{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,19]],"date-time":"2026-10-19T09:17:32Z","timestamp":1792401452736,"version":"4.4.0"},"reference-count":12,"publisher":"SAGE Publications","issue":"2","license":[{"start":{"date-parts":[[2013,10,4]],"date-time":"2013-10-04T00:00:00Z","timestamp":1380844800000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/journals.sagepub.com\/page\/policies\/text-and-data-mining-license"}],"content-domain":{"domain":["journals.sagepub.com"],"crossmark-restriction":true},"short-container-title":["J Child Neurol"],"published-print":{"date-parts":[[2014,2]]},"abstract":"<jats:p>\n                    The clinical spectrum associated with\n                    <jats:italic>ATP1A2<\/jats:italic>\n                    mutations is expanding and includes familial hemiplegic migraine, alternating hemiplegia of childhood, and epilepsy. We have identified a novel c.1766T&gt;C. (Ile589Thr) heterozygous mutation in the\n                    <jats:italic>ATP1A2<\/jats:italic>\n                    gene in a Saudi kindred with hemiplegic attacks and seizures. Our findings broaden the phenotypic spectrum of patients with\n                    <jats:italic>ATP1A2<\/jats:italic>\n                    mutations.\n                  <\/jats:p>","DOI":"10.1177\/0883073813504623","type":"journal-article","created":{"date-parts":[[2013,10,4]],"date-time":"2013-10-04T22:49:12Z","timestamp":1380926952000},"page":"265-268","update-policy":"https:\/\/doi.org\/10.1177\/sage-journals-update-policy","source":"Crossref","is-referenced-by-count":18,"title":["A Wide Clinical Phenotype Spectrum in Patients With\n                    <i>ATP1A2<\/i>\n                    Mutations"],"prefix":"10.1177","volume":"29","author":[{"given":"Bashaer","family":"Al-Bulushi","sequence":"first","affiliation":[{"name":"Divisions of Pediatric Neurology, Prince Sultan Military Medical City, Kingdom of Saudi Arabia"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Amal","family":"Al-Hashem","sequence":"additional","affiliation":[{"name":"Genetics, Department of Pediatrics, Prince Sultan Military Medical City, Kingdom of Saudi Arabia"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Brahim","family":"Tabarki","sequence":"additional","affiliation":[{"name":"Divisions of Pediatric Neurology, Prince Sultan Military Medical City, Kingdom of Saudi Arabia"}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"179","published-online":{"date-parts":[[2013,10,4]]},"reference":[{"issue":"8","key":"e_1_3_2_2_2","article-title":"Genetic effects of ATP1A2 in familial hemiplegic migraine type II and animal models","volume":"7","author":"Gritz SM","year":"2013","unstructured":"Gritz SM, Radcliffe RA. 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