{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,10,30]],"date-time":"2025-10-30T20:45:44Z","timestamp":1761857144123,"version":"build-2065373602"},"reference-count":5,"publisher":"Elsevier BV","issue":"9","license":[{"start":{"date-parts":[[2021,11,1]],"date-time":"2021-11-01T00:00:00Z","timestamp":1635724800000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"},{"start":{"date-parts":[[2021,11,1]],"date-time":"2021-11-01T00:00:00Z","timestamp":1635724800000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/legal\/tdmrep-license"}],"content-domain":{"domain":["clinicalkey.es","elsevier.es","elsevier.com","sciencedirect.com"],"crossmark-restriction":true},"short-container-title":["Medicina Cl\u00ednica"],"published-print":{"date-parts":[[2021,11]]},"DOI":"10.1016\/j.medcli.2020.09.011","type":"journal-article","created":{"date-parts":[[2020,11,30]],"date-time":"2020-11-30T16:46:03Z","timestamp":1606754763000},"page":"455-456","update-policy":"https:\/\/doi.org\/10.1016\/elsevier_cm_policy","source":"Crossref","is-referenced-by-count":0,"title":["Paraganglioma m\u00faltiple hereditario"],"prefix":"10.1016","volume":"157","author":[{"given":"Antonio","family":"Rosales-Castillo","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Antonio","family":"Bustos-Merlo","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Laura Gallo","family":"Padilla","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"78","reference":[{"key":"10.1016\/j.medcli.2020.09.011_bib0030","doi-asserted-by":"crossref","first-page":"933","DOI":"10.1016\/j.beem.2010.10.002","article-title":"Phaeochromocytomas and functional paragangliomas: Clinical management","volume":"24","author":"Plouin","year":"2010","journal-title":"Best Pract Res Clin Endocrinol Metab"},{"key":"10.1016\/j.medcli.2020.09.011_bib0035","doi-asserted-by":"crossref","first-page":"1541","DOI":"10.1210\/jc.2008-2419","article-title":"Clinically Guided Genetic Screening in a Large Cohort of Italian Patients with Pheochromocytomas and\/or Functional or Nonfunctional Paragangliomas","volume":"94","author":"Mannelli","year":"2009","journal-title":"J Clin Endocrinol Metab"},{"key":"10.1016\/j.medcli.2020.09.011_bib0040","doi-asserted-by":"crossref","first-page":"1","DOI":"10.1007\/s11864-020-00749-5","article-title":"Hereditary Syndromes in Neuroendocrine Tumors","volume":"21","author":"Lewis","year":"2020","journal-title":"Curr Treat Options Oncol"},{"key":"10.1016\/j.medcli.2020.09.011_bib0045","doi-asserted-by":"crossref","first-page":"270","DOI":"10.1007\/s12022-019-09594-1","article-title":"Malignant Intrarenal\/Renal Pelvis Paraganglioma with Co-Occurring SDHB and ATRX Mutations","volume":"30","author":"Irwin","year":"2019","journal-title":"Endocr Pathol"},{"key":"10.1016\/j.medcli.2020.09.011_bib0050","doi-asserted-by":"crossref","first-page":"91","DOI":"10.1530\/ERC-15-0268","article-title":"15 YEARS OF PARAGANGLIOMA: Clinical manifestations of paraganglioma syndromes types 1-5","volume":"22","author":"Benn","year":"2015","journal-title":"Endocr Relat Cancer"}],"container-title":["Medicina Cl\u00ednica"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S002577532030748X?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S002577532030748X?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2025,9,21]],"date-time":"2025-09-21T01:53:53Z","timestamp":1758419633000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S002577532030748X"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2021,11]]},"references-count":5,"journal-issue":{"issue":"9","published-print":{"date-parts":[[2021,11]]}},"alternative-id":["S002577532030748X"],"URL":"https:\/\/doi.org\/10.1016\/j.medcli.2020.09.011","relation":{},"ISSN":["0025-7753"],"issn-type":[{"type":"print","value":"0025-7753"}],"subject":[],"published":{"date-parts":[[2021,11]]},"assertion":[{"value":"Elsevier","name":"publisher","label":"This article is maintained by"},{"value":"Paraganglioma m\u00faltiple hereditario","name":"articletitle","label":"Article Title"},{"value":"Medicina Cl\u00ednica","name":"journaltitle","label":"Journal Title"},{"value":"https:\/\/doi.org\/10.1016\/j.medcli.2020.09.011","name":"articlelink","label":"CrossRef DOI link to publisher maintained version"},{"value":"simple-article","name":"content_type","label":"Content Type"},{"value":"\u00a9 2020 Elsevier Espa\u00f1a, S.L.U. All rights reserved.","name":"copyright","label":"Copyright"}]}}