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Marcus Quinkler, Bertil Ekman, Claudio Marelli, Sharif Uddin, Pierre Zelissen, Robert D Murray and on behalf of the EU-AIR Investigators

2009 94 4216 – 4223 . ( doi:10.1210/jc.2009-1097 ) 32 Zueger T Kirchner P Herren C Fischli S Zwahlen M Christ E Stettler C. Glucocorticoid replacement and mortality in patients with nonfunctioning pituitary adenoma

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Enrique Soto-Pedre, Paul J Newey, John S Bevan and Graham P Leese

visible pituitary adenomas and/or diagnosis of hyperprolactinaemia followed for 14 years but no increased risk of breast cancer was observed ( 12 ). However, several large case-controlled and population-based cohort studies have failed to show any

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Soraya Puglisi, Paola Perotti, Mattia Barbot, Paolo Cosio, Carla Scaroni, Antonio Stigliano, Pina Lardo, Valentina Morelli, Elisa Polledri, Iacopo Chiodini, Giuseppe Reimondo, Anna Pia and Massimo Terzolo

Introduction Cushing’s syndrome (CS) is a condition of endogenous hypercortisolism caused by different pathological entities that is classified in two variants: (i) ACTH-dependent CS, due to a corticotroph pituitary adenoma or an ectopic tumor

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Mikkel Andreassen, Anders Juul, Ulla Feldt-Rasmussen and Niels Jørgensen

supporting sufficient bioactivity. One previous study has investigated FSH bioactivity in male patients with non-functioning pituitary adenomas and found unchanged in vitro FSH bioactivity. By contrast clinically relevant changes in the bioactivity of

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K E Lines, R P Vas Nunes, M Frost, C J Yates, M Stevenson and R V Thakker

-0240 ) 23 Walls GV Lemos MC Javid M Bazan-Peregrino M Jeyabalan J Reed AA Harding B Tyler DJ Stuckey DJ Piret S MEN1 gene replacement therapy reduces proliferation rates in a mouse model of pituitary adenomas . Cancer

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Eeva M Ryhänen, Ilkka Heiskanen, Harri Sintonen, Matti J Välimäki, Risto P Roine and Camilla Schalin-Jäntti

pituitary adenomas having surgery as primary treatment . Clinical Endocrinology 2015 82 412 – 421 . ( doi:10.1111/cen.12550 ). 12 Kluger N Matikainen N Sintonen H Ranki A Roine RP Schalin-Jäntti C . Impaired health-related quality of life

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Marco Marino, Valentina Cirello, Valentina Gnarini, Carla Colombo, Elisa Pignatti, Livio Casarini, Chiara Diazzi, Vincenzo Rochira, Katia Cioni, Bruno Madeo, Cesare Carani, Manuela Simoni and Laura Fugazzola

Z Liu J Liu Y . Pituitary tumor transforming gene-1 haplotypes and risk of pituitary adenoma: a case–control study . BMC Medical Genetics 2011 12 44 . ( doi:10.1186/1471-2350-12-44 ). 16 Wondergem B Zhang Z Huang D Ong CK Koeman

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Alberto Giacinto Ambrogio, Massimiliano Andrioli, Martina De Martin, Francesco Cavagnini and Francesca Pecori Giraldi

-secreting cells derived from a rapidly growing pituitary adenoma . Brain Tumor Pathology 2000 17 133 – 138 . ( doi:10.1007/BF02484284 ) 10.1007/BF02484284 11310920 19 Leal Cerro A Martin Rodriguez JF Ibañez-Costa A Madrazo-Atutxa AM

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Charlotte Höybye, Laia Faseh, Christos Himonakos, Tomasz Pielak and Jesper Eugen-Olsen

GHD was identified. Twenty-nine patients had previously been treated for non-functioning pituitary adenomas (NFPA); four patients for GH producing adenoma, five patients for ACTH producing adenoma, seven for prolactinoma, four patients for

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Elizaveta Mamedova, Natalya Mokrysheva, Evgeny Vasilyev, Vasily Petrov, Ekaterina Pigarova, Sergey Kuznetsov, Nikolay Kuznetsov, Liudmila Rozhinskaya, Galina Melnichenko, Ivan Dedov and Anatoly Tiulpakov

after surgical treatment and seven patients had pituitary adenomas, neuroendocrine tumors or other tumors diagnosed after PHPT. Nobody had a histological diagnosis of parathyroid carcinoma or atypical parathyroid adenoma. Table 4 Clinical