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Journal Abstract Search

365 related items for PubMed ID: 18692402

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  • 3. Clinical and molecular characteristics of Pendred syndrome.
    Kopp P, Bizhanova A.
    Ann Endocrinol (Paris); 2011 Apr; 72(2):88-94. PubMed ID: 21511235
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  • 5. Pendred syndrome.
    Glaser B.
    Pediatr Endocrinol Rev; 2003 Dec; 1 Suppl 2():199-204; discussion 204. PubMed ID: 16444159
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  • 10. Analysis of the SLC26A4 gene in patients with Pendred syndrome in Taiwan.
    Lai CC, Chiu CY, Shiao AS, Tso YC, Wu YC, Tu TY, Jap TS.
    Metabolism; 2007 Sep; 56(9):1279-84. PubMed ID: 17697873
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  • 11. TSH regulates pendrin membrane abundance and enhances iodide efflux in thyroid cells.
    Pesce L, Bizhanova A, Caraballo JC, Westphal W, Butti ML, Comellas A, Kopp P.
    Endocrinology; 2012 Jan; 153(1):512-21. PubMed ID: 22109890
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  • 13. Hereditary hearing loss with thyroid abnormalities.
    Choi BY, Muskett J, King KA, Zalewski CK, Shawker T, Reynolds JC, Butman JA, Brewer CC, Stewart AK, Alper SL, Griffith AJ.
    Adv Otorhinolaryngol; 2011 Jan; 70():43-49. PubMed ID: 21358184
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  • 15. Congenital goitrous hypothyroidism, deafness and iodide organification defect in four siblings: Pendred or pseudo-Pendred syndrome?
    Kara C, Kılıç M, Uçaktürk A, Aydın M.
    J Clin Res Pediatr Endocrinol; 2010 Jan; 2(2):81-4. PubMed ID: 21274344
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  • 17. Differential diagnosis between Pendred and pseudo-Pendred syndromes: clinical, radiologic, and molecular studies.
    Fugazzola L, Cerutti N, Mannavola D, Crino A, Cassio A, Gasparoni P, Vannucchi G, Beck-Peccoz P.
    Pediatr Res; 2002 Apr; 51(4):479-84. PubMed ID: 11919333
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  • 20. Expression of pendrin and the Pendred syndrome (PDS) gene in human thyroid tissues.
    Bidart JM, Mian C, Lazar V, Russo D, Filetti S, Caillou B, Schlumberger M.
    J Clin Endocrinol Metab; 2000 May; 85(5):2028-33. PubMed ID: 10843192
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