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Cochlear Synaptopathy and Noise-Induced Hidden Hearing Loss
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inferredcites →https://doi.org/10.1002/(sici)1096-9861(19960722)371:2<208::aid-cne2>3.0.co;2-6openalex-snapshot
Ultrastructural differences among afferent synapses on cochlear hair cells: Correlations with spontaneous discharge rate
inferredcites →https://doi.org/10.1002/jnr.21259openalex-snapshot
Primary afferent dendrite degeneration as a cause of tinnitus
inferredcites →https://doi.org/10.1002/jnr.23152openalex-snapshot
Hyperexcitability of inferior colliculus neurons caused by acute noise exposure
inferredcites →https://doi.org/10.1007/bf00318554openalex-snapshot
Intermediate stages in the disassembly of synaptic ribbons in cone photoreceptors of the crucian carp, Carassius carassius
inferredcites →https://doi.org/10.1007/s00232-005-0854-4openalex-snapshot
Structure and Function of the Hair Cell Ribbon Synapse
inferredcites →https://doi.org/10.1007/s00441-015-2177-9openalex-snapshot
Basic response properties of auditory nerve fibers: a review
inferredcites →https://doi.org/10.1007/s10162-005-5029-6openalex-snapshot
Effects of Age, Age-Related Hearing Loss, and Contralateral Cafeteria Noise on the Discrimination of Small Frequency Changes: Psychoacoustic and Electrophysiological Measures
inferredcites →https://doi.org/10.1007/s10162-011-0277-0openalex-snapshot
Primary Neural Degeneration in the Guinea Pig Cochlea After Reversible Noise-Induced Threshold Shift
inferredcites →https://doi.org/10.1007/s10162-011-0283-2openalex-snapshot
Age-Related Primary Cochlear Neuronal Degeneration in Human Temporal Bones
inferredcites →https://doi.org/10.1007/s10162-012-0344-1openalex-snapshot
Brainstem Auditory Evoked Potentials Suggest a Role for the Ventral Cochlear Nucleus in Tinnitus
inferredcites →https://doi.org/10.1007/s10162-015-0510-3openalex-snapshot
Dynamics of cochlear synaptopathy after acoustic overexposure
inferredcites →https://doi.org/10.1007/s10162-015-0539-3openalex-snapshot
Towards a Diagnosis of Cochlear Neuropathy with Envelope Following Responses
inferredcites →https://doi.org/10.1007/s101620020028openalex-snapshot
Dynamics of Noise-Induced Cellular Injury and Repair in the Mouse Cochlea
inferredcites →https://doi.org/10.1007/s12035-012-8372-8openalex-snapshot
Noise-Induced Inner Hair Cell Ribbon Loss Disturbs Central Arc Mobilization: A Novel Molecular Paradigm for Understanding Tinnitus
inferredcites →https://doi.org/10.1016/0378-5955(83)90031-xopenalex-snapshot
Functional significance of dendritic swelling after loud sounds in the guinea pig cochlea
inferredcites →https://doi.org/10.1016/0378-5955(85)90008-5openalex-snapshot
Characteristics of tone-pip response patterns in relationship to spontaneous rate in cat auditory nerve fibers
inferredcites →https://doi.org/10.1016/0378-5955(90)90096-8openalex-snapshot
Changes in the synaptic region of auditory hair cells during noise-induced temporary threshold shift
inferredcites →https://doi.org/10.1016/0378-5955(92)90099-9openalex-snapshot
Effects of various noise exposures on endocochlear potentials correlated with cochlear gross responses
inferredcites →https://doi.org/10.1016/0378-5955(95)00014-uopenalex-snapshot
Afferent synaptic changes in auditory hair cells during noise-induced temporary threshold shift
inferredcites →https://doi.org/10.1016/0378-5955(95)00115-kopenalex-snapshot
Noise exposure alters the response of outer hair cells to ATP
inferredcites →https://doi.org/10.1016/0378-5955(95)00225-1openalex-snapshot
The effects of continuous versus interrupted noise exposures on distortion product otoacoustic emissions in guinea pigs
inferredcites →https://doi.org/10.1016/j.bbrc.2011.05.049openalex-snapshot
Dynamic changes in hair cell stereocilia and cochlear transduction after noise exposure
inferredcites →https://doi.org/10.1016/j.brainres.2012.02.008openalex-snapshot
