{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,16]],"date-time":"2026-09-16T04:58:14Z","timestamp":1789534694551,"version":"build-2803163510"},"reference-count":15,"publisher":"Springer Science and Business Media LLC","issue":"4","license":[{"start":{"date-parts":[[2016,11,12]],"date-time":"2016-11-12T00:00:00Z","timestamp":1478908800000},"content-version":"unspecified","delay-in-days":0,"URL":"http:\/\/www.springer.com\/tdm"}],"content-domain":{"domain":["link.springer.com"],"crossmark-restriction":false},"short-container-title":["Endocr Pathol"],"published-print":{"date-parts":[[2017,12]]},"DOI":"10.1007\/s12022-016-9460-5","type":"journal-article","created":{"date-parts":[[2016,11,12]],"date-time":"2016-11-12T06:53:15Z","timestamp":1478933595000},"page":"302-307","update-policy":"https:\/\/doi.org\/10.1007\/springer_crossmark_policy","source":"Crossref","is-referenced-by-count":33,"title":["Pathological and Genetic Characterization of Bilateral Adrenomedullary Hyperplasia in a Patient with Germline MAX Mutation"],"prefix":"10.1007","volume":"28","author":[{"given":"Pauline","family":"Romanet","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Carole","family":"Guerin","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Pascal","family":"Pedini","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Wassim","family":"Essamet","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Fr\u00e9d\u00e9ric","family":"Castinetti","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Fr\u00e9deric","family":"Sebag","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Philippe","family":"Roche","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Alberto","family":"Cascon","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Arthur S.","family":"Tischler","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Karel","family":"Pacak","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Anne","family":"Barlier","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"David","family":"Ta\u00efeb","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"297","published-online":{"date-parts":[[2016,11,12]]},"reference":[{"key":"9460_CR1","doi-asserted-by":"crossref","first-page":"647","DOI":"10.1136\/jmedgenet-2015-103218","volume":"52","author":"M Curras-Freixes","year":"2015","unstructured":"Curras-Freixes M, Inglada-Perez L, Mancikova V et al. Recommendations for somatic and germline genetic testing of single pheochromocytoma and paraganglioma based on findings from a series of 329 patients. J Med Genet 52: 647\u2013656, 2015.","journal-title":"J Med Genet"},{"key":"9460_CR2","doi-asserted-by":"crossref","first-page":"868","DOI":"10.1016\/j.neo.2014.09.002","volume":"16","author":"E Korpershoek","year":"2014","unstructured":"Korpershoek E, Petri BJ, Post, E et al. Adrenal medullary hyperplasia is a precursor lesion for pheochromocytoma in MEN2 syndrome. Neoplasia 16: 868\u2013873, 2014.","journal-title":"Neoplasia"},{"key":"9460_CR3","doi-asserted-by":"crossref","first-page":"e200","DOI":"10.1200\/JCO.2010.32.2156","volume":"29","author":"RH Grogan","year":"2011","unstructured":"Grogan RH, Pacak K, Pasche L, Huynh TT, Greco RS Bilateral adrenal medullary hyperplasia associated with an SDHB mutation. J Clin Oncol 29: e200\u2013202, 2011.","journal-title":"J Clin Oncol"},{"key":"9460_CR4","doi-asserted-by":"crossref","first-page":"663","DOI":"10.1038\/ng.861","volume":"43","author":"I Comino-Mendez","year":"2011","unstructured":"Comino-Mendez I, Gracia-Aznarez FJ, Schiavi F et al. Exome sequencing identifies MAX mutations as a cause of hereditary pheochromocytoma. Nat Genet 43: 663\u2013667, 2011.","journal-title":"Nat Genet"},{"key":"9460_CR5","doi-asserted-by":"crossref","first-page":"153","DOI":"10.1007\/978-1-4939-2715-9_12","volume":"1315","author":"CT Kwok","year":"2015","unstructured":"Kwok CT, Hitchins MP Allele Quantification Pyrosequencing (R) at Designated SNP Sites to Detect Allelic Expression Imbalance and Loss-of-Heterozygosity. Methods Mol Biol 1315: 153\u2013171, 2015.","journal-title":"Methods Mol Biol"},{"key":"9460_CR6","doi-asserted-by":"crossref","first-page":"L1","DOI":"10.1530\/ERC-12-0339","volume":"20","author":"A Cascon","year":"2013","unstructured":"Cascon A, Inglada-Perez L, Comino-Mendez, I et al. Genetics of pheochromocytoma and paraganglioma in Spanish pediatric patients. Endocr Relat Cancer 20: