{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,4,4]],"date-time":"2026-04-04T01:41:54Z","timestamp":1775266914160,"version":"3.50.1"},"reference-count":24,"publisher":"Wiley","issue":"1","license":[{"start":{"date-parts":[[2011,3,1]],"date-time":"2011-03-01T00:00:00Z","timestamp":1298937600000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Epileptic Disorders"],"published-print":{"date-parts":[[2011,3]]},"abstract":"<jats:title>ABSTRACT<\/jats:title>\n                  <jats:p>\n                    Creutzfeldt\u2010Jakob disease (CJD) is a rare form of rapidly progressive neurodegenerative disorder. Literature survey reveals only four reported cases of CJD with epilepsia partialis continua. Here, we present a review and a case study, with video\u2010EEG sequences and characteristic MRI findings, of a fifth patient who presented with epilepsia partialis continua in the very early stage of the disease and followed a fatal course which was faster than expected.\n                    <jats:italic>[Published with video sequences]<\/jats:italic>\n                  <\/jats:p>","DOI":"10.1684\/epd.2011.0400","type":"journal-article","created":{"date-parts":[[2019,8,2]],"date-time":"2019-08-02T09:24:19Z","timestamp":1564737859000},"page":"82-87","source":"Crossref","is-referenced-by-count":10,"title":["Epilepsia partialis continua as the presenting symptom in probable sporadic Creutzfeldt\u2010Jakob disease"],"prefix":"10.1002","volume":"13","author":[{"given":"Aslihan","family":"Taskiran","sequence":"first","affiliation":[{"name":"Department of Neurology School of Medicine Hacettepe University Ankara Turkey"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"F. Irsel","family":"Tezer","sequence":"additional","affiliation":[{"name":"Department of Neurology School of Medicine Hacettepe University Ankara Turkey"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Serap","family":"Saygi","sequence":"additional","affiliation":[{"name":"Department of Neurology School of Medicine Hacettepe University Ankara Turkey"}],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"311","published-online":{"date-parts":[[2011,3]]},"reference":[{"key":"e_1_2_5_2_1","doi-asserted-by":"publisher","DOI":"10.1002\/ana.410150220"},{"key":"e_1_2_5_3_1","doi-asserted-by":"publisher","DOI":"10.1212\/WNL.30.6.611"},{"key":"e_1_2_5_4_1","doi-asserted-by":"publisher","DOI":"10.1002\/ana.410200507"},{"key":"e_1_2_5_5_1","doi-asserted-by":"publisher","DOI":"10.1001\/archneur.1972.00490110062006"},{"key":"e_1_2_5_6_1","doi-asserted-by":"publisher","DOI":"10.1093\/brain\/119.2.393"},{"key":"e_1_2_5_7_1","first-page":"108","article-title":"Seizures and Creutzfeldt\u2010Jakob disease. A case report and series review","volume":"60","author":"Cokgor I","year":"1999","journal-title":"N C Med J"},{"key":"e_1_2_5_8_1","doi-asserted-by":"publisher","DOI":"10.1016\/S0987-7053(88)80069-8"},{"key":"e_1_2_5_9_1","doi-asserted-by":"publisher","DOI":"10.1002\/mds.20502"},{"key":"e_1_2_5_10_1","doi-asserted-by":"publisher","DOI":"10.1002\/ana.410080323"},{"key":"e_1_2_5_11_1","doi-asserted-by":"publisher","DOI":"10.1177\/155005940103200103"},{"key":"e_1_2_5_12_1","doi-asserted-by":"publisher","DOI":"10.3109\/00207459008987162"},{"key":"e_1_2_5_13_1","doi-asserted-by":"publisher","DOI":"10.1056\/NEJM199812313392707"},{"key":"e_1_2_5_14_1","doi-asserted-by":"publisher","DOI":"10.1034\/j.1600-0404.2000.102006398.x"},{"key":"e_1_2_5_15_1","doi-asserted-by":"crossref","first-page":"271","DOI":"10.1684\/epd.2008.0216","article-title":"Familial Creutzfeldt\u2010Jakob disease presenting as epilepsia partialis continua","volume":"10","author":"Lowden MR","year":"2008","journal-title":"Epileptic Disord"},{"key":"e_1_2_5_16_1","doi-asserted-by":"publisher","DOI":"10.1053\/seiz.2001.0646"},{"key":"e_1_2_5_17_1","doi-asserted-by":"publisher","DOI":"10.1054\/jocn.2000.0845"},{"key":"e_1_2_5_18_1","doi-asserted-by":"publisher","DOI":"10.1001\/archneurpsyc.1929.02220020174010"},{"key":"e_1_2_5_19_1","doi-asserted-by":"publisher","DOI":"10.1093\/brain\/122.12.2345"},{"key":"e_1_2_5_20_1","doi-asserted-by":"publisher","DOI":"10.1038\/nrneurol.2009.118"},{"key":"e_1_2_5_21_1","doi-asserted-by":"publisher","DOI":"10.1001\/archneur.1977.00500170020003"},{"key":"e_1_2_5_22_1","doi-asserted-by":"publisher","DOI":"10.1016\/0987-7053(96)80168-7"},{"key":"e_1_2_5_23_1","doi-asserted-by":"publisher","DOI":"10.1016\/j.clinph.2005.12.007"},{"key":"e_1_2_5_24_1","unstructured":"World Health Organisation.Global Surveillance Diagnosis and Therapy of Human Transmissible Spongiform Encephalopathies: Report of a WHO Consultation. Geneva Switzerland. 9\u201011 February1998."},{"key":"e_1_2_5_25_1","doi-asserted-by":"publisher","DOI":"10.1093\/brain\/awp191"}],"container-title":["Epileptic Disorders"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/onlinelibrary.wiley.com\/doi\/pdf\/10.1684\/epd.2011.0400","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2024,7,21]],"date-time":"2024-07-21T12:53:08Z","timestamp":1721566388000},"score":1,"resource":{"primary":{"URL":"https:\/\/onlinelibrary.wiley.com\/doi\/10.1684\/epd.2011.0400"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2011,3]]},"references-count":24,"journal-issue":{"issue":"1","published-print":{"date-parts":[[2011,3]]}},"alternative-id":["10.1684\/epd.2011.0400"],"URL":"https:\/\/doi.org\/10.1684\/epd.2011.0400","archive":["Portico"],"relation":{"is-cited-by":[{"id-type":"doi","id":"10.1155\/2018\/3092018","asserted-by":"object"}]},"ISSN":["1294-9361","1950-6945"],"issn-type":[{"value":"1294-9361","type":"print"},{"value":"1950-6945","type":"electronic"}],"subject":[],"published":{"date-parts":[[2011,3]]}}}