{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,10,26]],"date-time":"2025-10-26T21:29:31Z","timestamp":1761514171760,"version":"build-2065373602"},"reference-count":18,"publisher":"Elsevier BV","issue":"3","license":[{"start":{"date-parts":[[2018,9,1]],"date-time":"2018-09-01T00:00:00Z","timestamp":1535760000000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"},{"start":{"date-parts":[[2018,9,1]],"date-time":"2018-09-01T00:00:00Z","timestamp":1535760000000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/legal\/tdmrep-license"}],"content-domain":{"domain":["ajkd.org","clinicalkey.com","clinicalkey.com.au","clinicalkey.es","clinicalkey.fr","clinicalkey.jp","elsevier.com","sciencedirect.com"],"crossmark-restriction":true},"short-container-title":["American Journal of Kidney Diseases"],"published-print":{"date-parts":[[2018,9]]},"DOI":"10.1053\/j.ajkd.2017.12.020","type":"journal-article","created":{"date-parts":[[2018,3,18]],"date-time":"2018-03-18T19:12:34Z","timestamp":1521400354000},"page":"457-461","update-policy":"https:\/\/doi.org\/10.1016\/elsevier_cm_policy","source":"Crossref","is-referenced-by-count":4,"title":["Dialysis as a Treatment Option for a Patient With Normal Kidney Function and Familial Tumoral Calcinosis Due to a Compound Heterozygous FGF23 Mutation"],"prefix":"10.1053","volume":"72","author":[{"given":"Patr\u00edcia T.","family":"Goldenstein","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Precil D.","family":"Neves","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Bruno E.","family":"Balbo","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Rosilene M.","family":"Elias","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Alexandre C.","family":"Pereira","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Luiz F.","family":"Onuchic","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Harald","family":"J\u00fcppner","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Vanda","family":"Jorgetti","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Hugo","family":"Abensur","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Rosa Maria","family":"Moys\u00e9s","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"78","reference":[{"issue":"3","key":"10.1053\/j.ajkd.2017.12.020_bib1","doi-asserted-by":"crossref","first-page":"652","DOI":"10.1038\/jid.2009.337","article-title":"Familial tumoral calcinosis: from characterization of a rare pheynotype to the pathogenesis of ectopic calcification","volume":"130","author":"Sprecher","year":"2010","journal-title":"J\u00a0Invest Dermatol"},{"key":"10.1053\/j.ajkd.2017.12.020_bib2","doi-asserted-by":"crossref","first-page":"248","DOI":"10.1038\/nmeth0410-248","article-title":"A\u00a0method and server for predicting damaging missense mutations","volume":"7","author":"Adzhubei","year":"2010","journal-title":"Nat Methods"},{"key":"10.1053\/j.ajkd.2017.12.020_bib3","first-page":"1015","article-title":"Sur la calcification tibernale","volume":"10","author":"Giard","year":"1898","journal-title":"CR Soc Biol"},{"key":"10.1053\/j.ajkd.2017.12.020_bib4","first-page":"725","article-title":"Tumeurs multiples and singuliers de bourses sereuses","volume":"74","author":"Duret","year":"1899","journal-title":"Bull M\u00e9m Soc Anat Paris"},{"key":"10.1053\/j.ajkd.2017.12.020_bib5","doi-asserted-by":"crossref","first-page":"490","DOI":"10.1001\/jama.1943.02840070018005","article-title":"Tumoral calcinosis","volume":"121","author":"Inclan","year":"1943","journal-title":"J\u00a0Am Med Assoc"},{"issue":"1","key":"10.1053\/j.ajkd.2017.12.020_bib6","doi-asserted-by":"crossref","first-page":"215","DOI":"10.1148\/radiology.174.1.2294551","article-title":"Imaging of tumoral calcinosis: new observations","volume":"174","author":"Martinez","year":"1990","journal-title":"Radiology"},{"issue":"5637","key":"10.1053\/j.ajkd.2017.12.020_bib7","doi-asserted-by":"crossref","first-page":"153","DOI":"10.1136\/bmj.1.5637.142-a","article-title":"Tumoral calcinosis\u2013an unrecognized disease","volume":"1","author":"McClatchie","year":"1969","journal-title":"Br Med J"},{"key":"10.1053\/j.ajkd.2017.12.020_bib8","doi-asserted-by":"crossref","first-page":"105","DOI":"10.1016\/0002-9343(65)90164-6","article-title":"Tumoral calcinosis: a metabolic disease of obscure etiology","volume":"38","author":"Lafferty","year":"1965","journal-title":"Am J Med"},{"issue":"3","key":"10.1053\/j.ajkd.2017.12.020_bib9","doi-asserted-by":"crossref","first-page":"871","DOI":"10.1148\/rg.263055099","article-title":"Tumoral