Noise exposure enhances auditory cortex responses related to hyperacusis behavior
inferredcites →https://doi.org/10.1016/j.clinph.2014.01.011openalex-snapshot
Rapid acquisition of auditory subcortical steady state responses using multichannel recordings
inferredcites →https://doi.org/10.1016/j.heares.2004.08.016openalex-snapshot
Mechanisms of noise-induced hearing loss potentiation by hypoxia
inferredcites →https://doi.org/10.1016/j.heares.2006.06.007openalex-snapshot
Effects of intense noise exposure on the outer hair cell plasma membrane fluidity
inferredcites →https://doi.org/10.1016/j.heares.2006.08.017openalex-snapshot
Physiology, pharmacology and plasticity at the inner hair cell synaptic complex
inferredcites →https://doi.org/10.1016/j.heares.2010.03.002openalex-snapshot
Timing is everything: Temporal processing deficits in the aged auditory brainstem
inferredcites →https://doi.org/10.1016/j.heares.2012.02.002openalex-snapshot
Spontaneous hyperactivity in the auditory midbrain: Relationship to afferent input
inferredcites →https://doi.org/10.1016/j.heares.2015.02.009openalex-snapshot
Synaptopathy in the noise-exposed and aging cochlea: Primary neural degeneration in acquired sensorineural hearing loss
inferredcites →https://doi.org/10.1016/j.heares.2015.11.015openalex-snapshot
Functional-structural reorganisation of the neuronal network for auditory perception in subjects with unilateral hearing loss: Review of neuroimaging studies
inferredcites →https://doi.org/10.1016/j.heares.2016.05.008openalex-snapshot
Acquired hearing loss and brain plasticity
inferredcites →https://doi.org/10.1016/j.ijpsycho.2014.03.011openalex-snapshot
Animal models of auditory temporal processing
inferredcites →https://doi.org/10.1016/j.neuropsychologia.2012.08.013openalex-snapshot
Relationship between brainstem, cortical and behavioral measures relevant to pitch salience in humans
inferredcites →https://doi.org/10.1016/j.neuroscience.2006.05.057openalex-snapshot
Synaptic organization in cochlear inner hair cells deficient for the CaV1.3 (α1D) subunit of L-type Ca2+ channels
inferredcites →https://doi.org/10.1016/j.neuroscience.2007.08.010openalex-snapshot
Detection and differentiation of sensorineural hearing loss in mice using auditory steady-state responses and transient auditory brainstem responses
inferredcites →https://doi.org/10.1016/j.neuroscience.2009.08.036openalex-snapshot
Hyperactivity in the auditory midbrain after acoustic trauma: dependence on cochlear activity
inferredcites →https://doi.org/10.1016/j.neuroscience.2015.07.066openalex-snapshot
Noise-induced damage to ribbon synapses without permanent threshold shifts in neonatal mice
inferredcites →https://doi.org/10.1016/j.pneurobio.2013.08.002openalex-snapshot
Advances in the neurobiology of hearing disorders: Recent developments regarding the basis of tinnitus and hyperacusis
inferredcites →https://doi.org/10.1016/j.tins.2005.11.002openalex-snapshot
How to build a central synapse: clues from cell culture
inferredcites →https://doi.org/10.1016/s0378-5955(97)00006-3openalex-snapshot
Speech recognition in noise and presbycusis: relations to possible neural mechanisms
inferredcites →https://doi.org/10.1016/s0378-5955(99)00175-6openalex-snapshot
Threshold shifts and enhancement of cortical evoked responses after noise exposure in rats
inferredcites →https://doi.org/10.1016/s0959-4388(03)00098-9openalex-snapshot
The afferent synapse of cochlear hair cells
inferredcites →https://doi.org/10.1016/s0959-4388(97)80026-8openalex-snapshot
Mechanical amplification of stimuli by hair cells
inferredcites →https://doi.org/10.1016/s0960-9822(02)01384-2openalex-snapshot
Synapse Formation: Let's Stick Together
inferredcites →https://doi.org/10.1038/nature03418openalex-snapshot
Hair cell synaptic ribbons are essential for synchronous auditory signalling
inferredcites →https://doi.org/10.1038/srep25200openalex-snapshot
