Browsing Centre for Endocrinology by Author "Gadelha, MR"
Now showing items 1-7 of 7
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AIP mutations in brazilian patients with sporadic pituitary adenomas: A single-center evaluation
Araujo, PB; Kasuki, L; de Azeredo Lima, CH; Ogino, L; Camacho, AHS; Chimelli, L; Korbonits, M; Gadelha, MR (2017-11-01)© 2017 The authors Published by Bioscientifica Ltd. Aryl hydrocarbon receptor-interacting protein (AIP) gene mutations (AIPmut) are the most frequent germline mutations found in apparently sporadic pituitary adenomas (SPA). ... -
The genetic background of acromegaly.
Gadelha, MR; Kasuki, L; Korbonits, M (2017-02)Acromegaly is caused by a somatotropinoma in the vast majority of the cases. These are monoclonal tumors that can occur sporadically or rarely in a familial setting. In the last few years, novel familial syndromes have ... -
Pituitary MRI Features in Acromegaly Resulting From Ectopic GHRH Secretion From a Neuroendocrine Tumor: Analysis of 30 Cases
Potorac, I; Bonneville, J-F; Daly, AF; de Herder, W; Fainstein-Day, P; Chanson, P; Korbonits, M; Cordido, F; Lamback, EB; Abid, M (2022) -
Pituitary MRI Features in Acromegaly Resulting From Ectopic GHRH Secretion From a Neuroendocrine Tumor: Analysis of 30 Cases (vol 107, pg e3313, 2022)
Potorac, I; Bonneville, J-F; Daly, AF; de Herder, W; Fainstein-Day, P; Chanson, P; Korbonits, M; Cordido, F; Lamback, EB; Abid, M (2022) -
Polymorphism or mutation? - The role of the R304Q missense AIP mutation in the predisposition to pituitary adenoma
Mothojakan, NB; Ferrau, F; Dang, MN; Barlier, A; Chanson, P; Occhi, G; Daly, AF; Schofl, C; Dal, J; Gadelha, MR (2016-10-14) -
Regulation of Aryl Hydrocarbon Receptor Interacting Protein (AIP) Protein Expression by MiR-34a in Sporadic Somatotropinomas
Denes, J; Kasuki, L; Trivellin, G; Colli, LM; Takiya, CM; Stiles, CE; Barry, S; de Castro, M; Gadelha, MR; Korbonits, M (2015-02-06) -
Somatic USP8 mutations are frequent events in corticotroph tumor progression causing Nelson's tumor.
Pérez-Rivas, LG; Theodoropoulou, M; Puar, TH; Fazel, J; Stieg, MR; Ferraù, F; Assié, G; Gadelha, MR; Deutschbein, T; Fragoso, MC (2018-01)OBJECTIVE: Somatic mutations in the ubiquitin-specific protease 8 (USP8) gene are frequent in corticotroph tumors causing Cushing's disease (CD). Corticotroph tumor progression, the so-called Nelson's syndrome (NS), is a ...