{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,8,7]],"date-time":"2026-08-07T16:15:30Z","timestamp":1786119330672,"version":"build-2736575974"},"reference-count":12,"publisher":"Ovid Technologies (Wolters Kluwer Health)","issue":"3","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[2010,5]]},"DOI":"10.1097\/nrl.0b013e3181a3cb6c","type":"journal-article","created":{"date-parts":[[2010,5,5]],"date-time":"2010-05-05T04:44:42Z","timestamp":1273034682000},"page":"203-205","source":"Crossref","is-referenced-by-count":4,"title":["A Case of Paramyotonia Congenita Without Periodic Paralysis"],"prefix":"10.1097","volume":"16","author":[{"given":"Jeong Ho","family":"Park","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Young Wha","family":"Lee","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Sun Ah","family":"Park","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Tae Kyeong","family":"Lee","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Hak Jae","family":"Rho","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Ki Bum","family":"Sung","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"276","reference":[{"key":"R1-10-20210211","doi-asserted-by":"crossref","first-page":"772","DOI":"10.1046\/j.1523-1755.2000.00914.x","article-title":"Spectrum of sodium channel disturbances in the nondystrophic myotonias and periodic paralyses.","volume":"57","author":"Cannon","year":"2000","journal-title":"Kidney Int"},{"key":"R2-10-20210211","doi-asserted-by":"crossref","first-page":"58","DOI":"10.1016\/S0002-9343(98)00123-5","article-title":"The familial periodic paralyses and nondystrophic myotonias.","volume":"105","author":"Ptacek","year":"1998","journal-title":"Am J Med"},{"key":"R3-10-20210211","doi-asserted-by":"crossref","first-page":"700","DOI":"10.1002\/mus.880090804","article-title":"Lack of cold sensitivity in hyperkalemic periodic paralysis.","volume":"9","author":"Subramony","year":"1986","journal-title":"Muscle Nerve"},{"key":"R4-10-20210211","doi-asserted-by":"crossref","first-page":"21","DOI":"10.1002\/mus.880130106","article-title":"Paramyotonia congenita or hyperkalemic periodic paralysis? Clinical and electrophysiological features of each entity in one family.","volume":"13","author":"de Silva","year":"1990","journal-title":"Muscle Nerve"},{"key":"R5-10-20210211","doi-asserted-by":"crossref","first-page":"94","DOI":"10.2302\/kjm.43.94","article-title":"Paramyotonia congenita without cold paralysis: a case report.","volume":"43","author":"Izumi","year":"1994","journal-title":"Keio J Med"},{"key":"R6-10-20210211","doi-asserted-by":"crossref","first-page":"2","DOI":"10.1159\/000114781","article-title":"Paramyotonia congenita without cold paralysis and myotonia levoir. A genetic and clinical study.","volume":"15","author":"Brungger","year":"1977","journal-title":"Eur Neurol"},{"key":"R7-10-20210211","doi-asserted-by":"crossref","first-page":"2001","DOI":"10.1097\/00001756-199510010-00012","article-title":"Paramyotonia congenita without paralysis on exposure to cold: a novel mutation in the SCN4A gene (Val1293Ile).","volume":"6","author":"Koch","year":"1995","journal-title":"Neuroreport"},{"key":"R8-10-20210211","doi-asserted-by":"crossref","first-page":"504","DOI":"10.1136\/jnnp.68.4.504","article-title":"Clinical, electrophysiological, and molecular genetic studies in a new family with paramyotonia congenita.","volume":"68","author":"Davies","year":"2000","journal-title":"J Neurol Neurosurg Psychiatry"},{"key":"R9-10-20210211","doi-asserted-by":"crossref","first-page":"533","DOI":"10.1016\/S0960-8966(02)00007-X","article-title":"An expanding view for the molecular basis of familial periodic paralysis.","volume":"12","author":"Cannon","year":"2002","journal-title":"Neuromuscul Disord"},{"key":"R10-10-20210211","doi-asserted-by":"crossref","first-page":"769","DOI":"10.1016\/0092-8674(92)90151-2","article-title":"Temperature-sensitive mutations in the III\u2013IV cytoplasmic loop region of the skeletal muscle sodium channel gene in paramyotonia congenita.","volume":"68","author":"McClatchey","year":"1992","journal-title":"Cell"},{"key":"R11-10-20210211","doi-asserted-by":"crossref","first-page":"763","DOI":"10.1002\/mus.880170710","article-title":"Paramyotonia congenita: abnormal short exercise test, and improvement after mexiletine therapy.","volume":"17","author":"Jackson","year":"1994","journal-title":"Muscle Nerve"},{"key":"R12-10-20210211","doi-asserted-by":"crossref","first-page":"238","DOI":"10.1016\/j.nurt.2007.01.012","article-title":"The nondystrophic myotonias.","volume":"4","author":"Heatwole","year":"2007","journal-title":"Neurotherapeutics"}],"container-title":["The Neurologist"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/www.ovid.com\/10.1097\/NRL.0b013e3181a3cb6c","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2026,8,6]],"date-time":"2026-08-06T18:17:27Z","timestamp":1786040247000},"score":1,"resource":{"primary":{"URL":"https:\/\/www.ovid.com\/00127893-201005000-00010"}},"subtitle":["Electrophysiological and Molecular Genetic Studies"],"short-title":[],"issued":{"date-parts":[[2010,5]]},"references-count":12,"journal-issue":{"issue":"3","published-print":{"date-parts":[[2010]]}},"URL":"https:\/\/doi.org\/10.1097\/nrl.0b013e3181a3cb6c","relation":{},"ISSN":["1074-7931"],"issn-type":[{"value":"1074-7931","type":"print"}],"subject":[],"published":{"date-parts":[[2010,5]]}}}