Coding deficits in hidden hearing loss induced by noise: the nature and impacts
inferredcites →https://doi.org/10.1046/j.0022-7722.2002.00030.xopenalex-snapshot
Birth, growth and elimination of a single synapse
inferredcites →https://doi.org/10.1055/s-0040-1715963openalex-snapshot
Sources of the Scalp-Recorded Amplitude-Modulation Following Response
inferredcites →https://doi.org/10.1073/pnas.1108912108openalex-snapshot
Normal hearing is not enough to guarantee robust encoding of suprathreshold features important in everyday communication
inferredcites →https://doi.org/10.1080/1047322x.1996.10389319openalex-snapshot
Advances in Our Understanding of Noise-Induced Hearing Loss
inferredcites →https://doi.org/10.1097/00003446-199408000-00004openalex-snapshot
The Relationship Among Distortion-Product Otoacoustic Emissions, Evoked Potential Thresholds, and Outer Hair Cells Following Interrupted Noise Exposures
inferredcites →https://doi.org/10.1097/aud.0000000000000107openalex-snapshot
Auditory Function in Normal-Hearing, Noise-Exposed Human Ears
inferredcites →https://doi.org/10.1097/moo.0000000000000085openalex-snapshot
Noise-induced hearing loss
inferredcites →https://doi.org/10.1098/rsta.2011.0192openalex-snapshot
Nonlinear models of development, amplification and compression in the mammalian cochlea
inferredcites →https://doi.org/10.1111/j.1460-9568.2004.03198.xopenalex-snapshot
Mouse photoreceptor synaptic ribbons lose and regain material in response to illumination changes
inferredcites →https://doi.org/10.1111/j.1749-6632.1999.tb08646.xopenalex-snapshot
Excitotoxicity, Synaptic Repair, and Functional Recovery in the Mammalian Cochlea: A Review of Recent Findings
inferredcites →https://doi.org/10.1121/1.1487841openalex-snapshot
Word recognition in competing babble and the effects of age, temporal processing, and absolute sensitivity
inferredcites →https://doi.org/10.1121/1.1798354openalex-snapshot
Human temporal auditory acuity as assessed by envelope following responses
inferredcites →https://doi.org/10.1121/1.381736openalex-snapshot
Auditory-nerve response from cats raised in a low-noise chamber
inferredcites →https://doi.org/10.1121/1.393530openalex-snapshot
Rate responses of auditory nerve fibers to tones in noise near masked threshold
inferredcites →https://doi.org/10.1126/science.7079757openalex-snapshot
Single-Neuron Labeling in the Cat Auditory Nerve
inferredcites →https://doi.org/10.1126/science.7079767openalex-snapshot
Noise-Induced Hearing Loss Can Alter Neural Coding and Increase Excitability in the Central Nervous System
inferredcites →https://doi.org/10.1152/jn.00164.2013openalex-snapshot
Noise-induced cochlear neuropathy is selective for fibers with low spontaneous rates
inferredcites →https://doi.org/10.1152/jn.00371.2012openalex-snapshot
Long-term, but not transient, threshold shifts alter the morphology and increase the excitability of cortical pyramidal neurons
inferredcites →https://doi.org/10.1152/jn.00738.2013openalex-snapshot
Contribution of auditory nerve fibers to compound action potential of the auditory nerve
inferredcites →https://doi.org/10.1155/2016/2162105openalex-snapshot
Neural Hyperactivity of the Central Auditory System in Response to Peripheral Damage
inferredcites →https://doi.org/10.1177/1073858409340253openalex-snapshot
The Making of Synaptic Ribbons: How They Are Built and What They Do
inferredcites →https://doi.org/10.1177/2331216514550621openalex-snapshot
Perceptual Consequences of “Hidden” Hearing Loss
inferredcites →https://doi.org/10.1242/jcs.162099openalex-snapshot
Unconventional molecular regulation of synaptic vesicle replenishment in cochlear inner hair cells
inferredcites →https://doi.org/10.1371/journal.pone.0049550openalex-snapshot
Silent Damage of Noise on Cochlear Afferent Innervation in Guinea Pigs and the Impact on Temporal Processing
inferredcites →https://doi.org/10.1371/journal.pone.0081566openalex-snapshot
Ribbon Synapse Plasticity in the Cochleae of Guinea Pigs after Noise-Induced Silent Damage
