Works about WERMER syndrome


Results: 143
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    A MEN1 syndrome with a paraganglioma.

    Published in:
    European Journal of Human Genetics, 2014, v. 22, n. 2, p. 283, doi. 10.1038/ejhg.2013.128
    By:
    • Jamilloux, Yvan;
    • Favier, Judith;
    • Pertuit, Morgane;
    • Delage-Corre, Manuela;
    • Lopez, Stéphanie;
    • Teissier, Marie-Pierre;
    • Mathonnet, Muriel;
    • Galinat, Sophie;
    • Barlier, Anne;
    • Archambeaud, Françoise
    Publication type:
    Article
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    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
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