{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,4,16]],"date-time":"2026-04-16T08:55:10Z","timestamp":1776329710577,"version":"3.50.1"},"reference-count":12,"publisher":"Baskent University","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Exp Clin Transplant"],"DOI":"10.6002\/ect.2017.0163","type":"journal-issue","created":{"date-parts":[[2018,3,14]],"date-time":"2018-03-14T07:25:35Z","timestamp":1521012335000},"source":"Crossref","is-referenced-by-count":0,"title":[],"prefix":"10.6002","member":"4021","published-online":{"date-parts":[[2018,3,9]]},"reference":[{"issue":"1","key":"ref0","doi-asserted-by":"publisher","first-page":"53","DOI":"10.1001\/archopht.1973.01000050055011","article-title":"Werner syndrome","volume":"90","author":"JD","year":"1973","unstructured":"1. Bullock JD, Howard RO. Werner syndrome. Arch Ophthalmol. 1973;90(1):53-56.","journal-title":"Arch Ophthalmol"},{"issue":"3","key":"ref1","doi-asserted-by":"publisher","first-page":"331","DOI":"10.4103\/2230-8210.95659","article-title":"The eye as a window to rare endocrine disorders","volume":"16","author":"Chopra","year":"2012","unstructured":"2. Chopra R, Chander A, Jacob JJ. The eye as a window to rare endocrine disorders. Indian J Endocrinol Metab. 2012;16(3):331-338.","journal-title":"Indian J Endocrinol Metab"},{"issue":"6","key":"ref2","doi-asserted-by":"publisher","first-page":"558","DOI":"10.1002\/humu.20337","article-title":"The spectrum of WRN mutations in Werner syndrome patients","volume":"27","author":"Huang","year":"2006","unstructured":"3. Huang S, Lee L, Hanson NB, et al. The spectrum of WRN mutations in Werner syndrome patients. Hum Mutat. 2006;27(6):558-567.","journal-title":"Hum Mutat"},{"issue":"1","key":"ref3","doi-asserted-by":"publisher","first-page":"107","DOI":"10.1016\/S0039-6257(02)00400-9","article-title":"Ocular manifestations in the inherited DNA repair disorders","volume":"48","author":"Dollfus","year":"2003","unstructured":"4. Dollfus H, Porto F, Caussade P, et al. Ocular manifestations in the inherited DNA repair disorders. Surv Ophthalmol. 2003;48(1):107-122.","journal-title":"Surv Ophthalmol"},{"key":"ref4","doi-asserted-by":"publisher","first-page":"31","DOI":"10.1186\/1471-2415-14-31","article-title":"Werner syndrome with refractory cystoid macular edema and immunohistochemical analysis of WRN proteins in human retinas","volume":"14","author":"Oshitari","year":"2014","unstructured":"5. Oshitari T, Kitahashi M, Mizuno S, et al. Werner syndrome with refractory cystoid macular edema and immunohistochemical analysis of WRN proteins in human retinas. BMC Ophthalmol. 2014;14:31.","journal-title":"BMC Ophthalmol"},{"issue":"2","key":"ref5","doi-asserted-by":"publisher","first-page":"92","DOI":"10.1097\/ICB.0000000000000011","article-title":"Bilateral retinal detachment in Werner syndrome","volume":"8","author":"Sasoh","year":"2014","unstructured":"6. Sasoh M, Tsukitome H, Matsui Y, Furuta M, Kondo M. Bilateral retinal detachment in Werner syndrome. Retin Cases Brief Rep. 2014;8(2):92-94.","journal-title":"Retin Cases Brief Rep"},{"key":"ref6","unstructured":"7. Kocabora MS, Kurkcuoglu AR, Engin G, Yilmazli C, Arslan O. [Cataract surgery by phacoemulsification in Werner's syndrome]. J Fr Ophtalmol. 2000;23(10):1012-1015."},{"key":"ref7","unstructured":"8. Mine T, Ashida Y. [Werner's syndrome and its cataract operation]. Nihon Ganka Kiyo. 1968;19(11):1068-1075."},{"key":"ref8","doi-asserted-by":"crossref","unstructured":"9. Jonas JB, Ruprecht KW, Schmitz-Valckenberg P, et al. Ophthalmic surgical complications in Werner's syndrome: report on 18 eyes of nine patients. Ophthalmic Surg. 1987;18(10):760-764.","DOI":"10.3928\/1542-8877-19871001-14"},{"issue":"6","key":"ref9","doi-asserted-by":"publisher","first-page":"570","DOI":"10.4103\/0301-4738.103802","article-title":"Endothelial cell study in a case of Werner's syndrome undergoing phacoemulsification and Yettrium-Aluminum-Garnet laser capsulotomy","volume":"60","author":"Kemmanu","year":"2012","unstructured":"10. Kemmanu V, Nagappa S, Hegde K, Yadav NK, Shetty BK. Endothelial cell study in a case of Werner's syndrome undergoing phacoemulsification and Yettrium-Aluminum-Garnet laser capsulotomy. Indian J Ophthalmol. 2012;60(6):570-572.","journal-title":"Indian J Ophthalmol"},{"issue":"3","key":"ref10","doi-asserted-by":"publisher","first-page":"263","DOI":"10.1016\/0167-4943(89)90045-9","article-title":"Ophthalmological aspects in patients with Werner's syndrome","volume":"9","author":"Ruprecht","year":"1989","unstructured":"11. Ruprecht KW. Ophthalmological aspects in patients with Werner's syndrome. Arch Gerontol Geriatr. 1989;9(3):263-270.","journal-title":"Arch Gerontol Geriatr"},{"issue":"6","key":"ref11","doi-asserted-by":"publisher","first-page":"503","DOI":"10.3143\/geriatrics.30.503","article-title":"[Two cases of Werner's syndrome treated with penetrating keratoplasty]","volume":"30","author":"Shintani","year":"1993","unstructured":"12. Shintani M, Ikegami H, Kawaguchi Y, Hosotani H, Miki T, Ogihara T. [Two cases of Werner's syndrome treated with penetrating keratoplasty]. Nihon Ronen Igakkai Zasshi. 1993;30(6):503-505.","journal-title":"Nihon Ronen Igakkai Zasshi"}],"container-title":["Experimental and Clinical Transplantation"],"original-title":[],"deposited":{"date-parts":[[2022,8,15]],"date-time":"2022-08-15T20:40:20Z","timestamp":1660596020000},"score":1,"resource":{"primary":{"URL":"http:\/\/ectrx.org\/forms\/ectrxcontentshow.php?doi_id=10.6002\/ect.2017.0163"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2018,3,9]]},"references-count":12,"URL":"https:\/\/doi.org\/10.6002\/ect.2017.0163","relation":{},"ISSN":["1304-0855","2146-8427"],"issn-type":[{"value":"1304-0855","type":"print"},{"value":"2146-8427","type":"electronic"}],"subject":[],"published":{"date-parts":[[2018,3,9]]}}}