{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,13]],"date-time":"2026-10-13T11:19:02Z","timestamp":1791890342755,"version":"4.3.4"},"reference-count":39,"publisher":"Wiley","issue":"6","license":[{"start":{"date-parts":[[2005,3,3]],"date-time":"2005-03-03T00:00:00Z","timestamp":1109808000000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Movement Disorders"],"published-print":{"date-parts":[[2005,6]]},"abstract":"<jats:title>Abstract<\/jats:title><jats:p>Fifty Japanese and European families with cortical myoclonic tremor and epilepsy have been reported under various names. Unfamiliarity with the syndrome often leads to an initial misdiagnosis of essential tremor or progressive myoclonus epilepsy. A detailed overview of the literature is lacking and is the scope of this study. Disease characteristics are adult onset, distal action tremor and myoclonus, epileptic seizures, autosomal dominant inheritance, benign course, effectiveness of antiepileptic drugs, and possibly cognitive decline. A channelopathy is hypothesized to be the basis of the disease. Despite phenotypic and genetic differences between the Japanese and European pedigrees, the clinical and electrophysiological data point toward one syndrome. To avoid confusion in literature and possible misdiagnosis of patients, we propose to use one description and suggest \u201cfamilial cortical myoclonic tremor with epilepsy\u201d (FCMTE). In addition, we put forward diagnostic criteria to give a starting point from which to conduct genetic studies. \u00a9 2005 Movement Disorder Society<\/jats:p>","DOI":"10.1002\/mds.20413","type":"journal-article","created":{"date-parts":[[2005,3,3]],"date-time":"2005-03-03T19:16:29Z","timestamp":1109877389000},"page":"665-673","source":"Crossref","is-referenced-by-count":96,"title":["Familial cortical myoclonic tremor with epilepsy: A single syndromic classification for a group of pedigrees bearing common features"],"prefix":"10.1002","volume":"20","author":[{"given":"Anne\u2010Fleur","family":"Van Rootselaar","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Ivo N.","family":"van Schaik","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Arn M.J.M.","family":"van den Maagdenberg","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Johannes H.T.M.","family":"Koelman","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Petra M.C.","family":"Callenbach","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Marina A.J.","family":"Tijssen","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"311","published-online":{"date-parts":[[2005,3,3]]},"reference":[{"key":"e_1_2_6_2_2","doi-asserted-by":"publisher","DOI":"10.1007\/s00415-002-0729-x"},{"issue":"8","key":"e_1_2_6_3_2","first-page":"128","article-title":"A Dutch family with \u2018Familial Cortical Tremor with Epilepsy\u2019: exclusion of linkage to chromosomes 8q and 2p","volume":"43","author":"Brouwer OF","year":"2002","journal-title":"Epilepsia"},{"key":"e_1_2_6_4_2","doi-asserted-by":"publisher","DOI":"10.1212\/01.WNL.0000055874.24000.4A"},{"issue":"12","key":"e_1_2_6_5_2","first-page":"2459","article-title":"Autosomal dominant cortical myoclonus and epilepsy (ADCME) with complex partial and generalized seizures: a newly recognized epilepsy syndrome with linkage to chromosome 2p11","volume":"124","author":"Guerrini R","year":"2001","journal-title":"1\u2010q12.2. 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