Filtros de búsqueda

Lista de obras de Byung Yoon Choi

A clinical guidance to DFNA22 drawn from a Korean cohort study with an autosomal dominant deaf population: A retrospective cohort study

artículo científico publicado en 2018

A comparative study of audiological outcomes and compliance between the Osia system and other bone conduction hearing implants

scientific article published in 2022

A comparison study of audiological outcome and compliance of bone conduction implantable hearing implants

scientific article published on 13 May 2020

A new technique for correcting cryptotia: V-Y swing flap

artículo científico publicado en 2007

A novel mutation of TMPRSS3 related to milder auditory phenotype in Korean postlingual deafness: a possible future implication for a personalized auditory rehabilitation

artículo científico publicado en 2014

ATP1A3 mutations can cause progressive auditory neuropathy: a new gene of auditory synaptopathy

artículo científico publicado en 2017

Analysis of the long-term hearing results after the surgical repair of aural atresia

artículo científico publicado en 2006

Application of next generation sequencing upon the molecular genetic diagnosis of deafness.

scientific article published on 30 April 2012

Appropriate Imaging Modality for the Etiologic Diagnosis of Congenital Single-Sided Deafness in Children

Atlantoaxial rotary subluxation after tympanoplasty

artículo científico publicado en 2011

Audiologic presentation of enlargement of the vestibular aqueduct according to the SLC26A4 genotypes

artículo científico publicado en 2014

Audiological and surgical evidence for the presence of a third window effect for the conductive hearing loss in DFNX2 deafness irrespective of types of mutations

artículo científico publicado en 2013

Auditory Phenotype and Histopathologic Findings of a Mutant Nlrp3 Expression Mouse Model

artículo científico publicado en 2022

Beware of a Fragile Footplate: Lessons from Ossiculoplasty in Patients with Ossicular Anomalies Related to Second Pharyngeal Arch Defects

scientific article published on 03 December 2019

CHARGE syndrome with oculomotor nerve palsy

artículo científico publicado en 2015

CSF gusher in cochlear implantation

scientific article published on 01 September 2004

Can magnetic resonance imaging provide clues to the inner ear functional status of enlarged vestibular aqueduct subjects with PDS mutation?

artículo científico publicado en 2008

Changes in Vestibulo-Ocular Reflex Gain After Surgical Plugging of Superior Semicircular Canal Dehiscence

artículo científico publicado en 2020

Characterization of Detailed Audiological Features of Cytomegalovirus Infection: A Composite Cohort Study from Groups with Distinct Demographics

scientific article published on 30 August 2018

Characterization of an induced pluripotent stem cell line (UMi040-A) bearing an auditory neuropathy spectrum disorder-associated variant in TMEM43

artículo científico publicado en 2022

Clarification of glycosylphosphatidylinositol anchorage of OTOANCORIN and human OTOA variants associated with deafness

scientific article published on 28 February 2019

ClinGen expert clinical validity curation of 164 hearing loss gene–disease pairs

artículo científico publicado en 2019

Clinical characteristics of patients with narrow bony cochlear nerve canal: is the bilateral case just a duplicate of the unilateral case?

artículo científico publicado en 2013

Clinical implication of ocular torsion in peripheral vestibulopathy

artículo científico

Clinical observations and molecular variables of patients with hearing loss and incomplete partition type III.

artículo científico publicado en 2015

Clinical predictors for satisfaction with incus vibroplasty: a preliminary study.

artículo científico publicado en 2017

Clinical utility and improved speed of analysis by automated variant prioritization system in genetic hearing loss

scientific article published in 2021

Cochlear implantation in chronic ear disease

artículo científico publicado en 2004

Cochlear implantation in chronic ear disease.

artículo científico publicado en 2004

Cochlear reimplantation in device failure: effectiveness and safety

artículo científico publicado en 2004

Cochlear reimplantation in device failure: effectiveness and safety

artículo científico publicado en 2004

Combining Cep290 and Mkks ciliopathy alleles in mice rescues sensory defects and restores ciliogenesis

artículo científico publicado en 2012

Combining Cep290 and Mkksciliopathy alleles in mice rescues sensory defects and restores ciliogenesis.

artículo científico publicado en 2012

Construction of an MRI-based decision tree to differentiate autoimmune and autoinflammatory inner ear disease from chronic otitis media with sensorineural hearing loss

artículo científico publicado en 2021

Cortical Oscillatory Signatures Reveal the Prerequisites for Tinnitus Perception: A Comparison of Subjects With Sudden Sensorineural Hearing Loss With and Without Tinnitus

artículo científico publicado en 2020

Craniometaphyseal dysplasia.