inferredcites →https://doi.org/10.1515/jbcpp.1997.8.3.113openalex-snapshot
Pathophysiological Mechanisms of Hearing Loss
inferredcites →https://doi.org/10.1523/jneurosci.0389-10.2010openalex-snapshot
Onset Coding Is Degraded in Auditory Nerve Fibers from Mutant Mice Lacking Synaptic Ribbons
inferredcites →https://doi.org/10.1523/jneurosci.05-12-03261.1985openalex-snapshot
Representation of tones in noise in the responses of auditory nerve fibers in cats. I. Comparison with detection thresholds
inferredcites →https://doi.org/10.1523/jneurosci.1014-10.2010openalex-snapshot
Molecular Anatomy of the Hair Cell's Ribbon Synapse
inferredcites →https://doi.org/10.1523/jneurosci.1964-08.2008openalex-snapshot
Multiple RIBEYE–RIBEYE Interactions Create a Dynamic Scaffold for the Formation of Synaptic Ribbons
inferredcites →https://doi.org/10.1523/jneurosci.2156-11.2011openalex-snapshot
Tinnitus with a Normal Audiogram: Physiological Evidence for Hidden Hearing Loss and Computational Model
inferredcites →https://doi.org/10.1523/jneurosci.2845-09.2009openalex-snapshot
Adding Insult to Injury: Cochlear Nerve Degeneration after “Temporary” Noise-Induced Hearing Loss
inferredcites →https://doi.org/10.1523/jneurosci.3389-10.2011openalex-snapshot
Opposing Gradients of Ribbon Size and AMPA Receptor Expression Underlie Sensitivity Differences among Cochlear-Nerve/Hair-Cell Synapses
inferredcites →https://doi.org/10.1523/jneurosci.3411-05.2005openalex-snapshot
Few Ca V 1.3 Channels Regulate the Exocytosis of a Synaptic Vesicle at the Hair Cell Ribbon Synapse
inferredcites →https://doi.org/10.1523/jneurosci.3491-12.2013openalex-snapshot
Disruption of the Presynaptic Cytomatrix Protein Bassoon Degrades Ribbon Anchorage, Multiquantal Release, and Sound Encoding at the Hair Cell Afferent Synapse
inferredcites →https://doi.org/10.1523/jneurosci.3915-14.2015openalex-snapshot
Individual Differences Reveal Correlates of Hidden Hearing Deficits
inferredcites →https://doi.org/10.1523/jneurosci.4460-15.2016openalex-snapshot
Auditory Brainstem Response Latency in Noise as a Marker of Cochlear Synaptopathy
inferredcites →https://doi.org/10.3109/00016487109125346openalex-snapshot
Primary Structural Changes in the Organ of Corti After Acoustic Overstimulation
inferredcites →https://doi.org/10.3109/00016489.2015.1061699openalex-snapshot
Noise induced reversible changes of cochlear ribbon synapses contribute to temporary hearing loss in mice
inferredcites →https://doi.org/10.3109/00016489309135819openalex-snapshot
Pathophysiology of the Glutamatergic Synapses in the Cochlea
inferredcites →https://doi.org/10.3109/00016489709117773openalex-snapshot
Synaptic Repair Mechanisms Responsible for Functional Recovery in Various Cochlear Pathologies
inferredcites →https://doi.org/10.3389/fnagi.2015.00008openalex-snapshot
Cochlear Injury and Adaptive Plasticity of the Auditory Cortex
inferredcites →https://doi.org/10.3389/fnmol.2014.00003openalex-snapshot
Presynaptic [Ca2+] and GCAPs: aspects on the structure and function of photoreceptor ribbon synapses
inferredcites →https://doi.org/10.3766/jaaa.23.8.5openalex-snapshot
Central Presbycusis: A Review and Evaluation of the Evidence
inferredcites →https://doi.org/10.7874/kja.2013.17.2.45openalex-snapshot
Pathophysiology of Age-Related Hearing Loss (Peripheral and Central)
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Applying technical guidance from the USA for management of impacts of anthropogenic noise on wildlife in other countries: the Canadian context
inferred← citeshttps://doi.org/10.1001/jamanetworkopen.2021.24100openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/978-3-030-40413-0_2openalex-snapshot
Noise-Induced Hearing Loss and Drug Therapy: Basic and Translational Science
inferred← citeshttps://doi.org/10.1007/s00106-019-0640-8openalex-snapshot
„Hidden hearing loss“ – Schäden der Hörverarbeitung auch bei niederschwelliger Lärmbelastung?
