{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,11,7]],"date-time":"2025-11-07T06:35:42Z","timestamp":1762497342906,"version":"build-2065373602"},"reference-count":21,"publisher":"Elsevier BV","issue":"3","license":[{"start":{"date-parts":[[2019,5,1]],"date-time":"2019-05-01T00:00:00Z","timestamp":1556668800000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"},{"start":{"date-parts":[[2019,5,1]],"date-time":"2019-05-01T00:00:00Z","timestamp":1556668800000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/legal\/tdmrep-license"},{"start":{"date-parts":[[2020,10,9]],"date-time":"2020-10-09T00:00:00Z","timestamp":1602201600000},"content-version":"vor","delay-in-days":527,"URL":"http:\/\/creativecommons.org\/licenses\/by-nc-nd\/4.0\/"}],"content-domain":{"domain":["aaceclinicalcasereports.com","elsevier.com","sciencedirect.com"],"crossmark-restriction":true},"short-container-title":["AACE Clinical Case Reports"],"published-print":{"date-parts":[[2019,5]]},"DOI":"10.4158\/accr-2018-0555","type":"journal-article","created":{"date-parts":[[2019,3,13]],"date-time":"2019-03-13T15:45:17Z","timestamp":1552491917000},"page":"e222-e225","update-policy":"https:\/\/doi.org\/10.1016\/elsevier_cm_policy","source":"Crossref","is-referenced-by-count":3,"title":["Ovarian Granulosa cell Tumor in a Patient with a Pathogenic Variant in the CDC73 Gene (Hyperparathyroidism-Jaw Tumor Syndrome)"],"prefix":"10.1016","volume":"5","author":[{"given":"Rowella Licup","family":"Sirbiladze","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Denise","family":"Uyar","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Jennifer L.","family":"Geurts","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Joseph L.","family":"Shaker","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"78","reference":[{"key":"10.4158\/ACCR-2018-0555_bb0010","first-page":"1006","article-title":"Hereditary hyperparathyroidism and multiple ossifying jaw fibromas: a clinically and genetically distinct syndrome","volume":"108","author":"Jackson","year":"1990","journal-title":"Surgery"},{"key":"10.4158\/ACCR-2018-0555_bb0015","doi-asserted-by":"crossref","first-page":"829","DOI":"10.7326\/0003-4819-49-4-829","article-title":"Hereditary hyperparathyroidism associated with recurrent pancreatitis","volume":"49","author":"Jackson","year":"1958","journal-title":"Ann Int Med"},{"key":"10.4158\/ACCR-2018-0555_bb0020","doi-asserted-by":"crossref","first-page":"676","DOI":"10.1038\/ng1048","article-title":"HRPT2, encoding parafibromin, is mutated in the hyperparathyroidism-jaw tumor syndrome","volume":"32","author":"Carpten","year":"2002","journal-title":"Nature Genet"},{"key":"10.4158\/ACCR-2018-0555_bb0025","first-page":"167","article-title":"The hyperparathyroidism-jaw tumour (HPT-JT) syndrome","volume":"3","author":"Bradley","year":"2006","journal-title":"Clin Cases Miner Bone Metab"},{"key":"10.4158\/ACCR-2018-0555_bb0030","doi-asserted-by":"crossref","first-page":"R229","DOI":"10.1530\/ERC-16-0059","article-title":"Endocrine neoplasms in familial syndromes of hyperparathyroidism","volume":"23","author":"Li","year":"2016","journal-title":"Endocr Relat Cancer"},{"key":"10.4158\/ACCR-2018-0555_bb0035","unstructured":"NM_024529.4(CDC73):c.687_688dupAG (p.Val230Glufs). Available at: https:\/\/www.ncbi.nlm.nih.gov\/clinvar\/variation\/241496\/. Accessed Month 1, 2019."},{"key":"10.4158\/ACCR-2018-0555_bb0040","doi-asserted-by":"crossref","first-page":"44","DOI":"10.1007\/s12672-011-0100-8","article-title":"Frequent germ-line mutations of the MEN1, CASR, and HRPT2\/CDC73 genes in young patients with clinically non-familial primary hyperparathyroidism","volume":"3","author":"Starker","year":"2012","journal-title":"Horm Cancer"},{"key":"10.4158\/ACCR-2018-0555_bb0045","doi-asserted-by":"crossref","first-page":"494","DOI":"10.1016\/0002-9610(81)90382-2","article-title":"Fibroosseous tumors of the facial skeleton in association with primary hyperparathyroidism: an endocrine syndrome or coincidence?","volume":"142","author":"Rosen","year":"1981","journal-title":"Am J Surg"},{"key":"10.4158\/ACCR-2018-0555_bb0050","first-page":"944","article-title":"Hereditary hyperparathyroidism-jaw tumor syndrome: the endocrine tumor gene HRPT2 maps to chromosome 1q21-q31","volume":"56","author":"Szab\u00f3","year":"1995","journal-title":"Am J Hum Genet"},{"key":"10.4158\/ACCR-2018-0555_bb0055","doi-asserted-by":"crossref","first-page":"477","DOI":"10.1530\/EJE-11-0003","article-title":"CDC73-related hereditary hyperparathyroidism: five new mutations and the clinical spectrum","volume":"165","author":"Frank-Raue","year":"2011","journal-title":"Euro J Endocrinol"},{"key":"10.4158\/ACCR-2018-0555_bb0060","doi-asserted-by":"crossref","first-page":"1","DOI":"10.1097\/00005792-200201000-00001","article-title":"Familial