{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,6,27]],"date-time":"2026-06-27T23:24:07Z","timestamp":1782602647410,"version":"3.54.5"},"reference-count":21,"publisher":"Springer Science and Business Media LLC","issue":"1","license":[{"start":{"date-parts":[[1987,1,1]],"date-time":"1987-01-01T00:00:00Z","timestamp":536457600000},"content-version":"tdm","delay-in-days":0,"URL":"http:\/\/www.springer.com\/tdm"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Eye"],"published-print":{"date-parts":[[1987,1]]},"DOI":"10.1038\/eye.1987.21","type":"journal-article","created":{"date-parts":[[2011,7,4]],"date-time":"2011-07-04T10:14:42Z","timestamp":1309774482000},"page":"146-153","source":"Crossref","is-referenced-by-count":44,"title":["Ocular signs in Alport's syndrome"],"prefix":"10.1038","volume":"1","author":[{"given":"S M","family":"Thompson","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"J P","family":"Deady","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"H E","family":"Willshaw","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"R H R","family":"White","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"297","reference":[{"key":"BFeye198721_CR1","first-page":"213","volume":"69","author":"GS Spear","year":"1972","unstructured":"Spear GS and Slusser RJ : Alport's syndrome: emphasizing electron microscopic studies of the glomerulus. Am. J. Pathol. 1972, 69: 213.","journal-title":"Am. J. Pathol."},{"key":"BFeye198721_CR2","doi-asserted-by":"publisher","first-page":"199","DOI":"10.1002\/path.1711350305","volume":"135","author":"N Yoshikawa","year":"1981","unstructured":"Yoshikawa N, Cameron AH and White RHR : The glomerular basal lamina in hereditary nephritis. Br. J. Pathol. 1981, 135: 199\u2013209.","journal-title":"Br. J. Pathol."},{"key":"BFeye198721_CR3","first-page":"172","volume":"17","author":"N Yoshikawa","year":"1982","unstructured":"Yoshikawa N, White RHR and Cameron AH : Familial haematuria: clinico-pathological correlations. Clin. Nephrol 1982, 17: 172\u201382.","journal-title":"Clin. Nephrol"},{"key":"BFeye198721_CR4","doi-asserted-by":"publisher","first-page":"1","DOI":"10.1159\/000308468","volume":"165","author":"R Faggioni","year":"1972","unstructured":"Faggioni R, Scouras J and Streiff EB : Alport's syndrome: clinicopathological considerations. Ophthalmologica 1972, 165: 1\u201314.","journal-title":"Ophthalmologica"},{"key":"BFeye198721_CR5","first-page":"163","volume":"13","author":"D Perrin","year":"1980","unstructured":"Perrin D, Jungers P, Grunefeld JP, Delons S, Noel L-H and Zenatti C : Perimacular changes in Alport's syndrome. Clin. Nephrol. 1980, 13: 163\u20137.","journal-title":"Clin. Nephrol."},{"key":"BFeye198721_CR6","doi-asserted-by":"publisher","first-page":"493","DOI":"10.1016\/0002-9343(81)90571-4","volume":"70","author":"M Gubler","year":"1981","unstructured":"Gubler M, Levy M, Broyer M, Naizot C, Gonzales G, Perrin D and Habib R : Alport's syndrome. A report of 58 cases and a review of the literature. Am. J. Med. 1981, 70: 493\u2013505.","journal-title":"Am. J. Med."},{"key":"BFeye198721_CR7","doi-asserted-by":"publisher","first-page":"204","DOI":"10.1159\/000309287","volume":"186","author":"R Sabates","year":"1983","unstructured":"Sabates R, Krachmer JH and Weingeist TA : Ocular findings in Alport's syndrome. Ophthalmologica 1983, 186: 204\u2013210.","journal-title":"Ophthalmologica"},{"key":"BFeye198721_CR8","doi-asserted-by":"publisher","first-page":"532","DOI":"10.1016\/0002-9394(77)90447-0","volume":"84","author":"BCP Polak","year":"1977","unstructured":"Polak BCP and Hogewind BL : Macular lesions in Alport's disease. Am. J. Ophthalmol. 1977, 84: 532\u20135.","journal-title":"Am. J. Ophthalmol."},{"key":"BFeye198721_CR9","doi-asserted-by":"publisher","first-page":"627","DOI":"10.1001\/archinte.1956.00250230121013","volume":"97","author":"E Sohar","year":"1956","unstructured":"Sohar E : Renal disease, inner ear deafness, and ocular changes. Arch. Intern. Med. 1956, 97: 627\u201330.","journal-title":"Arch. Intern. Med."},{"key":"BFeye198721_CR10","doi-asserted-by":"publisher","first-page":"557","DOI":"10.1136\/bjo.54.8.557","volume":"54","author":"PD Davies","year":"1970","unstructured":"Davies PD : Pigment dispersion in a case of Alport's syndrome. Br. J. Ophthalmol. 1970, 54: 557\u201361.","journal-title":"Br. J. Ophthalmol."},{"key":"BFeye198721_CR11","doi-asserted-by":"publisher","first-page":"493","DOI":"10.1136\/bjo.67.8.493","volume":"67","author":"JAA Govan","year":"1983","unstructured":"Govan JAA : Ocular manifestations of Alport's syndrome: a hereditary disorder of basement membranes? Br. J. Ophthalmol. 