{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,7,28]],"date-time":"2026-07-28T07:14:14Z","timestamp":1785222854410,"version":"3.55.0"},"reference-count":13,"publisher":"Scientific Scholar","issue":"5","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Indian J Nephrol"],"published-print":{"date-parts":[[2020]]},"DOI":"10.4103\/ijn.ijn_347_19","type":"journal-article","created":{"date-parts":[[2021,2,8]],"date-time":"2021-02-08T09:18:36Z","timestamp":1612775916000},"page":"342","source":"Crossref","is-referenced-by-count":3,"title":["Atypical HUS associated With CFH\/CFHR-1 hybrid gene"],"prefix":"10.25259","volume":"30","author":[{"given":"Valentine","family":"Lobo","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Sharon","family":"Negi","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Vipul","family":"Chakurkar","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Meenal","family":"Agarwal","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"10894","reference":[{"key":"key-10.4103\/0971-4065.293645-1","doi-asserted-by":"crossref","first-page":"539","DOI":"10.1016\/j.kint.2016.10.005","article-title":"Conference Participants.Atypical hemolytic uremic syndrome and C3 glomerulopathy: Conclusions from a \u201cKidney Disease: Improving Global Outcomes\u201d (KDIGO) controversies conference","author":"Goodship","year":"2017","journal-title":"Kidney Int"},{"key":"key-10.4103\/0971-4065.293645-2","doi-asserted-by":"crossref","first-page":"240","DOI":"10.1681\/ASN.2017050518","article-title":"Factor H competitor generated by gene conversion events associates with atypical hemolytic uremic syndrome","author":"Goicoechea","year":"2018","journal-title":"J Am Soc Nephrol"},{"key":"key-10.4103\/0971-4065.293645-3","doi-asserted-by":"crossref","first-page":"81","DOI":"10.1016\/j.molimm.2004.01.003","article-title":"Functional analysis in serum from atypical Hemolytic Uremic Syndrome patients reveals impaired protection of host cells associated with mutations in factor H","author":"S\u00e1nchez-Corral","year":"2004","journal-title":"Mol Immunol"},{"key":"key-10.4103\/0971-4065.293645-4","first-page":"1847","article-title":"Syndromes of thrombotic microangiopathy","author":"George","year":"2014","journal-title":"N Engl J Med"},{"key":"key-10.4103\/0971-4065.293645-5","first-page":"895","article-title":"Pregnancy-associated hemolytic uremic syndrome revisited in the era of complement gene mutations","author":"Fakhouri","year":"2010","journal-title":"J Am Soc Nephrol"},{"key":"key-10.4103\/0971-4065.293645-6","doi-asserted-by":"crossref","first-page":"508","DOI":"10.1016\/j.semnephrol.2013.08.003","article-title":"Atypical hemolytic uremic syndrome","author":"Kavanagh","year":"2013","journal-title":"Semin Nephrol"},{"key":"key-10.4103\/0971-4065.293645-7","doi-asserted-by":"crossref","first-page":"1844","DOI":"10.2215\/CJN.02210310","article-title":"Relative role of genetic complement abnormalities in sporadic and familial aHUS and their impact on clinical phenotype","author":"Noris","year":"2010","journal-title":"Clin J Am Soc Nephrol"},{"key":"key-10.4103\/0971-4065.293645-8","doi-asserted-by":"crossref","first-page":"170","DOI":"10.1016\/j.molimm.2013.06.001","article-title":"Complement factor H related proteins (CFHRs)","author":"Skerka","year":"2013","journal-title":"Mol Immunol"},{"key":"key-10.4103\/0971-4065.293645-9","doi-asserted-by":"crossref","first-page":"359","DOI":"10.1053\/j.ajkd.2015.03.040","article-title":"Glomerular diseases dependent on complement activation, including atypical hemolytic uremic syndrome, membranoproliferative glomerulonephritis, and C3 glomerulopathy: Core curriculum 2015","author":"Noris","year":"2015","journal-title":"Am J Kidney Dis"},{"key":"key-10.4103\/0971-4065.293645-10","doi-asserted-by":"crossref","first-page":"60","DOI":"10.1186\/1750-1172-6-60","article-title":"Atypical hemolytic uremic syndrome","author":"Loirat","year":"2011","journal-title":"Orphanet J Rare Dis"},{"key":"key-10.4103\/0971-4065.293645-11","doi-asserted-by":"crossref","first-page":"475","DOI":"10.1681\/ASN.2012090884","article-title":"Combined complement gene mutations in atypical hemolytic uremic syndrome influence clinical phenotype","author":"Bresin","year":"2013","journal-title":"J Am Soc Nephrol"},{"key":"key-10.4103\/0971-4065.293645-12","doi-asserted-by":"crossref","first-page":"2221","DOI":"10.1007\/s00467-013-2560-2","article-title":"A novel hybrid CFHR1\/CFH gene causes atypical hemolytic uremic syndrome","author":"Eyler","year":"2013","journal-title":"Pediatr Nephrol"},{"key":"key-10.4103\/0971-4065.293645-13","doi-asserted-by":"crossref","first-page":"209","DOI":"10.1681\/ASN.2013121339","article-title":"A novel atypical hemolytic uremic syndrome-associated hybrid CFHR1\/CFH gene encoding a fusion protein that antagonizes factor H-dependent complement regulation","author":"Valoti","year":"2015","journal-title":"J Am Soc Nephrol"}],"container-title":["Indian Journal of Nephrology"],"original-title":[],"language":"en","deposited":{"date-parts":[[2024,4,3]],"date-time":"2024-04-03T19:47:29Z","timestamp":1712173649000},"score":1,"resource":{"primary":{"URL":"https:\/\/indianjnephrol.org\/atypical-hus-associated-with-cfh-cfhr-1-hybrid-gene\/"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2020]]},"references-count":13,"journal-issue":{"issue":"5","published-print":{"date-parts":[[2020]]}},"alternative-id":["293645"],"URL":"https:\/\/doi.org\/10.4103\/ijn.ijn_347_19","relation":{},"ISSN":["0971-4065"],"issn-type":[{"value":"0971-4065","type":"print"}],"subject":[],"published":{"date-parts":[[2020]]}}}