isolated hyperparathyroidism: clinical and genetic characteristics of 36 kindreds","volume":"81","author":"Simonds","year":"2002","journal-title":"Medicine"},{"key":"10.4158\/ACCR-2018-0555_bb0065","doi-asserted-by":"crossref","first-page":"634","DOI":"10.1046\/j.1365-2796.2003.01168.x","article-title":"Hyperparathroidism-jaw tumour syndrome","volume":"253","author":"Chen","year":"2003","journal-title":"J Int Med"},{"key":"10.4158\/ACCR-2018-0555_bb0070","doi-asserted-by":"crossref","first-page":"54","DOI":"10.7326\/0003-4819-107-1-54","article-title":"Familial cystic parathyroid adenomatosis","volume":"107","author":"Malette","year":"1987","journal-title":"Ann Int Med"},{"key":"10.4158\/ACCR-2018-0555_bb0075","doi-asserted-by":"crossref","first-page":"2827","DOI":"10.1210\/jc.2005-1239","article-title":"Diagnosis of parathyroid tumors in familial isolated hyperparathyroidism with HRPT2 mutation: implications for cancer surveillance","volume":"91","author":"Guarnieri","year":"2006","journal-title":"J Clin Endocrinol Metab"},{"key":"10.4158\/ACCR-2018-0555_bb0080","doi-asserted-by":"crossref","first-page":"186","DOI":"10.1530\/EC-13-0046","article-title":"CDC73 mutational status and loss of parafibromin in the outcome of parathyroid cancer","volume":"2","author":"Cetani","year":"2013","journal-title":"Endocr Connect"},{"key":"10.4158\/ACCR-2018-0555_bb0085","doi-asserted-by":"crossref","first-page":"1140","DOI":"10.1097\/01.pas.0000209827.39477.4f","article-title":"Loss of nuclear expression of parafibromin distinguishes parathyroid carcinomas and hyperparathyroidism-jaw tumor (HPT-JT) syndrome-related adenomas from sporadic parathyroid adenomas and hyperplasias","volume":"30","author":"Gill","year":"2006","journal-title":"Am J Surg Pathol"},{"key":"10.4158\/ACCR-2018-0555_bb0090","first-page":"4204","article-title":"Autosomal dominant primary hyperparathyroidism and jaw tumor syndrome associated with renal hamartomas and cystic kidney disease: linkage to 1q21-q32 and loss of the wild type allele in renal hamartomas","volume":"81","author":"Teh","year":"1996","journal-title":"J Clin Endocrinol Metab"},{"key":"10.4158\/ACCR-2018-0555_bb0095","doi-asserted-by":"crossref","first-page":"18","DOI":"10.1111\/j.1365-2796.2004.01421.x","article-title":"Uterine tumours are a phenotypic manifestation of the hyperparathyroidism-jaw tumour syndrome","volume":"257","author":"Bradley","year":"2005","journal-title":"J Int Med"},{"key":"10.4158\/ACCR-2018-0555_bb0100","doi-asserted-by":"crossref","first-page":"2719","DOI":"10.1056\/NEJMoa0902542","article-title":"Mutation of FOXL2 in granulosa-cell tumors of the ovary","volume":"360","author":"Shah","year":"2009","journal-title":"N Engl J Med"},{"key":"10.4158\/ACCR-2018-0555_bb0105","doi-asserted-by":"crossref","first-page":"109","DOI":"10.1210\/er.2011-0014","article-title":"Molecular pathogenesis of granulosa cell tumors of the ovary","volume":"33","author":"Jamieson","year":"2012","journal-title":"Endocr Rev"},{"key":"10.4158\/ACCR-2018-0555_bb0110","doi-asserted-by":"crossref","first-page":"2909","DOI":"10.1007\/s13277-015-4103-x","article-title":"The roles of parafibromin expression in ovarian epithelial carcinomas: a marker for differentiation and prognosis and a target for gene therapy","volume":"37","author":"Shen","year":"2016","journal-title":"Tumor Biol"}],"container-title":["AACE Clinical Case Reports"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S237606052030403X?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S237606052030403X?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2025,11,7]],"date-time":"2025-11-07T06:30:47Z","timestamp":1762497047000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S237606052030403X"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2019,5]]},"references-count":21,"journal-issue":{"issue":"3","published-print":{"date-parts":[[2019,5]]}},"alternative-id":["S237606052030403X"],"URL":"https:\/\/doi.org\/10.4158\/accr-2018-0555","relation":{},"ISSN":["2376-0605"],"issn-type":[{"type":"print","value":"2376-0605"}],"subject":[],"published":{"date-parts":[[2019,5]]},"assertion":[{"value":"Elsevier","name":"publisher","label":"This article is maintained by"},{"value":"Ovarian Granulosa cell Tumor in a Patient with a Pathogenic Variant in the CDC73 Gene (Hyperparathyroidism-Jaw Tumor Syndrome)","name":"articletitle","label":"Article Title"},{"value":"AACE Clinical Case Reports","name":"journaltitle","label":"Journal Title"},{"value":"https:\/\/doi.org\/10.4158\/ACCR-2018-0555","name":"articlelink","label":"CrossRef DOI link to publisher maintained version"},{"value":"article","name":"content_type","label":"Content Type"},{"value":"Copyright \u00a9 2019 Elsevier Inc.","name":"copyright","label":"Copyright"}]}}