{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,8,14]],"date-time":"2026-08-14T14:28:15Z","timestamp":1786717695385,"version":"build-2736575974"},"reference-count":8,"publisher":"Ovid Technologies (Wolters Kluwer Health)","issue":"1","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["J Pediatr Neurosci"],"published-print":{"date-parts":[[2017]]},"DOI":"10.4103\/jpn.jpn_165_16","type":"journal-article","created":{"date-parts":[[2017,5,4]],"date-time":"2017-05-04T02:29:11Z","timestamp":1493864951000},"page":"85","source":"Crossref","is-referenced-by-count":7,"title":["Glutaric aciduria type I: A rare metabolic disorder mimicking as choreoathetoid cerebral palsy"],"prefix":"10.4103","volume":"12","author":[{"given":"LulupKumar","family":"Sahoo","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"PradoshKumar","family":"Sarangi","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"AshokKumar","family":"Mallick","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"PrafullaKumar","family":"Dash","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"276","reference":[{"key":"key-10.4103\/1817-1745.205640-1","first-page":"1194","volume-title":"Glutaryl-coenzyme A dehydrogenase deficiency: A distinct encephalopathy","author":"Hoffmann","year":"1991","journal-title":"Pediatrics"},{"key":"key-10.4103\/1817-1745.205640-2","first-page":"675","volume-title":"CT and MR of the brain in glutaric acidemia type I: A review of 59 published cases and a report of 5 new patients","author":"Brismar","year":"1995","journal-title":"AJNR Am J Neuroradiol"},{"key":"key-10.4103\/1817-1745.205640-3","first-page":"38","volume-title":"Two cases of glutaric aciduria type 1: Clinical and neuropathological findings","author":"Kimura","year":"1994","journal-title":"J Neurol Sci"},{"key":"key-10.4103\/1817-1745.205640-4","first-page":"228","volume-title":", Zitelli BJ, Claassen D, Scarano J, et al. Acute profound dystonia in infants with glutaric acidemia","author":"Bergman","year":"1989","journal-title":"Pediatrics"},{"key":"key-10.4103\/1817-1745.205640-5","first-page":"381","volume-title":"Glutaric aciduria type I: From clinical, biochemical and molecular diversity to successful therapy","author":"Hoffmann","year":"1999","journal-title":"J Inherit Metab Dis"},{"key":"key-10.4103\/1817-1745.205640-6","first-page":"5","volume-title":"Guideline for the diagnosis and management of glutaryl-CoA dehydrogenase deficiency (glutaric aciduria type I)","author":"K\u00f6lker","year":"2007","journal-title":"J Inherit Metab Dis"},{"key":"key-10.4103\/1817-1745.205640-7","first-page":"1654","volume-title":"Glutaric aciduria type I: Clinical heterogeneity and neuroradiologic features","author":"Amir","year":"1987","journal-title":"Neurology"},{"key":"key-10.4103\/1817-1745.205640-8","unstructured":"Nyhan WL, Ozand PT, editors. Glutaric aciduria (type I). In: Atlas of Metabolic Diseases. London: Chapman and Hall; 1998. p. 46-52."}],"container-title":["Journal of Pediatric Neurosciences"],"original-title":[],"language":"en","deposited":{"date-parts":[[2026,8,14]],"date-time":"2026-08-14T13:27:27Z","timestamp":1786714047000},"score":1,"resource":{"primary":{"URL":"https:\/\/www.ovid.com\/10.4103\/jpn.JPN_165_16"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2017]]},"references-count":8,"journal-issue":{"issue":"1","published-print":{"date-parts":[[2017]]}},"alternative-id":["205640"],"URL":"https:\/\/doi.org\/10.4103\/jpn.jpn_165_16","relation":{},"ISSN":["1817-1745"],"issn-type":[{"value":"1817-1745","type":"print"}],"subject":[],"published":{"date-parts":[[2017]]}}}