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(2007) Pituitary autoantibodies in autoimmune polyendocrine syndrome type 1. <i>Proc Natl Acad Sci U S A<\/i> 104: 949-954.","DOI":"10.1073\/pnas.0610070104"},{"key":"35","doi-asserted-by":"crossref","unstructured":"35. Iwama S, Welt CK, Romero CJ, Radovick S, Caturegli P (2013) Isolated prolactin deficiency associated with serum autoantibodies against prolactin-secreting cells. <i>J Clin Endocrinol Metab <\/i>98: 3920-3925.","DOI":"10.1210\/jc.2013-2411"},{"key":"36","doi-asserted-by":"crossref","unstructured":"36. Krude H, Biebermann H, Luck W, Horn R, Brabant G, et al. (1998) Severe early-onset obesity, adrenal insufficiency and red hair pigmentation caused by POMC mutations in humans. <i>Nat Genet <\/i>19: 155-157.","DOI":"10.1038\/509"},{"key":"37","doi-asserted-by":"crossref","unstructured":"37. Vallette-Kasic S, Brue T, Pulichino AM, Gueydan M, Barlier A, et al. (2005) Congenital isolated adrenocorticotropin deficiency: an underestimated cause of neonatal death, explained by TPIT gene mutations. <i>J Clin Endocrinol Metab <\/i>90: 1323-1331.","DOI":"10.1210\/jc.2004-1300"}],"container-title":["Endocrine Journal"],"original-title":[],"language":"en","deposited":{"date-parts":[[2022,4,20]],"date-time":"2022-04-20T17:42:35Z","timestamp":1650476555000},"score":1,"resource":{"primary":{"URL":"https:\/\/www.jstage.jst.go.jp\/article\/endocrj\/62\/2\/62_EJ14-0369\/_article"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2015]]},"references-count":37,"journal-issue":{"issue":"2","published-print":{"date-parts":[[2015]]}},"URL":"https:\/\/doi.org\/10.1507\/endocrj.ej14-0369","relation":{},"ISSN":["0918-8959","1348-4540"],"issn-type":[{"value":"0918-8959","type":"print"},{"value":"1348-4540","type":"electronic"}],"subject":[],"published":{"date-parts":[[2015]]}}}