{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,10,1]],"date-time":"2025-10-01T15:38:44Z","timestamp":1759333124181},"reference-count":7,"publisher":"Ovid Technologies (Wolters Kluwer Health)","issue":"2","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[2010]]},"DOI":"10.1097\/icb.0b013e3181ad3944","type":"journal-article","created":{"date-parts":[[2010,3,24]],"date-time":"2010-03-24T08:15:21Z","timestamp":1269418521000},"page":"150-153","source":"Crossref","is-referenced-by-count":5,"title":["PIGMENTARY MACULOPATHY IN TWO SIBLINGS WITH WOLFRAM SYNDROME"],"prefix":"10.1097","volume":"4","author":[{"given":"Tran Thi Ha","family":"Chau","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Delepine","family":"Bertrand","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Delobel","family":"Bruno","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"276","reference":[{"key":"R1-18-20210126","first-page":"715","article-title":"Diabetes mellitus and simple optic atrophy among siblings: report of four cases.","volume":"13","author":"Wolfram","year":"1938","journal-title":"Mayo Clin Proc"},{"key":"R2-18-20210126","doi-asserted-by":"crossref","first-page":"99","DOI":"10.1002\/humu.9300","article-title":"Wolfram syndrome in French population: characterization of novel mutations and polymorphisms in the WFS1 gene.","volume":"25","author":"Giuliano","year":"2005","journal-title":"Hum Mutat"},{"key":"R3-18-20210126","doi-asserted-by":"crossref","first-page":"84","DOI":"10.1177\/112067210201200202","article-title":"Ophthalmologic findings in fifteen patients with Wolfram syndrome.","volume":"12","author":"Al-Till","year":"2002","journal-title":"Eur J Ophthalmol"},{"key":"R4-18-20210126","doi-asserted-by":"crossref","first-page":"838","DOI":"10.1136\/jmg.34.10.838","article-title":"Wolfram (DIDMOAD) syndrome.","volume":"34","author":"Barrett","year":"1997","journal-title":"J Med Genet"},{"key":"R5-18-20210126","doi-asserted-by":"crossref","first-page":"38","DOI":"10.1016\/S0008-4182(06)80064-5","article-title":"Pigmentary maculopathy in a patient with Wolfram syndrome.","volume":"41","author":"Dhalla","year":"2006","journal-title":"Can J Ophthalmol"},{"key":"R6-18-20210126","doi-asserted-by":"crossref","first-page":"1821","DOI":"10.1016\/S0161-6420(99)90356-1","article-title":"Prevalence of macular pattern dystrophy in maternally inherited diabetes and deafness.","volume":"106","author":"Massin","year":"1999","journal-title":"GEDIAM Group. Ophthalmology"},{"key":"R7-18-20210126","doi-asserted-by":"crossref","first-page":"1","DOI":"10.1002\/cne.21734","article-title":"Wolfram syndrome 1 (Wfs1) gene expression in the normal mouse visual system.","volume":"510","author":"Kawano","year":"2008","journal-title":"J Comp Neurol"}],"container-title":["RETINAL Cases & Brief Reports"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/journals.lww.com\/10.1097\/ICB.0b013e3181ad3944","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2021,5,14]],"date-time":"2021-05-14T00:57:07Z","timestamp":1620953827000},"score":1,"resource":{"primary":{"URL":"https:\/\/journals.lww.com\/01271216-201000420-00018"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2010]]},"references-count":7,"journal-issue":{"issue":"2","published-print":{"date-parts":[[2010]]}},"URL":"https:\/\/doi.org\/10.1097\/icb.0b013e3181ad3944","relation":{},"ISSN":["1935-1089"],"issn-type":[{"value":"1935-1089","type":"print"}],"subject":[],"published":{"date-parts":[[2010]]}}}