Works matching IS 09456317 AND DT 2017 AND VI 471 AND IP 3


Results: 18
    1
    2
    3
    4

    MEN1 mutations and potentially MEN1-targeting miRNAs are responsible for menin deficiency in sporadic and MEN1 syndrome-associated primary hyperparathyroidism.

    Published in:
    2017
    By:
    • Grolmusz, Vince;
    • Borka, Katalin;
    • Kövesdi, Annamária;
    • Németh, Kinga;
    • Balogh, Katalin;
    • Dékány, Csaba;
    • Kiss, András;
    • Szentpéteri, Anna;
    • Sármán, Beatrix;
    • Somogyi, Anikó;
    • Csajbók, Éva;
    • Valkusz, Zsuzsanna;
    • Tóth, Miklós;
    • Igaz, Péter;
    • Rácz, Károly;
    • Patócs, Attila;
    • Grolmusz, Vince Kornél;
    • Kövesdi, Annamária;
    • Németh, Kinga;
    • Dékány, Csaba
    Publication type:
    journal article
    5
    7
    8
    9
    10
    11
    12
    14
    15
    16
    17
    18

    In this issue.

    Published in:
    Virchows Archiv: European Journal of Pathology, 2017, v. 471, n. 3, p. 309, doi. 10.1007/s00428-017-2228-6
    Publication type:
    Article