artículo científico publicado en 2005

De novo large genomic deletions involving POU3F4 in incomplete partition type III inner ear anomaly in East Asian populations and implications for genetic counseling

artículo científico publicado en 2015

Destabilization and mislocalization of POU3F4 by C-terminal frameshift truncation and extension mutation

artículo científico publicado en 2013

Development of novel noninvasive prenatal testing protocol for whole autosomal recessive disease using picodroplet digital PCR

artículo científico publicado en 2016

Diagnostic application of targeted resequencing for familial nonsyndromic hearing loss

artículo científico publicado en 2013

Differential disruption of autoinhibition and defect in assembly of cytoskeleton during cell division decide the fate of human DIAPH1-related cytoskeletopathy

scientific article published on 31 August 2019

Discovery of CDH23 as a Significant Contributor to Progressive Postlingual Sensorineural Hearing Loss in Koreans.

artículo científico publicado en 2016

Discovery of MYH14 as an important and unique deafness gene causing prelingually severe autosomal dominant nonsyndromic hearing loss

artículo científico publicado en 2017

Distinct vestibular phenotypes in DFNA9 families with COCH variants

artículo científico publicado en 2016

Diverse etiologies manifesting auditory neuropathy characteristics from infants with profound hearing loss and clinical implications

artículo científico publicado en 2016

Dizziness and vestibular function before and after cochlear implantation

artículo científico publicado en 2016

Dopamine increases Na+ absorption in the Reissner's membrane of the gerbil cochlea

artículo científico publicado en 2012

Downsloping high-frequency hearing loss due to inner ear tricellular tight junction disruption by a novel ILDR1 mutation in the Ig-like domain

artículo científico publicado en 2015

Early combination treatment with intratympanic steroid injection in severe to profound sudden sensorineural hearing loss improves speech discrimination performance

artículo científico publicado en 2011

Effect of initial switch-on within 24 hours of cochlear implantation using slim modiolar electrodes

artículo científico publicado en 2021

Effects of CoQ10 Replacement Therapy on the Audiological Characteristics of Pediatric Patients with COQ6 Variants

artículo científico publicado en 2022

Effects of in vivo repositioning of slim modiolar electrodes on electrical thresholds and speech perception

artículo científico publicado en 2021

Efficacy of cochlear implants in children with borderline hearing who have already achieved significant language development with hearing aids

scientific article published in 2022

Efficiency of Exploration of Molecular Genetic Etiology for Cochlear Implantees and Its Implication

artículo científico publicado en 2014

Efficient molecular genetic diagnosis of enlarged vestibular aqueducts in East Asians.

artículo científico publicado en 2009

Electrocochleographic findings in superior canal dehiscence syndrome.

artículo científico publicado en 2015

Elucidation of the unique mutation spectrum of severe hearing loss in a Vietnamese pediatric population

artículo científico publicado en 2019

Erratum to: Clinical implication of ocular torsion in peripheral vestibulopathy

artículo científico publicado en 2015

Establishment of a Flexible Real-Time Polymerase Chain Reaction-Based Platform for Detecting Prevalent Deafness Mutations Associated with Variable Degree of Sensorineural Hearing Loss in Koreans.

artículo científico publicado en 2016

Expansion of phenotypic spectrum of MYO15A pathogenic variants to include postlingual onset of progressive partial deafness

artículo científico publicado en 2018

Exploration of molecular genetic etiology for Korean cochlear implantees with severe to profound hearing loss and its implication

artículo científico publicado en 2014

Expression of osmotic stress protein 94 in murine endolymphatic hydrops model.

artículo científico publicado en 2012

Extremely common radiographic finding of cochlear nerve deficiency among infants with prelingual single-sided deafness and its clinical implications

scientific article published on 10 July 2018

Flexible Real-Time Polymerase Chain Reaction-Based Platforms for Detecting Deafness Mutations in Koreans: A Proposed Guideline for the Etiologic Diagnosis of Auditory Neuropathy Spectrum Disorder

artículo científico publicado en 2020

Full etiologic spectrum of pediatric severe to profound hearing loss of consecutive 119 cases

artículo científico publicado en 2022

Functional characterization of a novel loss-of-function mutation of PRPS1 related to early-onset progressive nonsyndromic hearing loss in Koreans (DFNX1): Potential implications on future therapeutic intervention.

