References
- Thakker RV , NeweyPJ, WallsGVet al. Clinical practice guidelines for multiple endocrine neoplasia type 1 (MEN1). J. Clin. Endocrinol. Metab. 97(9), 2990–3011 (2012).
- Chandrasekharappa SC , GuruSC, ManickamPet al. Positional cloning of the gene for multiple endocrine neoplasia-type 1. Science 276(5311), 404–407 (1997).
- Agarwal SK , KennedyPA, ScacheriPCet al. Menin molecular interactions: insights into normal functions and tumorigenesis. Horm. Metab. Res. 37(6), 369–374 (2005).
- Lemos MC , ThakkerRV. Multiple endocrine neoplasia type 1 (MEN1): analysis of 1336 mutations reported in the first decade following identification of the gene. Hum. Mutat.29(1), 22–32 (2008).
- Thevenon J , BourredjemA, FaivreLet al. Higher risk of death among MEN1 patients with mutations in the JunD interacting domain: a Groupe d‘etude des Tumeurs Endocrines (GTE) cohort study. Hum. Mol. Genet. 22(10), 1940–1948 (2013).
- Syro LV , ScheithauerBW, KovacsKet al. Pituitary tumors in patients with MEN1 syndrome. Clinics (Sao Paulo) 67(Suppl. 1), 43–48 (2012).
- Elston MS , McDonaldKL, Clifton-BlighRJ, RobinsonBG. Familial pituitary tumor syndromes. Nat. Rev. Endocrinol.5(8), 453–461 (2009).
- Nunes VS , SouzaGL, PeroneD, CondeSJ, NogueiraCR. Frequency of multiple endocrine neoplasia type 1 in a group of patients with pituitary adenoma: genetic study and familial screening.Pituitary doi:10.1007/s11102-013-0462-8 (2013) (Epub ahead of print).
- Goudet P , Bonithon-KoppC, MuratAet al. Gender-related differences in MEN1 lesion occurrence and diagnosis: a cohort study of 734 cases from the Groupe d‘etude des Tumeurs Endocrines. Eur. J. Endocrinol. 165(1), 97–105 (2011).
- Delemer B . MEN1 and pituitary adenomas. Ann. Endocrinol. (Paris)73(2), 59–61 (2012).
- Vergès B , BoureilleF, GoudetPet al. Pituitary disease in MEN type 1 (MEN1): data from the France–Belgium MEN1 multicenter study. J. Clin. Endocrinol. Metab. 87(2), 457–465 (2002).
- Trouillas J , Labat-MoleurF, SturmNet al. Pituitary tumors and hyperplasia in multiple endocrine neoplasia type 1 syndrome (MEN1): a case–control study in a series of 77 patients versus 2509 non-MEN1 patients. Am. J. Surg. Pathol. 32(4), 534–543 (2008).
- Cuny T , PertuitM, Sahnoun-FathallahMet al. Genetic analysis in young patients with sporadic pituitary macroadenomas: besides AIP don‘t forget MEN1 genetic analysis. Eur. J. Endocrinol. 168(4), 533–541 (2013).
- Raverot G , CastinettiF, JouanneauEet al. Pituitary carcinomas and aggressive pituitary tumours: merits and pitfalls of temozolomide treatment. Clin. Endocrinol. (Oxf) 76(6), 769–775 (2012).
- Mete O , EzzatS, AsaSL. Biomarkers of aggressive pituitary adenomas. J. Mol. Endocrinol.49(2), R69–R78 (2012).
- Philippon M , MorangeI, BarrieMet al. Long-term control of a MEN1 prolactin secreting pituitary carcinoma after temozolomide treatment. Ann. Endocrinol. (Paris) 73(3), 225–229 (2012).
- Scheithauer BW , KovacsK, NoseVet al. Multiple endocrine neoplasia type 1-associated thyrotropin-producing pituitary carcinoma: report of a probable de novo example. Hum. Pathol. 40(2), 270–278 (2009).
- Vroonen L , Jaffrain-ReaML, PetrossiansPet al. Prolactinomas resistant to standard doses of cabergoline: a multicenter study of 92 patients. Eur. J. Endocrinol. 167(5), 651–662 (2012).
- Walls GV , LemosMC, JavidMet al. MEN1 gene replacement therapy reduces proliferation rates in a mouse model of pituitary adenomas. Cancer Res.72(19), 5060–5068 (2012).
- Trouillas J , RoyP, SturmNet al. A new prognostic clinicopathological classification of pituitary adenomas: a multicentric case–control study of 410 patients with 8 years post-operative follow-up. Acta Neuropathol. 126(1), 123–135 (2013).