{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,9,12]],"date-time":"2025-09-12T19:10:26Z","timestamp":1757704226430},"reference-count":14,"publisher":"BMJ","issue":"2","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Journal of Neurology, Neurosurgery &amp; Psychiatry"],"published-print":{"date-parts":[[1996,8,1]]},"DOI":"10.1136\/jnnp.61.2.139","type":"journal-article","created":{"date-parts":[[2008,11,10]],"date-time":"2008-11-10T22:20:59Z","timestamp":1226355659000},"page":"139-142","source":"Crossref","is-referenced-by-count":15,"title":["Creutzfeldt-Jakob disease in Austria."],"prefix":"10.1136","volume":"61","author":[{"given":"J A","family":"Hainfellner","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"K","family":"Jellinger","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"H","family":"Diringer","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"M","family":"Guentchev","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"R","family":"Kleinert","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"P","family":"Pilz","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"H","family":"Maier","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"H","family":"Budka","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"239","reference":[{"key":"ref_1","first-page":"174","article-title":"Epidemiology of Creutzfeldt-Jakob disease in the United States","volume":"14","author":"Holman, R.C.; Khan, A.S.; Kent, J.; Strine, T.W.; Schonberger, L.B.","year":"1995","unstructured":"Holman RC, Khan AS, Kent J, Strine TW, Schonberger LB. Epidemiology of Creutzfeldt-Jakob disease in the United States. Neuroepidemiology 1995;14: 174-81.","journal-title":"Neuroepidemiology"},{"key":"ref_2","first-page":"898","volume":"346","author":"Delasnerie-Laupretre, N.; Poser, S.; Pocchiari, M.; Wientiens, D.P.W.M.; Will, R.","year":"1995","unstructured":"Delasnerie-Laupretre N, Poser S, Pocchiari M, Wientiens DPWM, Will R. Creutzfeldt-Jakob disease in Europe. Lancet 1995;346:898.","journal-title":"Creutzfeldt-Jakob disease in Europe. Lancet"},{"key":"ref_3","first-page":"918","article-title":"Incidence of Creutzfeldt-Jakob disease in","volume":"343","author":"Alperovitch, A.; Brown, P.; Weber, T.; Pocchiari, M.; Hofman, A.; Will, R.","year":"1994","unstructured":"Alperovitch A, Brown P, Weber T, Pocchiari M, Hofman A, Will R. Incidence of Creutzfeldt-Jakob disease in Europe in 1993. Lancet 1994;343:918.","journal-title":"Europe in 1993. Lancet"},{"key":"ref_4","doi-asserted-by":"crossref","first-page":"1229","DOI":"10.1016\/S0140-6736(94)92441-4","article-title":"Incidence of Creutzfeldt-Jakob disease","volume":"343","author":"Desgrandchamps, D.; Rieder, H.L.; Marti, B.","year":"1994","unstructured":"Desgrandchamps D, Rieder HL, Marti B. Incidence of Creutzfeldt-Jakob disease. Lancet 1994;343:1229.","journal-title":"Lancet"},{"key":"ref_5","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, C.L.; Harris, J.O.; Gajdusek, D.C.; CJf, Gibbs; Bernoulli, C.; Asher, D.M.","year":"1979","unstructured":"Masters CL, Harris JO, Gajdusek DC, Gibbs CJf, Bernoulli C, Asher DM. Creutzfeldt-Jakob disease: patterns of worldwide occurrence and the significance of familial and sporadic clustering. Ann Neurol 1979; 5:177-88.","journal-title":"Ann Neurol"},{"key":"ref_6","doi-asserted-by":"crossref","first-page":"749","DOI":"10.1136\/jnnp.49.7.749","article-title":"A retrospective study of Creutzfeldt-Jakob disease in England and Wales 1970-1979 II: epidemiology","volume":"49","author":"Will, R.G.; Matthews, W.B.; Smith, P.G.; Hudson, C.","year":"1986","unstructured":"Will RG, Matthews WB, Smith PG, Hudson C. A retrospective study of Creutzfeldt-Jakob disease in England and Wales 1970-1979 II: epidemiology. J Neurol Neurosurg Psychiatry 1986;49:749-55.","journal-title":"J Neurol Neurosurg Psychiatry"},{"key":"ref_7","doi-asserted-by":"crossref","first-page":"895","DOI":"10.1212\/WNL.37.6.895","article-title":"The epidemiology of Creutzfeldt-Jakob disease: conclusion of a 15-year investigation in France and review of the world literature","volume":"37","author":"Brown, P.; Cathala, F.; Raubertas, R.F.; Gajdusek, D.C.; Castaigne, P.","year":"1987","unstructured":"Brown P, Cathala F, Raubertas RF, Gajdusek DC, Castaigne P. The epidemiology of Creutzfeldt-Jakob disease: conclusion of a 15-year investigation in France and review of the world literature. Neurology 1987;37: 