177 related articles for article (PubMed ID: 25488846)
1. Audiologic presentation of enlargement of the vestibular aqueduct according to the SLC26A4 genotypes.
Rah YC; Kim AR; Koo JW; Lee JH; Oh SH; Choi BY
Laryngoscope; 2015 Jun; 125(6):E216-22. PubMed ID: 25488846
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. 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; 127(7):E238-E243. PubMed ID: 27859305
[TBL] [Abstract][Full Text] [Related]
4. 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; 120(2):384-9. PubMed ID: 19998422
[TBL] [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
[TBL] [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; 9():167. PubMed ID: 21961810
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. 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]
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; 14():56. PubMed ID: 23705809
[TBL] [Abstract][Full Text] [Related]
10. A common
Chattaraj P; Munjal T; Honda K; Rendtorff ND; Ratay JS; Muskett JA; Risso DS; Roux I; Gertz EM; Schäffer AA; Friedman TB; Morell RJ; Tranebjærg L; Griffith AJ
J Med Genet; 2017 Oct; 54(10):665-673. PubMed ID: 28780564
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. 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]
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. Diagnostic Value of SLC26A4 Mutation Status in Hereditary Hearing Loss With EVA: A PRISMA-Compliant Meta-Analysis.
Lu YJ; Yao J; Wei QJ; Xing GQ; Cao X
Medicine (Baltimore); 2015 Dec; 94(50):e2248. PubMed ID: 26683941
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. Mutation analysis of SLC26A4 in mainland Chinese patients with enlarged vestibular aqueduct.
Reyes S; Wang G; Ouyang X; Han B; Du LL; Yuan HJ; Yan D; Dai P; Liu XZ
Otolaryngol Head Neck Surg; 2009 Oct; 141(4):502-8. PubMed ID: 19786220
[TBL] [Abstract][Full Text] [Related]
17. 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; 90():170-174. PubMed ID: 27729126
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. 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; 139(9):907-13. PubMed ID: 24051746
[TBL] [Abstract][Full Text] [Related]
20. 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; 24(4):639-48. PubMed ID: 24224479
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
