volume":"5","author":"Burbelo","year":"1995","journal-title":"Curr Biol"},{"key":"10.1054\/jocn.1999.0191_RF60","doi-asserted-by":"crossref","first-page":"498","DOI":"10.1016\/0968-0004(92)90339-B","article-title":"14\u20133\u20133 proteins: a highly conserved, widespread family of eukaryotic proteins","volume":"17","author":"Aitken","year":"1992","journal-title":"Trends Biochem Sci"},{"key":"10.1054\/jocn.1999.0191_RF61","doi-asserted-by":"crossref","first-page":"955","DOI":"10.1016\/S0140-6736(96)24040-1","article-title":"Cerebrospinal-fluid test for new-variant Creutzfeldt-Jakob disease","volume":"348","author":"Will","year":"1996","journal-title":"Lancet"},{"key":"10.1054\/jocn.1999.0191_RF62","doi-asserted-by":"crossref","first-page":"177","DOI":"10.1002\/ana.410050212","article-title":"Creutzfeldt-Jakob disease: patterns of worldwide occurrence and the significance of familial and sporadic clustering","volume":"5","author":"Masters","year":"1979","journal-title":"Ann Neurol"},{"key":"10.1054\/jocn.1999.0191_RF63","doi-asserted-by":"crossref","first-page":"593","DOI":"10.1212\/WNL.49.2.593","article-title":"Detection of 14\u20133\u20133 protein in the CSF of genetic Creutzfeldt-Jakob disease","volume":"49","author":"Rosenmann","year":"1997","journal-title":"Neurology"},{"key":"10.1054\/jocn.1999.0191_RF64","doi-asserted-by":"crossref","first-page":"577","DOI":"10.1136\/bmj.316.7131.577","article-title":"Diagnosis of Creutzfeldt-Jakob disease by measurement of S100 protein in serum: prospective case-control study","volume":"316","author":"Otto","year":"1998","journal-title":"BMJ"},{"key":"10.1054\/jocn.1999.0191_RF65","doi-asserted-by":"crossref","first-page":"409","DOI":"10.1002\/elps.1150190308","article-title":"A diagnostic test for scrapie-infected sheep using a capillary electrophoresis immunoassay with fluorescent-labeled peptides","volume":"19","author":"Schmerr","year":"1998","journal-title":"Electrophoresis"},{"key":"10.1054\/jocn.1999.0191_RF66","doi-asserted-by":"crossref","first-page":"207","DOI":"10.1016\/S0021-9673(99)00514-2","article-title":"Use of capillary electrophoresis and fluorescent labeled peptides to detect the abnormal prion protein in the blood of animals that are infected with a transmissible spongiform encephalopathy","volume":"853","author":"Schmerr","year":"1999","journal-title":"J Chromatogr"},{"key":"10.1054\/jocn.1999.0191_RF67","doi-asserted-by":"crossref","first-page":"1157","DOI":"10.1038\/2654","article-title":"Eight prion strains have PrPscmolecules with different conformations","volume":"4","author":"Safar","year":"1998","journal-title":"Nat Med"},{"key":"10.1054\/jocn.1999.0191_RF68","doi-asserted-by":"crossref","first-page":"657","DOI":"10.1093\/infdis\/146.5.657","article-title":"Natural infection of Suffolk sheep with scrapie virus","volume":"146","author":"Hadlow","year":"1982","journal-title":"J Infect Dis"},{"key":"10.1054\/jocn.1999.0191_RF69","doi-asserted-by":"crossref","first-page":"154","DOI":"10.1128\/IAI.41.1.154-161.1983","article-title":"Creutzfeldt-Jakob disease in ice: persistent viremia and preferential replication of virus in low-density lymphocytes","volume":"41","author":"Kuroda","year":"1983","journal-title":"Infect Immun"},{"key":"10.1054\/jocn.1999.0191_RF70","doi-asserted-by":"crossref","first-page":"111","DOI":"10.1111\/j.1574-6968.1985.tb00844.x","article-title":"Long-term persistence of scrapie infection in mouse spleens in the absence of clinical disease","volume":"29","author":"Collis","year":"1985","journal-title":"FEMS Microbiol Lett"},{"key":"10.1054\/jocn.1999.0191_RF71","doi-asserted-by":"crossref","first-page":"563","DOI":"10.1038\/381563a0","article-title":"Preclinical test for prion disease","volume":"381","author":"Schreuder","year":"1996","journal-title":"Nature"},{"key":"10.1054\/jocn.1999.0191_RF72","doi-asserted-by":"crossref","first-page":"99","DOI":"10.1016\/S0140-6736(97)24002-X","article-title":"Diagnosis