895-904.","journal-title":"Neurology"},{"key":"ref_8","first-page":"45","article-title":"Neuropathological diagnostic criteria for Creutzfeldt-Jakob disease (CJD) and other human spongiform encephalopathies (prion diseases)","volume":"5","author":"Budka, H.; Aguzzi, A.; Brown, P.","year":"1995","unstructured":"Budka H, Aguzzi A, Brown P, et al. Neuropathological diagnostic criteria for Creutzfeldt-Jakob disease (CJD) and other human spongiform encephalopathies (prion diseases). Brain Pathol 1995;5:45-66.","journal-title":"Brain Pathol"},{"key":"ref_9","doi-asserted-by":"crossref","first-page":"53","DOI":"10.1111\/j.1750-3639.1995.tb00577.x","article-title":"Inherited prion diseases and transmission to rodents","volume":"5","author":"Tateishi, J.; Kitamoto, T.","year":"1995","unstructured":"Tateishi J, Kitamoto T. Inherited prion diseases and transmission to rodents. Brain Pathol 1995;5:53-9.","journal-title":"Brain Pathol"},{"key":"ref_10","first-page":"1285","article-title":"Abnormal isoform of prion proteins accumulates in the synaptic structures of the central nervous system in patients with Creutzfeldt-Jakob disease","volume":"140","author":"Kitamoto, T.; Shin, R.W.; Doh-ura, K.","year":"1992","unstructured":"Kitamoto T, Shin RW, Doh-ura K, et al. Abnormal isoform of prion proteins accumulates in the synaptic structures of the central nervous system in patients with Creutzfeldt-Jakob disease. Am J Pathol 1992;140: 1285-94.","journal-title":"Am J Pathol"},{"key":"ref_11","doi-asserted-by":"crossref","first-page":"738","DOI":"10.1093\/oxfordjournals.bmb.a072645","article-title":"Neuropathology of spongiform encephalopathies in humans","volume":"49","author":"Bell, J.E.; Ironside, J.W.","year":"1993","unstructured":"Bell JE, Ironside JW. Neuropathology of spongiform encephalopathies in humans. Br Med Bull 1993;49: 738-77.","journal-title":"Br Med Bull"},{"key":"ref_12","doi-asserted-by":"crossref","first-page":"99","DOI":"10.1007\/BF01538820","article-title":"Characterisation of antisera raised against species-specific peptide sequences from scrapie-associated fibril protein and their application for post-mortem immunodiagnosis of spongiform encephalopathies","volume":"136","author":"Oberdieck, U.; Xi, Y.-G.; Pocchiari, M.; Diringer, H.","year":"1994","unstructured":"Oberdieck U, Xi Y-G, Pocchiari M, Diringer H. Characterisation of antisera raised against species-specific peptide sequences from scrapie-associated fibril protein and their application for post-mortem immunodiagnosis of spongiform encephalopathies. Arch Virol 1994;136: 99-110.","journal-title":"Arch Virol"},{"key":"ref_13","doi-asserted-by":"crossref","first-page":"319","DOI":"10.1111\/j.1750-3639.1995.tb00609.x","article-title":"Tissue handling in suspected Creutzfeldt-Jakob disease (CJD) and other human spongiform encephalopathies (prion diseases)","volume":"5","author":"Budka, H.; Aguzzi, A.; Brown, P.","year":"1995","unstructured":"Budka H, Aguzzi A, Brown P, et al. Tissue handling in suspected Creutzfeldt-Jakob disease (CJD) and other human spongiform encephalopathies (prion diseases). Brain Pathol 1995;5:319-22.","journal-title":"Brain Pathol"},{"key":"ref_14","first-page":"11","article-title":"Epidemiology of CJD in the UK. International Symposium prion diseases: epidemiology, biochemistry and molecular biology. Gottingen, Germany: Medien in der Medizin","volume-title":"Universitat Gottingen,","author":"Will, R.","year":"1995","unstructured":"Will R. Epidemiology of CJD in the UK. International Symposium prion diseases: epidemiology, biochemistry and molecular biology. Gottingen, Germany: Medien in der Medizin, Universitat Gottingen, 1995:11."}],"container-title":["Journal of Neurology, Neurosurgery &amp; Psychiatry"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/syndication.highwire.org\/content\/doi\/10.1136\/jnnp.61.2.139","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2020,9,26]],"date-time":"2020-09-26T02:53:50Z","timestamp":1601088830000},"score":1,"resource":{"primary":{"URL":"https:\/\/jnnp.bmj.com\/lookup\/doi\/10.1136\/jnnp.61.2.139"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[1996,8,1]]},"references-count":14,"journal-issue":{"issue":"2","published-print":{"date-parts":[[1996,8,1]]}},"URL":"https:\/\/doi.org\/10.1136\/jnnp.61.2.139","relation":{},"ISSN":["0022-3050"],"issn-type":[{"value":"0022-3050","type":"print"}],"subject":[],"published":{"date-parts":[[1996,8,1]]}}}