Disease: Auditory neuropathy
- <em>AIFM1</em> variants associated with auditory neuropathy spectrum disorder cause apoptosis due to impaired apoptosis-inducing factor dimerization
- <em>FDXR</em>-Associated Oculopathy: Congenital Amaurosis and Early-Onset Severe Retinal Dystrophy as Common Presenting Features in a Chinese Population
- A 15-Year Review of 260 Children With Auditory Neuropathy Spectrum Disorder: I. Demographic and Diagnostic Characteristics
- A 15-year Review of 260 Children With Auditory Neuropathy Spectrum Disorder: II. Management and Outcomes
- A Case Report of Riboflavin Treatment and Cochlear Implants in a 4-Year-Old Girl with Progressive Hearing Loss and Delayed Speech Development: Brown-Vialetto-Van Laere Syndrome
- A dominant variant in apoptosis-related gene XKR8 is relevant to hereditary auditory neuropathy
- A Rare Case of Unilateral Auditory Neuropathy Induced by Proton Therapy
- AIF translocation into nucleus caused by Aifm1 R450Q mutation: generation and characterization of a mouse model for AUNX1
- AIFM1 variants associated with auditory neuropathy spectrum disorder cause apoptosis due to impaired apoptosis-inducing factor dimerization
- An Umbrella Review of Cochlear Implant Outcomes in Children With Auditory Neuropathy
- Apoptosis of type I spiral ganglion neuron cells in Otof-mutant mice
- Audiogram Configuration, Molecular Etiology, and Outcome of Cochlear Implantation in Postlingual Auditory Neuropathy Spectrum Disorder
- Auditory neuropathy in mice and humans with Friedreich ataxia
- Auditory Neuropathy Spectrum Disorder in the White Sutton Syndrome
- Auditory Neuropathy Spectrum Disorder Progressing with Motor and Sensory Neuropathy Caused by an ATP1A1 Variant
- Axonal polyneuropathy and ataxia in children: consider Perrault Syndrome, a case report
- Case report: Clinical and genetic analysis of a family with nonsyndromic auditory neuropathy
- Case report: Mohr-Tranebjaerg syndrome: hearing impairment as the onset of an insidious disorder with high recurrence risk
- Case report: Novel insights into hemorrhagic destruction of the brain, subependymal calcification, and cataracts disease
- Case Report: Transient Auditory Neuropathy (TAN) with resurgence of electrophysiologic waveforms observed between the neonatal period and age 3 years
- Clinical and genetic architecture of a large cohort with auditory neuropathy
- Clinical protocol: audiological assessment of infants in Russian Federation. Part II
- Cochlear Implantation in Charcot-Marie-Tooth Patients: Speech Perception and Quality of Life
- Cochlear implantation in children with auditory neuropathy spectrum disorder: an updated systematic review
- Cochlear Implantation in Children with Auditory Neuropathy: Meta-Analysis
- Cochlear implantation in patients with Charcot-Marie-Tooth disease: two cases with a review of the literature
- Comparing Auditory Brain Stem Responses and Transient Otoacoustic Emissions in Premature Infants with Auditory Developmental Delay: Evidence of Temporary Auditory Neuropathy
- Comparison of Otoacoustic Emission (OAE) and Brainstem Evoked Response Audiometry (BERA) in High Risk Infants and Children under 5 Years of Age for Hearing Assessment in Western India: A Modification in Screening Protocol
- Cortical Auditory Evoked Potential Testing in Children With Auditory Neuropathy Spectrum Disorder
- Current Advances in Gene Therapies of Genetic Auditory Neuropathy Spectrum Disorder
- Deletion of the Notch ligand Jagged1 during cochlear maturation leads to inner hair cell defects and hearing loss
- Distribution characteristics and correlation analysis of <em>GJB2</em> variation in patients with auditory neuropathy
- Distribution characteristics and correlation analysis of GJB2 variation in patients with auditory neuropathy
- Duration of Cochlear Microphonics in Click and Toneburst-Evoked Auditory Brainstem Response in Individuals With Auditory Neuropathy Spectrum Disorder and Normal Hearing
- Dynamics of the association between visual and auditory functional changes in glaucoma. Preliminary results
- Efficacy of vestibular rehabilitation program in children with balance disorders and sensorineural hearing loss
- Electrocochleography
- Epidemiology, aetiology and diagnosis of congenital hearing loss via hearing screening of 153 913 newborns
- Establishment of Reference Values for Early Auditory Preverbal Skills of Children with Cochlear Implants
- Expanding Understanding of Electrocochleography in Cochlear Implantation: Auditory Neuropathy Spectrum Disorder With Normal Pure Tone Average
- Factors associated with congenital cytomegalovirus infection detected by dried blood spot testing in children with hearing loss
- FDXR-associated disease: a challenging differential diagnosis with inflammatory peripheral neuropathy
- Genetic etiological analysis of auditory neuropathy spectrum disorder by next-generation sequencing
- Hearing impairment in systemic sclerosis patients-what do we really know?