inferred← citeshttps://doi.org/10.1007/s10162-020-00762-3openalex-snapshot
The Genetics of Variation of the Wave 1 Amplitude of the Mouse Auditory Brainstem Response
inferred← citeshttps://doi.org/10.1016/b978-0-12-813724-6.00040-2openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.anl.2021.03.015openalex-snapshot
The possibility of cochlear synaptopathy in young people using a personal listening device
inferred← citeshttps://doi.org/10.1016/j.arr.2021.101423openalex-snapshot
Diabetes mellitus and hearing loss: A review
inferred← citeshttps://doi.org/10.1016/j.bbrep.2025.102044openalex-snapshot
Recombinant human Neuritin protects cochlear ribbon synapses and hearing function via ERK1/2 activation post noise-induced injury
inferred← citeshttps://doi.org/10.1016/j.celrep.2020.108431openalex-snapshot
Noise Exposures Causing Hearing Loss Generate Proteotoxic Stress and Activate the Proteostasis Network
inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2019.02.022openalex-snapshot
Targeting dysregulation of redox homeostasis in noise-induced hearing loss: Oxidative stress and ROS signaling
inferred← citeshttps://doi.org/10.1016/j.heares.2019.03.016openalex-snapshot
Rising-frequency chirp stimulus to effectively enhance wave-I amplitude of auditory brainstem response
inferred← citeshttps://doi.org/10.1016/j.heares.2020.107980openalex-snapshot
How low must you go? Effects of low-level noise on cochlear neural response
inferred← citeshttps://doi.org/10.1016/j.heares.2021.108208openalex-snapshot
Temporal characteristics of the cochlear response after noise exposure
inferred← citeshttps://doi.org/10.1016/j.heares.2021.108279openalex-snapshot
The increase in the degree of neural forward masking of cochlea following salicylate application
inferred← citeshttps://doi.org/10.1016/j.heares.2022.108459openalex-snapshot
Review of blast noise and the auditory system
inferred← citeshttps://doi.org/10.1016/j.heares.2026.109704openalex-snapshot
Frequency-specific and level-dependent alteration in cochlear nucleus following prolonged moderate noise exposure
inferred← citeshttps://doi.org/10.1016/j.joto.2018.05.001openalex-snapshot
Hidden cochlear impairments
inferred← citeshttps://doi.org/10.1016/j.neulet.2020.134910openalex-snapshot
Nicotinamide riboside protects noise-induced hearing loss by recovering the hair cell ribbon synapses
inferred← citeshttps://doi.org/10.1016/j.neuroscience.2018.09.026openalex-snapshot
Noise-induced Cochlear Synaptopathy and Signal Processing Disorders
inferred← citeshttps://doi.org/10.1016/j.neuroscience.2019.12.049openalex-snapshot
Repeated Moderate Sound Exposure Causes Accumulated Trauma to Cochlear Ribbon Synapses in Mice
inferred← citeshttps://doi.org/10.1016/j.neuroscience.2024.09.011openalex-snapshot
Cortical region-specific recovery of auditory temporal processing following noise-induced hearing loss
inferred← citeshttps://doi.org/10.1016/j.neuroscience.2026.02.004openalex-snapshot
Extracellular signal-regulated kinases 1/2 (ERK1/2) is a key regulator of noise-induced hidden hearing loss
inferred← citeshttps://doi.org/10.1016/j.tins.2019.03.006openalex-snapshot
Mechanisms of Hair Cell Damage and Repair
inferred← citeshttps://doi.org/10.1021/acsnano.3c11049openalex-snapshot
Complete Restoration of Hearing Loss and Cochlear Synaptopathy via Minimally Invasive, Single-Dose, and Controllable Middle Ear Delivery of Brain-Derived Neurotrophic Factor–Poly( dl -lactic acid- co -glycolic acid)-Loaded Hydrogel
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Prevalence of Pre-Existing Hearing Loss Among Patients With Drug-Resistant Tuberculosis in South Africa
