M. Kirschner, R. Powell, &. Jr, and M. Lipsett, Cushing's Syndrome: Nodular Cortical Hyperplasia of Adrenal Glands with Clinical and Pathological Features Suggesting Adrenocortical Tumor, The Journal of Clinical Endocrinology & Metabolism, vol.24, issue.10, pp.947-955, 1964.
DOI : 10.1210/jcem-24-10-947

G. Alencar, A. Lerario, M. Nishi, B. Mariani, M. Almeida et al., Mutations Are a Frequent Cause of Primary Macronodular Adrenal Hyperplasia, The Journal of Clinical Endocrinology & Metabolism, vol.99, issue.8, pp.1501-1509, 1210.
DOI : 10.1210/jc.2013-4237

J. Swain, C. Grant, R. Schlinkert, G. Thompson, J. Lloyd et al., Corticotropin-Independent Macronodular Adrenal Hyperplasia, Archives of Surgery, vol.133, issue.5, pp.541-546, 1998.
DOI : 10.1001/archsurg.133.5.541

D. Venanzi, A. Alencar, G. Bourdeau, I. Fragoso, and M. Lacroix, Primary bilateral macronodular adrenal hyperplasia, Current Opinion in Endocrinology & Diabetes and Obesity, vol.21, issue.3, pp.177-184, 2014.
DOI : 10.1097/MED.0000000000000061

M. Fragoso, G. Alencar, A. Lerario, I. Bourdeau, M. Almeida et al., Genetics of primary macronodular adrenal hyperplasia, Journal of Endocrinology, vol.224, issue.1, pp.31-43, 2015.
DOI : 10.1530/JOE-14-0568

F. Swords, L. Noon, P. King, and A. Clark, Constitutive activation of the human ACTH receptor resulting from a synergistic interaction between two naturally occurring missense mutations in the MC2R gene, Molecular and Cellular Endocrinology, vol.213, issue.2, pp.149-154, 2004.
DOI : 10.1016/j.mce.2003.10.052

A. Lacroix, I. Bourdeau, A. Lampron, T. Mazzuco, J. Tremblay et al., Aberrant G-protein coupled receptor expression in relation to adrenocortical overfunction, Clinical Endocrinology, vol.73, pp.1-15, 2010.
DOI : 10.1111/j.1365-2265.2009.03689.x

R. Libé, J. Coste, L. Guignat, F. Tissier, H. Lefebvre et al., Aberrant cortisol regulations in bilateral macronodular adrenal hyperplasia: a frequent finding in a prospective study of 32 patients with overt or subclinical Cushing's syndrome, European Journal of Endocrinology, vol.163, issue.1, pp.129-138, 2010.
DOI : 10.1530/EJE-10-0195

H. Lefebvre, C. Duparc, N. Chartrel, S. Jegous, A. Pellerin et al., Intraadrenal Adrenocorticotropin Production in a Case of Bilateral Macronodular Adrenal Hyperplasia Causing Cushing???s Syndrome, The Journal of Clinical Endocrinology & Metabolism, vol.88, issue.7, pp.3035-3042, 1210.
DOI : 10.1210/jc.2002-030014

E. Louiset, C. Duparc, J. Young, S. Renouf, M. Tetsi et al., Intraadrenal Corticotropin in Bilateral Macronodular Adrenal Hyperplasia, Intradrenal corticotropin in bilateral macronodular adrenal hyperplasia, pp.2115-2125, 2013.
DOI : 10.1056/NEJMoa1215245

J. Findlay, L. Sheeler, W. Engeland, and D. Aron, Familial adrenocorticotropin-independent Cushing syndrome with bilateral macronodular adrenal hyperplasia, Journal of Clinical Endocrinology and Metabolism, vol.76, pp.189-191, 1993.
DOI : 10.1210/jc.76.1.189

S. Minami, H. Sugihara, J. Sato, A. Tatsukuchi, and Y. Sugisaki, ACTH independent Cushing's syndrome occurring in siblings, Clinical Endocrinology, vol.44, issue.4, pp.483-488
DOI : 10.1046/j.1365-2265.1996.682504.x

L. Drougat, S. Espiard, and J. Bertherat, Genetics of primary bilateral macronodular adrenal hyperplasia: a model for early diagnosis of Cushing's syndrome?, European Journal of Endocrinology, vol.173, issue.4, pp.121-131, 2015.
DOI : 10.1530/EJE-15-0532

G. Assie, R. Libe, S. Espiard, M. Rizk-rabin, A. Guimier et al., Mutations in Macronodular Adrenal Hyperplasia with Cushing's Syndrome, New England Journal of Medicine, vol.369, issue.22, pp.2105-2114, 1304603.
DOI : 10.1056/NEJMoa1304603

F. Faucz, M. Zilbermint, M. Lodish, E. Szarek, G. Trivellin et al., ) Gene: A Clinical and Genetic Investigation, The Journal of Clinical Endocrinology & Metabolism, vol.99, issue.6, pp.1113-1119
DOI : 10.1210/jc.2013-4280

L. Gagliard, A. Schreider, C. Hahn, J. Feng, T. Cranston et al., Mutations Are Common in Familial Bilateral Macronodular Adrenal Hyperplasia, ARMC5 mutations are common in familial bilateral macronodular adrenal hyperplasia, pp.1784-1792, 1210.
DOI : 10.1210/jc.2014-1265

U. Elbelt, A. Trovato, M. Kloth, E. Gentz, R. Finke et al., Tumor Syndrome: Concurrent Inactivating Germline and Somatic Mutations Are Associated With Both Primary Macronodular Adrenal Hyperplasia and Meningioma, The Journal of Clinical Endocrinology & Metabolism, vol.100, issue.1, pp.119-128, 1210.
DOI : 10.1210/jc.2014-2648
URL : http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4283009

S. Espiard, L. Drougat, R. Libé, G. Assié, K. Perlemoine et al., Mutations in a Large Cohort of Primary Macronodular Adrenal Hyperplasia: Clinical and Functional Consequences, The Journal of Clinical Endocrinology & Metabolism, vol.100, issue.6, pp.926-935
DOI : 10.1210/jc.2014-4204