L1-L6, 2013.","journal-title":"Endocr Relat Cancer"},{"key":"9460_CR7","doi-asserted-by":"crossref","first-page":"3119","DOI":"10.1158\/0008-5472.CAN-11-3891","volume":"72","author":"A Cascon","year":"2012","unstructured":"Cascon A, Robledo M MAX and MYC: a heritable breakup. Cancer Res 72: 3119\u20133124, 2012.","journal-title":"Cancer Res"},{"key":"9460_CR8","doi-asserted-by":"crossref","unstructured":"Casey SC, Tong L, Li, Y et al. 2016 MYC regulates the antitumor immune response through CD47 and PD-L1. Science","DOI":"10.1126\/science.aac9935"},{"key":"9460_CR9","doi-asserted-by":"crossref","first-page":"2828","DOI":"10.1158\/1078-0432.CCR-12-0160","volume":"18","author":"N Burnichon","year":"2012","unstructured":"Burnichon N, Cascon A, Schiavi F, et al. MAX mutations cause hereditary and sporadic pheochromocytoma and paraganglioma. Clinical cancer research : an official journal of the American Association for Cancer Research 18: 2828\u20132837, 2012.","journal-title":"Clinical cancer research : an official journal of the American Association for Cancer Research"},{"key":"9460_CR10","doi-asserted-by":"crossref","first-page":"817","DOI":"10.1111\/cen.12218","volume":"79","author":"M Peczkowska","year":"2013","unstructured":"Peczkowska M, Kowalska A, Sygut J et al. Testing new susceptibility genes in the cohort of apparently sporadic phaeochromocytoma\/paraganglioma patients with clinical characteristics of hereditary syndromes. Clinical Endocrinology 79: 817\u2013823, 2013.","journal-title":"Clinical Endocrinology"},{"key":"9460_CR11","doi-asserted-by":"crossref","unstructured":"Kimura N A Pathologist\u2019s view: molecular profiles for diagnosing pheochromocytomas and paragangliomas. Int J Endocrine Onc: 193\u2013200, 2015.","DOI":"10.2217\/ije.15.16"},{"key":"9460_CR12","doi-asserted-by":"crossref","first-page":"1034","DOI":"10.1210\/jc.2015-3889","volume":"101","author":"A Flynn","year":"2016","unstructured":"Flynn A, Dwight T, Harris, J et al. Pheo-Type: A Diagnostic Gene-expression Assay for the Classification of Pheochromocytoma and Paraganglioma. J Clin Endocrinol Metab 101: 1034\u20131043, 2016.","journal-title":"J Clin Endocrinol Metab"},{"key":"9460_CR13","doi-asserted-by":"crossref","first-page":"231","DOI":"10.55418\/9781881041016-09","volume-title":"Tumors of the Adrenal Gland and Extraadrenal Paraganglia","author":"EE Lack","year":"2007","unstructured":"Lack EE Tumors of the Adrenal Gland and Extraadrenal Paraganglia. Washington, DC: American Registry Of Pathology: 231\u2013240, 2007."},{"key":"9460_CR14","first-page":"177","volume":"83","author":"RA DeLellis","year":"1976","unstructured":"DeLellis RA, Wolfe HJ, Gagel, R.F et al. Adrenal medullary hyperplasia. A morphometric analysis in patients with familial medullary thyroid carcinoma. Am J Pathol 83: 177\u2013196, 1976.","journal-title":"Am J Pathol"},{"key":"9460_CR15","doi-asserted-by":"crossref","first-page":"101","DOI":"10.1038\/nrendo.2014.188","volume":"11","author":"J Favier","year":"2015","unstructured":"Favier J, Amar L, Gimenez-Roqueplo AP Paraganglioma and phaeochromocytoma: from genetics to personalized medicine. Nat Rev Endocrinol 11: 101\u2013111, 2015.","journal-title":"Nat Rev Endocrinol"}],"container-title":["Endocrine Pathology"],"original-title":[],"language":"en","link":[{"URL":"http:\/\/link.springer.com\/article\/10.1007\/s12022-016-9460-5\/fulltext.html","content-type":"text\/html","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/link.springer.com\/content\/pdf\/10.1007\/s12022-016-9460-5.pdf","content-type":"application\/pdf","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/link.springer.com\/content\/pdf\/10.1007\/s12022-016-9460-5.pdf","content-type":"application\/pdf","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2023,8,20]],"date-time":"2023-08-20T22:00:29Z","timestamp":1692568829000},"score":1,"resource":{"primary":{"URL":"http:\/\/link.springer.com\/10.1007\/s12022-016-9460-5"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2016,11,12]]},"references-count":15,"journal-issue":{"issue":"4","published-print":{"date-parts":[[2017,12]]}},"alternative-id":["9460"],"URL":"https:\/\/doi.org\/10.1007\/s12022-016-9460-5","relation":{},"ISSN":["1046-3976","1559-0097"],"issn-type":[{"value":"1046-3976","type":"print"},{"value":"1559-0097","type":"electronic"}],"subject":[],"published":{"date-parts":[[2016,11,12]]}}}