{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,5,3]],"date-time":"2026-05-03T10:06:08Z","timestamp":1777802768219,"version":"3.51.4"},"reference-count":11,"publisher":"SAGE Publications","issue":"7","license":[{"start":{"date-parts":[[1999,7,1]],"date-time":"1999-07-01T00:00:00Z","timestamp":930787200000},"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":["J Child Neurol"],"published-print":{"date-parts":[[1999,7]]},"abstract":"<jats:p>Seven subjects with Chiari I malformations and seizures (four males, three females; age range 11 years, 7 months to 36 years; mean, 22.28 \u00b1 7.58 years; median, 21) were identified in four different centers from among a group of 10 patients. Our aim was to analyze clinical and electroencephalographic characteristics of seizures in this etiologically homogeneous group of patients. Most of the seizures were of the complex partial type, and paroxysmal abnormalities were mainly localized over the frontal and temporal regions. The course of the epilepsy was rather benign, with complete control of seizures in four patients and an important reduction in frequency in the remaining three subjects. Other cortical alterations are not usually associated with the typical abnormalities of the posterior fossa in Chiari I malformation; thus, it is possible to hypothesize that cerebral microdysgenesis or, alternatively, a cerebellar dysfunction could underlie epileptogenesis in these patients. (J Child Neurol 1999;14:446-450).<\/jats:p>","DOI":"10.1177\/088307389901400707","type":"journal-article","created":{"date-parts":[[2008,1,24]],"date-time":"2008-01-24T19:24:33Z","timestamp":1201202673000},"page":"446-450","source":"Crossref","is-referenced-by-count":23,"title":["Seizures in Chiari I Malformation: A Clinical and Electroencephalographic Study"],"prefix":"10.1177","volume":"14","author":[{"given":"Maurizio","family":"Elia","sequence":"first","affiliation":[{"name":"Department of Neurology, OASI Institute for Research on Mental Retardation and Brain Aging Troina,"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Roberto","family":"Biondi","sequence":"additional","affiliation":[{"name":"Department of Neurology, University of Catania"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Vito","family":"Sofia","sequence":"additional","affiliation":[{"name":"Department of Neurology, University of Catania"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Sebastiano A.","family":"Musumeci","sequence":"additional","affiliation":[{"name":"Department of Neurology, OASI Institute for Research on Mental Retardation and Brain Aging Troina"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Raffaele","family":"Ferri","sequence":"additional","affiliation":[{"name":"Department of Neurology, OASI Institute for Research on Mental Retardation and Brain Aging Troina"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Giuseppe","family":"Capovilla","sequence":"additional","affiliation":[{"name":"Children's Neuropsychiatric Unit \"C. 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