Reply: Both mitochondrial DNA and mitonuclear gene mutations cause hearing loss through cochlear dysfunction.

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Patient care standards for primary mitochondrial disease: a consensus statement from the Mitochondrial Medicine Society.Hearing impairment in MELAS: new prospective in clinical use of microRNA, a systematic review.

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Reply: Both mitochondrial DNA and mitonuclear gene mutations cause hearing loss through cochlear dysfunction.

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Elona Cama

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Maria Lucia Valentino

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Information from cochlear potentials and genetic mutations helps localize the lesion site in auditory neuropathy.

Mitochondrial DNA: impacting central and peripheral nervous systems.

Psychophysical evaluation of cochlear hair cell damage due to the A3243G mitochondrial DNA mutation.

Pathophysiological mechanisms and functional hearing consequences of auditory neuropathy.

Cochlear origin of hearing loss in MELAS syndrome.

Are inner or outer hair cells the source of summating potentials recorded from the round window?

Both mitochondrial DNA and mitonuclear gene mutations cause hearing loss through cochlear dysfunction.

Frequency-specific electrocochleography indicates that presynaptic and postsynaptic mechanisms of auditory neuropathy exist.

Abnormal brainstem auditory evoked responses in mitochondrial neurogastrointestinal encephalomyopathy (MNGIE): evidence of delayed central conduction time.

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