Daly, A.F., Rixhon, M., Adam, C., Dempegioti, A., Tichomirowa, M.A., Beckers, A., High prevalence of pituitary adenomas: A cross-sectional study in the province of Liège Belgium. J Clin Endocrinol Metab. 91 (2006), 4769–4775.
Peverelli, E., Mantovani, G., Lania, A.G., Spada, A., cAMP in the pituitary: an old messenger for multiple signals. J Mol Endocrinol. 52 (2014), R67–R77.
Hernández-Ramírez, L.C., Stratakis, C.A., Genetics of Cushing's Syndrome. Endocrinol Metab Clin North Am. 47 (2018), 275–297.
Daly, A.F., Beckers, A., Chapter 21 – Genetics of Pituitary Tumor Syndromes. Pituitary, 2017, 619–630.
Goudie, C., Hannah-Shmouni, F., Kavak, M., Stratakis, C.A., Foulkes, W.D., 65 YEARS OF THE DOUBLE HELIX: Endocrine tumour syndromes in children and adolescents. Endocr Relat Cancer. 25 (2018), T221–T244.
Caimari, F., Korbonits, M., Novel Genetic Causes of Pituitary Adenomas. Clin Cancer Res. 22 (2016), 5030–5042.
Daly, A.F., Beckers, A., Familial isolated pituitary adenomas (FIPA) and mutations in the aryl hydrocarbon receptor interacting protein (AIP) gene. Endocrinol Metab Clin North Am. 44 (2015), 19–25.
Thakker, R.V., Newey, P.J., Walls, G.V., Bilezikian, J., Dralle, H., Ebeling, P.R., et al. Clinical Practice Guidelines for Multiple Endocrine Neoplasia Type 1 (MEN1). J Clin Endocrinol Metab. 97 (2012), 2990–3011.
Beckers, A., Petrossians, P., Hanson, J., Daly, A.F., The causes and consequences of pituitary gigantism. Nat Rev Endocrinol. 14 (2018), 705–720.
Trivellin, G., Daly, A.F., Faucz, F.R., Yuan, B., Rostomyan, L., Larco, D.O., et al. Gigantism and acromegaly due to Xq26 microduplications and GPR101 mutation. N Engl J Med. 371 (2014), 2363–2374.
Beckers, A., Lodish, M.B., Trivellin, G., Rostomyan, L., Lee, M., Faucz, F.R., et al. X-linked acrogigantism syndrome: Clinical profile and therapeutic responses. Endocr Relat Cancer. 22 (2015), 353–367.
Daly, A.F., Yuan, B., Fina, F., Caberg, J.-H., Trivellin, G., Rostomyan, L., et al. Somatic mosaicism underlies X-linked acrogigantism syndrome in sporadic male subjects. Endocr Relat Cancer. 23 (2016), 221–233.
Romanet, P., Philibert, P., Fina, F., Cuny, T., Roche, C., Ouafik, L., et al. Using Digital Droplet Polymerase Chain Reaction to Detect the Mosaic GNAS Mutations in Whole Blood DNA or Circulating Cell-Free DNA in Fibrous Dysplasia and McCune-Albright Syndrome. J Pediatr., 2018.
Xekouki, P., Brennand, A., Whitelaw, B., Pacak, K., Stratakis, C.A., The 3PAs: An Update on the Association of Pheochromocytomas Paragangliomas, and Pituitary Tumors. Horm Metab Res., 2018.
Daly, A.F., Castermans, E., Oudijk, L., Guitelman, M.A., Beckers, P., Potorac, I., et al. Pheochromocytomas and pituitary adenomas in three patients with MAX exon deletions. Endocr Relat Cancer. 25 (2018), L37–L42.
