{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2024,12,11]],"date-time":"2024-12-11T00:25:12Z","timestamp":1733876712152,"version":"3.30.1"},"reference-count":16,"publisher":"Medknow","issue":"1","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Saudi J Kidney Dis Transpl"],"published-print":{"date-parts":[[2018]]},"DOI":"10.4103\/1319-2442.225193","type":"journal-article","created":{"date-parts":[[2018,2,12]],"date-time":"2018-02-12T03:06:24Z","timestamp":1518404784000},"page":"167","source":"Crossref","is-referenced-by-count":1,"title":["Alport\u2019s syndrome with focal segmental glomerulosclerosis lesion \u2013 Pattern to recognize"],"prefix":"10.4103","volume":"29","author":[{"given":"AbdullahA","family":"Al Sayyari","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"AfnanA","family":"Alsahli","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"SaraI","family":"Alshahwan","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"AmalO","family":"Alotaibi","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"KhaledO","family":"Alsaad","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Nourah","family":"Aloudah","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Mahfooz","family":"Farooqui","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"2581","reference":[{"key":"key-10.4103\/1319-2442.225193-1","first-page":"357","volume-title":"Mammalian collagen IV","author":"Khoshnoodi","year":"2008","journal-title":"Microsc Res Tech"},{"key":"key-10.4103\/1319-2442.225193-2","first-page":"1081","volume-title":"Pathology vs.Molecular genetics: (re)defining the spectrum of Alport syndrome","author":"Miner","year":"2014","journal-title":"Kidney Int"},{"key":"key-10.4103\/1319-2442.225193-3","first-page":"1217","volume-title":"A comparison of the clinical, histopathologic, and ultrastructural phenotypes in carriers of X-linked and autosomal recessive Alport\u2019s syndrome","author":"Dagher","year":"2001","journal-title":"Am J Kidney Dis"},{"key":"key-10.4103\/1319-2442.225193-4","first-page":"626","volume-title":"Glomerular diseases: FSGS","author":"Bose","year":"2014","journal-title":"Clin J Am Soc Nephrol"},{"key":"key-10.4103\/1319-2442.225193-5","first-page":"517","volume-title":"FSGS: From pathogenesis to the histological lesion","author":"Angioi","year":"2016","journal-title":"J Nephrol"},{"key":"key-10.4103\/1319-2442.225193-6","first-page":"1205","volume-title":"The spectrum of podocytopathies: A unifying view of glomerular diseases","author":"Wiggins","year":"2007","journal-title":"Kidney Int"},{"key":"key-10.4103\/1319-2442.225193-7","doi-asserted-by":"crossref","unstructured":"Reiser J, Altintas MM. Podocytes. F1000Res 2016;5. pii: F1000 Faculty Rev-114.","DOI":"10.12688\/f1000research.7255.1"},{"key":"key-10.4103\/1319-2442.225193-8","first-page":"1253","volume-title":"Rare hereditary COL4A3\/COL4A4 variants may be mistaken for familial focal segmental glomerulosclerosis","author":"Malone","year":"2014","journal-title":"Kidney Int"},{"key":"key-10.4103\/1319-2442.225193-9","first-page":"498","volume-title":"COL4A3 mutations cause focal segmental glomerulosclerosis","author":"Xie","year":"2014","journal-title":"J Mol Cell Biol"},{"key":"key-10.4103\/1319-2442.225193-10","first-page":"373","volume-title":"Study of a family affected with focal segmental glomerulosclerosis due to mutation of COL4A5 gene","author":"Zhang","year":"2017","journal-title":"Zhonghua Yi Xue Yi Chuan Xue Za Zhi"},{"key":"key-10.4103\/1319-2442.225193-11","first-page":"2328","volume-title":"A novel heterozygous COL4A4 missense mutation in a Chinese family with focal segmental glomerulosclerosis","author":"Wu","year":"2016","journal-title":"J Cell Mol Med"},{"key":"key-10.4103\/1319-2442.225193-12","first-page":"1630365","volume-title":"Secondary focal segmental glomerulosclerosis: From podocyte injury to glomerulosclerosis","author":"Kim","year":"2016","journal-title":"Biomed Res Int"},{"key":"key-10.4103\/1319-2442.225193-13","first-page":"629","volume-title":"Obesity-associated focal segmental glomerulosclerosis: Pathological features of the lesion and relationship with cardiomegaly and hyperlipidemia","author":"Verani","year":"1992","journal-title":"Am J Kidney Dis"},{"key":"key-10.4103\/1319-2442.225193-14","first-page":"82","volume-title":"Familial focal segmental glomerulosclerosis: Mutation in inverted formin 2 mimicking Alport syndrome","author":"Rood","year":"2016","journal-title":"Neth J Med"},{"key":"key-10.4103\/1319-2442.225193-15","first-page":"1291","volume-title":"Mutation in the alpha 5(IV) collagen chain in juvenile-onset Alport syndrome without hearing loss or ocular lesions: Detection by denaturing gradient gel electrophoresis of a PCR product","author":"Zhou","year":"1992","journal-title":"Am J Hum Genet"},{"key":"key-10.4103\/1319-2442.225193-16","first-page":"249","volume-title":"Mapping of Alport syndrome to the long arm of the X chromosome","author":"Atkin","year":"1988","journal-title":"Am J Hum Genet"}],"container-title":["Saudi Journal of Kidney Diseases and Transplantation"],"original-title":[],"language":"en","deposited":{"date-parts":[[2019,10,10]],"date-time":"2019-10-10T16:19:51Z","timestamp":1570724391000},"score":1,"resource":{"primary":{"URL":"http:\/\/www.sjkdt.org\/text.asp?2018\/29\/1\/167\/225193"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2018]]},"references-count":16,"journal-issue":{"issue":"1","published-print":{"date-parts":[[2018]]}},"alternative-id":["225193"],"URL":"https:\/\/doi.org\/10.4103\/1319-2442.225193","relation":{},"ISSN":["1319-2442"],"issn-type":[{"type":"print","value":"1319-2442"}],"subject":[],"published":{"date-parts":[[2018]]}}}