{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,4,30]],"date-time":"2026-04-30T17:37:01Z","timestamp":1777570621861,"version":"3.51.4"},"reference-count":10,"publisher":"SAGE Publications","issue":"1","license":[{"start":{"date-parts":[[2003,1,1]],"date-time":"2003-01-01T00:00:00Z","timestamp":1041379200000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/journals.sagepub.com\/page\/policies\/text-and-data-mining-license"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Clinical Electroencephalography"],"published-print":{"date-parts":[[2003,1]]},"abstract":"<jats:p>Benign neonatal sleep myoclonus (BNSM), characterized by myoclonic jerks of the extremities only in non-REM sleep, occurs in the first months of life with spontaneous disappearance within 3\u20134 months. We examined five siblings with typical BNSM, at the 3\u201310 years follow-up neurological examination. Psychomotor development, cognitive functions and EEG were completely normal. These cases confirm that BNSM is a self limited and nonepileptic disorder.<\/jats:p>","DOI":"10.1177\/155005940303400107","type":"journal-article","created":{"date-parts":[[2015,11,24]],"date-time":"2015-11-24T20:52:23Z","timestamp":1448398343000},"page":"15-17","source":"Crossref","is-referenced-by-count":21,"title":["Benign Neonatal Sleep Myoclonus: Case Report and Follow-up of Four Members of an Affected Family"],"prefix":"10.1177","volume":"34","author":[{"given":"M. Luigia","family":"Vaccario","sequence":"first","affiliation":[{"name":"M. Luigia Vaccario, MD, Maria A. Valenti, MD, Anna Carullo, MD, Rosseta Di Bartolomeo, MD, and Salvatore Mazza, MD, are from the Institute of Neurology, Catholic University of Rome, and Policlinico Agostino Gemelli, Rome, Italy"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Maria A.","family":"Valenti","sequence":"additional","affiliation":[{"name":"M. 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