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Examining the Profile of Noise-Induced Cochlear Synaptopathy Using iPhone Health App Data and Cochlear and Brainstem Electrophysiological Responses to Fast Clicks Rates
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Change in gene expression levels of GABA, glutamate and neurosteroid pathways due to acoustic trauma in the cochlea
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Association between occupational noise exposure level and pure-tone audiometry abnormalities among Metropolitan Manila Development Authority employees: A cross-sectional study
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Speech perception in noise, gap detection and amplitude modulation detection in suspected hidden hearing loss
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Listening effort in individuals with noise-induced hearing loss
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Urban noise levels are high enough to damage auditory sensorineural health
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Noise Damage Accelerates Auditory Aging and Tinnitus: A Canadian Population-Based Study
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inferred← citeshttps://doi.org/10.1101/311407openalex-snapshot
Genome-wide Association Study for Noise-induced Cochlear Synaptopathy
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Altered protein quality control contributes to noise-induced hearing loss
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Occupational noise exposure: A review of its effects, epidemiology, and impact with recommendations for reducing its burden
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Inner-hair-cell induced hearing loss: A biophysical modeling perspective
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Susceptibility of Diabetic Mice to Noise Trauma
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Exposição ao ruído em call center: headsets, sintomas auditivos e extra-auditivos de operadores de telemarketing
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Investigação dos efeitos da exposição ao ruído ocupacional nas vias auditivas periférica e central de indivíduos normo-ouvintes
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Potenciais evocados auditivos de estado estável e de longa latência em indivíduos normo-ouvintes expostos ao ruído ocupacional
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Optimal scheduling to minimize noise exposure in an oil and gas field
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Current insights in noise-induced hearing loss: A literature review of the underlying mechanism, pathophysiology, asymmetry, and management options
inferred← citeshttps://doi.org/10.1186/s43163-025-00885-5openalex-snapshot
Tinnitus and cochlear synaptopathy: exploring listening effort, speech perception in noise, and auditory brainstem response in normal-hearing adults
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Preferred music-listening level in musicians and non-musicians
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Speech-in-noise discriminability after noise exposure: Insights from a gerbil model of acoustic trauma
inferred← citeshttps://doi.org/10.1523/jneurosci.0759-18.2018openalex-snapshot
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Auditory Synaptopathy and Masking Psychometric Function Slope: A Conjecture
inferred← citeshttps://doi.org/10.21848/asr.220086openalex-snapshot
Recommended Auditory Brainstem Responses to Stimulation and Recording Parameters for Hidden Hearing Loss: A Systematic Review and Meta-Analysis
inferred← citeshttps://doi.org/10.22038/ijbms.2021.59970.13296openalex-snapshot
Metabotropic glutamate receptor: A new possible therapeutic target for cochlear synaptopathy.
