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Glezer A, Bronstein MD. Pituitary autoimmune disease: nuances in clinical presentation. Endocrine 42: 74-79, 2012."},{"key":"2","doi-asserted-by":"crossref","unstructured":"2. Hamano H, Kawa S, Horiuchi A, et al. High serum IgG4 concentrations in patients with sclerosing pancreatitis. N Engl J Med 344: 732-738, 2001.","DOI":"10.1056\/NEJM200103083441005"},{"key":"3","doi-asserted-by":"crossref","unstructured":"3. Stone JH, Zen Y, Deshpande V. IgG4-related disease. N Engl J Med 366: 539-551, 2012.","DOI":"10.1056\/NEJMra1104650"},{"key":"4","unstructured":"4. Raina A, Yadav D, Krasinskas AM, et al. Evaluation and management of autoimmune pancreatitis: experience at a large US center. Am J Gastroenterol 104: 2295-2306, 2009."},{"key":"5","doi-asserted-by":"crossref","unstructured":"5. Stone JH, Khosroshahi A, Deshpande V, et al. Recommendations for the nomenclature of IgG4-related disease and its individual organ system manifestations. 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Inflammatory pseudotumors in multiple organs associated with elevated serum IgG4 level: recovery by only a small replacement dose of steroid. Intern Med 47: 1139-1142, 2008."},{"key":"18","doi-asserted-by":"crossref","unstructured":"18. Isaka Y, Yoshioka K, Nishio M, et al. A case of IgG4-related multifocal fibrosclerosis complicated by central diabetes insipidus. Endocr J 55: 723-728, 2008.","DOI":"10.1507\/endocrj.K08E-034"},{"key":"19","unstructured":"19. Miyoshi T, Otsuka F, Tsukamoto N, et al. A case of suspected hypothalamo hypophyseal dysfunction due to IgG4-related diseases. Folia Endocrinol Jpn 84 (Suppl.): 87-89, 2008 (in Japanese)."},{"key":"20","unstructured":"20. Taji H, Takamura T, Mohri K, et al. A male case of lymphocytic hypophysitis accompanied by IgG4- related disease. Folia Endocrinol Jpn 85 (Suppl.): 42-44, 2009 (in Japanese)."},{"key":"21","unstructured":"21. Osawa S, Ogawa Y, Watanabe M, Tominaga T. 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