| CLINICAL AND EXPERIMENTAL OTORHINOLARYNGOLOGY |
Association Between Hearing Impairment and Albuminuria With or Without Diabetes Mellitus
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| INTERNATIONAL JOURNAL OF PEDIATRIC OTORHINOLARYNGOLOGY |
Protective effects of 1,2,3-triazole derivative KPR-A020 against cisplatin-induced ototoxicity in murine cochlear cultures
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| CLINICAL AND EXPERIMENTAL OTORHINOLARYNGOLOGY |
A Novel Frameshift Mutation of SLC26A4 in a Korean Family With Nonsyndromic Hearing Loss and Enlarged Vestibular Aqueduct
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| Journal of Audiology & Otology |
Clinical Aspects and Surgical Outcomes of Congenital Cholesteatoma in 93 Children: Increasing Trends of Congenital Cholesteatoma from 1997 through 2012
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| Clinical and Experimental Otorhinolaryngology |
Association of Bone Mineral Density With Hearing Impairment in Postmenopausal Women in Korea
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| Genes and genetic systems |
A novel missense variant in the DIAPH1 gene in a Korean family with autosomal dominant nonsyndromic hearing loss
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| GENE |
Genetic association of MYH genes with hereditary hearing loss in Korea
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| GENES GENOMICS |
Genetic analysis of COL11A2 in Korean patients with autosomal dominant non-syndromic hearing loss
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| LARYNGOSCOPE |
The efficacy of combination therapy for idiopathic sudden sensorineural hearing loss
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| 대한이비인후과학회지 두경부외과학 |
선천성 난청 소아들의 인공와우 이식 후 언어 발달: 장기 추적 관찰 결과
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| 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
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| ANTIOXIDANTS REDOX SIGNALING |
Methionine Sulfoxide Reductase B3-Targeted In Utero Gene Therapy Rescues Hearing Function in a Mouse Model of Congenital Sensorineural Hearing Loss
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| Toxicology letters |
Galangin prevents aminoglycoside-induced ototoxicity by decreasing mitochondrial production of reactive oxygen species in mouse cochlear cultures.
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| INTERNATIONAL JOURNAL OF PEDIATRIC OTORHINOLARYNGOLOGY |
Identification of a nonsense mutation in the STRC gene in a Korean family with moderate hearing loss
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| 임상이비인후과학회지 |
이식형 보청기
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| FASEB JOURNAL |
Pannexin 3 is required for normal progression of skeletal development in vertebrates
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| 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
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| 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.
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| OTOLOGY NEUROTOLOGY |
The Prevalence of Preauricular Sinus and Associated Factors in a Nationwide Population-Based Survey of South Korea
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| NEUROIMAGE |
Functional mapping of the auditory tract in rodent tinnitus model using manganese-enhanced magnetic resonance imaging
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| ANNALS OF CLINICAL AND LABORATORY SCIENCE |
Identification of Causative Mutation in a Korean Family with Crouzon Syndrome Using Whole Exome Sequencing
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| korean journal of audiology |
A case of a cholesterol granuloma occluding the external auditory canal in a 12-year-old girl
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| POULTRY SCIENCE |
Molecular cloning, characterization, and expression of pannexin genes in chicken
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| HEARING RESEARCH |
Comparison of auditory responses determined by acoustic stimulation and by mechanical round window stimulation at equivalent stapes velocities
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| 대한이비인후과학회 두경부외과 |
Mechanism of Tinnitus Generation
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| BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS |
Alpha-lipoic acid protects against cisplatin-induced ototoxicity via the regulation of MAPKs and proinflammatory cytokines
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| PLOS ONE |
Genetic Analysis of Genes Related to Tight Junction Function in the Korean Population with Non-Syndromic Hearing Loss
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| Human molecular genetics |
Methionine sulfoxide reductase B3 deficiency causes hearing loss due to stereocilia degeneration and apoptotic cell death in cochlear hair cells.
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| LARYNGOSCOPE |
Surgical Outcomes of Early Congenital Cholesteatoma: Minimally Invasive Transcanal Approach
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| GENE |
Genetic analysis of TMPRSS3 gene in the Korean population with autosomal recessive nonsyndromic hearing loss
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| The Korean Audiological Society |
Pathophysiology of Age-Related Hearing Loss(Peripheral and Central)
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| GENE |
Genetic analysis of auditory neuropathy spectrum disorder in the Korean population
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| PLOS ONE |
A Rapid Method for Simultaneous Screening of Multi-Gene Mutations Associated with Hearing Loss in the Korean Population
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| ORPHANET JOURNAL OF RARE DISEASES |
Targeted massive parallel sequencing: the effective detection of novel causative mutations associated with hearing loss in small families
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| PLOS ONE |
Molecular and Clinical Characterization of the Variable Phenotype in Korean Families with Hearing Loss Associated with the Mitochondrial A1555G Mutation
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| GENE |
A novel insertion-induced frameshift mutation of the SLC26A4 gene in a Korean family with Pendred syndrome
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| 대한이비인후과학회지 두경부외과학 |
마우스 와우의 형태학적 검사방법
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| 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
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| Human Mutation |
Different functional consequences of two missense mutations in the GJB2 gene associated with non-syndromic hearing loss
|
| 대한이비이후과학회지 |
골형성 부전증 환자에 시행한 인공와우 이식술 1예
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| International journal of pediatric otorhinolaryngology |
Molecular analysis of the GJB2, GJB6 and SLC26A4 genes in Korean deafness patients
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| International Journal of Molecular Medicine |
Molecular analysis of mitochondrial gene mutations in Korean patients with nonsyndromic hearing loss
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| 2007 |
Evaluation of white matter structures in patients with tinnitus using diffusion tensor imaging
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| 2007 |
Novel EYA1 mutation in a Korean branchio-oto-renal syndrome family
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