Pathology and physiology of auditory neuropathy with a novel mutation in the MPZ gene (Tyr145->Ser).
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Auditory processing in individuals with auditory neuropathy.Ouabain-induced cochlear degeneration in rat.Acoustically evoked auditory change complex in children with auditory neuropathy spectrum disorder: a potential objective tool for identifying cochlear implant candidatesIntertrial auditory neural stability supports beat synchronization in preschoolers.Central recruitment in individual with auditory neuropathy.Cervical and Ocular Vestibular Evoked Myogenic Potentials Test Results in Individuals with Auditory Neuropathy Spectrum Disorders.Auditory neuropathy/dys-synchrony and its perceptual consequences.Gap detection measured with electrically evoked auditory event-related potentials and speech-perception abilities in children with auditory neuropathy spectrum disorder.Loudness adaptation accompanying ribbon synapse and auditory nerve disorders.Temporal processing and speech perception in noise by listeners with auditory neuropathyAuditory cortical N100 in pre- and post-synaptic auditory neuropathy to frequency or intensity changes of continuous tonesInformation from cochlear potentials and genetic mutations helps localize the lesion site in auditory neuropathy.Abnormal cochlear potentials from deaf patients with mutations in the otoferlin geneSynchronous auditory nerve activity in the carboplatin-chinchilla model of auditory neuropathy.N100 cortical potentials accompanying disrupted auditory nerve activity in auditory neuropathy (AN): effects of signal intensity and continuous noise.A dominantly inherited progressive deafness affecting distal auditory nerve and hair cells.Speech identification and cortical potentials in individuals with auditory neuropathy.Auditory nerve is affected in one of two different point mutations of the neurofilament light gene.Lack of Tff3 peptide results in hearing impairment and accelerated presbyacusis.Human Cochlear Histopathology Reflects Clinical Signatures of Primary Neural DegenerationGenotype-phenotype characteristics and baseline natural history of heritable neuropathies caused by mutations in the MPZ gene.Human cytomegalovirus (HCMV) and hearing impairment: infection of fibroblast cells with HCMV induces chromosome breaks at 1q23.3, between loci DFNA7 and DFNA49 -- both involved in dominantly inherited, sensorineural, hearing impairment.Cochlear microphonic potential recorded by transtympanic electrocochleography in normally-hearing and hearing-impaired earsA Novel Asp121Asn Mutation of Myelin Protein Zero Is Associated with Late-Onset Axonal Charcot-Marie-Tooth Disease, Hearing Loss and Pupil Abnormalities.Temporal Response Properties of the Auditory Nerve in Implanted Children with Auditory Neuropathy Spectrum Disorder and Implanted Children with Sensorineural Hearing Loss.Glial cell line-derived neurotrophic factor (GDNF) induces neuritogenesis in the cochlear spiral ganglion via neural cell adhesion molecule (NCAM)The mitochondrial connection in auditory neuropathy.Vestibular test findings in individuals with auditory neuropathy: review.The audiological journey and early outcomes of twelve infants with auditory neuropathy spectrum disorder from birth to two years of age.Pathophysiological mechanisms and functional hearing consequences of auditory neuropathy.Auditory neuropathy--neural and synaptic mechanisms.Acquired auditory neuropathy spectrum disorder after an attack of chikungunya: case study.Perceptual consequences of disrupted auditory nerve activity.Deep band modulated phrase perception in quiet and noise in individuals with auditory neuropathy spectrum disorder and sensorineural hearing loss.Selective hair cell ablation and noise exposure lead to different patterns of changes in the cochlea and the cochlear nucleus.Multi-site diagnosis and management of 260 patients with auditory neuropathy/dys-synchrony (auditory neuropathy spectrum disorder).Involvement of peripheral vestibular nerve in individuals with auditory neuropathy.Individual Differences in Human Auditory Processing: Insights From Single-Trial Auditory Midbrain Activity in an Animal Model.ATP1A3 mutations can cause progressive auditory neuropathy: a new gene of auditory synaptopathy.Characteristics of clinical and electrophysiological pattern of Charcot-Marie-Tooth 4C.
P2860
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P2860
Pathology and physiology of auditory neuropathy with a novel mutation in the MPZ gene (Tyr145->Ser).
description
2003 nî lūn-bûn
@nan
2003年の論文
@ja
2003年学术文章
@wuu
2003年学术文章
@zh
2003年学术文章
@zh-cn
2003年学术文章
@zh-hans
2003年学术文章
@zh-my
2003年学术文章
@zh-sg
2003年學術文章
@yue
2003年學術文章
@zh-hant
name
Pathology and physiology of au ...... in the MPZ gene (Tyr145->Ser).
@en
Pathology and physiology of auditory neuropathy with a novel mutation in the MPZ gene
@nl
type
label
Pathology and physiology of au ...... in the MPZ gene (Tyr145->Ser).
@en
Pathology and physiology of auditory neuropathy with a novel mutation in the MPZ gene
@nl
prefLabel
Pathology and physiology of au ...... in the MPZ gene (Tyr145->Ser).
@en
Pathology and physiology of auditory neuropathy with a novel mutation in the MPZ gene
@nl
P2093
P356
P1433
P1476
Pathology and physiology of au ...... in the MPZ gene (Tyr145->Ser).
@en
P2093
Arnold Starr
Bronya Keats
Chong S Kim
Deidre Winnier
Fan-Gang Zeng
Fred Linthicum
Henry J Michalewski
Sharon Fujikawa-Brooks
P304
P356
10.1093/BRAIN/AWG156
P407
P577
2003-05-06T00:00:00Z