{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,12,6]],"date-time":"2025-12-06T05:01:25Z","timestamp":1764997285986},"reference-count":11,"publisher":"Springer Science and Business Media LLC","issue":"2","license":[{"start":{"date-parts":[[2020,2,12]],"date-time":"2020-02-12T00:00:00Z","timestamp":1581465600000},"content-version":"tdm","delay-in-days":0,"URL":"http:\/\/www.springer.com\/tdm"},{"start":{"date-parts":[[2020,2,12]],"date-time":"2020-02-12T00:00:00Z","timestamp":1581465600000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/www.springer.com\/tdm"}],"content-domain":{"domain":["link.springer.com"],"crossmark-restriction":false},"short-container-title":["Familial Cancer"],"published-print":{"date-parts":[[2020,4]]},"DOI":"10.1007\/s10689-019-00152-6","type":"journal-article","created":{"date-parts":[[2020,2,12]],"date-time":"2020-02-12T09:02:47Z","timestamp":1581498167000},"page":"189-192","update-policy":"http:\/\/dx.doi.org\/10.1007\/springer_crossmark_policy","source":"Crossref","is-referenced-by-count":11,"title":["Co-occurrence of multiple endocrine neoplasia type 4 and spinal neurofibromatosis: a case report"],"prefix":"10.1007","volume":"19","author":[{"given":"Pamela","family":"Brock","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Jean","family":"Bustamante Alvarez","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Amir","family":"Mortazavi","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Sameek","family":"Roychowdhury","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"John","family":"Phay","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Raheela A.","family":"Khawaja","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Manisha H.","family":"Shah","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Bhavana","family":"Konda","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"297","published-online":{"date-parts":[[2020,2,12]]},"reference":[{"issue":"10","key":"152_CR1","doi-asserted-by":"publisher","first-page":"T195","DOI":"10.1530\/ERC-17-0243","volume":"24","author":"R Alrezk","year":"2017","unstructured":"Alrezk R, Hannah-Shmouni F, Stratakis CA (2017) MEN4 and CDKN1B mutations: the latest of the MEN syndromes. Endocr Relat Cancer 24(10):T195\u2013T208","journal-title":"Endocr Relat Cancer"},{"issue":"42","key":"152_CR2","doi-asserted-by":"publisher","first-page":"15558","DOI":"10.1073\/pnas.0603877103","volume":"103","author":"N Pellegata","year":"2006","unstructured":"Pellegata N, Quintanilla-Martinez L, Siggelkow H, Samson E, Bink K, Hofler H, Fend F, Graw J, Atkinson M (2006) Germ-line mutations in p27Kip1 cause a multiple endocrine neoplasia syndrome in rats and humans. Proc Natl Acad Sci USA 103(42):15558\u201315563","journal-title":"Proc Natl Acad Sci USA"},{"key":"152_CR3","doi-asserted-by":"publisher","first-page":"1923","DOI":"10.1212\/WNL.41.12.1923","volume":"41","author":"S Pulst","year":"1991","unstructured":"Pulst S, Riccardi V, Fain P, Korenberg J (1991) Familial spinal neurofibromatosis: clinical and DNA linkage analysis. Neurology 41:1923\u20131927","journal-title":"Neurology"},{"issue":"1","key":"152_CR4","doi-asserted-by":"publisher","first-page":"45","DOI":"10.1186\/s13052-018-0483-z","volume":"44","author":"G Corsello","year":"2018","unstructured":"Corsello G, Antona V, Serra G, Zara F, Giambrone C, Lagalla L, Piccione M, Piro E (2018) Clinical and molecular characterization of 112 single-center patients with Neurofibromatosis type 1. Ital J Pediatr 44(1):45","journal-title":"Ital J Pediatr"},{"issue":"9","key":"152_CR5","doi-asserted-by":"publisher","first-page":"3637","DOI":"10.1210\/jc.2019-00082","volume":"104","author":"A Frederiksen","year":"2019","unstructured":"Frederiksen A, Rossing M, Hermann P, Ejersed C, Thakker R, Frost M (2019) Clinical features of multiple endocrine neoplasia type 4: novel pathogenic variant and review of published cases. J Clin Endocrinol Metab 104(9):3637\u20133646","journal-title":"J Clin Endocrinol Metab"},{"issue":"7","key":"152_CR6","doi-asserted-by":"publisher","first-page":"1169","DOI":"10.1093\/hmg\/6.7.1169","volume":"6","author":"S Agarwal","year":"1997","unstructured":"Agarwal S, Kester M, Debelenko L, Heppner C, Emmert-Buck