Auditory neuropathy--neural and synaptic mechanisms (Q38739507)

6 September 2017

Auditory neuropathy--neural and synaptic mechanisms (English)

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6 September 2017

1

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6 September 2017

2

Arnold Starr

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PubMed ID

26891769

6 September 2017

language of work or name

English

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publication date

19 February 2016

1 reference

6 September 2017

Nature Reviews Neurology

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6 September 2017

12

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6 September 2017

135-149

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6 September 2017

3

1 reference

https://scigraph.springernature.com/pub.10.1038/nrneurol.2016.10

6 September 2017

0 references

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.10

Perceptual consequences of disrupted auditory nerve activity.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.10

[Diagnosis and therapy of auditory synaptopathy/neuropathy].

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.10

Prevalence of auditory neuropathy spectrum disorder in an auditory health care service

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.10

Clinical findings for a group of infants and young children with auditory neuropathy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.10

Prevalence of auditory neuropathy/synaptopathy in a population of children with profound hearing loss.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.10

A multicenter study on the prevalence and spectrum of mutations in the otoferlin gene (OTOF) in subjects with nonsyndromic hearing impairment and auditory neuropathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.10

Phenotypic characterization of hereditary hearing impairment linked to DFNA25.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.10

The diverse roles of ribbon synapses in sensory neurotransmission

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.10

Loss-of-function mutations in a calcium-channel alpha1-subunit gene in Xp11.23 cause incomplete X-linked congenital stationary night blindness

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.10

An L-type calcium-channel gene mutated in incomplete X-linked congenital stationary night blindness

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.10

Mutations in CABP4, the gene encoding the Ca2+-binding protein 4, cause autosomal recessive night blindness

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.10

Hair cell synaptic ribbons are essential for synchronous auditory signalling.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.10

Onset coding is degraded in auditory nerve fibers from mutant mice lacking synaptic ribbons

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.10

Disruption of adaptor protein 2μ (AP-2μ) in cochlear hair cells impairs vesicle reloading of synaptic release sites and hearing

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.10

Hearing requires otoferlin-dependent efficient replenishment of synaptic vesicles in hair cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.10

Mutant beta-spectrin 4 causes auditory and motor neuropathies in quivering mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.10

BetaIVSigma1 spectrin stabilizes the nodes of Ranvier and axon initial segments

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.10

Relating structure and function of inner hair cell ribbon synapses

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.10

Time and intensity coding at the hair cell's ribbon synapse

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.10

Mechanisms underlying the temporal precision of sound coding at the inner hair cell ribbon synapse

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.10

Otoferlin: a multi-C2 domain protein essential for hearing

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.10

Exocytosis at the hair cell ribbon synapse apparently operates without neuronal SNARE proteins

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.10

Complexin-I is required for high-fidelity transmission at the endbulb of Held auditory synapse.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.10

Molecular anatomy of the hair cell's ribbon synapse

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.10

Unconventional molecular regulation of synaptic vesicle replenishment in cochlear inner hair cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.10

Otoferlin, defective in a human deafness form, is essential for exocytosis at the auditory ribbon synapse

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.10

Sensorineural deafness and seizures in mice lacking vesicular glutamate transporter 3.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.10

Impairment of SLC17A8 encoding vesicular glutamate transporter-3, VGLUT3, underlies nonsyndromic deafness DFNA25 and inner hair cell dysfunction in null mice.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.10

Congenital deafness and sinoatrial node dysfunction in mice lacking class D L-type Ca2+ channels

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.10

Dendrotoxin-sensitive K(+) currents contribute to accommodation in murine spiral ganglion neurons.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.10

Spike encoding of neurotransmitter release timing by spiral ganglion neurons of the cochlea.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.10

Transmitter release at the hair cell ribbon synapse

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.10

Uniquantal release through a dynamic fusion pore is a candidate mechanism of hair cell exocytosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.10

Where is the spike generator of the cochlear nerve? Voltage-gated sodium channels in the mouse cochlea.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.10

A mutation in OTOF, encoding otoferlin, a FER-1-like protein, causes DFNB9, a nonsyndromic form of deafness

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.10

OTOF mutations revealed by genetic analysis of hearing loss families including a potential temperature sensitive auditory neuropathy allele

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.10

Temperature-sensitive auditory neuropathy associated with an otoferlin mutation: Deafening fever!

