{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,5,3]],"date-time":"2026-05-03T10:17:46Z","timestamp":1777803466125,"version":"3.51.4"},"reference-count":12,"publisher":"SAGE Publications","issue":"6","license":[{"start":{"date-parts":[[2011,5,24]],"date-time":"2011-05-24T00:00:00Z","timestamp":1306195200000},"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":[[2011,6]]},"abstract":"<jats:p>Macrocerebellum, a neuroradiological and clinical entity of unknown etiology characterized by an isolated, disproportionately large cerebellum, has to date been reported in only a few cases. It has been suggested that the condition could represent a marker for disturbed cerebral development, however, longitudinal reports are lacking. We describe a 19-month-old patient with agenesis of the corpus callosum, who developed enlargement of the cerebellum without clinical signs of cerebellar impairment, a picture that has not been previously described.<\/jats:p>","DOI":"10.1177\/0883073810387140","type":"journal-article","created":{"date-parts":[[2011,5,24]],"date-time":"2011-05-24T13:35:34Z","timestamp":1306244134000},"page":"756-760","update-policy":"https:\/\/doi.org\/10.1177\/sage-journals-update-policy","source":"Crossref","is-referenced-by-count":4,"title":["Cerebellum Enlargement and Corpus Callosum Agenesis: A Longitudinal Case Report"],"prefix":"10.1177","volume":"26","author":[{"given":"Anna","family":"Pichiecchio","sequence":"first","affiliation":[{"name":"Neuroradiology Department, IRCCS C. 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