1983, 67: 493\u2013503.Ocular manifestations of Alport's syndrome: a hereditary disorder of basement membranes? Br. J. Ophthalmol. 1983, 67: 493-503.","journal-title":"Br. J. Ophthalmol."},{"key":"BFeye198721_CR12","first-page":"211","volume":"94","author":"RC Tripathi","year":"1974","unstructured":"Tripathi RC, Casey TA and Wise G : Hereditary posterior polymorphous dystrophy, an ultrastructural and clinical report. Trans. OphthalmoL Soc. UK 1974, 94: 211\u201325.","journal-title":"Trans. OphthalmoL Soc. UK"},{"key":"BFeye198721_CR13","doi-asserted-by":"publisher","first-page":"481","DOI":"10.1001\/archopht.1964.00970010497007","volume":"71","author":"RD Brownell","year":"1964","unstructured":"Brownell RD and Wolter JR : Anterior lenticonus in familial hemorrhagic nephritis. Arch. Ophthalmol. 1964, 71: 481\u20133.","journal-title":"Arch. Ophthalmol."},{"key":"BFeye198721_CR14","first-page":"762","volume":"78","author":"WS Peterson","year":"1974","unstructured":"Peterson WS and Albert DM : Fundus changes in the hereditary nephropathies. Trans. Am. Acad. Ophthal. Otolaryngol. 1974, 78: 762\u201371.","journal-title":"Trans. Am. Acad. Ophthal. Otolaryngol."},{"key":"BFeye198721_CR15","first-page":"3","volume":"21","author":"GS Spear","year":"1984","unstructured":"Spear GS : Hereditary nephritis (Alport's syndrome)\u20141983. Clin. Nephrol 1984, 21: 3\u20136.","journal-title":"Clin. Nephrol"},{"key":"BFeye198721_CR16","first-page":"817","volume":"101","author":"GF Dibona","year":"1983","unstructured":"Dibona GF : Alport's syndrome: a genetic defect in biochemical composition of basement membrane of glomerulus, lens and inner ear? J. Lab. and Clin. Med. 1983, 101: 817\u201320.Alport's syndrome: a genetic defect in biochemical composition of basement membrane of glomerulus, lens and inner ear? J. Lab. and Clin. Med. 1983, 101: 817-20.","journal-title":"J. Lab. and Clin. Med."},{"key":"BFeye198721_CR17","doi-asserted-by":"publisher","first-page":"733","DOI":"10.1001\/archinte.1958.00260220049005","volume":"102","author":"GT Perkoff","year":"1958","unstructured":"Perkoff GT, Nugent CA, Dolowitz DA, Stephens FE, Carnes WH and Tyler FH : A follow-up study of hereditary chronic nephritis. Arch. Intern. Med. 1958, 102: 733\u201346.","journal-title":"Arch. Intern. Med."},{"key":"BFeye198721_CR18","doi-asserted-by":"publisher","first-page":"672","DOI":"10.1038\/ki.1985.63","volume":"27","author":"J Feingold","year":"1985","unstructured":"Feingold J, Bois E, Chompret A, Broyer M, Gubler M-C and Grunfeld J-P : Genetic heterogeneity of Alport syndrome. Kid. Internat. 1985, 27: 672\u20137.","journal-title":"Kid. Internat."},{"key":"BFeye198721_CR19","first-page":"1241","volume":"35","author":"SJ Hasstedt","year":"1983","unstructured":"Hasstedt SJ and Atkin CL : X-linked inheritance of Alport syndrome: family P revisited. Am. J. Hum. Genet. 1983, 35: 1241\u201351.","journal-title":"Am. J. Hum. Genet."},{"key":"BFeye198721_CR20","doi-asserted-by":"publisher","first-page":"285","DOI":"10.1111\/j.1399-0004.1980.tb00149.x","volume":"17","author":"SH Evans","year":"1980","unstructured":"Evans SH, Erickson RP, Kelsch R and Peirce JC : Apparently changing patterns of inheritance in Alport's hereditary nephritis: genetic heterogeneity versus altered diagnostic criteria. Clin. Genet. 1980, 17: 285\u201392.","journal-title":"Clin. Genet."},{"key":"BFeye198721_CR21","first-page":"379","volume":"13","author":"MM Cohen","year":"1961","unstructured":"Cohen MM, Cassady G and Hanna BL : A genetic study of hereditary renal dysfunction with associated nerve deafness. Am. J. Hum. Genet. 1961, 13: 379\u201389.","journal-title":"Am. J. Hum. Genet."}],"container-title":["Eye"],"original-title":[],"language":"en","link":[{"URL":"http:\/\/www.nature.com\/articles\/eye198721.pdf","content-type":"application\/pdf","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/www.nature.com\/articles\/eye198721","content-type":"text\/html","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/www.nature.com\/articles\/eye198721.pdf","content-type":"application\/pdf","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2023,5,18]],"date-time":"2023-05-18T17:22:23Z","timestamp":1684430543000},"score":1,"resource":{"primary":{"URL":"https:\/\/www.nature.com\/articles\/eye198721"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[1987,1]]},"references-count":21,"journal-issue":{"issue":"1","published-print":{"date-parts":[[1987,1]]}},"alternative-id":["BFeye198721"],"URL":"https:\/\/doi.org\/10.1038\/eye.1987.21","relation":{},"ISSN":["0950-222X","1476-5454"],"issn-type":[{"value":"0950-222X","type":"print"},{"value":"1476-5454","type":"electronic"}],"subject":[],"published":{"date-parts":[[1987,1]]}}}