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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

275 related items for PubMed ID: 32910226

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  • 12. Subgroups of enlarged vestibular aqueduct in relation to SLC26A4 mutations and hearing loss.
    Okamoto Y, Mutai H, Nakano A, Arimoto Y, Sugiuchi T, Masuda S, Morimoto N, Sakamoto H, Ogahara N, Takagi A, Taiji H, Kaga K, Ogawa K, Matsunaga T.
    Laryngoscope; 2014 Apr; 124(4):E134-40. PubMed ID: 24105851
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  • 13. 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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  • 19. Study on the relationship between the pathogenic mutations of SLC26A4 and CT phenotypes of inner ear in patient with sensorineural hearing loss.
    Wu L, Liu Y, Wu J, Chen S, Tang S, Jiang Y, Dai P.
    Biosci Rep; 2019 Mar 29; 39(3):. PubMed ID: 30842343
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  • 20. The Natural History of Hearing Loss in Pendred Syndrome and Non-Syndromic Enlarged Vestibular Aqueduct.
    Mey K, Bille M, Rye Rasmussen SH, Tranebjærg L, Cayé-Thomasen P.
    Otol Neurotol; 2019 Mar 29; 40(3):e178-e185. PubMed ID: 30741891
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