{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2024,3,28]],"date-time":"2024-03-28T17:09:40Z","timestamp":1711645780386},"reference-count":6,"publisher":"BMJ","issue":"1","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Journal of Neurology, Neurosurgery &amp; Psychiatry"],"published-print":{"date-parts":[[1996,7,1]]},"DOI":"10.1136\/jnnp.61.1.111","type":"journal-article","created":{"date-parts":[[2008,11,10]],"date-time":"2008-11-10T22:20:59Z","timestamp":1226355659000},"page":"111-112","source":"Crossref","is-referenced-by-count":6,"title":["Codon 200 mutation in a new family of Chilean origin with Creutzfeldt-Jakob disease."],"prefix":"10.1136","volume":"61","author":[{"given":"M","family":"Salvatore","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"M","family":"Pocchiari","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"F","family":"Cardone","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"R","family":"Petraroli","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"M","family":"D'Alessandro","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"S","family":"Galvez","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"P","family":"Brown","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"G","family":"Macchi","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"C","family":"Fieschi","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"C","family":"Colosimo","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"239","reference":[{"key":"ref_1","doi-asserted-by":"crossref","first-page":"477","DOI":"10.1007\/BF00143125","article-title":"Creutzfeldt-jakob disease associated with the PRNP codon 200' ! mutation: an analysis of 45 families","volume":"7","author":"Goldfarb, L.G.; Brown, P.; Mitrova, E.","year":"1991","unstructured":"Goldfarb LG, Brown P, Mitrova E, et al. Creutzfeldt-jakob disease associated with the PRNP codon 200' ! mutation: an analysis of 45 families. EurY Epidemiol 1991;7:477-86.","journal-title":"EurY Epidemiol"},{"issue":"12","key":"ref_2","first-page":"65","article-title":"Familial Creutzfeldt-Jakob disease in Chile is associated with the","volume-title":"mutation of the PRNP amyloid precursor gene on chromosome 20. Y7Neurol Sci","volume":"1","author":"Brown, P.; Galvez, S.; Goldfarb, L.G.","year":"1992","unstructured":"Brown P, Galvez S, Goldfarb LG, et al. Familial Creutzfeldt-Jakob disease in Chile is associated with the codon 200 mutation of the PRNP amyloid precursor gene on chromosome 20.Y7Neurol Sci 1992;1 12:65-7."},{"key":"ref_3","doi-asserted-by":"crossref","first-page":"923","DOI":"10.1016\/S0140-6736(94)92272-1","article-title":"Small virus-like structure in brains from cases of sporadic and familial Creutzfeldt-Jakob disease","volume":"344","author":"Ozel, M.; Xi, Y.G.; Baldauf, E.; Diringer, H.; Pocchiari, M.","year":"1994","unstructured":"Ozel M, Xi YG, Baldauf E, Diringer H, Pocchiari M. Small virus-like structure in brains from cases of sporadic and familial Creutzfeldt-Jakob disease. Lanicet 1994;344: 923-4.","journal-title":"Lanicet"},{"key":"ref_4","first-page":"828","article-title":"Mutation and polymorphism of the prion protein gene in Libyan Jews with Creutzfeldt-Jakob disease (CJD)","volume":"53","author":"Gabizon, R.; Rosenmann, H.; Meiner, Z.","year":"1993","unstructured":"Gabizon R, Rosenmann H, Meiner Z, et al. Mutation and polymorphism of the prion protein gene in Libyan Jews with Creutzfeldt-Jakob disease (CJD). Ant.7 Hunt Geniet 1993;53:828-35.","journal-title":"Ant.7 Hunt Geniet"},{"key":"ref_5","first-page":"299","article-title":"Japanese family with Creutzfeldt-Jakob disease with","volume":"44","author":"Inoue, I.; Kitamoto, T.; Doh-ura, K.; Shii, H.; Goto, I.; Tateishi, J.","year":"1994","unstructured":"Inoue I, Kitamoto T, Doh-ura K, Shii H, Goto I, Tateishi J. Japanese family with Creutzfeldt-Jakob disease with codon 200 point mutation of the prion protein gene. NTeutrologyi 1994;44:299-301.","journal-title":"NTeutrologyi; point mutation of the prion protein gene"},{"key":"ref_6","first-page":"1109","article-title":"Clinical heterogeneity and unusual presentations of Creutzfeldt-Jakob disease in Jewish patients with the PRNP","volume":"56","author":"Chapman, J.; Brown, P.; Goldfarb, L.G.; Arlazoroff, A.; Gajdusek, D.C.; Korczyn, A.D.","year":"1993","unstructured":"Chapman J, Brown P, Goldfarb LG, Arlazoroff A, Gajdusek DC, Korczyn AD. Clinical heterogeneity and unusual presentations of Creutzfeldt-Jakob disease in Jewish patients with the PRNP codon 200 mutation..7 Neuirol NVeu'11tstisug Psychiatty 1993;56: 1109-12.","journal-title":"Psychiatty"}],"container-title":["Journal of Neurology, Neurosurgery &amp; Psychiatry"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/syndication.highwire.org\/content\/doi\/10.1136\/jnnp.61.1.111","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2020,9,26]],"date-time":"2020-09-26T02:53:29Z","timestamp":1601088809000},"score":1,"resource":{"primary":{"URL":"https:\/\/jnnp.bmj.com\/lookup\/doi\/10.1136\/jnnp.61.1.111"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[1996,7,1]]},"references-count":6,"journal-issue":{"issue":"1","published-print":{"date-parts":[[1996,7,1]]}},"URL":"https:\/\/doi.org\/10.1136\/jnnp.61.1.111","relation":{},"ISSN":["0022-3050"],"issn-type":[{"value":"0022-3050","type":"print"}],"subject":[],"published":{"date-parts":[[1996,7,1]]}}}