about
Auditory processing deficits in children with Friedreich ataxia.A new locus for X-linked dominant Charcot-Marie-Tooth disease (CMTX6) is caused by mutations in the pyruvate dehydrogenase kinase isoenzyme 3 (PDK3) gene.Perceptual characterization of children with auditory neuropathy.Speech perception in noise for children with auditory neuropathy/dys-synchrony type hearing loss.Speech perception in children with auditory neuropathy/dyssynchrony managed with either hearing AIDS or cochlear implants.Auditory and visual temporal processing disruption in open angle glaucoma.Auditory perception in individuals with Friedreich's ataxia.Auditory function in individuals within Leber's hereditary optic neuropathy pedigrees.The use of listening devices to ameliorate auditory deficit in children with autism.Clinical findings for a group of infants and young children with auditory neuropathy.A comparison of 40 Hz auditory steady-state response (ASSR) and cortical auditory evoked potential (CAEP) thresholds in awake adult subjects.Steady-state evoked potential and behavioral hearing thresholds in a group of children with absent click-evoked auditory brain stem response.Auditory function in children with Charcot-Marie-Tooth disease.Interhemispheric transfer time in patients with auditory hallucinations: an auditory event-related potential study.Maturation of auditory steady-state responses in normal babies.Binaural speech processing in individuals with auditory neuropathy.Auditory processing deficits in individuals with primary open-angle glaucoma.Long-term hearing deficits after childhood middle ear disease.Auditory neuropathy in individuals with Type 1 diabetes.Successful treatment of auditory perceptual disorder in individuals with Friedreich ataxia.Speech and language outcomes in children with auditory neuropathy/dys-synchrony managed with either cochlear implants or hearing aids.The extent of hearing impairment amongst Australian Indigenous prisoners in Victoria, and implications for the correctional system.Speech perception ability in individuals with Friedreich ataxia.Receptive language and speech production in children with auditory neuropathy/dyssynchrony type hearing loss.Comparison of auditory steady-state responses and tone-burst auditory brainstem responses in normal babies.The test of everyday attention reveals significant sustained volitional attention and working memory deficits in friedreich ataxia.Interhemispheric EEG coherence is reduced in auditory cortical regions in schizophrenia patients with auditory hallucinations.Neuro-otological findings in patients with migraine- and nonmigraine-related dizzinessVestibular rehabilitation outcomes in patients with and without vestibular migraineAuditory neuropathyAuditory pathway changes mirror overall disease progress in individuals with Friedreich ataxia
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description
hulumtues
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Gary Rance
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Gary Rance
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Gary Rance
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Gary Rance
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Gary Rance
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Gary Rance
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Gary Rance
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Gary Rance
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Gary Rance
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Gary Rance
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Gary Rance
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Gary Rance
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Gary Rance
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Gary Rance
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Gary Rance
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