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Asa SL, Ezzat S (2009) The pathogenesis of pituitary tumors. <i>Annu Rev Pathol Mech Dis<\/i> 4: 97-126.","DOI":"10.1146\/annurev.pathol.4.110807.092259"},{"key":"2","unstructured":"2. Marx SJ, Agarwal SK, Kester MB, Heppner C, Kim YS, Skarulis MC, James LA, Goldsmith PK, Saggar SK, Park SY, Spiegel AM, Burns AL, Debelenko LV, Zhuang Z, Lubensky IA, Liotta LA, Emmert-Buck MR, Guru SC, Manickam P, Crabtree J, Erdos MR, Collins FS, Chandrasekharappa SC (1999) Multiple endocrine neoplasia type 1: clinical and genetic features of the hereditary endocrine neoplasias. <i>Recent Prog Horm Res<\/i> 54: 397-438."},{"key":"3","doi-asserted-by":"publisher","DOI":"10.1210\/jc.87.2.457"},{"key":"4","doi-asserted-by":"crossref","unstructured":"4. 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Horrocks PM, Franks S, Hockley AD, Rolfe EB, Van Noorden S, London DR (1982) An ACTH-secreting pituitary tumour arising in a patient with congenital adrenal hyperplasia. <i>Clin Endocrinol<\/i> 17: 457-468.","DOI":"10.1111\/j.1365-2265.1982.tb01613.x"},{"key":"8","doi-asserted-by":"crossref","unstructured":"8. Boronat M, Carrillo A, Ojeda A, Estrada J, Ezquieta B, Marin F, Novoa FJ (2004) Clinical manifestations and hormonal profile of two women with Cushing&rsquo;s disease and mild deficiency of 21-hydroxlyase. <i>J Endocrinol Invest<\/i> 27: 583-590.","DOI":"10.1007\/BF03347484"},{"key":"9","doi-asserted-by":"publisher","DOI":"10.1210\/jc.2008-0125"},{"key":"10","doi-asserted-by":"crossref","unstructured":"10. 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Herman V, Fagin J, Gonsky R, Kovacs K, Melmed S (1990) Clonal origin of pituitary adenomas. <i>J Clin Endocrinol Metab<\/i> 71: 1427-1433.","DOI":"10.1210\/jcem-71-6-1427"},{"key":"18","doi-asserted-by":"crossref","unstructured":"18. Assi&eacute; G, Bahurel H, Bertherat J, Kujas M, Legmann P, Bertagna X (2004) The Nelson&rsquo;s syndrome... revisited. <i>Pituitary<\/i> 7: 209-215.","DOI":"10.1007\/s11102-005-1403-y"},{"key":"19","doi-asserted-by":"crossref","unstructured":"19. Ghannam NN, Hammami MM, Muttair Z, Bakheet SM (1999) Primary hypothyroidism-asscociated TSH-secreting pituitary adenoma\/hyperplasia presenting as a bleeding nasal mass and extremely elevated TSH level. <i>J Endocrinol Invest<\/i> 22: 419-423.","DOI":"10.1007\/BF03343584"},{"key":"20","doi-asserted-by":"crossref","unstructured":"20. 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Benoit I, Drui D, Chaillous L, Dupas B, Mosnier JF, Charbonnel B, Cariou B (2009) A corticotroph pituitary adenoma as the initial presentation of familial glucocorticoid deficiency. <i>Eur J Endocrinol<\/i> 161: 195-199.","DOI":"10.1530\/EJE-09-0100"},{"key":"31","doi-asserted-by":"publisher","DOI":"10.1210\/jc.81.1.124"},{"key":"32","doi-asserted-by":"crossref","unstructured":"32. Mazarakis N, Kontogeorgos G, Kovacs K, Horvath E, Borboli N, Piaditis G (2001) Composite somatotroph--ACTH-immunoreactive pituitary adenoma with transformation of hyperplasia to adenoma. <i>Pituitary<\/i> 4: 215-221.","DOI":"10.1023\/A:1020764013137"},{"key":"33","doi-asserted-by":"publisher","DOI":"10.1515\/CCLM.2010.239"},{"key":"34","doi-asserted-by":"crossref","unstructured":"34. 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