{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2022,4,1]],"date-time":"2022-04-01T10:52:34Z","timestamp":1648810354512},"reference-count":10,"publisher":"Springer Science and Business Media LLC","issue":"7","license":[{"start":{"date-parts":[[2000,7,1]],"date-time":"2000-07-01T00:00:00Z","timestamp":962409600000},"content-version":"tdm","delay-in-days":0,"URL":"http:\/\/www.springer.com\/tdm"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Indian J Pediatr"],"published-print":{"date-parts":[[2000,7]]},"DOI":"10.1007\/bf02760490","type":"journal-article","created":{"date-parts":[[2008,3,11]],"date-time":"2008-03-11T11:38:07Z","timestamp":1205235487000},"page":"539-540","source":"Crossref","is-referenced-by-count":0,"title":["Rett syndrome"],"prefix":"10.1007","volume":"67","author":[{"given":"M.","family":"Ghofrani","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"T.","family":"Mahmoodian","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"297","reference":[{"key":"BF02760490_CR1","doi-asserted-by":"crossref","first-page":"761","DOI":"10.1001\/archpedi.1986.02140220043029","volume":"140","author":"Al-Mateenm","year":"1986","unstructured":"Al-Mateenmet al. Rett syndrome: A commonly over looked progressive encephalopathy in girls.Am J Dis Child 1986; 140: 761","journal-title":"Am J Dis Child"},{"key":"BF02760490_CR2","doi-asserted-by":"crossref","first-page":"573","DOI":"10.1016\/S0387-7604(85)80003-6","volume":"7","author":"J Wahlstrom","year":"1985","unstructured":"Wahlstrom J. Genetic implication of Rett syndrome.Brain Dev 1985; 7: 573","journal-title":"Brain Dev"},{"key":"BF02760490_CR3","doi-asserted-by":"crossref","first-page":"383","DOI":"10.1002\/ajmg.1320250540","volume":"24","author":"DE Comings","year":"1986","unstructured":"Comings DE. The genetics of Rett syndrome: The consequences of a disorder where every case is a new mutation.Am J Med Genet 1986; 24:383","journal-title":"Am J Med Genet"},{"key":"BF02760490_CR4","doi-asserted-by":"crossref","first-page":"5","DOI":"10.1016\/0887-8994(94)90082-5","volume":"11","author":"BA Hagberg","year":"1994","unstructured":"Hagberg BAet al. Rett variants: A suggested model for inclusion criteria.Pediatric Neurol 1994 11: 5\u201311","journal-title":"Pediatric Neurol"},{"key":"BF02760490_CR5","doi-asserted-by":"crossref","first-page":"424","DOI":"10.1177\/088307389400900419","volume":"9","author":"ME Cornford","year":"1994","unstructured":"Cornford MEet al. Neuropathology of Rett syndrome: Case report with neuronal and mitochondrial abnormalities in the brain.J Child Neurol 1994; 9: 424\u2013431","journal-title":"J Child Neurol"},{"key":"BF02760490_CR6","doi-asserted-by":"crossref","unstructured":"Coker SB. Rett syndrome and mitochondrial enzyme deficiency. 1991; 6: 164\u2013165","DOI":"10.1177\/088307389100600216"},{"key":"BF02760490_CR7","doi-asserted-by":"crossref","first-page":"210","DOI":"10.1177\/088307389000500311","volume":"5","author":"Eeg-Olofsson","year":"1990","unstructured":"Eeg-Olofsson. Rett syndrome: A mitochondrial disease.J Child Neurol 1990; 5: 210\u2013214","journal-title":"J Child Neurol"},{"key":"BF02760490_CR8","doi-asserted-by":"crossref","first-page":"26","DOI":"10.1177\/088307389400900105","volume":"9","author":"T Matsuishi","year":"1994","unstructured":"Matsuishi Tet al. Abnormal carbohydrate metabolism in cerebrospinal fluid in Rett syndrome.J Child Neurol 1994; 9: 26\u201330","journal-title":"J Child Neurol"},{"key":"BF02760490_CR9","doi-asserted-by":"crossref","first-page":"81","DOI":"10.1016\/S0387-7604(12)80183-5","volume":"12","author":"SS Budden","year":"1990","unstructured":"Budden SSet al. Cerebrospinal fluid studies in the Rett syndrome: Biogenic amines and beta endorphin.Brain Dev 1990; 12: 81","journal-title":"Brain Dev"},{"key":"BF02760490_CR10","doi-asserted-by":"crossref","first-page":"234","DOI":"10.1016\/S0022-3476(88)80060-X","volume":"112","author":"TL Perry","year":"1988","unstructured":"Perry TLet al. Cerebrospinal fluid values for monoamine metabolism, 8-aminobutyric acid and other amino compounds in Rett syndrome.J Pediatr 1988; 112: 234\u2013238","journal-title":"J Pediatr"}],"container-title":["The Indian Journal of Pediatrics"],"original-title":[],"language":"en","link":[{"URL":"http:\/\/link.springer.com\/content\/pdf\/10.1007\/BF02760490.pdf","content-type":"application\/pdf","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/link.springer.com\/article\/10.1007\/BF02760490\/fulltext.html","content-type":"text\/html","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/link.springer.com\/content\/pdf\/10.1007\/BF02760490","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2019,5,20]],"date-time":"2019-05-20T13:22:16Z","timestamp":1558358536000},"score":1,"resource":{"primary":{"URL":"http:\/\/link.springer.com\/10.1007\/BF02760490"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2000,7]]},"references-count":10,"journal-issue":{"issue":"7","published-print":{"date-parts":[[2000,7]]}},"alternative-id":["BF02760490"],"URL":"https:\/\/doi.org\/10.1007\/bf02760490","relation":{},"ISSN":["0019-5456","0973-7693"],"issn-type":[{"value":"0019-5456","type":"print"},{"value":"0973-7693","type":"electronic"}],"subject":[],"published":{"date-parts":[[2000,7]]}}}