{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,10,22]],"date-time":"2025-10-22T20:43:44Z","timestamp":1761165824527,"version":"build-2065373602"},"reference-count":9,"publisher":"Elsevier BV","issue":"2","license":[{"start":{"date-parts":[[2011,4,1]],"date-time":"2011-04-01T00:00:00Z","timestamp":1301616000000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"},{"start":{"date-parts":[[2011,4,1]],"date-time":"2011-04-01T00:00:00Z","timestamp":1301616000000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/legal\/tdmrep-license"}],"content-domain":{"domain":["clinicalkey.com","clinicalkey.com.au","clinicalkey.es","clinicalkey.fr","clinicalkey.jp","jaapos.org","elsevier.com","sciencedirect.com"],"crossmark-restriction":true},"short-container-title":["Journal of American Association for Pediatric Ophthalmology and Strabismus"],"published-print":{"date-parts":[[2011,4]]},"DOI":"10.1016\/j.jaapos.2011.02.004","type":"journal-article","created":{"date-parts":[[2011,5,22]],"date-time":"2011-05-22T21:39:03Z","timestamp":1306100343000},"page":"205-207","update-policy":"https:\/\/doi.org\/10.1016\/elsevier_cm_policy","source":"Crossref","is-referenced-by-count":26,"title":["Uveitis in Blau syndrome from a de novo mutation of the NOD2\/CARD15 gene"],"prefix":"10.1016","volume":"15","author":[{"given":"Veena Rao","family":"Raiji","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Marijean M.","family":"Miller","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"L.K.","family":"Jung","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"78","reference":[{"key":"10.1016\/j.jaapos.2011.02.004_bib1","doi-asserted-by":"crossref","first-page":"801","DOI":"10.1016\/0002-9343(85)90286-4","article-title":"Familial granulomatous synovitis, uveitis, and cranial neuropathies","volume":"78","author":"Jabs","year":"1985","journal-title":"Am J Med"},{"key":"10.1016\/j.jaapos.2011.02.004_bib2","doi-asserted-by":"crossref","first-page":"3041","DOI":"10.1002\/art.10618","article-title":"CARD15 mutations in familial granulomatosis syndromes: A study of the original Blau syndrome kindred and other families with large-vessel arteritis and cranial neuropathy","volume":"46","author":"Wang","year":"2002","journal-title":"Arthritis Rheum"},{"key":"10.1016\/j.jaapos.2011.02.004_bib3","doi-asserted-by":"crossref","first-page":"2040","DOI":"10.1016\/S0161-6420(03)00717-6","article-title":"Ocular manifestations in Blau syndrome associated with a CARD15\/Nod2 mutation","volume":"110","author":"Kurokawa","year":"2003","journal-title":"Ophthalmology"},{"key":"10.1016\/j.jaapos.2011.02.004_bib4","doi-asserted-by":"crossref","first-page":"729","DOI":"10.1016\/S0002-9394(03)00569-5","article-title":"With a mere nod, uveitis enters a new era","volume":"136","author":"Rosenbaum","year":"2003","journal-title":"Am J Ophthalmol"},{"key":"10.1016\/j.jaapos.2011.02.004_bib5","doi-asserted-by":"crossref","first-page":"3805","DOI":"10.1002\/art.22966","article-title":"NOD2 gene-associated pediatric granulomatous arthritis: Clinical diversity, novel and recurrent mutations, and evidence of clinical improvement with Interleukin-1 blockade in a Spanish cohort","volume":"56","author":"Arostegui","year":"2007","journal-title":"Arthritis and Rheumatism"},{"key":"10.1016\/j.jaapos.2011.02.004_bib6","doi-asserted-by":"crossref","first-page":"3455","DOI":"10.1073\/pnas.0530276100","article-title":"Gene\u2013environment interaction modulated by allelic heterogeneity in inflammatory diseases","volume":"100","author":"Chamaillard","year":"2003","journal-title":"Proc Natl Acad Sci U S A"},{"key":"10.1016\/j.jaapos.2011.02.004_bib7","doi-asserted-by":"crossref","first-page":"242","DOI":"10.1002\/art.24134","article-title":"Role of the NOD2 genotype in the clinical phenotype of Blau syndrome and early-onset sarcoidosis","volume":"60","author":"Okafujim","year":"2009","journal-title":"Arth Rheum"},{"key":"10.1016\/j.jaapos.2011.02.004_bib8","doi-asserted-by":"crossref","first-page":"515","DOI":"10.1111\/j.1442-200X.1994.tb03237.x","article-title":"Preschool sarcoidosis manifesting as juvenile rheumatoid arthritis: A case report and a review of the literature of Japanese cases","volume":"36","author":"Ukae","year":"1994","journal-title":"Acta Paediatrica Japonica (Overseas Edition)"},{"key":"10.1016\/j.jaapos.2011.02.004_bib9","doi-asserted-by":"crossref","first-page":"1195","DOI":"10.1182\/blood-2004-07-2972","article-title":"Early-onset sarcoidosis and CARD15 mutations with constitutive nuclear factor-B activation: Common genetic etiology with Blau syndrome","volume":"105","author":"Kanazawa","year":"2005","journal-title":"Blood"}],"container-title":["Journal of American Association for Pediatric Ophthalmology and Strabismus"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S1091853111002527?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S1091853111002527?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2025,10,21]],"date-time":"2025-10-21T20:17:38Z","timestamp":1761077858000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S1091853111002527"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2011,4]]},"references-count":9,"journal-issue":{"issue":"2","published-print":{"date-parts":[[2011,4]]}},"alternative-id":["S1091853111002527"],"URL":"https:\/\/doi.org\/10.1016\/j.jaapos.2011.02.004","relation":{},"ISSN":["1091-8531"],"issn-type":[{"type":"print","value":"1091-8531"}],"subject":[],"published":{"date-parts":[[2011,4]]},"assertion":[{"value":"Elsevier","name":"publisher","label":"This article is maintained by"},{"value":"Uveitis in Blau syndrome from a de novo mutation of the NOD2\/CARD15 gene","name":"articletitle","label":"Article Title"},{"value":"Journal of American Association for Pediatric Ophthalmology and Strabismus","name":"journaltitle","label":"Journal Title"},{"value":"https:\/\/doi.org\/10.1016\/j.jaapos.2011.02.004","name":"articlelink","label":"CrossRef DOI link to publisher maintained version"},{"value":"article","name":"content_type","label":"Content Type"},{"value":"Copyright \u00a9 2011 American Association for Pediatric Ophthalmology and Strabismus. Published by Mosby, Inc. All rights reserved.","name":"copyright","label":"Copyright"}]}}