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Resmini E, Minuto F, Colao A, et al. Secondary diabetes associated with principal endocrinopathies: the impact of new treatment modalities. Acta Diabetol 46: 85-95, 2009.","DOI":"10.1007\/s00592-009-0112-9"},{"key":"2","doi-asserted-by":"crossref","unstructured":"2. Terzolo M, Reimondo G, Chiodini I, et al. Screening of Cushing's syndrome in outpatients with type 2 diabetes: results of a prospective multicentric study in Italy. J Clin Endocrinol Metab 97: 3467-3475, 2012.","DOI":"10.1210\/jc.2012-1323"},{"key":"3","doi-asserted-by":"crossref","unstructured":"3. Fieffe S, Morange I, Petrossians P, et al. Diabetes in acromegaly, prevalence, risk factors, and evolution: data from the French Acromegaly Registry. Eur J Endocrinol 164: 877-884, 2011.","DOI":"10.1530\/EJE-10-1050"},{"key":"4","doi-asserted-by":"crossref","unstructured":"4. Kim SK, Suh S, Lee JI, et al. The ability of β-cells to compensate for insulin resistance is restored with a reduction in excess growth hormone in Korean acromegalic patients. J Korean Med Sci 27: 177-183, 2012.","DOI":"10.3346\/jkms.2012.27.2.177"},{"key":"5","unstructured":"5. Hansen I, Tsalikian E, Beaufrere B, et al. Insulin resistance in acromegaly: defects in both hepatic and extrahepatic insulin action. Am J Physiol 250: 269-273, 1986."},{"key":"6","doi-asserted-by":"crossref","unstructured":"6. Muggeo M, Bar RS, Roth J, et al. The insulin resistance of Acromegaly: evidence for two alterations in the insulin receptor on circulating monocytes. J Clin Endocrinol Metab 48: 17-25, 1979.","DOI":"10.1210\/jcem-48-1-17"},{"key":"7","doi-asserted-by":"crossref","unstructured":"7. Ogo A, Matoba Y, Matsuda Y, et al. A decrease in the dose of pegvisomant was needed for the treatment of acromegaly after adrenalectomy in a patient with coexisting preclinical Cushing's syndrome. 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Alzahrani AS, Al-Khaldi N, Shi Y, et al. Diagnosis by serendipity: Cushing syndrome attributable to cortisol-producing adrenal adenoma as the initial manifestation of multiple endocrine neoplasia type 1 due to a rare splicing site MEN1 gene mutation. Endocr Pract 14: 595-602, 2008.","DOI":"10.4158\/EP.14.5.595"},{"key":"12","doi-asserted-by":"crossref","unstructured":"12. Thakker RV, Newey PJ, Walls GV, et al. Clinical practice guidelines for multiple endocrine neoplasia type 1 (MEN1). J Clin Endocrinol Metab 97: 2990-3011, 2012.","DOI":"10.1210\/jc.2012-1230"},{"key":"13","doi-asserted-by":"crossref","unstructured":"13. Daly AF, Tichomirowa MA, Beckers A. The epidemiology and genetics of pituitary adenomas. Best Pract Res Clin Endocrinol Metab 23: 543-554, 2009.","DOI":"10.1016\/j.beem.2009.05.008"},{"key":"14","doi-asserted-by":"crossref","unstructured":"14. Nakagawa K, Akikawa K, Matsubara M, Kubo M. Effect of dexamethasone on growth hormone (GH) response to growth hormone releasing hormone in acromegaly. J Clin Endocrinol Metab 60: 306-310, 1985.","DOI":"10.1210\/jcem-60-2-306"},{"key":"15","doi-asserted-by":"crossref","unstructured":"15. Reid TJ, Post KD, Bruce JN, et al. Features at diagnosis of 324 patients with acromegaly did not change from 1981 to 2006: acromegaly remains under-recognized and under-diagnosed. Clin Endocrinol 72: 203-208, 2010.","DOI":"10.1111\/j.1365-2265.2009.03626.x"},{"key":"16","doi-asserted-by":"crossref","unstructured":"16. Nieman LK, Biller BM, Findling JW, et al. The diagnosis of Cushing's syndrome: an endocrine society clinical practice guideline. 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