artículo científico publicado en 2016

Genetic Information and Precision Medicine in Hearing Loss

artículo científico publicado en 2020

Genetic Load of Alternations of Transcription Factor Genes in Non-Syndromic Deafness and the Associated Clinical Phenotypes: Experience from Two Tertiary Referral Centers

artículo científico publicado en 2022

Head position dependency of induced nystagmus to ice-water irrigation in peripheral vestibulopathy.

artículo científico publicado en 2005

Head-shaking and Vibration-induced Nystagmus During and Between the Attacks of Unilateral Ménière's Disease

artículo científico

Healthcare consumption among subjects with otitis media undergoing middle ear surgery—analysis of cost drivers

artículo científico publicado en 2022

Hereditary hearing loss with thyroid abnormalities

scientific article published on 24 February 2011

How to Maximize the Outcomes of Cochlear Implantation in Common Cavity and Cochlear Aplasia With Dilated Vestibule, the Most Severe Inner Ear Anomalies?

artículo científico publicado en 2022

Hypo-functional SLC26A4 variants associated with nonsyndromic hearing loss and enlargement of the vestibular aqueduct: genotype-phenotype correlation or coincidental polymorphisms?

artículo científico publicado en 2009

Identification and Clinical Implications of Novel MYO15A Mutations in a Non-consanguineous Korean Family by Targeted Exome Sequencing

artículo científico publicado en 2015

Identification of a Novel Frameshift Variant of POU3F4 and Genetic Counseling of Korean Incomplete Partition Type III Subjects Based on Detailed Genotypes

scientific article published on 07 May 2019

Identification of a Potential Founder Effect of a Novel PDZD7 Variant Involved in Moderate-to-Severe Sensorineural Hearing Loss in Koreans ⬇️

scientific article published on 26 August 2019

Identification of a novel splice site variant of OTOF in the Korean nonsyndromic hearing loss population with low prevalence of the OTOF mutations

artículo científico publicado en 2014

Identification of a novel truncation mutation of EYA4 in moderate degree hearing loss by targeted exome sequencing

artículo científico publicado en 2015

Identification of novel functional null allele of SLC26A4 associated with enlarged vestibular aqueduct and its possible implication

artículo científico publicado en 2014

Improving genetic diagnosis by disease-specific, ACMG/AMP variant interpretation guidelines for hearing loss

artículo científico publicado en 2022

Incus footplate assembly: Indication and surgical outcome

artículo científico publicado en 2016

Inflammatory and Immune Proteins in Umbilical Cord Blood: Association with Hearing Screening Test Failure in Preterm Neonates

artículo científico publicado en 2018

Intralabyrinthine Schwannoma: Distinct Features for Differential Diagnosis

scientific article published on 23 July 2019

Intravenous administration of human mesenchymal stem cells after noise- or drug-induced hearing loss in rats.

artículo científico publicado en 2012

Involvement of the Internal Auditory Canal in Subjects With Cochlear Otosclerosis

artículo científico publicado en 2019

Is the posterior cingulate cortex an on-off switch for tinnitus?: A comparison between hearing loss subjects with and without tinnitus

artículo científico publicado en 2021

Jugular Bulb Resurfacing With Bone Cement for Patients With High Dehiscent Jugular Bulb and Ipsilateral Pulsatile Tinnitus

artículo científico publicado en 2019

Long term results of postoperative canal stenosis in congenital aural atresia surgery.

artículo científico publicado en 2007

Longitudinal analysis of surgical outcome in subjects with pulsatile tinnitus originating from the sigmoid sinus

artículo científico publicado en 2020

Long‐term audiologic outcomes and potential outcome predictors of cochlear implantation in cochlear aplasia with dilated vestibule: A case series

artículo científico publicado en 2022

Management of intractable Ménière's disease after intratympanic injection of gentamicin

artículo científico publicado en 2014

Maternal and Placental Factors Associated with Congenital Hearing Loss in Very Preterm Neonates

artículo científico publicado en 2016

Modiolar Proximity of Slim Modiolar Electrodes and Cochlear Duct Length: Correlation for Potential Basis of Customized Cochlear Implantation With Perimodiolar Electrodes

artículo científico publicado en 2020

Molecular Etiology of Hereditary Single-Side Deafness: Its Association With Pigmentary Disorders and Waardenburg Syndrome

artículo científico publicado en 2015

Molecular aetiology of ski-slope hearing loss and audiological course of cochlear implantees

artículo científico publicado en 2022

Mouse model of enlarged vestibular aqueducts defines temporal requirement of Slc26a4 expression for hearing acquisition

artículo científico publicado en 2011

Multiphasic analysis of whole exome sequencing data identifies a novel mutation of ACTG1 in a nonsyndromic hearing loss family

artículo científico publicado en 2013

Mutational and phenotypic spectrum of OTOF-related auditory neuropathy in Koreans: eliciting reciprocal interaction between bench and clinics

