{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,6,23]],"date-time":"2026-06-23T13:23:22Z","timestamp":1782221002328,"version":"3.54.5"},"reference-count":17,"publisher":"International Research and Cooperation Association for Bio & Socio-Sciences Advancement (IRCA-BSSA)","issue":"4","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["IRDR"],"published-print":{"date-parts":[[2016]]},"DOI":"10.5582\/irdr.2016.01058","type":"journal-article","created":{"date-parts":[[2016,9,11]],"date-time":"2016-09-11T22:04:56Z","timestamp":1473631496000},"page":"297-300","source":"Crossref","is-referenced-by-count":8,"title":["Dent's disease complicated by nephrotic syndrome: A case report"],"prefix":"10.5582","volume":"5","author":[{"given":"Guohua","family":"He","sequence":"first","affiliation":[{"name":"Pediatrics, Peking University First Hospital"},{"name":"Pediatrics, Foshan Maternal and Children's Hospital"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Hongwen","family":"Zhang","sequence":"additional","affiliation":[{"name":"Pediatrics, Peking University First Hospital"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Shanshan","family":"Cao","sequence":"additional","affiliation":[{"name":"Pediatrics, Peking University First Hospital"},{"name":"Health Center, Beijing Entry-Exit Inspection and Quarantine Bureau"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Huijie","family":"Xiao","sequence":"additional","affiliation":[{"name":"Pediatrics, Peking University First Hospital"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Yong","family":"Yao","sequence":"additional","affiliation":[{"name":"Pediatrics, Peking University First Hospital"}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"3542","reference":[{"key":"1","unstructured":"1. Wrong OM, Norden AG, Feest TG. Dent's disease; a familial proximal renal tubular syndrome with low-molecular-weight proteinuria, hypercalciuria, nephrocalcinosis, metabolic bone disease, progressive renal failure and a marked male predominance. QJM. 1994; 87:473-493."},{"key":"2","doi-asserted-by":"crossref","unstructured":"2. Frymoyer PA, Scheinman SJ, Dunham PB, Jones DB, Hueber P, Schroeder ET. X-linked recessive nephrolithiasis with renal failure. N Engl J Med. 1991; 325:681-686.","DOI":"10.1056\/NEJM199109053251003"},{"key":"3","doi-asserted-by":"crossref","unstructured":"3. Devuyst O, Thakker RV. Dent's disease. Orphanet J Rare Dis. 2010; 5:28.","DOI":"10.1186\/1750-1172-5-28"},{"key":"4","doi-asserted-by":"crossref","unstructured":"4. Reinhart SC, Norden AG, Lapsley M, Thakker RV, Pang J, Moses AM, Frymoyer PA, Favus MJ, Hoepner JA, Scheinman SJ. Characterization of carrier females and affected males with X-linked recessive nephrolithiasis. J Am Soc Nephrol. 1995; 5:1451-1461.","DOI":"10.1681\/ASN.V571451"},{"key":"5","doi-asserted-by":"crossref","unstructured":"5. Wu F, Reed AA, Williams SE, Loh NY, et al. Mutational analysis of CLC-5, cofilin and CLC-4 in patients with Dent's disease. Nephron Physiol. 2009; 112:p53-p62.","DOI":"10.1159\/000225944"},{"key":"6","doi-asserted-by":"crossref","unstructured":"6. Frishberg Y, Dinour D, Belostotsky R, Becker-Cohen R, Rinat C, Feinstein S, Navon-Elkan P, Ben-Shalom E. Dent's disease manifesting as focal glomerulosclerosis: Is it the tip of the iceberg? Pediatr Nephrol. 2009; 24:2369-2373.","DOI":"10.1007\/s00467-009-1299-2"},{"key":"7","doi-asserted-by":"crossref","unstructured":"7. Valina MR, Larsen CP, Kanosky S, Suchy SF, Nield LS, Onder AM. A novel CLCN5 mutation in a boy with asymptomatic proteinuria and focal global glomerulosclerosis. Clin Nephrol. 