{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2024,3,29]],"date-time":"2024-03-29T00:09:54Z","timestamp":1711670994144},"reference-count":6,"publisher":"Ovid Technologies (Wolters Kluwer Health)","issue":"5","content-domain":{"domain":["neurology.org"],"crossmark-restriction":true},"short-container-title":["Neurology"],"published-print":{"date-parts":[[2013,1,29]]},"DOI":"10.1212\/wnl.0b013e31827f1346","type":"journal-article","created":{"date-parts":[[2013,1,29]],"date-time":"2013-01-29T00:14:53Z","timestamp":1359418493000},"update-policy":"http:\/\/dx.doi.org\/10.1212\/crossmarkpolicy","source":"Crossref","is-referenced-by-count":0,"title":["Clinical Reasoning: A girl presenting with stiffness episodes during sleep, caf\u00e9-au-lait spots, and flecked retina"],"prefix":"10.1212","volume":"80","author":[{"given":"Romina","family":"Moavero","sequence":"first","affiliation":[{"name":"From the Pediatric Neurology Unit (R.M., P.C.), Neuroscience Department, Tor Vergata University Hospital, Rome; and Division of Neurology (R.C., F.V.) and Cytogenetics and Molecular Genetics Unit (M.C.R.), \u201cBambino Ges\u00f9\u201d Children's Hospital, IRCCS, Rome, Italy."}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Raffaella","family":"Cusmai","sequence":"additional","affiliation":[{"name":"From the Pediatric Neurology Unit (R.M., P.C.), Neuroscience Department, Tor Vergata University Hospital, Rome; and Division of Neurology (R.C., F.V.) and Cytogenetics and Molecular Genetics Unit (M.C.R.), \u201cBambino Ges\u00f9\u201d Children's Hospital, IRCCS, Rome, Italy."}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Maria Cristina","family":"Roberti","sequence":"additional","affiliation":[{"name":"From the Pediatric Neurology Unit (R.M., P.C.), Neuroscience Department, Tor Vergata University Hospital, Rome; and Division of Neurology (R.C., F.V.) and Cytogenetics and Molecular Genetics Unit (M.C.R.), \u201cBambino Ges\u00f9\u201d Children's Hospital, IRCCS, Rome, Italy."}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Federico","family":"Vigevano","sequence":"additional","affiliation":[{"name":"From the Pediatric Neurology Unit (R.M., P.C.), Neuroscience Department, Tor Vergata University Hospital, Rome; and Division of Neurology (R.C., F.V.) and Cytogenetics and Molecular Genetics Unit (M.C.R.), \u201cBambino Ges\u00f9\u201d Children's Hospital, IRCCS, Rome, Italy."}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Paolo","family":"Curatolo","sequence":"additional","affiliation":[{"name":"From the Pediatric Neurology Unit (R.M., P.C.), Neuroscience Department, Tor Vergata University Hospital, Rome; and Division of Neurology (R.C., F.V.) and Cytogenetics and Molecular Genetics Unit (M.C.R.), \u201cBambino Ges\u00f9\u201d Children's Hospital, IRCCS, Rome, Italy."}],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"276","reference":[{"key":"e_1_3_4_2_2","doi-asserted-by":"crossref","first-page":"327","DOI":"10.1684\/epd.2007.0121","article-title":"Ring chromosome 17 epilepsy may resemble that of ring chromosome 20 syndrome","volume":"9","author":"Ricard-Mousnier B","year":"2007","unstructured":"Ricard-Mousnier B, N'Guyen S, Dubas F, Pouplard F, Guichet A. Ring chromosome 17 epilepsy may resemble that of ring chromosome 20 syndrome. Epileptic Disord 2007;9:327\u2013331.","journal-title":"Epileptic Disord"},{"key":"e_1_3_4_3_2","doi-asserted-by":"publisher","DOI":"10.1111\/j.1399-0004.2009.01203.x"},{"key":"e_1_3_4_4_2","doi-asserted-by":"publisher","DOI":"10.1034\/j.1399-0004.2003.00146.x"},{"key":"e_1_3_4_5_2","doi-asserted-by":"publisher","DOI":"10.1136\/bjo.75.2.125"},{"key":"e_1_3_4_6_2","doi-asserted-by":"publisher","DOI":"10.1001\/archopht.1994.01090180036013"},{"key":"e_1_3_4_7_2","first-page":"234","article-title":"Ring chromosome 17 in a mentally retarded boy","volume":"22","author":"Qazi OH","year":"1979","unstructured":"Qazi OH, Madahar C, Kanchanapoomi R, Giridharan R, Beller E. Ring chromosome 17 in a mentally retarded boy. Ann Genet 1979;22:234\u2013238.","journal-title":"Ann Genet"}],"container-title":["Neurology"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/www.neurology.org\/doi\/pdfdirect\/10.1212\/WNL.0b013e31827f1346","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2024,3,28]],"date-time":"2024-03-28T13:14:59Z","timestamp":1711631699000},"score":1,"resource":{"primary":{"URL":"https:\/\/www.neurology.org\/doi\/10.1212\/WNL.0b013e31827f1346"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2013,1,29]]},"references-count":6,"journal-issue":{"issue":"5","published-print":{"date-parts":[[2013,1,29]]}},"alternative-id":["10.1212\/WNL.0b013e31827f1346"],"URL":"https:\/\/doi.org\/10.1212\/wnl.0b013e31827f1346","relation":{},"ISSN":["0028-3878","1526-632X"],"issn-type":[{"value":"0028-3878","type":"print"},{"value":"1526-632X","type":"electronic"}],"subject":[],"published":{"date-parts":[[2013,1,29]]}}}