Natural Course of Residual Hearing with Reference to GJB2 and SLC26A4 Genotypes: Clinical Implications for Hearing Rehabilitation

artículo científico publicado en 2021

Natural course of residual hearing preservation with a slim, modiolar cochlear implant electrode array

artículo científico publicado en 2022

Novel KCNQ4 variants in different functional domains confer genotype- and mechanism-based therapeutics in patients with nonsyndromic hearing loss

scientific article published in 2021

Novel Molecular Genetic Etiology of Asymmetric Hearing Loss: Autosomal-Dominant LMX1A Variants

artículo científico publicado en 2022

Novel Splice Site Pathogenic Variant of EFTUD2 Is Associated with Mandibulofacial Dysostosis with Microcephaly and Extracranial Symptoms in Korea

artículo científico publicado en 2020

Novel TECTA mutations identified in stable sensorineural hearing loss and their clinical implications

artículo científico publicado en 2014

Novel genotype-phenotype correlation of functionally characterized LMX1A variants linked to sensorineural hearing loss

artículo científico publicado en 2020

Objectification and Differential Diagnosis of Vascular Pulsatile Tinnitus by Transcanal Sound Recording and Spectrotemporal Analysis: A Preliminary Study.

artículo científico publicado en 2016

One-step noninvasive prenatal testing (NIPT) for autosomal recessive homozygous point mutations using digital PCR.

artículo científico publicado en 2018

Otological aspects of NLRP3-related autoinflammatory disorder focusing on the responsiveness to anakinra

artículo científico publicado en 2020

Outcome of Cochlear Implantation in NLRP3-related Autoinflammatory Inner Ear Disorders

scientific article published on 04 November 2020

Outcome of Cochlear Implantation in Prelingually Deafened Children According to Molecular Genetic Etiology

artículo científico

Outcome of cochlear implantation in the worse ear of post-lingual asymmetric hearing loss: elucidation of prognostic markers

artículo científico publicado en 2021

Outcomes and limitations of hospital-based newborn hearing screening.

artículo científico publicado en 2017

POLD1 variants leading to reduced polymerase activity can cause hearing loss without syndromic features

artículo científico publicado en 2020

Partial ossicular replacement versus type II tympanoplasty in congenital aural atresia surgery: a matched group study.

scientific article published on August 2009

Potential Implications of Slim Modiolar Electrodes for Severely Malformed Cochleae: A Comparison With the Straight Array With Circumferential Electrodes

artículo científico publicado en 2021

Powerful use of automated prioritization of candidate variants in genetic hearing loss with extreme etiologic heterogeneity

artículo científico publicado en 2021

Precision medicine approach to cochlear implantation

artículo científico publicado en 2022

Prediction of the Outcome of Cochlear Implantation in the Patients with Congenital Cytomegalovirus Infection based on Magnetic Resonance Imaging Characteristics

artículo científico publicado en 2019

Prenatal electroporation-mediated gene transfer restores Slc26a4 knock-out mouse hearing and vestibular function

artículo científico publicado en 2019

Preoperative Significance of Ipsilateral Manual Neck Compression in Patients With Pulsatile Tinnitus Secondary to Sigmoid Sinus Dehiscences and Diverticula

artículo científico publicado en 2022

Prevalence of p.V37I variant of GJB2 in mild or moderate hearing loss in a pediatric population and the interpretation of its pathogenicity

artículo científico publicado en 2013

Quantitative three-dimensional image analysis of the superior canal after surgical plugging to treat superior semicircular canal dehiscence

artículo científico publicado en 2021

Refinement of Molecular Diagnostic Protocol of Auditory Neuropathy Spectrum Disorder: Disclosure of Significant Level of Etiologic Homogeneity in Koreans and Its Clinical Implications

artículo científico publicado en 2015

Relation between amniotic fluid infection or cytokine levels and hearing screen failure in infants at 32 wk gestation or less

