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    Author
    Korbonits, M (12)
    Iacovazzo, D (2)Altieri, B (1)Anile, C (1)Artignan, A (1)Bajaj, A (1)Barry, S (1)Bianchi, A (1)Bidlingmaier, M (1)Biermasz, NR (1)... View MoreSubject
    Acromegaly (12)
    AIP (5)Humans (5)Female (4)Growth Hormone-Secreting Pituitary Adenoma (4)Adenoma (3)Male (3)Mutation (3)Adult (2)FIPA (2)... View MoreDate Issued2023 (3)2020 (2)2018 (1)2017 (2)2016 (3)
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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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    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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    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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    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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    AIP mutations in young patients with acromegaly and the Tampico Giant: the Mexican experience 

    Ramirez-Renteria, C; Hernandez-Ramirez, LC; Portocarrero-Ortiz, L; Vargas, G; Melgar, V; Espinosa, E; Laura Espinosa-de-los-Monteros, A; Sosa, E; Gonzalez, B; Zuniga, S;... (2016-08)
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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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    Patient-reported outcomes of parenteral somatostatin analogue injections in 195 patients with acromegaly. 

    Strasburger, CJ; Karavitaki, N; Störmann, S; Trainer, PJ; Kreitschmann-Andermahr, I; Droste, M; Korbonits, M; Feldmann, B; Zopf, K; Sanderson, VF;... (2016-03)
    BACKGROUND: Long-acting somatostatin analogues delivered parenterally are the most widely used medical treatment in acromegaly. This patient-reported outcomes survey was designed to assess the impact of chronic injections ...
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    Update on the Genetics of Pituitary Tumors 

    Barry, S; Korbonits, M (2020-09)
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    Novel AIP mutation in exon 6 causing acromegaly in a German family. 

    Detomas, M; Altieri, B; Flitsch, J; Saeger, W; Korbonits, M; Deutschbein, T (2023-08)
    The most frequent genetic alteration of familial isolated growth hormone producing pituitary neuroendocrine tumors is a germline mutation of the aryl hydrocarbon receptor-interacting protein (AIP) gene. Various AIP mutations ...
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    Macro-GH - A clinical entity causing a diagnostic challenge - A case report. 

    Stelmachowska-Banaś, M; Ostrowska, M; Goszczyński, TM; Kowalski, K; Korbonits, M; Kapuścińska, R; Zgliczyński, W; Glinicki, P (2023-06-01)
    AIM: Presentation of a new case of a patient with macro-GH, that may interfere with different GH assays leading to false-positive results in serum samples. CASE PRESENTATION: A 61-year-old female was referred with a pituitary ...
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