Detalhe da pesquisa
1.
Comprehensive Prediction Model, Including Genetic Testing, for the Outcomes of Cochlear Implantation.
Ear Hear
; 44(1): 223-231, 2023.
Artigo
Inglês
| MEDLINE | ID: mdl-35973050
2.
Distinct roles of stereociliary links in the nonlinear sound processing and noise resistance of cochlear outer hair cells.
Proc Natl Acad Sci U S A
; 117(20): 11109-11117, 2020 05 19.
Artigo
Inglês
| MEDLINE | ID: mdl-32358189
3.
Prevalence and Clinical Characteristics of Mitochondrial DNA Mutations in Korean Patients With Sensorineural Hearing Loss.
J Korean Med Sci
; 38(48): e355, 2023 Dec 11.
Artigo
Inglês
| MEDLINE | ID: mdl-38084023
4.
Surgical and nonsurgical treatment outcomes in traumatic facial nerve palsy.
Eur Arch Otorhinolaryngol
; 280(7): 3203-3208, 2023 Jul.
Artigo
Inglês
| MEDLINE | ID: mdl-36708423
5.
COCH-related autosomal dominant nonsyndromic hearing loss: a phenotype-genotype study.
Hum Genet
; 141(3-4): 889-901, 2022 Apr.
Artigo
Inglês
| MEDLINE | ID: mdl-34529116
6.
Differential genetic diagnoses of adult post-lingual hearing loss according to the audiogram pattern and novel candidate gene evaluation.
Hum Genet
; 141(3-4): 915-927, 2022 Apr.
Artigo
Inglês
| MEDLINE | ID: mdl-34519870
7.
The Effects of Preoperative Audiovisual Speech Perception on the Audiologic Outcomes of Cochlear Implantation in Patients with Postlingual Deafness.
Audiol Neurootol
; 26(3): 149-156, 2021.
Artigo
Inglês
| MEDLINE | ID: mdl-33352550
8.
Effect of Cochlear Implantation on Hearing Fluctuation in Patients with Biallelic SLC26A4 Variants.
Audiol Neurootol
; 26(2): 111-120, 2021.
Artigo
Inglês
| MEDLINE | ID: mdl-32877901
9.
Activation of KCNQ4 as a Therapeutic Strategy to Treat Hearing Loss.
Int J Mol Sci
; 22(5)2021 Mar 02.
Artigo
Inglês
| MEDLINE | ID: mdl-33801540
10.
Increased incidence of unilateral sudden sensorineural hearing loss in patients with hematological malignancies requiring hematopoietic stem cell transplantation.
Clin Otolaryngol
; 46(6): 1278-1281, 2021 11.
Artigo
Inglês
| MEDLINE | ID: mdl-34174171
11.
Bicarbonate permeation through anion channels: its role in health and disease.
Pflugers Arch
; 472(8): 1003-1018, 2020 08.
Artigo
Inglês
| MEDLINE | ID: mdl-32621085
12.
Genetic Inheritance of Late-Onset, Down-Sloping Hearing Loss and Its Implications for Auditory Rehabilitation.
Ear Hear
; 41(1): 114-124, 2020.
Artigo
Inglês
| MEDLINE | ID: mdl-31045651
13.
A recurrent mutation in KCNQ4 in Korean families with nonsyndromic hearing loss and rescue of the channel activity by KCNQ activators.
Hum Mutat
; 40(3): 335-346, 2019 03.
Artigo
Inglês
| MEDLINE | ID: mdl-30556268
14.
The TECTA mutation R1890C is identified as one of the causes of genetic hearing loss: a case report.
BMC Med Genet
; 20(1): 57, 2019 04 01.
Artigo
Inglês
| MEDLINE | ID: mdl-30935366
15.
ANO9/TMEM16J promotes tumourigenesis via EGFR and is a novel therapeutic target for pancreatic cancer.
Br J Cancer
; 117(12): 1798-1809, 2017 Dec 05.
Artigo
Inglês
| MEDLINE | ID: mdl-29024940
16.
Whole-exome sequencing identified a missense mutation in WFS1 causing low-frequency hearing loss: a case report.
BMC Med Genet
; 18(1): 151, 2017 12 19.
Artigo
Inglês
| MEDLINE | ID: mdl-29258540
17.
Mechanisms of CFTR functional variants that impair regulated bicarbonate permeation and increase risk for pancreatitis but not for cystic fibrosis.
PLoS Genet
; 10(7): e1004376, 2014 Jul.
Artigo
Inglês
| MEDLINE | ID: mdl-25033378
18.
Pore dilatation increases the bicarbonate permeability of CFTR, ANO1 and glycine receptor anion channels.
J Physiol
; 594(11): 2929-55, 2016 06 01.
Artigo
Inglês
| MEDLINE | ID: mdl-26663196
19.
Dynamic modulation of ANO1/TMEM16A HCO3(-) permeability by Ca2+/calmodulin.
Proc Natl Acad Sci U S A
; 110(1): 360-5, 2013 Jan 02.
Artigo
Inglês
| MEDLINE | ID: mdl-23248295
20.
Ventilation tube insertion is not effective to the treatment of hearing impairment in pediatric patients with Cornelia de Lange syndrome.
Am J Otolaryngol
; 37(3): 231-5, 2016.
Artigo
Inglês
| MEDLINE | ID: mdl-27178514