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.10

Screening mutations of OTOF gene in Chinese patients with auditory neuropathy, including a familial case of temperature-sensitive auditory neuropathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.10

Novel OTOF mutations in Brazilian patients with auditory neuropathy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.10

A prevalent founder mutation and genotype-phenotype correlations of OTOF in Japanese patients with auditory neuropathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.10

An emergency response team for membrane repair

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.10

Dysferlin, a novel skeletal muscle gene, is mutated in Miyoshi myopathy and limb girdle muscular dystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.10

Defective membrane repair in dysferlin-deficient muscular dystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.10

Otoferlin is a calcium sensor that directly regulates SNARE-mediated membrane fusion

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.10

Characterization of the lipid binding properties of Otoferlin reveals specific interactions between PI(4,5)P2 and the C2C and C2F domains

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.10

Direct interaction of otoferlin with syntaxin 1A, SNAP-25, and the L-type voltage-gated calcium channel Cav1.3.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.10

The crystal structure of the C₂A domain of otoferlin reveals an unconventional top loop region

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.10

Alternate splicing of dysferlin C2A confers Ca²⁺-dependent and Ca²⁺-independent binding for membrane repair

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.10

Audibility, speech perception and processing of temporal cues in ribbon synaptic disorders due to OTOF mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.10

Probing the functional equivalence of otoferlin and synaptotagmin 1 in exocytosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.10

Otoferlin is critical for a highly sensitive and linear calcium-dependent exocytosis at vestibular hair cell ribbon synapses

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.10

Non-syndromic recessive auditory neuropathy is the result of mutations in the otoferlin (OTOF) gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.10

A forward genetics screen in mice identifies recessive deafness traits and reveals that pejvakin is essential for outer hair cell function

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.10

Loudness adaptation accompanying ribbon synapse and auditory nerve disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.10

Otoferlin couples to clathrin-mediated endocytosis in mature cochlear inner hair cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.10

DFNA25, a novel locus for dominant nonsyndromic hereditary hearing impairment, maps to 12q21-24.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.10

Vesicular glutamate transporter 3 is required for synaptic transmission in zebrafish hair cells.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.10

Molecular characterization of a 12q22-q24 deletion associated with congenital deafness: confirmation and refinement of the DFNA25 locus.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.10

Loss of Ca(v)1.3 (CACNA1D) function in a human channelopathy with bradycardia and congenital deafness

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.10

Calcium, ageing, and neuronal vulnerability in Parkinson's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.10

The L-Type voltage-gated calcium channel Cav1.3 mediates consolidation, but not extinction, of contextually conditioned fear in mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.10

The Ca2+ channel subunit beta2 regulates Ca2+ channel abundance and function in inner hair cells and is required for hearing

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.10

Mutation in the auxiliary calcium-channel subunit CACNA2D4 causes autosomal recessive cone dystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.10

A mutation in CABP2, expressed in cochlear hair cells, causes autosomal-recessive hearing impairment

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.10

Essential role of Ca2+-binding protein 4, a Cav1.4 channel regulator, in photoreceptor synaptic function

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.10

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.10

Multi-system neurological disease is common in patients with OPA1 mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.10

Medical management of hereditary optic neuropathies

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.10

OPA1, encoding a dynamin-related GTPase, is mutated in autosomal dominant optic atrophy linked to chromosome 3q28

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.10

Nuclear gene OPA1, encoding a mitochondrial dynamin-related protein, is mutated in dominant optic atrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.10

Mitochondria: from cell death executioners to regulators of cell differentiation

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.10

Molecular screening of 980 cases of suspected hereditary optic neuropathy with a report on 77 novel OPA1 mutations.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.10

A splice site mutation in the murine Opa1 gene features pathology of autosomal dominant optic atrophy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.10

Brain potentials before and during memory scanning

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.10

Pathology and physiology of auditory neuropathy with a novel mutation in the MPZ gene (Tyr145->Ser).

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.10

Sensorineural hearing impairment in patients with Pmp22 duplication, deletion, and frameshift mutations.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.10

Anticipation in a unique family with Charcot-Marie-Tooth syndrome and deafness: delineation of the clinical features and review of the literature

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.10

Pathophysiological mechanisms and functional hearing consequences of auditory neuropathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.10

Mutations in the gene encoding pejvakin, a newly identified protein of the afferent auditory pathway, cause DFNB59 auditory neuropathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.10

High frequency of autosomal-recessive DFNB59 hearing loss in an isolated Arab population in Israel.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.10

Truncating mutation of the DFNB59 gene causes cochlear hearing impairment and central vestibular dysfunction

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.10

Novel mutations in the pejvakin gene are associated with autosomal recessive non-syndromic hearing loss in Iranian families.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.10

Involvement of DFNB59 mutations in autosomal recessive nonsyndromic hearing impairment.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.10

Hypervulnerability to Sound Exposure through Impaired Adaptive Proliferation of Peroxisomes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.10

A gene responsible for autosomal dominant auditory neuropathy (AUNA1) maps to 13q14-21.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.10

A dominantly inherited progressive deafness affecting distal auditory nerve and hair cells.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.10

Increased activity of Diaphanous homolog 3 (DIAPH3)/diaphanous causes hearing defects in humans with auditory neuropathy and in Drosophila

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.10

Diaphanous homolog 3 (Diap3) overexpression causes progressive hearing loss and inner hair cell defects in a transgenic mouse model of human deafness

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.10

Speech perception ability in individuals with Friedreich ataxia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.10

The frequency of auditory neuropathy detected by universal newborn hearing screening program

