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Journal Abstract Search

329 related items for PubMed ID: 21358184

  • 1. 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; 70():43-49. PubMed ID: 21358184
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  • 4. Mutations in the SLC26A4 (pendrin) gene in patients with sensorineural deafness and enlarged vestibular aqueduct.
    Bogazzi F, Russo D, Raggi F, Ultimieri F, Berrettini S, Forli F, Grasso L, Ceccarelli C, Mariotti S, Pinchera A, Bartalena L, Martino E.
    J Endocrinol Invest; 2004 May; 27(5):430-5. PubMed ID: 15279074
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  • 5. Pendred syndrome.
    Wémeau JL, Kopp P.
    Best Pract Res Clin Endocrinol Metab; 2017 Mar; 31(2):213-224. PubMed ID: 28648509
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  • 6. SLC26A4-linked CEVA haplotype correlates with phenotype in patients with enlargement of the vestibular aqueduct.
    Chao JR, Chattaraj P, Munjal T, Honda K, King KA, Zalewski CK, Chien WW, Brewer CC, Griffith AJ.
    BMC Med Genet; 2019 Jul 02; 20(1):118. PubMed ID: 31266487
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  • 8. Association of SLC26A4 mutations, morphology, and hearing in pendred syndrome and NSEVA.
    Mey K, Muhamad AA, Tranebjaerg L, Rendtorff ND, Rasmussen SH, Bille M, Cayé-Thomasen P.
    Laryngoscope; 2019 Nov 02; 129(11):2574-2579. PubMed ID: 31633822
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  • 10. Genetics and phenomics of Pendred syndrome.
    Bizhanova A, Kopp P.
    Mol Cell Endocrinol; 2010 Jun 30; 322(1-2):83-90. PubMed ID: 20298745
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  • 11. Enlarged vestibular aqueduct and Mondini Malformation: audiological, clinical, radiologic and genetic features.
    Forli F, Lazzerini F, Auletta G, Bruschini L, Berrettini S.
    Eur Arch Otorhinolaryngol; 2021 Jul 30; 278(7):2305-2312. PubMed ID: 32910226
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  • 16. Functional assessment of allelic variants in the SLC26A4 gene involved in Pendred syndrome and nonsyndromic EVA.
    Pera A, Dossena S, Rodighiero S, Gandía M, Bottà G, Meyer G, Moreno F, Nofziger C, Hernández-Chico C, Paulmichl M.
    Proc Natl Acad Sci U S A; 2008 Nov 25; 105(47):18608-13. PubMed ID: 19017801
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  • 17. Pendred syndrome and iodide transport in the thyroid.
    Kopp P, Pesce L, Solis-S JC.
    Trends Endocrinol Metab; 2008 Sep 25; 19(7):260-8. PubMed ID: 18692402
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  • 18. Lack of significant association between mutations of KCNJ10 or FOXI1 and SLC26A4 mutations in Pendred syndrome/enlarged vestibular aqueducts.
    Landa P, Differ AM, Rajput K, Jenkins L, Bitner-Glindzicz M.
    BMC Med Genet; 2013 Aug 21; 14():85. PubMed ID: 23965030
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  • 19. [Current status and perspectives of the research in Pendred syndrome].
    Matsunaga T, Fujioka M, Hosoya M.
    Nihon Rinsho; 2013 Dec 21; 71(12):2215-22. PubMed ID: 24437281
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