calcinosis: pearls, polemics, and alternative possibilities","volume":"26","author":"Olsen","year":"2006","journal-title":"Radiographics"},{"issue":"2","key":"10.1053\/j.ajkd.2017.12.020_bib10","doi-asserted-by":"crossref","first-page":"78","DOI":"10.1007\/s11914-015-0254-3","article-title":"Hyperphosphatemic familial tumoral calcinosis: genetic models of deficient FGF23 action","volume":"13","author":"Folsom","year":"2015","journal-title":"Curr Osteoporos Rep"},{"issue":"6","key":"10.1053\/j.ajkd.2017.12.020_bib11","doi-asserted-by":"crossref","first-page":"579","DOI":"10.1038\/ng1358","article-title":"Mutations in GALNT3, encoding a protein involved in O-linked glycosylation, cause familial tumoral calcinosis","volume":"36","author":"Topaz","year":"2004","journal-title":"Nat Genet"},{"issue":"3","key":"10.1053\/j.ajkd.2017.12.020_bib12","doi-asserted-by":"crossref","first-page":"385","DOI":"10.1093\/hmg\/ddi034","article-title":"An FGF23 missense mutation causes familial tumoral calcinosis with hyperphosphatemia","volume":"14","author":"Benet-Pag\u00e8s","year":"2005","journal-title":"Hum Mol Genet"},{"issue":"4","key":"10.1053\/j.ajkd.2017.12.020_bib13","doi-asserted-by":"crossref","first-page":"2424","DOI":"10.1210\/jc.2004-2238","article-title":"A\u00a0novel recessive mutation in fibroblast growth factor-23 causes familial tumoral calcinosis","volume":"90","author":"Larsson","year":"2005","journal-title":"J\u00a0Clin Endocrinol Metab"},{"issue":"4","key":"10.1053\/j.ajkd.2017.12.020_bib14","first-page":"318","article-title":"A\u00a0homozygous missense mutation in human KLOTHO causes severe tumoral calcinosis","volume":"7","author":"Ichikawa","year":"2007","journal-title":"J\u00a0Musculoskelet Neuronal Interact"},{"issue":"5","key":"10.1053\/j.ajkd.2017.12.020_bib15","doi-asserted-by":"crossref","first-page":"735","DOI":"10.1016\/j.berh.2011.10.020","article-title":"Hyperphosphatemic familial tumoral calcinosis (FGF23, GALNT3, \u03b1Klotho)","volume":"25","author":"Farrow","year":"2011","journal-title":"Best Pract Res Clin Rheumatol"},{"issue":"4","key":"10.1053\/j.ajkd.2017.12.020_bib16","doi-asserted-by":"crossref","first-page":"896","DOI":"10.1002\/ajmg.a.33337","article-title":"Clinical variability of familial tumoral calcinosis caused by novel GALNT3 mutations","volume":"152A","author":"Ichikawa","year":"2010","journal-title":"Am J Med Genet A"},{"issue":"4","key":"10.1053\/j.ajkd.2017.12.020_bib17","doi-asserted-by":"crossref","first-page":"648","DOI":"10.1210\/jcem-50-4-648","article-title":"Phosphorus excretion in tumoral calcinosis: response to parathyroid hormone and acetazolamide","volume":"50","author":"Lufkin","year":"1980","journal-title":"J\u00a0Clin Endocrinol Metab"},{"issue":"8","key":"10.1053\/j.ajkd.2017.12.020_bib18","doi-asserted-by":"crossref","first-page":"1244","DOI":"10.2106\/00004623-198971080-00019","article-title":"Tumoral calcinosis: successful medical treatment. A case report","volume":"71","author":"Gregosiewicz","year":"1989","journal-title":"J\u00a0Bone Joint Surg Am"}],"container-title":["American Journal of Kidney Diseases"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0272638618301239?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0272638618301239?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2025,10,3]],"date-time":"2025-10-03T03:16:05Z","timestamp":1759461365000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S0272638618301239"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2018,9]]},"references-count":18,"journal-issue":{"issue":"3","published-print":{"date-parts":[[2018,9]]}},"alternative-id":["S0272638618301239"],"URL":"https:\/\/doi.org\/10.1053\/j.ajkd.2017.12.020","relation":{},"ISSN":["0272-6386"],"issn-type":[{"type":"print","value":"0272-6386"}],"subject":[],"published":{"date-parts":[[2018,9]]},"assertion":[{"value":"Elsevier","name":"publisher","label":"This article is maintained by"},{"value":"Dialysis as a Treatment Option for a Patient With Normal Kidney Function and Familial Tumoral Calcinosis Due to a Compound Heterozygous FGF23 Mutation","name":"articletitle","label":"Article Title"},{"value":"American Journal of Kidney Diseases","name":"journaltitle","label":"Journal Title"},{"value":"https:\/\/doi.org\/10.1053\/j.ajkd.2017.12.020","name":"articlelink","label":"CrossRef DOI link to publisher maintained version"},{"value":"article","name":"content_type","label":"Content Type"},{"value":"\u00a9 2018 by the National Kidney Foundation, Inc.","name":"copyright","label":"Copyright"}]}}