Results 21 to 30 of about 114,029 (285)

Silencing mutated β-catenin inhibits cell proliferation and stimulates apoptosis in the adrenocortical cancer cell line H295R [PDF]

, 2013
Adrenocortical carcinoma (ACC) is a rare and highly aggressive endocrine neoplasm, with limited therapeutic options. Activating β-catenin somatic mutations are found in ACC and have been associated with a poor clinical outcome. In fact, activation of the
Bertherat, Jérôme, Beuschlein, Felix, Bonnet, Stéphane, Gaujoux, Sébastien, Guillaud-Bataille, Marine, Hantel, Constanze, Launay, Pierre, Lefèvre, Lucile, Perlemoine, Karine, Ragazzon, Bruno, Rizk-Rabin, Marthe, Tissier, Frédérique   +11 more
core   +9 more sources

Imaging findings of primary adrenal tumors in pediatric patients

Diagnostic and Interventional Radiology, 2021
Apart from neuroblastomas, adrenal tumors are rarely seen in children. The most common adrenal tumors are adrenocortical carcinoma and pheochromocytoma.
H. Nursun Özcan, Aziz Anil Tan, Burak Ardicli, Berna Oguz, Saniye Ekinci, Tezer Kutluk, Mithat Haliloglu   +6 more
doaj   +1 more source

Corticotropinoma as a Component of Carney Complex. [PDF]

, 2017
Known germline gene abnormalities cause one-fifth of the pituitary adenomas in children and adolescents, but, in contrast with other pituitary tumor types, the genetic causes of corticotropinomas are largely unknown.
Chittiboina, Prashant, Dimopoulos, Aggeliki, Faucz, Fabio R, Hernández-Ramírez, Laura C, Kay, Denise M, Lane, John, Lodish, Maya B, Mills, James L, Pankratz, Nathan, Stratakis, Constantine A, Tatsi, Christina, Valdés, Nuria   +11 more
core   +2 more sources

Adrenal Tumors

Therapeutische Umschau. Revue therapeutique, 2020
Adrenal tumors Abstract. The term 'adrenal tumor' describes benign and malignant mass lesions of the adrenal gland, including primary adrenal tumors and metastases from extra-adrenal origin. With the widespread use of imaging technique, adrenal tumors have become increasingly detected as 'incidentalomas'.
Lynn Model, Michael G. Caty, Emily R. Christison-Lagay   +2 more
openaire   +3 more sources

Hypogonadism and sexual function in men affected by adrenocortical carcinoma under mitotane therapy

Frontiers in Endocrinology
PurposeAdrenocortical carcinoma (ACC) is a rare and aggressive tumor. ACC male patients under adjuvant mitotane therapy (AMT) frequently develop hypogonadism, however sexual function has never been assessed in this setting.
Letizia Canu, Letizia Canu, Letizia Canu, Letizia Canu, Clotilde Sparano, Clotilde Sparano, Lara Naletto, Giuseppina De Filpo, Giulia Cantini, Giulia Cantini, Giulia Cantini, Elena Rapizzi, Elena Rapizzi, Elena Rapizzi, Serena Martinelli, Serena Martinelli, Serena Martinelli, Tonino Ercolino, Tonino Ercolino, Tonino Ercolino, Francesca Cioppi, Alessandro Fantoni, Lorenzo Zanatta, Lorenzo Zanatta, Alessandro Terreni, Massimo Mannelli, Massimo Mannelli, Massimo Mannelli, Michaela Luconi, Michaela Luconi, Michaela Luconi, Mario Maggi, Mario Maggi, Mario Maggi, Mario Maggi, Francesco Lotti   +35 more
doaj   +1 more source

Adrenal imaging (Part 1): Imaging techniques and primary cortical lesions

Indian Journal of Endocrinology and Metabolism, 2015
Adrenal glands can be affected by a variety of lesions. Adrenal lesions can either be primary, of adrenal origin, or secondary to other pathologies. Primary adrenal lesions can further be either of cortical or medullary origin.
Ananya Panda, Chandan J Das, Ekta Dhamija, Rakesh Kumar, A K Gupta   +4 more
doaj   +1 more source

Adrenal myelolipoma: Radiologic-pathologic correlation

Apollo Medicine, 2018
Myelolipomas are rare, benign tumors of adrenal gland. These tumors are generally asymptomatic and are diagnosed incidentally. Differentiating the tumor from other adrenal tumors such as liposarcoma, pheochromocytoma is important for management.
Ashish Sachan, Hirdaya Hulas Nag, Sandip Barmann, Ravindra Kumar Saran   +3 more
doaj   +1 more source

Adrenal schwannoma: An uncommon incidentaloma

Indian Journal of Pathology and Microbiology, 2021
WHO classification of adrenal tumors. Only a handful of cases have been reported so far. A 30-year-old lady presented with cerebrovascular accident.
Sumanta Bhattacharya, Ankit Kumar, Uttara Chatterjee, Dilip K Pal   +3 more
doaj   +1 more source

European multicentre study on outcome of surgery for sporadic primary hyperparathyroidism

BJS (British Journal of Surgery), EarlyView., 2020
Some 5861 patients undergoing first‐time surgery for sporadic primary hyperparathyroidism were registered in the Eurocrine® database between 2015 and 2018. The use of intraoperative parathyroid hormone measurement decreased the risk of conversion and persistent hypercalcaemia.
A. Bergenfelz, S. van Slycke, Ö. Makay, L. Brunaud   +3 more
wiley   +1 more source

Gel chromatographic characterization of immunoreactive adrenocorticotropin in patients with ACTH hypersecretion [PDF]

, 1989
We investigated the molecular size of circulating immunoreactive ACTH by gel chromatography in patients with ACTH hypersecretion due to various disorders of the hypothalamic-pituitary-adrenal axis.
A Chatelain, AC Hale, B Allolio, B. Allolio, H Imura, JL Doppmann, JW Findling, K Nakao, M Reincke, M Reincke, M Thoren, M. Reincke, PJ Fuller, RC Pedersen, RE Mains, RS Yalow, SJ Ratter, U. Deuß, W. Winkelmann, Y Yamada   +19 more
core   +1 more source