Detalhe da pesquisa
1.
Evaluation of vestibular function following endolymphatic sac surgery.
Eur Arch Otorhinolaryngol
; 279(3): 1193-1201, 2022 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-33740085
2.
SLC26A4 gene is frequently involved in nonsyndromic hearing impairment with enlarged vestibular aqueduct in Caucasian populations.
Eur J Hum Genet
; 14(6): 773-9, 2006 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-16570074
3.
GJB2 and GJB6 mutations: genotypic and phenotypic correlations in a large cohort of hearing-impaired patients.
Arch Otolaryngol Head Neck Surg
; 131(6): 481-7, 2005 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-15967879
4.
[The early medico-social center for hearing loss (Nantes University Hospital). A twenty two years experience]. / Le Centre d'Action Médico-Sociale Précoce spécialisé pour la déficience auditive de l'enfant (CHU de Nantes). Une expérience de vingt deux ans.
Bull Acad Natl Med
; 188(1): 77-84; discussion 85-6, 2004.
Artigo
em Francês
| MEDLINE | ID: mdl-15368927
5.
Complete exon sequencing of all known Usher syndrome genes greatly improves molecular diagnosis.
Orphanet J Rare Dis
; 6: 21, 2011 May 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-21569298
6.
Systematic screening for nonspecific autoantibodies in idiopathic sensorineural hearing loss: no association with steroid response.
Otol Neurotol
; 31(4): 687-90, 2010 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-20400925
7.
Screening of SLC26A4, FOXI1 and KCNJ10 genes in unilateral hearing impairment with ipsilateral enlarged vestibular aqueduct.
Int J Pediatr Otorhinolaryngol
; 74(9): 1049-53, 2010 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-20621367
8.
Large deletion of the GJB6 gene in deaf patients heterozygous for the GJB2 gene mutation: genotypic and phenotypic analysis.
Am J Med Genet A
; 127A(3): 263-7, 2004 Jun 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-15150777