Works matching Pendred syndrome


Results: 268
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    Pendred Syndrome, or Not Pendred Syndrome? That Is the Question.

    Published in:
    Genes, 2021, v. 12, n. 10, p. 1569, doi. 10.3390/genes12101569
    By:
    • Tesolin, Paola;
    • Fiorino, Sofia;
    • Lenarduzzi, Stefania;
    • Rubinato, Elisa;
    • Cattaruzzi, Elisabetta;
    • Ammar, Lydie;
    • Castro, Veronica;
    • Orzan, Eva;
    • Granata, Claudio;
    • Dell'Orco, Daniele;
    • Morgan, Anna;
    • Girotto, Giorgia
    Publication type:
    Article
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    Pendred’s Syndrome.

    Published in:
    European Neurology, 2007, v. 58, n. 3, p. 189, doi. 10.1159/000104724
    By:
    • Pearce, J. M. S.
    Publication type:
    Article
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    Incomplete partition type II in its various manifestations: isolated, in association with EVA, syndromic, and beyond; a multicentre international study.

    Published in:
    Neuroradiology, 2024, v. 66, n. 8, p. 1397, doi. 10.1007/s00234-024-03386-z
    By:
    • D'Arco, Felice;
    • Kandemirli, Sedat G.;
    • Dahmoush, Hisham M.;
    • Alves, Cesar A. P. F.;
    • Severino, Mariasavina;
    • Dellepiane, Francesco;
    • Robson, Caroline D.;
    • Lequin, Maarten H.;
    • Rossi-Espagnet, Camilla;
    • O'Brien, William T.;
    • Nash, Robert;
    • Clement, Emma;
    • Juliano, Amy F.
    Publication type:
    Article
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    Cochlear implantation in Pendred syndrome.

    Published in:
    Cochlear Implants International: An Interdisciplinary Journal, 2011, v. 12, n. 3, p. 157, doi. 10.1179/146701011X12950038111819
    By:
    • Kontorinis, Georgios;
    • Lenarz, Thomas;
    • Lesinski-Schiedat, Anke;
    • Neuburger, Juergen
    Publication type:
    Article
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    Pendredův syndrom v České republice.

    Published in:
    Otorhinolaryngology & Phoniatrics / Otorinolaryngologie a Foniatrie, 2011, v. 60, n. 2, p. 103
    By:
    • Katra, R.;
    • Pourová, R.;
    • Dytrych, P.;
    • Jelínková, H.;
    • Kabelka, Z.;
    • Dvořáková, M.;
    • Astl, J.
    Publication type:
    Article
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    Pendred syndrome.

    Published in:
    Expert Review of Endocrinology & Metabolism, 2008, v. 3, n. 5, p. 635, doi. 10.1586/17446651.3.5.635
    By:
    • Abeal, Joaquin Lado
    Publication type:
    Article
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    Functional Characterization of Wild-Type and a Mutated Form of SLC26A4 Identified in a Patient with Pendred Syndrome.

    Published in:
    Cellular Physiology & Biochemistry (Karger AG), 2006, v. 17, n. 5/6, p. 245, doi. 10.1159/000094137
    By:
    • Dossena, Silvia;
    • Vezzoli, Valeria;
    • Cerutti, Nadia;
    • Bazzini, Claudia;
    • Tosco, Marisa;
    • Sironi, Chiara;
    • Rodighiero, Simona;
    • Meyer, Giuliano;
    • Fascio, Umberto;
    • Fürst, Johannes;
    • Ritter, Markus;
    • Fugazzola, Laura;
    • Persani, Luca;
    • Zorowka, Patrick;
    • Storelli, Carlo;
    • Beck-Peccoz, Paolo;
    • Bottà, Guido;
    • Paulmichl, Markus
    Publication type:
    Article
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