{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2022,4,4]],"date-time":"2022-04-04T00:38:38Z","timestamp":1649032718799},"reference-count":8,"publisher":"Elsevier BV","issue":"6","license":[{"start":{"date-parts":[[2010,6,1]],"date-time":"2010-06-01T00:00:00Z","timestamp":1275350400000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Anales de Pediatr\u00eda"],"published-print":{"date-parts":[[2010,6]]},"DOI":"10.1016\/j.anpedi.2010.01.017","type":"journal-article","created":{"date-parts":[[2010,4,21]],"date-time":"2010-04-21T08:49:42Z","timestamp":1271839782000},"page":"424-427","source":"Crossref","is-referenced-by-count":0,"title":["Seudohipoparatiroidismo tipo Ia. Una mutaci\u00f3n original"],"prefix":"10.1016","volume":"72","author":[{"given":"M.","family":"Reis Oliveira","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"A.","family":"Oliveira Bandeira","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"P.","family":"Rendeiro","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"T.","family":"Silva Borges","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"H.","family":"Cardoso","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"78","reference":[{"key":"10.1016\/j.anpedi.2010.01.017_bib1","doi-asserted-by":"crossref","first-page":"308","DOI":"10.1542\/pir.26-8-308","article-title":"Understanding and recognizing pseudohypoparathyroidism","volume":"26","author":"Burgert","year":"2005","journal-title":"Pediatr Rev"},{"key":"10.1016\/j.anpedi.2010.01.017_bib2","doi-asserted-by":"crossref","first-page":"25","DOI":"10.1210\/er.2014-1034","article-title":"Identification of a novel GNSA mutation for pseudohypoparathyroidism in a Chinese family","volume":"36","author":"Sun","year":"2009","journal-title":"Endocrinology"},{"key":"10.1016\/j.anpedi.2010.01.017_bib3","series-title":"Brook's Clinical Pediatric Endocrinology","first-page":"263","article-title":"The parathyroid and disorders of calcium metabolism","author":"Allgrove","year":"2005"},{"key":"10.1016\/j.anpedi.2010.01.017_bib4","doi-asserted-by":"crossref","first-page":"749","DOI":"10.1203\/01.PDR.0000059752.07086.A2","article-title":"Molecular analysis of the GNAS1 gene for the correct diagnosis of Albright Hereditary Osteodystrophy and Pseudohypoparathyroidism","volume":"53","author":"Sanctis","year":"2003","journal-title":"Pediatr Res"},{"key":"10.1016\/j.anpedi.2010.01.017_bib5","doi-asserted-by":"crossref","first-page":"598","DOI":"10.1016\/S1695-4033(01)77602-3","article-title":"Osteodistrofia heredit\u00e1ria de Albright. Identificac\u00edon de una mutac\u00edon original en una familia","volume":"54","author":"Eizaguirre","year":"2001","journal-title":"An Esp Pediatr"},{"key":"10.1016\/j.anpedi.2010.01.017_bib6","first-page":"3254","article-title":"Identification of two novel deletion mutation within the Gs\u03b1 gene (GNSA1) in Albright Hereditary Osteodystrophy","volume":"84","author":"Yu","year":"1999","journal-title":"J Clin Endocrinol Metab"},{"key":"10.1016\/j.anpedi.2010.01.017_bib7","first-page":"65","article-title":"GNSA locus and pseudohypoparathyroidism","volume":"63","author":"Bastepe","year":"2005","journal-title":"Horm Res"},{"key":"10.1016\/j.anpedi.2010.01.017_bib8","doi-asserted-by":"crossref","first-page":"661","DOI":"10.1210\/jc.2007-0927","article-title":"A maternal epimutation of the GNAS leads to Albright Osteodystrophy and parathyroid hormone resistance","volume":"93","author":"Mariot","year":"2008","journal-title":"J Clin Endocrinol Metab"}],"container-title":["Anales de Pediatr\u00eda"],"original-title":[],"language":"es","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S169540331000130X?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S169540331000130X?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2018,7,26]],"date-time":"2018-07-26T14:09:21Z","timestamp":1532614161000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S169540331000130X"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2010,6]]},"references-count":8,"journal-issue":{"issue":"6","published-print":{"date-parts":[[2010,6]]}},"alternative-id":["S169540331000130X"],"URL":"https:\/\/doi.org\/10.1016\/j.anpedi.2010.01.017","relation":{},"ISSN":["1695-4033"],"issn-type":[{"value":"1695-4033","type":"print"}],"subject":[],"published":{"date-parts":[[2010,6]]}}}