of new variant Creutzfeldt-Jakob disease by tonsil biopsy","volume":"349","author":"Hill","year":"1997","journal-title":"Lancet"},{"key":"10.1054\/jocn.1999.0191_RF73","doi-asserted-by":"crossref","first-page":"703","DOI":"10.1016\/S0140-6736(98)24035-9","article-title":"Prion immunoreactivity in appendix before clinical onset of variant Creutzfeldt-Jakob disease","volume":"352","author":"Hilton","year":"1998","journal-title":"Lancet"},{"key":"10.1054\/jocn.1999.0191_RF74","doi-asserted-by":"crossref","first-page":"1322","DOI":"10.1016\/S0140-6736(05)62532-9","article-title":"Diagnosis of new variant Creutzfeldt-Jakob disease by tonsil biopsy","volume":"349","author":"Arya","year":"1997","journal-title":"Lancet"},{"key":"10.1054\/jocn.1999.0191_RF75","doi-asserted-by":"crossref","first-page":"68","DOI":"10.1016\/S0140-6736(05)66274-5","article-title":"Diagnosis of new variant Creutzfeldt-Jakob disease","volume":"350","author":"Kawashima","year":"1997","journal-title":"Lancet"},{"key":"10.1054\/jocn.1999.0191_RF76","doi-asserted-by":"crossref","first-page":"183","DOI":"10.1016\/S0140-6736(98)12075-5","article-title":"Investigation of variant Creutzfeldt-Jakob disease and other human prion diseases with tonsil biopsy samples","volume":"353","author":"Hill","year":"1999","journal-title":"Lancet"},{"key":"10.1054\/jocn.1999.0191_RF77","doi-asserted-by":"crossref","first-page":"538","DOI":"10.1136\/bmj.318.7182.538a","article-title":"Routine tonsil biopsy for diagnosis of new variant Creutzfeldt-Jakob disease is not justified","volume":"318","author":"Zeidler","year":"1999","journal-title":"BMJ"},{"key":"10.1054\/jocn.1999.0191_RF78","doi-asserted-by":"crossref","first-page":"1244","DOI":"10.1136\/jnnp.47.11.1244","article-title":"Computed tomography findings in 15 cases of Creutzfeldt-Jakob disease with histological verification","volume":"47","author":"G\u00e1lvez","year":"1984","journal-title":"J Neurol Neurosurg Psychiatr"},{"key":"10.1054\/jocn.1999.0191_RF79","doi-asserted-by":"crossref","first-page":"303","DOI":"10.1007\/BF00344171","article-title":"Serial computed tomography findings in Creutzfeldt-Jakob disease","volume":"31","author":"Schlenska","year":"1989","journal-title":"Neuroradiology"},{"key":"10.1054\/jocn.1999.0191_RF80","doi-asserted-by":"crossref","first-page":"793","DOI":"10.1148\/radiology.199.3.8638007","article-title":"MR imaging of Creutzfeldt-Jakob disease","volume":"199","author":"Finkenstaedt","year":"1996","journal-title":"Radiology"},{"key":"10.1054\/jocn.1999.0191_RF81","doi-asserted-by":"crossref","first-page":"125","DOI":"10.1097\/00004728-198501000-00023","article-title":"Cerebral MR and CT imaging in Creutzfeldt-Jakob disease","volume":"9","author":"Kovanen","year":"1985","journal-title":"J Comput Assist Tomogr"},{"key":"10.1054\/jocn.1999.0191_RF82","doi-asserted-by":"crossref","first-page":"65","DOI":"10.1007\/s002340050542","article-title":"MRI in sporadic Creutzfeldt-Jakob disease: correlation with clinical and neuropathological data","volume":"40","author":"Urbach","year":"1998","journal-title":"Neuroradiology"},{"key":"10.1054\/jocn.1999.0191_RF83","doi-asserted-by":"crossref","first-page":"423","DOI":"10.1007\/BF00867355","article-title":"Early MRI findings in Creutzfeldt-Jakob disease","volume":"240","author":"Onofrj","year":"1993","journal-title":"J Neurol"},{"key":"10.1054\/jocn.1999.0191_RF84","doi-asserted-by":"crossref","first-page":"584","DOI":"10.1007\/BF00588398","article-title":"MRI abnormalities in Creutzfeldt-Jakob disease","volume":"35","author":"Di Rocco","year":"1993","journal-title":"Neuroradiology"},{"key":"10.1054\/jocn.1999.0191_RF85","doi-asserted-by":"crossref","first-page":"155","DOI":"10.1016\/0720-048X(93)90095-5","article-title":"MRI alterations as an early finding in Creutzfeldt-Jakob