inferred← citeshttps://doi.org/10.23749/mdl.v116i6.17196openalex-snapshot
Steady-State Auditory Evoked Potentials in Workers Exposed to Occupational Noise
inferred← citeshttps://doi.org/10.33552/ojor.2020.04.000586openalex-snapshot
Cochlear Synaptopathy in Humans. Review of the Evidence and Future Directions
inferred← citeshttps://doi.org/10.3389/fcell.2020.635201openalex-snapshot
Differences in Calcium Clearance at Inner Hair Cell Active Zones May Underlie the Difference in Susceptibility to Noise-Induced Cochlea Synaptopathy of C57BL/6J and CBA/CaJ Mice
inferred← citeshttps://doi.org/10.3389/fncel.2024.1465216openalex-snapshot
Noise-induced cochlear synaptopathy in C57BL/6 N mice as a function of trauma strength: ribbons are more vulnerable than postsynapses
inferred← citeshttps://doi.org/10.3389/fnins.2016.00621openalex-snapshot
Inner Hair Cell Loss Disrupts Hearing and Cochlear Function Leading to Sensory Deprivation and Enhanced Central Auditory Gain
inferred← citeshttps://doi.org/10.3390/audiolres16030076openalex-snapshot
Potential Risk for Hearing from Prolonged Exposure to Sound at Conversation Levels
inferred← citeshttps://doi.org/10.3390/brainsci13060968openalex-snapshot
Evaluation of Subtle Auditory Impairments with Multiple Audiological Assessments in Normal Hearing Workers Exposed to Occupational Noise
inferred← citeshttps://doi.org/10.3390/ijms21228792openalex-snapshot
Changes in microRNA Expression in the Cochlear Nucleus and Inferior Colliculus after Acute Noise-Induced Hearing Loss
inferred← citeshttps://doi.org/10.3390/ijms22168807openalex-snapshot
Hearing Impairment in a Mouse Model of Diabetes Is Associated with Mitochondrial Dysfunction, Synaptopathy, and Activation of the Intrinsic Apoptosis Pathway
inferred← citeshttps://doi.org/10.3390/ijms24097840openalex-snapshot
Regeneration of Hair Cells from Endogenous Otic Progenitors in the Adult Mammalian Cochlea: Understanding Its Origins and Future Directions
inferred← citeshttps://doi.org/10.3390/ijms25105154openalex-snapshot
C-Phycocyanin Attenuates Noise-Induced Cochlear Synaptopathy via the Inhibition of Oxidative Stress and Intercellular Adhesion Molecule-1 in the Cochlea
inferred← citeshttps://doi.org/10.3390/jcm11030875openalex-snapshot
Possible Existence of Cochlear Synaptopathy in Patients Completely Recovered from Idiopathic Sudden Sensorineural Hearing Loss
inferred← citeshttps://doi.org/10.3390/jcm13154538openalex-snapshot
Changing Knowledge, Principles, and Technology in Contemporary Clinical Audiological Practice: A Narrative Review
inferred← citeshttps://doi.org/10.3390/molecules26123626openalex-snapshot
Ultrasound Microbubbles Enhance the Efficacy of Insulin-Like Growth Factor-1 Therapy for the Treatment of Noise-Induced Hearing Loss
inferred← citeshttps://doi.org/10.34034/tjahr.1034606openalex-snapshot
Gürültülü ortam çalışanlarında iş yaşamı ve genel yaşam kalitesinin ilişkisi
inferred← citeshttps://doi.org/10.3892/mi.2024.184openalex-snapshot
From sound waves to molecular and cellular mechanisms: Understanding noise‑induced hearing loss and pioneering preventive approaches (Review)
inferred← citeshttps://doi.org/10.4102/sajcd.v68i1.789openalex-snapshot
Patterns of noise exposure and prevalence of hearing loss amongst Cape Town Minstrel Carnival musicians
inferred← citeshttps://doi.org/10.4103/nah.nah_71_24openalex-snapshot
Individual and combined effects of noise exposure and diabetes mellitus on hearing
inferred← citeshttps://doi.org/10.4236/ijohns.2022.111006openalex-snapshot
Noise Exposure and Otological Morbidity in Military Musicians in Cotonou
inferred← citeshttps://doi.org/10.53846/goediss-10455openalex-snapshot
Synaptic mechanisms of noise-induced hearing loss
inferred← citeshttps://doi.org/10.6061/clinics/2020/e1845openalex-snapshot
Oxidative Stress as a Risk Factor for Hearing Changes in HIV-positive Normal Listeners
inferred← citeshttps://doi.org/10.62347/evde9449openalex-snapshot
ROS-induced oxidative stress and mitochondrial dysfunction: a possible mechanism responsible for noise-induced ribbon synaptic damage
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