• Login
    JavaScript is disabled for your browser. Some features of this site may not work without it.
    Search 
    •   QMRO Home
    • Search
    •   QMRO Home
    • Search
    ‌
    ‌

    Browse

    All of QMROCommunities & CollectionsBy Issue DateAuthorsTitlesSubjects
    ‌
    ‌

    Administrators only

    Login
    ‌
    ‌

    Discover

    Author
    Korbonits, M (9)
    Akker, SA (2)Dang, MN (2)Assié, G (1)Baldeweg, SE (1)Banerjee, A (1)Bertherat, J (1)Beuschlein, F (1)Bidlingmaier, M (1)Biermasz, NR (1)... View MoreSubject
    Adult (9)
    Humans (9)Female (8)Male (8)Middle Aged (5)Young Adult (5)Adenoma (4)Mutation (4)Aged (3)Germ-Line Mutation (3)... View MoreDate Issued2018 (3)2017 (4)2016 (2)
    ‌
    ‌

    Statistics

    Most Popular ItemsStatistics by CountryMost Popular Authors

    Search

    Show Advanced FiltersHide Advanced Filters

    Filters

    Use filters to refine the search results.

    Now showing items 1-9 of 9

    • Sort Options:
    • Relevance
    • Title Asc
    • Title Desc
    • Issue Date Asc
    • Issue Date Desc
    • Results Per Page:
    • 5
    • 10
    • 20
    • 40
    • 60
    • 80
    • 100
    Thumbnail

    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 ...
    Thumbnail

    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, ...
    Thumbnail

    Cantú syndrome with coexisting familial pituitary adenoma. 

    Marques, P; Spencer, R; Morrison, PJ; Carr, IM; Dang, MN; Bonthron, DT; Hunter, S; Korbonits, M (2018-03)
    CONTEXT: Pseudoacromegaly describes conditions with an acromegaly related physical appearance without abnormalities in the growth hormone (GH) axis. Acromegaloid facies, together with hypertrichosis, are typical manifestations ...
    Thumbnail

    Somatic USP8 mutations are frequent events in corticotroph tumor progression causing Nelson's tumor. 

    Pérez-Rivas, LG; Theodoropoulou, M; Puar, TH; Fazel, J; Stieg, MR; Ferraù, F; Assié, G; Gadelha, MR; Deutschbein, T; Fragoso, MC;... (2018-01)
    OBJECTIVE: Somatic mutations in the ubiquitin-specific protease 8 (USP8) gene are frequent in corticotroph tumors causing Cushing's disease (CD). Corticotroph tumor progression, the so-called Nelson's syndrome (NS), is a ...
    Thumbnail

    A novel DICER1 mutation in familial multinodular goitre. 

    Caimari, F; Kumar, AV; Kurzawinski, T; Butler, G; Sabbaghian, N; Foulkes, WD; Korbonits, M (2018-07)
    Thumbnail

    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 ...
    Thumbnail

    Novel Germline p.Gly42Val MEN1 Mutation in a Family with Multiple Endocrine Neoplasia Type 1 - Excellent Response of Prolactinoma to Cabergoline. 

    Koehler, VF; Jungheim, K; Groß, U; Iacovazzo, D; Mann, A; Korbonits, M (2017-09)
    We report on a 27-year-old male patient presenting with renal colic secondary to hyperparathyroidism. Further investigations confirmed a diagnosis of type 1 multiple endocrine neoplasia and revealed a 2.0 cm pancreatic ...
    Thumbnail

    Pituitary Carcinoma in a Patient with an SDHB Mutation. 

    Tufton, N; Roncaroli, F; Hadjidemetriou, I; Dang, MN; Dénes, J; Guasti, L; Thom, M; Powell, M; Baldeweg, SE; Fersht, N;... (2017-12)
    We present the first case of pituitary carcinoma occurring in a patient with a succinate dehydrogenase subunit B (SDHB) mutation and history of paraganglioma. She was initially treated for a glomus tumour with external ...
    Thumbnail

    Succinate Dehydrogenase B (SDHB)-Associated Bladder Paragangliomas. 

    Srirangalingam, U; Banerjee, A; Patki, P; Peters, J; George, E; Chew, SL; Kumar, VKA; Korbonits, M; Waterhouse, M; Druce, MR;... (2017-02)
    Twitter iconFollow QMUL on Twitter
    Twitter iconFollow QM Research
    Online on twitter
    Facebook iconLike us on Facebook
    • Site Map
    • Privacy and cookies
    • Disclaimer
    • Accessibility
    • Contacts
    • Intranet
    • Current students

    Modern Slavery Statement

    Queen Mary University of London
    Mile End Road
    London E1 4NS
    Tel: +44 (0)20 7882 5555

    © Queen Mary University of London.