{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,1,19]],"date-time":"2026-01-19T07:29:31Z","timestamp":1768807771232,"version":"3.49.0"},"reference-count":14,"publisher":"Ovid Technologies (Wolters Kluwer Health)","issue":"1","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Neurology"],"published-print":{"date-parts":[[1999,7]]},"DOI":"10.1212\/wnl.53.1.3","type":"journal-article","created":{"date-parts":[[2012,5,13]],"date-time":"2012-05-13T13:40:24Z","timestamp":1336916424000},"page":"3-3","source":"Crossref","is-referenced-by-count":160,"title":["<b>CACNA1A<\/b>\n            mutations"],"prefix":"10.1212","volume":"53","author":[{"given":"Elisabeth","family":"Tournier-Lasserve","sequence":"first","affiliation":[{"name":"From INSERM U25 and Laboratory of GeneticsHo\u0308pital Lariboisie\u0300re, Paris, France."}],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"276","reference":[{"key":"e_1_3_1_2_2","doi-asserted-by":"publisher","DOI":"10.1016\/S0092-8674(00)81373-2"},{"key":"e_1_3_1_3_2","doi-asserted-by":"publisher","DOI":"10.1002\/(SICI)1096-8628(19980526)77:4<298::AID-AJMG9>3.0.CO;2-J"},{"key":"e_1_3_1_4_2","doi-asserted-by":"publisher","DOI":"10.1086\/302192"},{"key":"e_1_3_1_5_2","doi-asserted-by":"publisher","DOI":"10.1212\/WNL.53.1.38"},{"key":"e_1_3_1_6_2","doi-asserted-by":"publisher","DOI":"10.1212\/WNL.53.1.26"},{"key":"e_1_3_1_7_2","doi-asserted-by":"publisher","DOI":"10.1212\/WNL.53.1.34"},{"key":"e_1_3_1_8_2","first-page":"1115","volume":"2","year":"1955","unstructured":"Blau JN, Whitty CWM. Familial hemiplegic migraine. Lancet 1955;2:1115\u20131116.","journal-title":"Lancet"},{"key":"e_1_3_1_9_2","first-page":"555","volume":"108","year":"1985","unstructured":"Fitzsimons RB, Wolfenden WH. Migraine coma. Meningitic migraine with cerebral oedema associated with a new form of autosomal dominant cerebellar ataxia. Brain 1985;108:555\u2013577.","journal-title":"Brain"},{"key":"e_1_3_1_10_2","first-page":"642","volume":"38","year":"1946","unstructured":"Parker HL. Periodic ataxia. Mayo Clin Proc 1946;38:642\u2013645.","journal-title":"Mayo Clin Proc"},{"key":"e_1_3_1_11_2","doi-asserted-by":"publisher","DOI":"10.1038\/ng0993-40"},{"key":"e_1_3_1_12_2","first-page":"A274.","volume":"53","year":"1999","unstructured":"Vahedi K, Denier C, Ducros A, et al. Sporadic hemiplegic migraine with de novo CACNA1A missense mutation. Neurology 1999;53 (suppl 2):A274. Abstract.","journal-title":"Neurology"},{"key":"e_1_3_1_13_2","first-page":"1816","volume":"53","year":"1999","unstructured":"Denier C, Ducros A, Vahedi K, et al. High prevalence of CACNA1A truncations and broader clinical spectrum in episodic ataxia type 2. Neurology 1999;53:1816\u20131821.","journal-title":"Neurology"},{"key":"e_1_3_1_14_2","doi-asserted-by":"publisher","DOI":"10.1038\/ng0197-62"},{"key":"e_1_3_1_15_2","doi-asserted-by":"publisher","DOI":"10.1074\/jbc.273.10.5586"}],"container-title":["Neurology"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/www.neurology.org\/doi\/pdfdirect\/10.1212\/WNL.53.1.3","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2024,3,28]],"date-time":"2024-03-28T17:31:27Z","timestamp":1711647087000},"score":1,"resource":{"primary":{"URL":"https:\/\/www.neurology.org\/doi\/10.1212\/WNL.53.1.3"}},"subtitle":["Hemiplegic migraine, episodic ataxia type 2, and the others"],"short-title":[],"issued":{"date-parts":[[1999,7]]},"references-count":14,"journal-issue":{"issue":"1","published-print":{"date-parts":[[1999,7]]}},"alternative-id":["10.1212\/WNL.53.1.3"],"URL":"https:\/\/doi.org\/10.1212\/wnl.53.1.3","relation":{},"ISSN":["0028-3878","1526-632X"],"issn-type":[{"value":"0028-3878","type":"print"},{"value":"1526-632X","type":"electronic"}],"subject":[],"published":{"date-parts":[[1999,7]]}}}