{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,3]],"date-time":"2026-10-03T11:45:47Z","timestamp":1791027947790,"version":"4.1.0"},"reference-count":29,"publisher":"Wiley","issue":"6","license":[{"start":{"date-parts":[[2004,2,12]],"date-time":"2004-02-12T00:00:00Z","timestamp":1076544000000},"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":[[2004,6]]},"abstract":"<jats:title>Abstract<\/jats:title><jats:p>Myoclonus\u2013dystonia syndrome (MDS) is an autosomal dominant disorder characterized by bilateral myoclonic jerks. An 8\u2010year\u2010old boy presenting with early onset, medically intractable, MDS due to a mutation in the \u03f5\u2010sarcoglycan gene (SGCE) underwent chronic bilateral stimulation of the globus pallidus internus, which eliminates both myoclonus and dystonia. We conclude that deep brain stimulation can be an effective and safe treatment for MDS. \u00a9 2004 Movement Disorder Society<\/jats:p>","DOI":"10.1002\/mds.20030","type":"journal-article","created":{"date-parts":[[2004,5,3]],"date-time":"2004-05-03T03:00:41Z","timestamp":1083553241000},"page":"724-727","source":"Crossref","is-referenced-by-count":89,"title":["Deep brain stimulation in myoclonus\u2013dystonia syndrome"],"prefix":"10.1002","volume":"19","author":[{"given":"Laura","family":"Cif","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Enza 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