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Long-term clinical course of IgG4-related systemic disease accompanied by hypophysitis. Endocr J 57: 485-492, 2010.","DOI":"10.1507\/endocrj.K09E-356"},{"key":"13","doi-asserted-by":"crossref","unstructured":"13. Carruthers MN, Topazian MD, Khosroshahi A, et al. Rituximab for IgG4-related disease: a prospective, open-label trial. Ann Rheum Dis 74: 1171-1177, 2015.","DOI":"10.1136\/annrheumdis-2014-206605"},{"key":"14","doi-asserted-by":"crossref","unstructured":"14. Bando H, Iguchi G, Fukuoka H, et al. The prevalence of IgG4-related hypophysitis in 170 consecutive patients with hypopituitarism and\/or central diabetes insipidus and review of the literature. Eur J Endocrinol 170: 161-172, 2014.","DOI":"10.1530\/EJE-13-0642"},{"key":"15","unstructured":"15. Nakasone Y, Oguchi K, Sato Y, Okubo Y, Yamauchi K, Aizawa T. Rapid conversion of autoimmune hypophysitis to an empty sella with immediate lowering of the serum IgG4 level. Case Report. 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