{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,8,14]],"date-time":"2026-08-14T16:43:36Z","timestamp":1786725816919,"version":"build-2736575974"},"reference-count":10,"publisher":"Ovid Technologies (Wolters Kluwer Health)","issue":"6","content-domain":{"domain":["lww.com","ovid.com"],"crossmark-restriction":true},"short-container-title":[],"published-print":{"date-parts":[[2023,11]]},"DOI":"10.4103\/aian.aian_666_23","type":"journal-article","created":{"date-parts":[[2023,9,27]],"date-time":"2023-09-27T11:02:36Z","timestamp":1695812556000},"page":"1011-1012","update-policy":"https:\/\/doi.org\/10.1097\/lww.0000000000001000","source":"Crossref","is-referenced-by-count":0,"title":["Ataxia with Vitamin E Deficiency: A Never to be Missed Treatable Ataxia"],"prefix":"10.4103","volume":"26","author":[{"given":"Ayush","family":"Agarwal","sequence":"first","affiliation":[{"name":"Department of Neurology, All India Institute of Medical Sciences, New Delhi, India"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Divyani","family":"Garg","sequence":"additional","affiliation":[{"name":"Department of Neurology, All India Institute of Medical Sciences, New Delhi, India"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Achal K.","family":"Srivastava","sequence":"additional","affiliation":[{"name":"Department of Neurology, All India Institute of Medical Sciences, New Delhi, India"}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"276","published-online":{"date-parts":[[2023,9,25]]},"reference":[{"key":"R1-20260511","doi-asserted-by":"crossref","first-page":"368","DOI":"10.1136\/jnnp.64.3.368","article-title":"Ataxia with isolated vitamin E deficiency presenting as mutation negative Friedreich\u2019s ataxia","volume":"64","author":"Hammans","year":"1998","journal-title":"J Neurol Neurosur Psychiatry"},{"key":"R2-20260511","doi-asserted-by":"crossref","first-page":"20","DOI":"10.4103\/0019-5359.13814","article-title":"Cerebellar ataxia due to isolated vitamin E deficiency","volume":"59","author":"Jayaram","year":"2005","journal-title":"Indian J Med Sci"},{"key":"R3-20260511","doi-asserted-by":"crossref","first-page":"267","DOI":"10.1055\/s-2008-1059657","article-title":"Neuromyopathy and vitamin E deficiency in man","volume":"12","author":"Burck","year":"1981","journal-title":"Neuropaediatrics"},{"key":"R4-20260511","doi-asserted-by":"crossref","first-page":"141","DOI":"10.1038\/ng0295-141","article-title":"Ataxia with isolated vitamin E deficiency is caused by mutations in the a\u0301-tocopherol transfer protein","volume":"9","author":"Ouahchi","year":"1995","journal-title":"Nat Genet"},{"key":"R5-20260511","doi-asserted-by":"crossref","first-page":"2179","DOI":"10.1212\/WNL.43.11.2179","article-title":"Friedreich\u2019s ataxia phenotype not linked to chromosome 9 and associated with selective autosomal recessive vitamin E deficiency in two inbred Tunisian families","volume":"43","author":"Ben Hamida","year":"1993","journal-title":"Neurology"},{"key":"R6-20260511","doi-asserted-by":"crossref","first-page":"503","DOI":"10.1056\/NEJM198102263040902","article-title":"A progressive neurological syndrome in children with chronic liver disease","volume":"304","author":"Rosenblum","year":"1981","journal-title":"N Engl J Med"},{"key":"R7-20260511","doi-asserted-by":"crossref","first-page":"402","DOI":"10.1093\/brain\/awt339","article-title":"Molecular, clinical and peripheral neuropathy study of Tunisian patients with ataxia with vitamin E deficiency","volume":"137","author":"El Euch-Fayache","year":"2014","journal-title":"Brain"},{"key":"R8-20260511","doi-asserted-by":"crossref","first-page":"372","DOI":"10.4103\/aian.AIAN_29_20","article-title":"Vitamin E deficiency: An under-recognized cause of dystonia and ataxia syndrome","volume":"23","author":"Gupta","year":"2020","journal-title":"Ann Ind Acad Neurol"},{"key":"R9-20260511","first-page":"39","article-title":"Friedreich\u2019s ataxia- vitamin E responsive type. The chromosome 8 locus","volume":"3","author":"Belal","year":"1995","journal-title":"Clin Neurosci"},{"key":"R10-20260511","doi-asserted-by":"crossref","first-page":"584","DOI":"10.1212\/WNL.49.2.584","article-title":"Alpha-Tocopherol transfer protein gene: Exon skipping of all transcripts causes ataxia","volume":"49","author":"Tamaru","year":"1997","journal-title":"Neurology"}],"container-title":["Annals of Indian Academy of Neurology"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/www.ovid.com\/10.4103\/aian.aian_666_23","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2026,8,14]],"date-time":"2026-08-14T16:26:07Z","timestamp":1786724767000},"score":1,"resource":{"primary":{"URL":"https:\/\/www.ovid.com\/10.4103\/aian.aian_666_23"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2023,9,25]]},"references-count":10,"journal-issue":{"issue":"6","published-print":{"date-parts":[[2023]]}},"URL":"https:\/\/doi.org\/10.4103\/aian.aian_666_23","relation":{},"ISSN":["0972-2327","1998-3549"],"issn-type":[{"value":"0972-2327","type":"print"},{"value":"1998-3549","type":"electronic"}],"subject":[],"published":{"date-parts":[[2023,9,25]]},"assertion":[{"value":"2023-07-28","name":"received","label":"Received","group":{"name":"publication_history","label":"Publication History"}},{"value":"2023-08-15","name":"accepted","label":"Accepted","group":{"name":"publication_history","label":"Publication History"}}]}}