artículo científico publicado en 2016

Residual Hearing in DFNB1 Deafness and Its Clinical Implication in a Korean Population

artículo científico publicado en 2015

Results of Active Middle Ear Implantation in Patients With Mixed Hearing Loss After Middle Ear Surgery: A Prospective Multicenter Study (the ROMEO Study)

scientific article published in 2022

Rising of <i>LOXHD1</i> as a signature causative gene of down-sloping hearing loss in people in their teens and 20s

scientific article published in 2021

Risk factors for failure in the newborn hearing screen test in very preterm twins

artículo científico publicado en 2018

SLC26A4 genotype, but not cochlear radiologic structure, is correlated with hearing loss in ears with an enlarged vestibular aqueduct ⬇️

artículo científico publicado en 2010

SLC26A4 genotypes and phenotypes associated with enlargement of the vestibular aqueduct

artículo científico publicado en 2011

SLC26A4 mutation testing for hearing loss associated with enlargement of the vestibular aqueduct

artículo científico publicado en 2013

Severe or Profound Sensorineural Hearing Loss Caused by Novel USH2A Variants in Korea: Potential Genotype-Phenotype Correlation

scientific article published on 02 November 2019

Significance of cytomegalovirus tests after three weeks of life in children with hearing loss

scientific article published in 2023

Significant Mendelian genetic contribution to pediatric mild-to-moderate hearing loss and its comprehensive diagnostic approach

artículo científico publicado en 2020

Simpler and effective radiological evaluations for modiolar proximity of a slim modiolar cochlear implant electrode

artículo científico publicado en 2020

Slc26a4-insufficiency causes fluctuating hearing loss and stria vascularis dysfunction

artículo científico publicado en 2014

Strategy for the customized mass screening of genetic sensorineural hearing loss in koreans

artículo científico publicado en 2014

Strong founder effect of p.P240L in CDH23 in Koreans and its significant contribution to severe-to-profound nonsyndromic hearing loss in a Korean pediatric population

artículo científico publicado en 2015

Structural analysis of pathogenic TMPRSS3 variants and their cochlear implantation outcomes of sensorineural hearing loss

scientific article published in 2023

Success rates in restoring hearing loss in patients with chronic otitis media: A systematic review

artículo científico publicado en 2021

TMC1 and TMC2 Localize at the Site of Mechanotransduction in Mammalian Inner Ear Hair Cell Stereocilia

artículo científico publicado en 2015

TMEM43, a novel passive conductance channel of cochlear glia is critical for maintenance of speech discrimination

artículo científico publicado en 2019

Targeted Exome Sequencing of Deafness Genes After Failure of Auditory Phenotype-Driven Candidate Gene Screening

artículo científico publicado en 2015

Tauroursodeoxycholic acid attenuates cisplatin-induced hearing loss in rats

scientific article published on 12 February 2020

The Analysis of A Frequent TMPRSS3 Allele Containing P.V116M and P.V291L in A Cis Configuration among Deaf Koreans

artículo científico publicado en 2017

The molecular etiology of deafness and auditory performance in the postlingually deafened cochlear implantees

artículo científico publicado en 2020

The semantic segmentation approach for normal and pathologic tympanic membrane using deep learning: Supplemental Figures

scholarly article published 8 January 2019

Tight modiolar proximity and feasibility of slim modiolar cochlear implant electrode array insertion in diverse etiologies of hearing loss

artículo científico publicado en 2021

Unraveling of Enigmatic Hearing-Impaired GJB2 Single Heterozygotes by Massive Parallel Sequencing: DFNB1 or Not?

scientific article published on April 2016

Update on CD164 and LMX1A genes to strengthen their causative role in autosomal dominant hearing loss

artículo científico publicado en 2022

Variable expressivity of FGF3 mutations associated with deafness and LAMM syndrome

artículo científico publicado en 2011

Whole exome sequencing for a patient with Rubinstein-Taybi syndrome reveals de novo variants besides an overt CREBBP mutation

artículo científico publicado en 2015

Whole-exome sequencing identifies a novel genotype-phenotype correlation in the entactin domain of the known deafness gene TECTA.

artículo científico publicado en 2014

Whole-exome sequencing reveals diverse modes of inheritance in sporadic mild to moderate sensorineural hearing loss in a pediatric population

artículo científico publicado en 2015

Dominio Público Uruguay está sostenido por:

Acerca de Dominio Público Uruguay

Ayuda