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    Author
    Korbonits, M (201)
    Iacovazzo, D (26)Dutta, P (21)Barry, S (19)Marques, P (19)Grossman, AB (18)Collier, D (14)Rai, A (13)Roncaroli, F (12)Chanson, P (11)... View MoreSubjectHumans (27)acromegaly (19)AIP (17)Acromegaly (12)Female (12)FIPA (12)Male (11)Adult (10)pituitary adenoma (9)Pituitary Neoplasms (9)... View MoreDate Issued2020 - 2023 (80)2010 - 2019 (98)2005 - 2009 (3)
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    Characterization of Aryl Hydrocarbon Receptor Interacting Protein (AIP) Mutations in Familial Isolated Pituitary Adenoma Families 

    Igreja, S; Chahal, HS; King, P; Bolger, GB; Srirangalingam, U; Guasti, L; Chapple, JP; Trivellin, G; Gueorguiev, M; Guegan, K;... (2010-08)
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    Genetics of pituitary adenomas 

    Shaid, M; Korbonits, M (2017-05-01)
    © 2017 Neurology India, Neurological Society of India. Clinically relevant pituitary tumors presenting with altered hormonal secretion or mass effect represent a significant proportion of patients in endocrinology clinics. ...
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    A Novel Mutation in the Upstream Open Reading Frame of the CDKN1B Gene Causes a MEN4 Phenotype 

    Occhi, G; Regazzo, D; Trivellin, G; Boaretto, F; Ciato, D; Bobisse, S; Ferasin, S; Cetani, F; Pardi, E; Korbonits, M;... (2013-03)
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    The Immunophilin-Like Protein XAP2 Is a Negative Regulator of Estrogen Signaling through Interaction with Estrogen Receptor alpha 

    Cai, W; Kramarova, TV; Berg, P; Korbonits, M; Pongratz, I (2011-10-03)
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    Additive Anti-Tumor Effects of Lovastatin and Everolimus In Vitro through Simultaneous Inhibition of Signaling Pathways 

    Noelting, S; Maurer, J; Spoettl, G; Prada, ETA; Reuther, C; Young, K; Korbonits, M; Goeke, B; Grossman, A; Auernhammer, CJ (2015-12-04)
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    Can immediate postoperative random growth hormone levels predict long-term cure in patients with acromegaly? 

    Dutta, P; Korbonits, M; Sachdeva, N; Gupta, P; Srinivasan, A; Devgun, JS; Bajaj, A; Mukherjee, KK (2016)
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    Germline and mosaic mutations causing pituitary tumours: genetic and molecular aspects. 

    Pepe, S; Korbonits, M; Iacovazzo, D (Bioscientifica, 2019-02-01)
    While 95% of pituitary adenomas arise sporadically without a known inheritable predisposing mutation, in about 5% of the cases they can arise in a familial setting, either isolated (familial isolated pituitary adenoma or ...
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    Rapid Proteasomal Degradation of Mutant Proteins Is the Primary Mechanism Leading to Tumorigenesis in Patients With Missense AIP Mutations 

    Hernandez-Ramirez, LC; Martucci, F; Morgan, RML; Trivellin, G; Tilley, D; Ramos-Guajardo, N; Iacovazzo, D; D'Acquisto, F; Prodromou, C; Korbonits, M (2016-08)
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    Common Genetic Variants of the Human Steroid 21-Hydroxylase Gene (CYP21A2) Are Related to Differences in Circulating Hormone Levels 

    Doleschall, M; Szabo, JA; Pazmandi, J; Szilagyi, A; Koncz, K; Farkas, H; Toth, M; Igaz, P; Glaz, E; Prohaszka, Z;... (2014-09-11)
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    The current landscape of European registries for rare endocrine conditions 

    Ali, SR; Bryce, J; Cools, M; Korbonits, M; Beun, JG; Taruscio, D; Danne, T; Dattani, M; Dekkers, OM; Linglart, A;... (BioScientifica, 2019-01)
    Objective To identify cross-border international registries for rare endocrine conditions that are led from Europe and to understand the extent of engagement with these registries within a network of reference centres ...
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