{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,10,5]],"date-time":"2025-10-05T19:56:08Z","timestamp":1759694168922},"reference-count":8,"publisher":"Elsevier BV","issue":"1","license":[{"start":{"date-parts":[[2004,1,1]],"date-time":"2004-01-01T00:00:00Z","timestamp":1072915200000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["European Journal of Paediatric Neurology"],"published-print":{"date-parts":[[2004,1]]},"DOI":"10.1016\/j.ejpn.2003.10.006","type":"journal-article","created":{"date-parts":[[2003,12,17]],"date-time":"2003-12-17T05:43:04Z","timestamp":1071639784000},"page":"55-59","source":"Crossref","is-referenced-by-count":4,"title":["Neonatal seizures and limb malformations associated with liver-specific complex IV respiratory chain deficiency"],"prefix":"10.1016","volume":"8","author":[{"given":"M.A","family":"Kurian","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"E.S","family":"O'Mahoney","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"P","family":"Rustin","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"G","family":"Brown","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"E.P","family":"Treacy","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"M.D","family":"King","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"78","reference":[{"issue":"4","key":"10.1016\/j.ejpn.2003.10.006_BIB1","doi-asserted-by":"crossref","first-page":"448","DOI":"10.1007\/BF00711360","article-title":"Metabolic disorders of embryogenesis","volume":"17","author":"Brown","year":"1994","journal-title":"J Inher Metab Dis"},{"key":"10.1016\/j.ejpn.2003.10.006_BIB2","doi-asserted-by":"crossref","first-page":"457","DOI":"10.1002\/(SICI)1096-8628(19961230)66:4<457::AID-AJMG15>3.0.CO;2-T","article-title":"Craniofacial anomalies and malformations in respiratory chain deficiency","volume":"66","author":"Cormier-Daire","year":"1996","journal-title":"Am J Med Genet"},{"issue":"2","key":"10.1016\/j.ejpn.2003.10.006_BIB3","doi-asserted-by":"crossref","first-page":"208","DOI":"10.1067\/S0022-3476(03)00130-6","article-title":"Antenatal manifestations of mitochondrial respiratory chain deficiency","volume":"143","author":"von Kleist-Retzow","year":"2003","journal-title":"J Pediatr"},{"key":"10.1016\/j.ejpn.2003.10.006_BIB4","series-title":"The metabolic and molecular bases of inherited disease","first-page":"2261","article-title":"Clinical presentation of respiratory chain deficiency","author":"Munnich","year":"2001"},{"key":"10.1016\/j.ejpn.2003.10.006_BIB5","doi-asserted-by":"crossref","first-page":"581","DOI":"10.1203\/00006450-200011000-00004","article-title":"Human cytochrome oxidase deficiency","volume":"48","author":"Robinson","year":"2000","journal-title":"Pediatr Res"},{"key":"10.1016\/j.ejpn.2003.10.006_BIB6","doi-asserted-by":"crossref","first-page":"337","DOI":"10.1038\/3804","article-title":"SURF1 encoding a factor involved in the biogenesis of cytochrome c oxidase is mutated in Leigh syndrome","volume":"20","author":"Zhu","year":"1998","journal-title":"Nat Genet"},{"key":"10.1016\/j.ejpn.2003.10.006_BIB7","doi-asserted-by":"crossref","first-page":"795","DOI":"10.1093\/hmg\/9.5.795","article-title":"Mutations in SCO2 are associated with a distinct form of hypertrophic cardiomyopathy and cytochrome c oxidase deficiency","volume":"9","author":"Jaksch","year":"2000","journal-title":"Hum Mol Genet"},{"key":"10.1016\/j.ejpn.2003.10.006_BIB8","first-page":"1104","article-title":"Mutations of the SCO1 gene in mitochondrial cytochrome c oxidase deficiency with neonatal-onset hepatic failure and encephalopathy","volume":"67","author":"Valnot","year":"2000","journal-title":"Am J Hum Genet"}],"container-title":["European Journal of Paediatric Neurology"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S1090379803001818?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S1090379803001818?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2019,2,15]],"date-time":"2019-02-15T23:21:56Z","timestamp":1550272916000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S1090379803001818"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2004,1]]},"references-count":8,"journal-issue":{"issue":"1","published-print":{"date-parts":[[2004,1]]}},"alternative-id":["S1090379803001818"],"URL":"https:\/\/doi.org\/10.1016\/j.ejpn.2003.10.006","relation":{},"ISSN":["1090-3798"],"issn-type":[{"value":"1090-3798","type":"print"}],"subject":[],"published":{"date-parts":[[2004,1]]}}}