{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,10,11]],"date-time":"2025-10-11T13:23:45Z","timestamp":1760189025833},"reference-count":6,"publisher":"BMJ","issue":"12","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Journal of Neurology, Neurosurgery &amp; Psychiatry"],"published-print":{"date-parts":[[1988,12,1]]},"DOI":"10.1136\/jnnp.51.12.1576","type":"journal-article","created":{"date-parts":[[2008,11,10]],"date-time":"2008-11-10T21:16:40Z","timestamp":1226351800000},"page":"1576-1577","source":"Crossref","is-referenced-by-count":2,"title":["Familial cerebellar ataxia and diabetes insipidus."],"prefix":"10.1136","volume":"51","author":[{"given":"I C","family":"Robinson","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"B P","family":"O'Malley","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"I D","family":"Young","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"239","reference":[{"key":"ref_1","doi-asserted-by":"crossref","first-page":"1151","DOI":"10.1016\/S0140-6736(83)92879-9","article-title":"Classification of the hereditary ataxias and paraplegias","volume":"i:","author":"Harding, A.E.","year":"1983","unstructured":"Harding AE. Classification of the hereditary ataxias and paraplegias. Lancet 1983;i:1151-5.","journal-title":"Lancet"},{"key":"ref_2","doi-asserted-by":"crossref","first-page":"1","DOI":"10.1093\/brain\/105.1.1","article-title":"The clinical features and classification ofthe late onset autosomal dominant cerebellar ataxias. A study of 11 families, including descendants of \"the Drew family of Walworth\"","volume":"105","author":"Harding, A.E.","year":"1982","unstructured":"Harding AE. The clinical features and classification ofthe late onset autosomal dominant cerebellar ataxias. A study of 11 families, including descendants of \"the Drew family of Walworth\". Brain 1982;105:1-28.","journal-title":"Brain"},{"key":"ref_3","doi-asserted-by":"crossref","first-page":"426","DOI":"10.1111\/j.1399-0004.1975.tb00353.x","article-title":"Autosomal recessive syndrome of cerebellar ataxia and hypogonadotropic hypogonadism","volume":"7","author":"Neuhauser, G.; Opitz, J.M.","year":"1975","unstructured":"Neuhauser G, Opitz JM. Autosomal recessive syndrome of cerebellar ataxia and hypogonadotropic hypogonadism. Clin Genet 1975;7:426-34.","journal-title":"Clin Genet"},{"key":"ref_4","doi-asserted-by":"crossref","first-page":"747","DOI":"10.1136\/jnnp.45.8.747","article-title":"Familial cerebellar ataxia and hypogonadotrophic hypogonadism: evidence for hypothalamic LHRH deficiency","volume":"45","author":"Berciano, J.; Amado, J.A.; Freijanes, J.; Rebollo, M.; Vaquero, A.","year":"1982","unstructured":"Berciano J, Amado JA, Freijanes J, Rebollo M, Vaquero A. Familial cerebellar ataxia and hypogonadotrophic hypogonadism: evidence for hypothalamic LHRH deficiency. J Neurol Neurosurg Psychiatry 1982;45: 747-51.","journal-title":"J Neurol Neurosurg Psychiatry"},{"key":"ref_5","doi-asserted-by":"crossref","first-page":"565","DOI":"10.1016\/S0022-3476(76)80387-3","article-title":"Juvenile diabetes mellitus, optic atrophy, sensory nerve deafness and diabetes insipidus-a syndrome","volume":"89","author":"Gunn, T.; Bortolussi, R.; Little, J.M.; Andermann, F.; Fraser, F.C.; Belmonte, M.M.","year":"1976","unstructured":"Gunn T, Bortolussi R, Little JM, Andermann F, Fraser FC, Belmonte MM. Juvenile diabetes mellitus, optic atrophy, sensory nerve deafness and diabetes insipidus-a syndrome. J Pediatr 1976;89:565-70.","journal-title":"J Pediatr"},{"key":"ref_6","first-page":"883","article-title":"Familial cranial diabetes insipidus: a report of five families. Genetic, diagnostic and therapeutic aspects","volume":"57","author":"Pedersen, E.B.; Lamm, L.U.; Albertsen, K.J.","year":"1985","unstructured":"Pedersen EB, Lamm LU, Albertsen KJ et al. Familial cranial diabetes insipidus: a report of five families. Genetic, diagnostic and therapeutic aspects. Q J Med 1985;57:883-96.","journal-title":"Q J Med"}],"container-title":["Journal of Neurology, Neurosurgery &amp; Psychiatry"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/syndication.highwire.org\/content\/doi\/10.1136\/jnnp.51.12.1576","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2020,9,26]],"date-time":"2020-09-26T04:20:59Z","timestamp":1601094059000},"score":1,"resource":{"primary":{"URL":"https:\/\/jnnp.bmj.com\/lookup\/doi\/10.1136\/jnnp.51.12.1576"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[1988,12,1]]},"references-count":6,"journal-issue":{"issue":"12","published-print":{"date-parts":[[1988,12,1]]}},"URL":"https:\/\/doi.org\/10.1136\/jnnp.51.12.1576","relation":{},"ISSN":["0022-3050"],"issn-type":[{"value":"0022-3050","type":"print"}],"subject":[],"published":{"date-parts":[[1988,12,1]]}}}