disease","volume":"17","author":"Tartaro","year":"1993","journal-title":"Eur J Radiol"},{"key":"10.1054\/jocn.1999.0191_RF86","doi-asserted-by":"crossref","first-page":"1481","DOI":"10.1212\/WNL.38.9.1481","article-title":"Creutzfeldt-Jakob disease: correlation of MRI and neuropathologic findings","volume":"38","author":"Gertz","year":"1988","journal-title":"Neurology"},{"key":"10.1054\/jocn.1999.0191_RF87","doi-asserted-by":"crossref","first-page":"1932","DOI":"10.1212\/WNL.45.10.1932","article-title":"MRI of Creutzfeldt-Jakob disease: asymmetric high signal intensity of the basal ganglia","volume":"45","author":"Yoon","year":"1995","journal-title":"Neurology"},{"key":"10.1054\/jocn.1999.0191_RF88","first-page":"403","article-title":"Creutzfeldt-Jakob disease: focal symmetrical cortical involvement demonstrated by MR imaging","volume":"13","author":"Falcone","year":"1992","journal-title":"AJNR"},{"key":"10.1054\/jocn.1999.0191_RF89","doi-asserted-by":"crossref","first-page":"114","DOI":"10.1002\/ana.410320124","article-title":"Increased signal in basal ganglia and white matter on magnetic resonance imaging in Creutzfeldt-Jakob disease","volume":"32","author":"Yamamoto","year":"1992","journal-title":"Ann Neurol"},{"key":"10.1054\/jocn.1999.0191_RF90","first-page":"583","article-title":"Rapid spongiform degeneration of the cerebrum and cerebellum in Creutzfeldt-Jakob encephalitis: serial MR findings","volume":"18","author":"Tzeng","year":"1997","journal-title":"AJNR"},{"key":"10.1054\/jocn.1999.0191_RF91","doi-asserted-by":"crossref","first-page":"364","DOI":"10.1007\/BF00587828","article-title":"Serial MR imaging in Creutzfeldt-Jakob disease","volume":"33","author":"Uchino","year":"1991","journal-title":"Neuroradiology"},{"key":"10.1054\/jocn.1999.0191_RF92","doi-asserted-by":"crossref","first-page":"115","DOI":"10.1159\/000117324","article-title":"Panencephalopathic type of Creutzfeldt-Jakob disease with primary extensive involvement of white matter","volume":"30","author":"Kr\u00fcger","year":"1990","journal-title":"Eur Neurol"},{"key":"10.1054\/jocn.1999.0191_RF93","doi-asserted-by":"crossref","first-page":"228","DOI":"10.1016\/0022-510X(94)90279-8","article-title":"Magnetic resonance imaging and neuropathological findings in two patients with Creutzfeldt-Jakob disease","volume":"126","author":"Iwasaki","year":"1994","journal-title":"J Neurol Sci"},{"key":"10.1054\/jocn.1999.0191_RF94","doi-asserted-by":"crossref","first-page":"577","DOI":"10.1001\/archneur.56.5.577","article-title":"Abnormal diffusion-weighted magnetic resonance images in Creutzfeldt-Jakob disease","volume":"56","author":"Bahn","year":"1999","journal-title":"Arch Neurol"},{"key":"10.1054\/jocn.1999.0191_RF95","doi-asserted-by":"crossref","first-page":"205","DOI":"10.1212\/WNL.52.1.205","article-title":"Diffusion-weighted MRI in sporadic Creutzfeldt-Jakob disease","volume":"52","author":"Demaerel","year":"1999","journal-title":"Neurology"},{"key":"10.1054\/jocn.1999.0191_RF96","doi-asserted-by":"crossref","first-page":"1514","DOI":"10.1212\/WNL.52.7.1514","article-title":"Diffusion-weighted MRI of right-hemisphere dysfunction in Creutzfeldt-Jakob disease","volume":"52","author":"Yee","year":"1999","journal-title":"Neurology"},{"key":"10.1054\/jocn.1999.0191_RF97","doi-asserted-by":"crossref","first-page":"269","DOI":"10.1148\/radiographics.13.2.8460220","article-title":"Bilateral basal ganglia lesions: pediatric differential considerations","volume":"13","author":"Ho","year":"1993","journal-title":"RadioGraphics"},{"key":"10.1054\/jocn.1999.0191_RF98","first-page":"1119","article-title":"Mitochondrail disorders: analysis of their clinical and imaging characteristics","volume":"14","author":"Barkovich","year":"1993","journal-title":"AJNR"},{"key":"10.1054\/jocn.1999.0191_RF99","first-page":"25","article-title":"Magnetic resonance imaging in Huntington\u2019s