2013; 80:377-384.","DOI":"10.5414\/CN107429"},{"key":"8","doi-asserted-by":"crossref","unstructured":"8. De Mutiis C, Pasini A, La Scola C, Pugliese F, Montini G. Nephrotic-range Albuminuria as the presenting symptom of Dent-2 disease. Ital J Pediatr. 2015; 41:46.","DOI":"10.1186\/s13052-015-0152-4"},{"key":"9","doi-asserted-by":"crossref","unstructured":"9. Cho HY, Lee BH, Choi HJ, Ha IS, Choi Y, Cheong HI. Renal manifestations of Dent disease and Lowe syndrome. Pediatr Nephrol. 2008; 23:243-249.","DOI":"10.1007\/s00467-007-0686-9"},{"key":"10","doi-asserted-by":"crossref","unstructured":"10. Mehta ZB, Pietka G, Lowe M. The cellular and physiological functions of the Lowe syndrome protein OCRL1.Traffic. 2014; 15:471-487.","DOI":"10.1111\/tra.12160"},{"key":"11","doi-asserted-by":"crossref","unstructured":"11. Norden AG, Lapsley M, Unwin RJ. Urine retinol-binding protein 4: A functional biomarker of the proximal renal tubule. Adv Clin Chem. 2014; 63:85-122.","DOI":"10.1016\/B978-0-12-800094-6.00003-0"},{"key":"12","doi-asserted-by":"crossref","unstructured":"12. Norden AG, Scheinman SJ, Deschodt-Lanckman MM, Lapsley M, Nortier JL, Thakker RV, Unwin RJ, Wrong O. Tubular proteinuria defined by a study of Dent's (CLCN5 mutation) and other tubular diseases. Kidney Int. 2000; 57:240-249.","DOI":"10.1046\/j.1523-1755.2000.00847.x"},{"key":"13","doi-asserted-by":"crossref","unstructured":"13. Vaisbich MH, Henriques Ldos S, Igarashi T, Sekine T, Seki G, Koch VH. The long-term use of enalapril and hydrochlorothiazide in two novel mutations patients with Dent's disease type 1. J Bras Nefrol. 2012; 34:78-81.","DOI":"10.1590\/S0101-28002012000100013"},{"key":"14","doi-asserted-by":"crossref","unstructured":"14. Blanchard A, Vargas-Poussou R, Peyrard S, Mogenet A, Baudouin V, Boudailliez B, Charbit M, Deschesnes G, Ezzhair N, Loirat C, Macher MA, Niaudet P, Azizi M. Effect of hydrochlorothiazide on urinary calcium excretion in Dent disease: An uncontrolled trial. Am J Kidney Dis. 2008; 52:1084-1095.","DOI":"10.1053\/j.ajkd.2008.08.021"},{"key":"15","doi-asserted-by":"crossref","unstructured":"15. Szczepanska M, Zaniew M, Recker F, Mizerska-Wasiak M, Zaluska-Lesniewska I, Kilis-Pstrusinska K, Adamczyk P, Zawadzki J, Pawlaczyk K, Ludwig M, Sikora P. Dent disease in children: Diagnostic and therapeutic considerations. Clin Nephrol. 2015; 84:222-230.","DOI":"10.5414\/CN108522"},{"key":"16","doi-asserted-by":"publisher","unstructured":"16. Liakos CI, Vyssoulis GP, Markou MI, Kafkas NV, Toutouzas KP, Tousoulis D. Twenty-four-hour urine alpha-microglobulin as a marker of hypertension-induced renal impairment and its response on different blood pressure-lowering drugs. J Clin Hypertens (Greenwich). 2016. doi: 10.1111\/jch.12811.","DOI":"10.1111\/jch.12811"},{"key":"17","doi-asserted-by":"crossref","unstructured":"17. Saif A, Soliman N. Urinary \u03b11-microglobulin and albumin excretion in children and adolescents with type 1 diabetes. J Diabetes. 2016. doi: 10.1111\/1753-0407.12383.","DOI":"10.1111\/1753-0407.12383"}],"container-title":["Intractable & Rare Diseases Research"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/www.jstage.jst.go.jp\/article\/irdr\/5\/4\/5_2016.01058\/_pdf","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2022,7,8]],"date-time":"2022-07-08T03:56:26Z","timestamp":1657252586000},"score":1,"resource":{"primary":{"URL":"https:\/\/www.jstage.jst.go.jp\/article\/irdr\/5\/4\/5_2016.01058\/_article"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2016]]},"references-count":17,"journal-issue":{"issue":"4","published-print":{"date-parts":[[2016]]}},"URL":"https:\/\/doi.org\/10.5582\/irdr.2016.01058","relation":{},"ISSN":["2186-361X","2186-3644"],"issn-type":[{"value":"2186-361X","type":"electronic"},{"value":"2186-3644","type":"print"}],"subject":[],"published":{"date-parts":[[2016]]}}}