243 related articles for article (PubMed ID: 26900070)
1. Vestibular function is associated with residual low-frequency hearing loss in patients with bi-allelic mutations in the SLC26A4 gene.
Jung J; Seo YW; Choi JY; Kim SH
Hear Res; 2016 May; 335():33-39. PubMed ID: 26900070
[TBL] [Abstract][Full Text] [Related]
2. 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
[TBL] [Abstract][Full Text] [Related]
3. 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
[TBL] [Abstract][Full Text] [Related]
4. 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; 20(1):118. PubMed ID: 31266487
[TBL] [Abstract][Full Text] [Related]
5. 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; 9():167. PubMed ID: 21961810
[TBL] [Abstract][Full Text] [Related]
6. 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
[TBL] [Abstract][Full Text] [Related]
7. Mono-allelic mutations of SLC26A4 is over-presented in deaf patients with non-syndromic enlarged vestibular aqueduct.
Pang X; Chai Y; Chen P; He L; Wang X; Wu H; Yang T
Int J Pediatr Otorhinolaryngol; 2015 Aug; 79(8):1351-3. PubMed ID: 26100058
[TBL] [Abstract][Full Text] [Related]
8. 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
[TBL] [Abstract][Full Text] [Related]
9. Genetic architecture and phenotypic landscape of SLC26A4-related hearing loss.
Honda K; Griffith AJ
Hum Genet; 2022 Apr; 141(3-4):455-464. PubMed ID: 34345941
[TBL] [Abstract][Full Text] [Related]
10. Molecular epidemiology and functional assessment of novel allelic variants of SLC26A4 in non-syndromic hearing loss patients with enlarged vestibular aqueduct in China.
Yuan Y; Guo W; Tang J; Zhang G; Wang G; Han M; Zhang X; Yang S; He DZ; Dai P
PLoS One; 2012; 7(11):e49984. PubMed ID: 23185506
[TBL] [Abstract][Full Text] [Related]
11. Identification of novel functional null allele of SLC26A4 associated with enlarged vestibular aqueduct and its possible implication.
Jang JH; Jung J; Kim AR; Cho YM; Kim MY; Lee SY; Choi JY; Lee JH; Choi BY
Audiol Neurootol; 2014; 19(5):319-26. PubMed ID: 25358692
[TBL] [Abstract][Full Text] [Related]
12. 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; 129(11):2574-2579. PubMed ID: 31633822
[TBL] [Abstract][Full Text] [Related]
13. Hypo-functional SLC26A4 variants associated with nonsyndromic hearing loss and enlargement of the vestibular aqueduct: genotype-phenotype correlation or coincidental polymorphisms?
Choi BY; Stewart AK; Madeo AC; Pryor SP; Lenhard S; Kittles R; Eisenman D; Kim HJ; Niparko J; Thomsen J; Arnos KS; Nance WE; King KA; Zalewski CK; Brewer CC; Shawker T; Reynolds JC; Butman JA; Karniski LP; Alper SL; Griffith AJ
Hum Mutat; 2009 Apr; 30(4):599-608. PubMed ID: 19204907
[TBL] [Abstract][Full Text] [Related]
14. 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; 133(12):1242-9. PubMed ID: 24245694
[TBL] [Abstract][Full Text] [Related]
15. SLC26A4 gene is frequently involved in nonsyndromic hearing impairment with enlarged vestibular aqueduct in Caucasian populations.
Albert S; Blons H; Jonard L; Feldmann D; Chauvin P; Loundon N; Sergent-Allaoui A; Houang M; Joannard A; Schmerber S; Delobel B; Leman J; Journel H; Catros H; Dollfus H; Eliot MM; David A; Calais C; Drouin-Garraud V; Obstoy MF; Tran Ba Huy P; Lacombe D; Duriez F; Francannet C; Bitoun P; Petit C; Garabédian EN; Couderc R; Marlin S; Denoyelle F
Eur J Hum Genet; 2006 Jun; 14(6):773-9. PubMed ID: 16570074
[TBL] [Abstract][Full Text] [Related]
16. Phenotypic analyses and mutation screening of the SLC26A4 and FOXI1 genes in 101 Taiwanese families with bilateral nonsyndromic enlarged vestibular aqueduct (DFNB4) or Pendred syndrome.
Wu CC; Lu YC; Chen PJ; Yeh PL; Su YN; Hwu WL; Hsu CJ
Audiol Neurootol; 2010; 15(1):57-66. PubMed ID: 19648736
[TBL] [Abstract][Full Text] [Related]
17. Molecular analysis of hearing loss associated with enlarged vestibular aqueduct in the mainland Chinese: a unique SLC26A4 mutation spectrum.
Hu H; Wu L; Feng Y; Pan Q; Long Z; Li J; Dai H; Xia K; Liang D; Niikawa N; Xia J
J Hum Genet; 2007; 52(6):492-497. PubMed ID: 17443271
[TBL] [Abstract][Full Text] [Related]
18. 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; 124(5):E194-202. PubMed ID: 24338212
[TBL] [Abstract][Full Text] [Related]
19. Spectrum and frequency of SLC26A4 mutations among Czech patients with early hearing loss with and without Enlarged Vestibular Aqueduct (EVA).
Pourová R; Janousek P; Jurovcík M; Dvoráková M; Malíková M; Rasková D; Bendová O; Leonardi E; Murgia A; Kabelka Z; Astl J; Seeman P
Ann Hum Genet; 2010 Jul; 74(4):299-307. PubMed ID: 20597900
[TBL] [Abstract][Full Text] [Related]
20. SLC26A4 genotypes and phenotypes associated with enlargement of the vestibular aqueduct.
Ito T; Choi BY; King KA; Zalewski CK; Muskett J; Chattaraj P; Shawker T; Reynolds JC; Butman JA; Brewer CC; Wangemann P; Alper SL; Griffith AJ
Cell Physiol Biochem; 2011; 28(3):545-52. PubMed ID: 22116369
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
