{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,30]],"date-time":"2026-10-30T17:58:05Z","timestamp":1793383085497,"version":"4.5.0"},"reference-count":16,"publisher":"Elsevier BV","issue":"6","license":[{"start":{"date-parts":[[2017,12,1]],"date-time":"2017-12-01T00:00:00Z","timestamp":1512086400000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"},{"start":{"date-parts":[[2017,12,1]],"date-time":"2017-12-01T00:00:00Z","timestamp":1512086400000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/legal\/tdmrep-license"}],"funder":[{"name":"Foundation of Jiangsu Province Hospital of Traditional Chinese Medicine","award":["Y17005, Y17065"],"award-info":[{"award-number":["Y17005, Y17065"]}]}],"content-domain":{"domain":["clinicalkey.com","clinicalkey.com.au","clinicalkey.es","clinicalkey.fr","clinicalkey.jp","jpurol.com","elsevier.com","sciencedirect.com"],"crossmark-restriction":true},"short-container-title":["Journal of Pediatric Urology"],"published-print":{"date-parts":[[2017,12]]},"DOI":"10.1016\/j.jpurol.2017.05.021","type":"journal-article","created":{"date-parts":[[2017,6,24]],"date-time":"2017-06-24T04:48:51Z","timestamp":1498279731000},"page":"629.e1-629.e5","update-policy":"https:\/\/doi.org\/10.1016\/elsevier_cm_policy","source":"Crossref","is-referenced-by-count":12,"title":["Clinical and genetic characterization of Chinese pediatric cystine stone patients"],"prefix":"10.1016","volume":"13","author":[{"given":"Luming","family":"Shen","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Xiaoming","family":"Cong","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Xin","family":"Zhang","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Ninghong","family":"Wang","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Ping","family":"Zhou","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Yan","family":"Xu","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Qingyi","family":"Zhu","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Xiaojian","family":"Gu","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"78","reference":[{"key":"10.1016\/j.jpurol.2017.05.021_bib1","series-title":"The metabolic and molecular bases of inherited disease","first-page":"4909","article-title":"Cystinuria","author":"Palacin","year":"2001"},{"key":"10.1016\/j.jpurol.2017.05.021_bib2","doi-asserted-by":"crossref","first-page":"723","DOI":"10.1016\/j.jpedsurg.2010.09.013","article-title":"Infrared spectroscopic analysis of urinary stones (including stones induced by melamine-contaminated milk powder) in 189 Chinese children","volume":"46","author":"Sun","year":"2011","journal-title":"J Pediatr Surg"},{"issue":"5","key":"10.1016\/j.jpurol.2017.05.021_bib3","doi-asserted-by":"crossref","first-page":"339","DOI":"10.1007\/s00240-011-0362-1","article-title":"Infrared spectroscopic analysis of 5248 urinary stones from Chinese patients with the first stone","volume":"39","author":"Sun","year":"2011","journal-title":"Urol Res"},{"key":"10.1016\/j.jpurol.2017.05.021_bib4","first-page":"75","article-title":"Simultaneous determination of oxalate and citric acid in 24 hours urine by ion-chromatography","volume":"28","author":"Zhang","year":"2007","journal-title":"Chin J Urol"},{"issue":"9","key":"10.1016\/j.jpurol.2017.05.021_bib5","doi-asserted-by":"crossref","first-page":"527","DOI":"10.1365\/s10337-007-0210-1","article-title":"Simple, rapid, and accurate RP-HPLC method for determination of cystine in human urine after derivatization with dansyl chloride","volume":"65","author":"Wang","year":"2007","journal-title":"Chromatographia"},{"issue":"4","key":"10.1016\/j.jpurol.2017.05.021_bib6","doi-asserted-by":"crossref","first-page":"255","DOI":"10.1159\/000282232","article-title":"Aspects on estimation of the risk of calcium oxalate crystallization in urine","volume":"47","author":"Tiselius","year":"1991","journal-title":"Urol Int"},{"issue":"1","key":"10.1016\/j.jpurol.2017.05.021_bib7","doi-asserted-by":"crossref","first-page":"162","DOI":"10.1016\/S0022-5347(05)67487-3","article-title":"A study of the etiology of idiopathic calcium urolithiasis in children: hypocitruria is the most important risk factor","volume":"164","author":"Tekin","year":"2000","journal-title":"J Urol"},{"key":"10.1016\/j.jpurol.2017.05.021_bib8","doi-asserted-by":"crossref","first-page":"27","DOI":"10.1016\/S0022-5347(05)64824-0","article-title":"The