- Hearing of Otof-deficient mice restored by trans-splicing of N- and C-terminal otoferlin
- Hereditary spastic paraplegia (SPG 48) with deafness and azoospermia: A case report
- Hidden hearing loss in a hereditary peripheral neuropathy: evidence from a mouse model of Charcot Marie Tooth type 1A
- Hidden hearing loss in hereditary demyelinating neuropathies: insights from Charcot-Marie-Tooth mouse models
- Hyperbilirobinemia and Its Effect on Auditory Perception and Speech Intelligibility in Cochlear Implanted Children (Cochlear Implantation Outcomes in Children Who Have Experienced Hyperbilirobinemia)
- Identification of a novel AIFM1 variant from a Chinese family with auditory neuropathy
- Impact of Prematurity on Auditory Processing in Children
- Impaired AIF-CHCHD4 interaction and mitochondrial calcium overload contribute to auditory neuropathy spectrum disorder in patient-iPSC-derived neurons with AIFM1 variant
- Increase in the natural hearing threshold after treatment with cochlear implants
- Indicators for cochlear implantation in children with auditory neuropathy spectrum disorder: A systematic review
- Inherited metabolic disorders in adults: systematic review on patient characteristics and diagnostic yield of broad sequencing techniques (exome and genome sequencing)
- Intracochlear electrocochleography findings in cochlear implant recipients with auditory neuropathy spectrum disorder
- Intronic <em>OTOF</em> mutation causes an atypical splicing defect resulting in auditory neuropathy spectrum disorder
- Intronic OTOF mutation causes an atypical splicing defect resulting in auditory neuropathy spectrum disorder
- Is Working Memory Compromised in Individuals with Sensorineural Hearing Loss with Auditory Neural Origin?
- Lack of neural contributions to the summating potential in humans with Meniere's disease
- Language and health-related quality of life outcomes of children early-detected with unilateral and mild bilateral hearing loss
- Middle Ear Muscle Reflex in Normal-Hearing Individuals with Occupational Noise Exposure
- Multiple cranial neuropathy due to varicella zoster virus reactivation without vesicular rash: a challenging diagnosis
- NADH improves AIF dimerization and inhibits apoptosis in iPSCs-derived neurons from patients with auditory neuropathy spectrum disorder
- New Frontiers in Newborn Hearing Screening: Understanding Auditory Neuropathy and its Predictive Trajectory
- Newborn hearing screening methodology impacts the timing of diagnosis for auditory neuropathy spectrum disorder
- Novel biallelic variants in the PLEC gene are associated with severe hearing loss
- Outcomes of cochlear implantation in 75 patients with auditory neuropathy
- Pathophysiological and Clinical Aspects of Hearing Loss Among 85-Year-Olds
- Peculiarities of CI processor fitting in children with auditory neuropathy spectrum disorders
- Photobiomodulation Can Enhance Stem Cell Viability in Cochlea with Auditory Neuropathy but Does Not Restore Hearing
- Preclinical Efficacy And Safety Evaluation of AAV-OTOF in DFNB9 Mouse Model And Nonhuman Primate
- Preclinical evaluation of the efficacy and safety of AAV1-hOTOF in mice and nonhuman primates
- Predicting the Impact of OTOF Gene Missense Variants on Auditory Neuropathy Spectrum Disorder
- Preparing for Otoferlin gene therapy trials: A survey of NHS Paediatric Audiology and Cochlear Implant services on diagnosis and management of Auditory Neuropathy Spectrum Disorder
- Prevalence and Auditory Characteristics of Auditory Neuropathy Spectrum Disorder in Adult Population with Sensory Neural Hearing Loss: A Hospital Based Study in South India
- Remediation of Perceptual Deficits in Progressive Auditory Neuropathy: A Case Study
- Results of cochlear implant surgery in patients with auditory neuropathy
- RNA base editing therapy cures hearing loss induced by OTOF gene mutation
- Short-term outcomes of infants with hyperbilirubinemia-associated auditory neuropathy spectrum disorder in neonatal intensive care unit
- Spatial rehabilitation using virtual auditory space training paradigm in individuals with sensorineural hearing impairment
- Speech and Language outcomes in Auditory Neuropathy Spectrum Disorder (ANSD) children managed with amplification
- Sudden Onset Auditory Neuropathy Spectrum Disorder: A Rare Case Report of Brown Vialetto Van Laere Syndrome
- Surgical outcomes of premeatal and retromeatal cerebellopontine angle meningioma in Vietnam: a single-center prospective cross-sectional study
- Systematic Literature Review and Early Benefit of Cochlear Implantation in Two Pediatric Auditory Neuropathy Cases
- Task force Guideline of Brazilian Society of Otology - hearing loss in children - Part II - Treatment
- Task force Guideline of Brazilian Society of Otology ‒ hearing loss in children - Part I ‒ Evaluation
- Temperature-Sensitive Auditory Neuropathy: Report of a Novel Variant of OTOF Gene and Review of Current Literature
- The audiological characteristics of infant auditory neuropathy patients without otoacoustic emission
- The challenge of a mature final diagnosis of hearing loss severity and early cochlear implantation
- The follow-up study on patients of children with auditory neuropathy
- The human OPA1(delTTAG) mutation induces adult onset and progressive auditory neuropathy in mice
- The human OPA1<sup>delTTAG</sup> mutation induces adult onset and progressive auditory neuropathy in mice
- The natural history, clinical outcomes, and genotype-phenotype relationship of otoferlin-related hearing loss: a systematic, quantitative literature review
- The role of CD4(+) CD25(+) Treg in the mechanism of autoimmune auditory neuropathy in SD rats
- The role of CD4<sup>+</sup> CD25<sup>+</sup> Treg in the mechanism of autoimmune auditory neuropathy in SD rats
- Therapeutic potential of NADH: in neurodegenerative diseases characterizde by mitochondrial dysfunction
- Tone-Burst Auditory Brainstem Response and Cortical Potentials in Diagnosis of Syndromic Auditory Neuropathy Spectrum Disorder
- Transmembrane proteins with unknown function (TMEMs) as ion channels: electrophysiological properties, structure, and pathophysiological roles
- Unraveling haplotype errors in the DFNA33 locus