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Journal Abstract Search

541 related items for PubMed ID: 24105851

  • 1. 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
    [Abstract] [Full Text] [Related]

  • 2. The influence of mutations in the SLC26A4 gene on the temporal bone in a population with enlarged vestibular aqueduct.
    Madden C, Halsted M, Meinzen-Derr J, Bardo D, Boston M, Arjmand E, Nishimura C, Yang T, Benton C, Das V, Smith R, Choo D, Greinwald J.
    Arch Otolaryngol Head Neck Surg; 2007 Feb; 133(2):162-8. PubMed ID: 17309986
    [Abstract] [Full Text] [Related]

  • 3. Significance of unilateral enlarged vestibular aqueduct.
    Greinwald J, DeAlarcon A, Cohen A, Uwiera T, Zhang K, Benton C, Halstead M, Meinzen-Derr J.
    Laryngoscope; 2013 Jun; 123(6):1537-46. PubMed ID: 23401162
    [Abstract] [Full Text] [Related]

  • 4. Enlarged vestibular aqueduct: Audiological and genetical features in children and adolescents.
    Aimoni C, Ciorba A, Cerritelli L, Ceruti S, Skarżyński PH, Hatzopoulos S.
    Int J Pediatr Otorhinolaryngol; 2017 Oct; 101():254-258. PubMed ID: 28780189
    [Abstract] [Full Text] [Related]

  • 5. Atypical patterns of segregation of familial enlargement of the vestibular aqueduct.
    Muskett JA, Chattaraj P, Heneghan JF, Reimold FR, Shmukler BE, Brewer CC, King KA, Zalewski CK, Shawker TH, Butman JA, Kenna MA, Chien WW, Alper SL, Griffith AJ.
    Laryngoscope; 2016 Jul; 126(7):E240-7. PubMed ID: 26485571
    [Abstract] [Full Text] [Related]

  • 6. Extremely discrepant mutation spectrum of SLC26A4 between Chinese patients with isolated Mondini deformity and enlarged vestibular aqueduct.
    Huang S, Han D, Yuan Y, Wang G, Kang D, Zhang X, Yan X, Meng X, Dong M, Dai P.
    J Transl Med; 2011 Sep 30; 9():167. PubMed ID: 21961810
    [Abstract] [Full Text] [Related]

  • 7. Correlation analysis of genotypes, auditory function, and vestibular size in Chinese children with enlarged vestibular aqueduct syndrome.
    Zhao FF, Lan L, Wang DY, Han B, Qi Y, Zhao Y, Zong L, Li Q, Wang QJ.
    Acta Otolaryngol; 2013 Dec 30; 133(12):1242-9. PubMed ID: 24245694
    [Abstract] [Full Text] [Related]

  • 8. Novel compound heterozygous mutations in SLC26A4 gene in a Chinese Han family with enlarged vestibular aqueduct.
    Wang M, Zhang F, Xu L, Xiao Y, Li J, Fan Z, Sun Q, Bai X, Wang H.
    Int J Pediatr Otorhinolaryngol; 2016 Nov 30; 90():170-174. PubMed ID: 27729126
    [Abstract] [Full Text] [Related]

  • 9. Pathogenic substitution of IVS15 + 5G > A in SLC26A4 in patients of Okinawa Islands with enlarged vestibular aqueduct syndrome or Pendred syndrome.
    Ganaha A, Kaname T, Yanagi K, Naritomi K, Tono T, Usami S, Suzuki M.
    BMC Med Genet; 2013 May 24; 14():56. PubMed ID: 23705809
    [Abstract] [Full Text] [Related]

  • 10. Use of SLC26A4 mutation testing for unilateral enlargement of the vestibular aqueduct.
    Chattaraj P, Reimold FR, Muskett JA, Shmukler BE, Chien WW, Madeo AC, Pryor SP, Zalewski CK, Butman JA, Brewer CC, Kenna MA, Alper SL, Griffith AJ.
    JAMA Otolaryngol Head Neck Surg; 2013 Sep 24; 139(9):907-13. PubMed ID: 24051746
    [Abstract] [Full Text] [Related]

  • 11. [Correlation of temporal bone HRCT, SLC26A4 gene and hearing loss in enlarged vestibular aqueduct].
    Zhao Z, Zhu Y, Fu Y, Jiang H.
    Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2022 Oct 24; 36(10):736-740. PubMed ID: 36217650
    [Abstract] [Full Text] [Related]

  • 12. 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
    [Abstract] [Full Text] [Related]

  • 13. Intrafamilial phenotypic variability in families with biallelic SLC26A4 mutations.
    Song MH, Shin JW, Park HJ, Lee KA, Kim Y, Kim UK, Jeon JH, Choi JY.
    Laryngoscope; 2014 May 02; 124(5):E194-202. PubMed ID: 24338212
    [Abstract] [Full Text] [Related]

  • 14. SLC26A4 genotype, but not cochlear radiologic structure, is correlated with hearing loss in ears with an enlarged vestibular aqueduct.
    King KA, Choi BY, Zalewski C, Madeo AC, Manichaikul A, Pryor SP, Ferruggiaro A, Eisenman D, Kim HJ, Niparko J, Thomsen J, Butman JA, Griffith AJ, Brewer CC.
    Laryngoscope; 2010 Feb 02; 120(2):384-9. PubMed ID: 19998422
    [Abstract] [Full Text] [Related]

  • 15. Analysis of the thyroid phenotype in 42 patients with Pendred syndrome and nonsyndromic enlargement of the vestibular aqueduct.
    Ladsous M, Vlaeminck-Guillem V, Dumur V, Vincent C, Dubrulle F, Dhaenens CM, Wémeau JL.
    Thyroid; 2014 Apr 02; 24(4):639-48. PubMed ID: 24224479
    [Abstract] [Full Text] [Related]

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  • 17. SLC26A4/PDS genotype-phenotype correlation in hearing loss with enlargement of the vestibular aqueduct (EVA): evidence that Pendred syndrome and non-syndromic EVA are distinct clinical and genetic entities.
    Pryor SP, Madeo AC, Reynolds JC, Sarlis NJ, Arnos KS, Nance WE, Yang Y, Zalewski CK, Brewer CC, Butman JA, Griffith AJ.
    J Med Genet; 2005 Feb 02; 42(2):159-65. PubMed ID: 15689455
    [No Abstract] [Full Text] [Related]

  • 18. Clinical and genetic analysis of children with hearing loss and bilateral enlarged vestibular aqueducts.
    Nakano A, Arimoto Y, Mutai H, Nara K, Inoue S, Matsunaga T.
    Int J Pediatr Otorhinolaryngol; 2022 Jan 02; 152():110975. PubMed ID: 34801268
    [Abstract] [Full Text] [Related]

  • 19. Hearing loss associated with enlarged vestibular aqueduct and zero or one mutant allele of SLC26A4.
    Rose J, Muskett JA, King KA, Zalewski CK, Chattaraj P, Butman JA, Kenna MA, Chien WW, Brewer CC, Griffith AJ.
    Laryngoscope; 2017 Jul 02; 127(7):E238-E243. PubMed ID: 27859305
    [Abstract] [Full Text] [Related]

  • 20. 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
    [Abstract] [Full Text] [Related]

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