impact of cystinuria on renal function","volume":"168","author":"Assimos","year":"2002","journal-title":"J Urol"},{"issue":"5","key":"10.1016\/j.jpurol.2017.05.021_bib9","doi-asserted-by":"crossref","first-page":"501","DOI":"10.1111\/j.1529-8817.2005.00185.x","article-title":"Molecular genetic analysis of SLC3A1 and SLC7A9 genes in Czech and Slovak cystinuric patients","volume":"69","author":"\u0160kopkov\u00e1","year":"2005","journal-title":"Ann Hum Genet"},{"issue":"4","key":"10.1016\/j.jpurol.2017.05.021_bib10","doi-asserted-by":"crossref","first-page":"305","DOI":"10.1093\/hmg\/10.4.305","article-title":"Functional analysis of mutations in SLC7A9, and genotype\u2013phenotype correlation in non-Type I cystinuria","volume":"10","author":"Font","year":"2001","journal-title":"Hum Mol Genet"},{"issue":"6","key":"10.1016\/j.jpurol.2017.05.021_bib11","doi-asserted-by":"crossref","first-page":"575","DOI":"10.1016\/j.jpurol.2005.11.011","article-title":"Identification of novel cystinuria mutations in pediatric patients","volume":"2","author":"Brauers","year":"2006","journal-title":"J Pediatr Urol"},{"issue":"6","key":"10.1016\/j.jpurol.2017.05.021_bib12","doi-asserted-by":"crossref","first-page":"417","DOI":"10.1007\/s00240-003-0366-6","article-title":"Urinary excretion of total cystine and the dibasic amino acids arginine, lysine and ornithine in relation to genetic findings in patients with cystinuria treated with sulfhydryl compounds","volume":"31","author":"Fjellstedt","year":"2003","journal-title":"Urol Res"},{"issue":"5","key":"10.1016\/j.jpurol.2017.05.021_bib13","doi-asserted-by":"crossref","first-page":"342","DOI":"10.5414\/CNP57342","article-title":"Analysis of the genes SLC7A9 and SLC3A1 in unclassified cystinurics: mutation detection rates and association between variants in SLC7A9 and the disease","volume":"57","author":"Schmidt","year":"2002","journal-title":"Clin Nephrol"},{"issue":"3","key":"10.1016\/j.jpurol.2017.05.021_bib14","doi-asserted-by":"crossref","first-page":"175","DOI":"10.1089\/gte.2005.9.175","article-title":"Identification of novel cystinuria mutations and polymorphisms in SLC3A1 and SLC7A9 genes: absence of SLC7A10 gene mutations in cystinuric patients","volume":"9","author":"Chatzikyriakidou","year":"2005","journal-title":"Genet Test"},{"issue":"6","key":"10.1016\/j.jpurol.2017.05.021_bib15","doi-asserted-by":"crossref","first-page":"1169","DOI":"10.1007\/s10545-005-0094-x","article-title":"Search for mutations in SLC1A5 (19q13) in cystinuria patients","volume":"28","author":"Brauers","year":"2005","journal-title":"J Inherit Metab Dis"},{"issue":"4","key":"10.1016\/j.jpurol.2017.05.021_bib16","doi-asserted-by":"crossref","first-page":"819","DOI":"10.1016\/S0022-5347(17)41019-6","article-title":"The spectrum of metabolic abnormalities in patients with cystine nephrolithiasis","volume":"141","author":"Sakhaee","year":"1989","journal-title":"J Urol"}],"container-title":["Journal of Pediatric Urology"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S1477513117302620?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S1477513117302620?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2025,10,26]],"date-time":"2025-10-26T13:44:08Z","timestamp":1761486248000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S1477513117302620"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2017,12]]},"references-count":16,"journal-issue":{"issue":"6","published-print":{"date-parts":[[2017,12]]}},"alternative-id":["S1477513117302620"],"URL":"https:\/\/doi.org\/10.1016\/j.jpurol.2017.05.021","relation":{},"ISSN":["1477-5131"],"issn-type":[{"value":"1477-5131","type":"print"}],"subject":[],"published":{"date-parts":[[2017,12]]},"assertion":[{"value":"Elsevier","name":"publisher","label":"This article is maintained by"},{"value":"Clinical and genetic characterization of Chinese pediatric cystine stone patients","name":"articletitle","label":"Article Title"},{"value":"Journal of Pediatric Urology","name":"journaltitle","label":"Journal Title"},{"value":"https:\/\/doi.org\/10.1016\/j.jpurol.2017.05.021","name":"articlelink","label":"CrossRef DOI link to publisher maintained version"},{"value":"article","name":"content_type","label":"Content Type"},{"value":"\u00a9 2017 Journal of Pediatric Urology Company. Published by Elsevier Ltd. All rights reserved.","name":"copyright","label":"Copyright"}]}}