disease","volume":"7","author":"Simmons","year":"1986","journal-title":"AJNR"},{"key":"10.1054\/jocn.1999.0191_RF100","doi-asserted-by":"crossref","first-page":"153","DOI":"10.1111\/j.1600-0404.1995.tb00424.x","article-title":"Regional cerebral glucose metabolism in autopsy-confirmed Creutzfeldt-Jakob disease","volume":"91","author":"Matochik","year":"1995","journal-title":"Acta Neurol Scand"},{"key":"10.1054\/jocn.1999.0191_RF101","doi-asserted-by":"crossref","first-page":"1035","DOI":"10.1001\/archneur.1990.00530090117024","article-title":"Positron emission tomography in Creutzfeldt-Jakob disease","volume":"47","author":"Holthoff","year":"1990","journal-title":"arch Neurol"},{"key":"10.1054\/jocn.1999.0191_RF102","doi-asserted-by":"crossref","first-page":"131","DOI":"10.1007\/BF03165066","article-title":"18F-fluorodeoxyglucose-PET and 99mTc-bicisate-SPECT in Creutzfeldt-Jakob disease","volume":"10","author":"Gr\u00fcnwald","year":"1996","journal-title":"Ann Nucl Med"},{"key":"10.1054\/jocn.1999.0191_RF103","doi-asserted-by":"crossref","first-page":"234","DOI":"10.1097\/00003072-199303000-00012","article-title":"Tc-99 m HMPAO brain SPECT findings in Creutzfeldt-Jakob disease","volume":"18","author":"Kao","year":"1993","journal-title":"Clin Nucl Med"},{"key":"10.1054\/jocn.1999.0191_RF104","first-page":"454","article-title":"The role of 99 m-Tc HMPAO SPECT in the diagnosis of Creutzfeldt-Jakob disease","volume":"19","author":"Miller","year":"1998","journal-title":"AJNR Am J Neuroradiol"},{"key":"10.1054\/jocn.1999.0191_RF105","first-page":"616","article-title":"SPECT diagnosis of Creutzfeldt-Jakob disease","volume":"36","author":"Aharon-Peretz","year":"1995","journal-title":"J Nucl Med"},{"key":"10.1054\/jocn.1999.0191_RF106","doi-asserted-by":"crossref","first-page":"593","DOI":"10.1136\/bmj.316.7131.593","article-title":"Single photon emission computed tomography in the identification of new variant Creutzfeldt-Jakob disease","volume":"316","author":"de Silva","year":"1998","journal-title":"BMJ"},{"key":"10.1054\/jocn.1999.0191_RF107","doi-asserted-by":"crossref","first-page":"808","DOI":"10.1097\/00003072-198911000-00004","article-title":"Brain SPECT imaging with Tc-99 m HMPAO in Creutzfeldt-Jakob disease","volume":"14","author":"Cohen","year":"1989","journal-title":"Clin Nucl Med"},{"key":"10.1054\/jocn.1999.0191_RF108","first-page":"1484","article-title":"Iodine-123 HIPDM brain imaging findings in subacute spongiform encephalopathy (Creutzfeldt-Jakob disease)","volume":"28","author":"Shih","year":"1987","journal-title":"J Nucl Med"},{"key":"10.1054\/jocn.1999.0191_RF109","doi-asserted-by":"crossref","first-page":"630","DOI":"10.1016\/0140-6736(91)90637-5","article-title":"Single photon emission tomography in growth-hormone related Creutzfeldt-Jakob disease","volume":"338","author":"Markus","year":"1991","journal-title":"Lancet"},{"key":"10.1054\/jocn.1999.0191_RF110","doi-asserted-by":"crossref","first-page":"236","DOI":"10.1097\/00003072-199603000-00010","article-title":"Brain SPECT of Creutzfeldt-Jakob disease","volume":"21","author":"Watanabe","year":"1996","journal-title":"Clin Nucl Med"}],"container-title":["Journal of Clinical Neuroscience"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0967586899901911?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0967586899901911?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2020,2,6]],"date-time":"2020-02-06T17:47:13Z","timestamp":1581011233000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S0967586899901911"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2000,5]]},"references-count":110,"journal-issue":{"issue":"3","published-print":{"date-parts":[[2000,5]]}},"alternative-id":["S0967586899901911"],"URL":"https:\/\/doi.org\/10.1054\/jocn.1999.0191","relation":{},"ISSN":["0967-5868"],"issn-type":[{"value":"0967-5868","type":"print"}],"subject":[],"published":{"date-parts":[[2000,5]]}}}