Byeonghyeon Lee

Daegu, Republic of Korea

Last Updated: 09/26/2026

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Found 25 publications

Correction to: Cochlear synaptic vulnerability scales with pathological noise intensity in a noise-induced hearing loss model.

Correction to: Cochlear synaptic vulnerability scales with pathological noise intensity in a noise-induced hearing loss model.

Journal: Genes & genomics

Published: June 16, 2026

Corrigendum to "Inhibition of the mitochondrial permeability transition pore as a promising target for protecting auditory function in cisplatin-induced hearing loss" [Biomed. Pharmacother. 182 (2025) 117767].

Corrigendum to "Inhibition of the mitochondrial permeability transition pore as a promising target for protecting auditory function in cisplatin-induced hearing loss" [Biomed. Pharmacother. 182 (2025) 117767].

Journal: Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie

Published: May 07, 2026

Cochlear synaptic vulnerability scales with pathological noise intensity in a noise-induced hearing loss model.

Cochlear synaptic vulnerability scales with pathological noise intensity in a noise-induced hearing loss model.

Journal: Genes & genomics

Published: January 07, 2026

Molecular remodeling of the central auditory pathway in tinnitus revealed by RNA sequencing.

Molecular remodeling of the central auditory pathway in tinnitus revealed by RNA sequencing.

Journal: Genes & genomics

Published: September 21, 2025

DCTN1-associated neurological disorder with symptoms similar to spinal bulbar muscular atrophy.

DCTN1-associated neurological disorder with symptoms similar to spinal bulbar muscular atrophy.

Journal: Journal of neuromuscular diseases

Published: July 16, 2025

NGS-based identification of a MYO7A mutation in a Korean family with DFNB2, a subtype of autosomal recessive non-syndromic hearing loss.

NGS-based identification of a MYO7A mutation in a Korean family with DFNB2, a subtype of autosomal recessive non-syndromic hearing loss.

Journal: Genes & genomics

Published: May 08, 2025

Inhibition of the mitochondrial permeability transition pore as a promising target for protecting auditory function in cisplatin-induced hearing loss.

Inhibition of the mitochondrial permeability transition pore as a promising target for protecting auditory function in cisplatin-induced hearing loss.

Journal: Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie

Published: September 10, 2024

Therapeutic effect of intraperitoneal dexamethasone on noise-induced permanent threshold shift in mice model.

Therapeutic effect of intraperitoneal dexamethasone on noise-induced permanent threshold shift in mice model.

Journal: Experimental brain research

Published: May 30, 2023

Identification of an in-frame homozygous KIF1A variant causing a mild SPG30 phenotype in a Korean family.

Identification of an in-frame homozygous KIF1A variant causing a mild SPG30 phenotype in a Korean family.

Journal: Gene

Published: February 09, 2023

Identification of novel missense mutation related with non-syndromic sensorineural deafness, DFNA11 in korean family by NGS.

Identification of novel missense mutation related with non-syndromic sensorineural deafness, DFNA11 in korean family by NGS.

Journal: Genes & genomics

Published: November 24, 2022

A novel REEP1 splicing mutation with broad clinical variability in a family with hereditary spastic paraplegia.

A novel REEP1 splicing mutation with broad clinical variability in a family with hereditary spastic paraplegia.

Journal: Gene

Published: May 06, 2020

An autosomal dominant ERLIN2 mutation leads to a pure HSP phenotype distinct from the autosomal recessive ERLIN2 mutations (SPG18).

An autosomal dominant ERLIN2 mutation leads to a pure HSP phenotype distinct from the autosomal recessive ERLIN2 mutations (SPG18).

Journal: Scientific reports

Published: November 09, 2019

Showing 1-12 of 25

Last Updated: 09/26/2026