Detalhe da pesquisa
1.
Deterioration in Distortion Product Otoacoustic Emissions in Auditory Neuropathy Patients With Distinct Clinical and Genetic Backgrounds.
Ear Hear
; 40(1): 184-191, 2019.
Artigo
em Inglês
| MEDLINE | ID: mdl-29688962
2.
Analysis of Streptococcus pneumoniae and Haemophilus influenzae isolated from middle ear fluid before and after the introduction of government subsidies for pneumococcal and H. influenzae type b vaccines in Japan.
J Infect Chemother
; 23(2): 85-89, 2017 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-27889249
3.
A novel frameshift variant of COCH supports the hypothesis that haploinsufficiency is not a cause of autosomal dominant nonsyndromic deafness 9.
Biochem Biophys Res Commun
; 469(2): 270-4, 2016 Jan 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-26631968
4.
[Cases of pediatric hearing impairment with bilateral stenosis of the bony cochlear nerve canal: bilateral stenosis of bony cochlear nerve canal].
Nihon Jibiinkoka Gakkai Kaiho
; 115(9): 849-54, 2012 Sep.
Artigo
em Japonês
| MEDLINE | ID: mdl-23198572
5.
Clinical and genetic analysis of children with hearing loss and bilateral enlarged vestibular aqueducts.
Int J Pediatr Otorhinolaryngol
; 152: 110975, 2022 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-34801268
6.
The influence of tonsillectomy on allergic diseases in pediatric patients.
Int J Pediatr Otorhinolaryngol
; 140: 110503, 2021 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-33223275
7.
Differences in hearing levels between siblings with hearing loss caused by GJB2 mutations.
Auris Nasus Larynx
; 47(6): 938-942, 2020 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-32553771
8.
High-level heteroplasmy for the m.7445A>G mitochondrial DNA mutation can cause progressive sensorineural hearing loss in infancy.
Int J Pediatr Otorhinolaryngol
; 108: 125-131, 2018 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-29605341
9.
The first sporadic case of DFNA11 identified by next-generation sequencing.
Int J Pediatr Otorhinolaryngol
; 100: 183-186, 2017 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-28802369
10.
Suppression of inflammation by dexamethasone prolongs adenoviral vector-mediated transgene expression in murine nasal mucosa.
Acta Otolaryngol
; 125(12): 1301-6, 2005 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-16303678
11.
High prevalence of CDH23 mutations in patients with congenital high-frequency sporadic or recessively inherited hearing loss.
Orphanet J Rare Dis
; 10: 60, 2015 May 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-25963016
12.
Effects of adenoviral vector-mediated BDNF expression on the bulbectomy-induced apoptosis of olfactory receptor neurons.
Brain Res Mol Brain Res
; 129(1-2): 88-95, 2004 Oct 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-15469885
13.
In vivo expression of adenovirus-mediated lacZ gene in murine nasal mucosa.
Acta Otolaryngol
; 122(6): 627-33, 2002 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-12403125
14.
Chronic constipation recognized as a sign of a SOX10 mutation in a patient with Waardenburg syndrome.
Gene
; 540(2): 258-62, 2014 May 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-24582978
15.
Subgroups of enlarged vestibular aqueduct in relation to SLC26A4 mutations and hearing loss.
Laryngoscope
; 124(4): E134-40, 2014 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-24105851
16.
Cochlear nerve deficiency and associated clinical features in patients with bilateral and unilateral hearing loss.
Otol Neurotol
; 34(3): 554-8, 2013 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-23449441
17.
GJB2-associated hearing loss undetected by hearing screening of newborns.
Gene
; 532(1): 41-5, 2013 Dec 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-24013081