Homozygous mutations in the fibroblast growth factor 3 (FGF3) gene have recently been discovered in an autosomal recessive form of syndromic deafness characterized by complete labyrinthine aplasia (Michel aplasia), microtia, and microdontia (OMIM 610706 - LAMM). In order to better characterize the phenotypic spectrum associated with FGF3 mutations, we sequenced...
The development and characteristics of cortical auditory evoked potentials from electrical stimulation of the cochlear nucleus by an auditory brainstem implant in 6 children with cochlear nerve aplasia
Effect of age on speech recognition in noise and on contralateral transient evoked otoacoustic emission suppression
We aimed to study the influence of age, in normal hearing individuals, on: the masking level difference test, the speech recognition in noise test, the transient evoked otoacoustic emissions test, and the contralateral transient evoked otoacoustic emission suppression test. We also aimed to research the effect of age when using...