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.10

Association Between Peak Serum Bilirubin and Neurodevelopmental Outcomes in Extremely Low Birth Weight Infants

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.10

Audiologic impairment associated with bilirubin-induced neurologic damage

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.10

Selective inner hair cell loss in premature infants and cochlea pathological patterns from neonatal intensive care unit autopsies.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.10

The Gunn rat: an experimental model for central deafness.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.10

Acute hyperbilirubinaemia induces presynaptic neurodegeneration at a central glutamatergic synapse

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.10

Changes in calcium-binding protein expression in the auditory brainstem nuclei of the jaundiced Gunn rat.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.10

Auditory system dysfunction due to infantile thiamine deficiency: long-term auditory sequelae.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.10

Targeted disruption of Slc19a2, the gene encoding the high-affinity thiamin transporter Thtr-1, causes diabetes mellitus, sensorineural deafness and megaloblastosis in mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.10

Deletion of SLC19A2, the high affinity thiamine transporter, causes selective inner hair cell loss and an auditory neuropathy phenotype

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.10

Afferent synaptic changes in auditory hair cells during noise-induced temporary threshold shift

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.10

Alpha-amino-3-hydroxy-5-methyl-4-isoxazole propionic acid electrophysiological and neurotoxic effects in the guinea-pig cochlea

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.10

Excitotoxicity and repair of cochlear synapses after noise-trauma induced hearing loss.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.10

Synaptic alterations at inner hair cells precede spiral ganglion cell loss in aging C57BL/6J mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.10

Adding insult to injury: cochlear nerve degeneration after "temporary" noise-induced hearing loss

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.10

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.10

Synaptopathy in the noise-exposed and aging cochlea: Primary neural degeneration in acquired sensorineural hearing loss.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.10

Tuning of synapse number, structure and function in the cochlea

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.10

Noise-induced cochlear neuropathy is selective for fibers with low spontaneous rates

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.10

Contribution of auditory nerve fibers to compound action potential of the auditory nerve

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.10

Neurotrophin-3 regulates ribbon synapse density in the cochlea and induces synapse regeneration after acoustic trauma

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.10

Tinnitus with a Normal Audiogram: Physiological Evidence for Hidden Hearing Loss and Computational Model

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.10

Absence of both auditory evoked potentials and auditory percepts dependent on timing cues

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.10

Cochlear receptor (microphonic and summating potentials, otoacoustic emissions) and auditory pathway (auditory brain stem potentials) activity in auditory neuropathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.10

Abnormal cochlear potentials from deaf patients with mutations in the otoferlin gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.10

Detection and differentiation of sensorineural hearing loss in mice using auditory steady-state responses and transient auditory brainstem responses.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.10

Massively Parallel Sequencing for Genetic Diagnosis of Hearing Loss: The New Standard of Care

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.10

Analysis of speech perception outcomes among patients receiving cochlear implants with auditory neuropathy spectrum disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.10

Does cochlear implantation improve speech recognition in children with auditory neuropathy spectrum disorder? A systematic review

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.10

Audiologic management of auditory neuropathy spectrum disorder in children: a systematic review of the literature

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.10

Auditory neuropathies: understanding their pathogenesis to illuminate intervention strategies

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.10

Speech and language outcomes in children with auditory neuropathy/dys-synchrony managed with either cochlear implants or hearing aids.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.10

Impact of the presence of auditory neuropathy spectrum disorder (ANSD) on outcomes of children at three years of age.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.10

Estimation of surviving spiral ganglion cells in the deaf rat using the electrically evoked auditory brainstem response.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.10

Results of cochlear implantation in two children with mutations in the OTOF gene.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.10

Optogenetic stimulation of the auditory pathway.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.10

Considering optogenetic stimulation for cochlear implants.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.10

Restoration of hearing in the VGLUT3 knockout mouse using virally mediated gene therapy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.10

CaV1.3 channels are essential for development and presynaptic activity of cochlear inner hair cells.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.10

In silico functional and structural characterisation of ferlin proteins by mapping disease-causing mutations and evolutionary information onto three-dimensional models of their C2 domains

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.10

Late-onset Charcot-Marie-Tooth type 2 disease with hearing impairment associated with a novel Pro105Thr mutation in the MPZ gene

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.10

Auditory brainstem response detects early bilirubin neurotoxicity at low indirect bilirubin values

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.10

Estimation of surviving spiral ganglion cells in the deaf rat using the electrically evoked auditory brainstem response

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.10

Electrically evoked auditory brainstem response in peripherally myelin-deficient mice

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.10

31 March 2020

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/26891769

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Exacerbation of noise-induced hearing loss in mice lacking the glutamate transporter GLAST

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/26891769

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Brain stem evoked response audiometry in newborn hearing screening

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/26891769

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1038/NRNEUROL.2016.10

1 reference

PubMed ID

26891769

Dimensions Publication ID

6 September 2017

0 references

1 reference

PubMed ID

26891769