M, Skarulis M, Doppman J, Kim Y, Lubensky I, Zhuang A et al (1997) Germline mutations of the MEN1 gene in familial multiple endocrine neoplasia type 1 and related states. Hum Mol Genet 6(7):1169\u20131175","journal-title":"Hum Mol Genet"},{"key":"152_CR7","doi-asserted-by":"publisher","first-page":"1177","DOI":"10.1093\/hmg\/6.7.1177","volume":"6","author":"European Consortium on MEN1","year":"1997","unstructured":"European Consortium on MEN1 (1997) Identification of the multiple endocrine neoplasia type 1 (MEN1) gene. Hum Mol Genet 6:1177\u20131183","journal-title":"Hum Mol Genet"},{"issue":"2","key":"152_CR8","doi-asserted-by":"publisher","first-page":"169","DOI":"10.1111\/j.1365-2265.2005.02190.x","volume":"62","author":"S Ellard","year":"2005","unstructured":"Ellard S, Hattersley AT, Brewer CM, Vaidya B (2005) Detection of an MEN1 gene mutation depends on clinical features and supports current referral criteria for diagnostic molecular genetic testing. Clin Endocrinol 62(2):169\u2013175","journal-title":"Clin Endocrinol"},{"key":"152_CR9","doi-asserted-by":"publisher","first-page":"1582","DOI":"10.1016\/S0022-5347(05)68171-2","volume":"162","author":"M Walther","year":"1999","unstructured":"Walther M, Herring J, Enquiest E, Keiser H, Linehand W (1999) Von Recklinghausen\u2019s disease and pheochromocytomas. J Urol 162:1582\u20131586","journal-title":"J Urol"},{"issue":"5","key":"152_CR10","doi-asserted-by":"publisher","first-page":"460","DOI":"10.1590\/2359-3997000000092","volume":"59","author":"AM Favere","year":"2015","unstructured":"Favere AM, Tsukumo DM, Matos PS, Santos SL, Lalli CA (2015) Association between atypical parathyroid adenoma and neurofibromatosis. Arch Endocrinol Metab 59(5):460\u2013466","journal-title":"Arch Endocrinol Metab"},{"issue":"5","key":"152_CR11","doi-asserted-by":"publisher","first-page":"401","DOI":"10.1111\/cge.12498","volume":"87","author":"M Ruggieri","year":"2015","unstructured":"Ruggieri M, Polizzi A, Spalice A, Salpietro V, Caltabiano R, D\u2019Orazi V, Pavone P, Pirrone C, Magro G, Platania N et al (2015) The natural history of spinal neurofibromatosis: a critical review of clinical and genetic features. Clin Genet 87(5):401\u2013410","journal-title":"Clin Genet"}],"container-title":["Familial Cancer"],"original-title":[],"language":"en","link":[{"URL":"http:\/\/link.springer.com\/content\/pdf\/10.1007\/s10689-019-00152-6.pdf","content-type":"application\/pdf","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/link.springer.com\/article\/10.1007\/s10689-019-00152-6\/fulltext.html","content-type":"text\/html","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/link.springer.com\/content\/pdf\/10.1007\/s10689-019-00152-6.pdf","content-type":"application\/pdf","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2021,2,11]],"date-time":"2021-02-11T14:37:31Z","timestamp":1613054251000},"score":1,"resource":{"primary":{"URL":"http:\/\/link.springer.com\/10.1007\/s10689-019-00152-6"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2020,2,12]]},"references-count":11,"journal-issue":{"issue":"2","published-print":{"date-parts":[[2020,4]]}},"alternative-id":["152"],"URL":"https:\/\/doi.org\/10.1007\/s10689-019-00152-6","relation":{},"ISSN":["1389-9600","1573-7292"],"issn-type":[{"value":"1389-9600","type":"print"},{"value":"1573-7292","type":"electronic"}],"subject":[],"published":{"date-parts":[[2020,2,12]]},"assertion":[{"value":"12 February 2020","order":1,"name":"first_online","label":"First Online","group":{"name":"ArticleHistory","label":"Article History"}},{"order":1,"name":"Ethics","group":{"name":"EthicsHeading","label":"Compliance with ethical standards"}},{"value":"Dr. Manisha Shah is an Institutional Principal Investigator for Merck & Co., Inc, and LOXO Oncology (commercial interest) and is an Advisory Board Member for Eisai Inc. All other authors report nothing to declare.","order":2,"name":"Ethics","group":{"name":"EthicsHeading","label":"Conflict of interest"}},{"value":"This project was exempt from Institutional Review Board review. This case report received approval from the Ohio State University Privacy Officer.","order":3,"name":"Ethics","group":{"name":"EthicsHeading","label":"Ethical approval"}}]}}