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    Korbonits, M (153)
    Iacovazzo, D (25)Grossman, AB (17)Marques, P (17)Dutta, P (15)Barry, S (14)Collier, D (13)Ellard, S (11)Roncaroli, F (11)Dang, MN (10)... View MoreSubjectHumans (20)acromegaly (16)AIP (16)FIPA (12)Female (11)Male (11)Acromegaly (9)Adult (9)pituitary adenoma (9)Adenoma (7)... View MoreDate Issued2020 - 2022 (51)2010 - 2019 (98)2005 - 2009 (3)
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    Characterisation of myocardial structure and function in adult-onset growth hormone deficiency using cardiac magnetic resonance. 

    Thomas, JDJ; Dattani, A; Zemrak, F; Burchell, T; Akker, SA; Gurnell, M; Grossman, AB; Davies, LC; Korbonits, M (2016-12)
    Growth hormone (GH) can profoundly influence cardiac function. While GH excess causes well-defined cardiac pathology, fewer data are available regarding the more subtle cardiac changes seen in GH deficiency (GHD). This ...
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    Pseudoacromegaly 

    Marques, P; Korbonits, M (Elsevier/Science Direct, 2018-11-15)
    © 2018 Elsevier Inc. Individuals with acromegaloid physical appearance or tall stature may be referred to endocrinologists to exclude growth hormone (GH) excess. While some of these subjects could be healthy individuals ...
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    International Union of Basic and Clinical Pharmacology. CV. Somatostatin Receptors: Structure, Function, Ligands, and New Nomenclature. 

    Günther, T; Tulipano, G; Dournaud, P; Bousquet, C; Csaba, Z; Kreienkamp, H-J; Lupp, A; Korbonits, M; Castaño, JP; Wester, H-J;... (2018-10)
    Somatostatin, also known as somatotropin-release inhibitory factor, is a cyclopeptide that exerts potent inhibitory actions on hormone secretion and neuronal excitability. Its physiologic functions are mediated by five G ...
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    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 ...
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    A unique haplotype of RCCX copy number variation: from the clinics of congenital adrenal hyperplasia to evolutionary genetics. 

    Doleschall, M; Luczay, A; Koncz, K; Hadzsiev, K; Erhardt, É; Szilágyi, Á; Doleschall, Z; Németh, K; Török, D; Prohászka, Z;... (2017-06)
    There is a difficulty in the molecular diagnosis of congenital adrenal hyperplasia (CAH) due to the c.955C>T (p.(Q319*), formerly Q318X, rs7755898) variant of the CYP21A2 gene. Therefore, a systematic assessment of the ...
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    Fatal Carney Complex in Siblings Due to De Novo Large Gene Deletion. 

    Stelmachowska-Banas, M; Zgliczynski, W; Tutka, P; Carney, JA; Korbonits, M (2017-11-01)
    Context: Carney complex (CNC) is a rare multiple neoplasia syndrome involving cardiac, endocrine, neural, and cutaneous tumors and a variety of pigmented skin lesions. CNC can be inherited as an autosomal dominant trait, ...
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    Somatic GPR101 Duplication Causing X-Linked Acrogigantism (XLAG)-Diagnosis and Management 

    Rodd, C; Millette, M; Iacovazzo, D; Stiles, CE; Barry, S; Evanson, J; Albrecht, S; Caswell, R; Bunce, B; Jose, S;... (2016-05)
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    Reduced protein expression of the phosphodiesterases PDE4A4 and PDE4A8 in AIP mutation positive somatotroph adenomas 

    Bizzi, MF; Pinheiro, SVB; Bolger, GB; Schweizer, JRDOL; Giannetti, AV; Dang, MN; Ribeiro-Oliveira, A; Korbonits, M
    © 2018 Type 4 phosphodiesterases (PDE4s) of the large PDE enzyme superfamily have unique specificity for cAMP and may, therefore, be relevant for somatotroph tumorigenesis. Somatotroph adenomas typically overexpress PDEs ...
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    Metabolic Syndrome in Cushing's Syndrome Patients. 

    Ferraù, F; Korbonits, M (2018)
    Cushing's syndrome (CS), including visceral obesity, dyslipidemia, hypertension and diabetes among its many manifestations, is "a model" of metabolic syndrome. Glucocorticoid (GC) excess, through a combination of effects ...
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    Macimorelin as a Diagnostic Test for Adult GH Deficiency 

    Garcia, JM; Biller, BMK; Korbonits, M; Popovic, V; Luger, A; Strasburger, CJ; Chanson, P; Medic-Stojanoska, M; Schopohl, J; Zakrzewska, A;... (2018-08)
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