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2007 Evaluation of white matter structures in patients with tinnitus using diffusion tensor imaging

2007 Novel EYA1 mutation in a Korean branchio-oto-renal syndrome family

CLINICAL AND EXPERIMENTAL OTORHINOLARYNGOLOGY A Novel Frameshift Mutation of SLC26A4 in a Korean Family With Nonsyndromic Hearing Loss and Enlarged Vestibular Aqueduct

INTERNATIONAL JOURNAL OF PEDIATRIC OTORHINOLARYNGOLOGY Protective effects of 1,2,3-triazole derivative KPR-A020 against cisplatin-induced ototoxicity in murine cochlear cultures

CLINICAL AND EXPERIMENTAL OTORHINOLARYNGOLOGY Association Between Hearing Impairment and Albuminuria With or Without Diabetes Mellitus

INTERNATIONAL JOURNAL OF PEDIATRIC OTORHINOLARYNGOLOGY Identification of a nonsense mutation in the STRC gene in a Korean family with moderate hearing loss

Toxicology letters Galangin prevents aminoglycoside-induced ototoxicity by decreasing mitochondrial production of reactive oxygen species in mouse cochlear cultures.

ANTIOXIDANTS REDOX SIGNALING Methionine Sulfoxide Reductase B3-Targeted In Utero Gene Therapy Rescues Hearing Function in a Mouse Model of Congenital Sensorineural Hearing Loss

CLINICAL AND EXPERIMENTAL OTORHINOLARYNGOLOGY Is Body Mass Index Associated With the Development of Age-Related Hearing Impairment in Koreans? The Korean National Health and Nutrition Examination Survey 2009-2012

대한이비인후과학회지 두경부외과학 선천성 난청 소아들의 인공와우 이식 후 언어 발달: 장기 추적 관찰 결과

LARYNGOSCOPE The efficacy of combination therapy for idiopathic sudden sensorineural hearing loss

GENES GENOMICS Genetic analysis of COL11A2 in Korean patients with autosomal dominant non-syndromic hearing loss

GENE Genetic association of MYH genes with hereditary hearing loss in Korea

Genes and genetic systems A novel missense variant in the DIAPH1 gene in a Korean family with autosomal dominant nonsyndromic hearing loss

Clinical and Experimental Otorhinolaryngology Association of Bone Mineral Density With Hearing Impairment in Postmenopausal Women in Korea

Journal of Audiology & Otology Clinical Aspects and Surgical Outcomes of Congenital Cholesteatoma in 93 Children: Increasing Trends of Congenital Cholesteatoma from 1997 through 2012

EUROPEAN JOURNAL OF HUMAN GENETICS A missense variant of the ATP1A2 gene is associated with a novel phenotype of progressive sensorineural hearing loss associated with migraine

FASEB JOURNAL Pannexin 3 is required for normal progression of skeletal development in vertebrates

임상이비인후과학회지 이식형 보청기

LARYNGOSCOPE Surgical Outcomes of Early Congenital Cholesteatoma: Minimally Invasive Transcanal Approach

Human molecular genetics Methionine sulfoxide reductase B3 deficiency causes hearing loss due to stereocilia degeneration and apoptotic cell death in cochlear hair cells.

PLOS ONE Genetic Analysis of Genes Related to Tight Junction Function in the Korean Population with Non-Syndromic Hearing Loss

BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS Alpha-lipoic acid protects against cisplatin-induced ototoxicity via the regulation of MAPKs and proinflammatory cytokines

대한이비인후과학회 두경부외과 Mechanism of Tinnitus Generation

HEARING RESEARCH Comparison of auditory responses determined by acoustic stimulation and by mechanical round window stimulation at equivalent stapes velocities

POULTRY SCIENCE Molecular cloning, characterization, and expression of pannexin genes in chicken

korean journal of audiology A case of a cholesterol granuloma occluding the external auditory canal in a 12-year-old girl

ANNALS OF CLINICAL AND LABORATORY SCIENCE Identification of Causative Mutation in a Korean Family with Crouzon Syndrome Using Whole Exome Sequencing

NEUROIMAGE Functional mapping of the auditory tract in rodent tinnitus model using manganese-enhanced magnetic resonance imaging

OTOLOGY NEUROTOLOGY The Prevalence of Preauricular Sinus and Associated Factors in a Nationwide Population-Based Survey of South Korea

Human mutation Identification of Pathogenic Mechanisms of COCH Mutations, Abolished Cochlin Secretion, and Intracellular Aggregate Formation: Genotype-Phenotype Correlations in DFNA9 Deafness and Vestibular Disorder.

PLOS ONE A Rapid Method for Simultaneous Screening of Multi-Gene Mutations Associated with Hearing Loss in the Korean Population

GENE Genetic analysis of auditory neuropathy spectrum disorder in the Korean population

The Korean Audiological Society Pathophysiology of Age-Related Hearing Loss(Peripheral and Central)

GENE Genetic analysis of TMPRSS3 gene in the Korean population with autosomal recessive nonsyndromic hearing loss

PLOS ONE Molecular and Clinical Characterization of the Variable Phenotype in Korean Families with Hearing Loss Associated with the Mitochondrial A1555G Mutation

ORPHANET JOURNAL OF RARE DISEASES Targeted massive parallel sequencing: the effective detection of novel causative mutations associated with hearing loss in small families

GENE A novel insertion-induced frameshift mutation of the SLC26A4 gene in a Korean family with Pendred syndrome

대한이비인후과학회지 두경부외과학 마우스 와우의 형태학적 검사방법

INTERNATIONAL JOURNAL OF MOLECULAR MEDICINE Application of allele-specific primer extension-based microarray for simultaneous multi-gene mutation screening in patients with non-syndromic hearing loss

대한이비이후과학회지 골형성 부전증 환자에 시행한 인공와우 이식술 1예

Human Mutation Different functional consequences of two missense mutations in the GJB2 gene associated with non-syndromic hearing loss

International Journal of Molecular Medicine Molecular analysis of mitochondrial gene mutations in Korean patients with nonsyndromic hearing loss

International journal of pediatric otorhinolaryngology Molecular analysis of the GJB2, GJB6 and SLC26A4 genes in Korean deafness patients