Different cortical metabolic activation by visual stimuli possibly due to different time courses of hearing loss in patients withGJB2 and SLC26A4 mutation
Contains fulltext : 47828.pdf (publisher's version ) (Closed access)Hearing impair...
Deafness can occur due to damage to the ear, especially the inner ear. In other cases, the cause is ...
In many world populations, mutations in the GJB2 gene (codifyng for Connexin 26) are the most common...
Conclusion. We have demonstrated differences in cortical activation with language-related visual sti...
Mutations in GJB2 gene are the most common cause of genetic deafness. More than 100 mutations have b...
The SLC26A4 gene has been described as the second gene involved in most cases of sensorineural non-s...
The aim of this study was to screen 349 patients affected by sensorineural hearing loss (SNHL), most...
The SLC26A4 gene has been described as the second gene involved in most cases of sensorineural non-s...
Results in studies concerning cortical changes in idiopathic sudden sensorineural hearing loss (ISSN...
We recorded cochlear potentials by transtympanic electrocochleography (ECochG) in three hearing-impa...
The common GJB2 (Connexin 26) 35delG mutation might contribute to the development of age-related hea...
Mutations in the GJB2 gene (encoding for Connexin 26 protein) represent a leading cause of genetic h...
We recorded cochlear potentials by transtympanic electrocochleography (ECochG) in three hearing-impa...
<p>CI, cochlear implantation; AgeHL, age at detection of hearing loss; AgeCI, age at implantation; M...
INTRODUCTION: Mutations in GJB2 are the most common cause of non-syndromic autosomal recessive heari...
Contains fulltext : 47828.pdf (publisher's version ) (Closed access)Hearing impair...
Deafness can occur due to damage to the ear, especially the inner ear. In other cases, the cause is ...
In many world populations, mutations in the GJB2 gene (codifyng for Connexin 26) are the most common...
Conclusion. We have demonstrated differences in cortical activation with language-related visual sti...
Mutations in GJB2 gene are the most common cause of genetic deafness. More than 100 mutations have b...
The SLC26A4 gene has been described as the second gene involved in most cases of sensorineural non-s...
The aim of this study was to screen 349 patients affected by sensorineural hearing loss (SNHL), most...
The SLC26A4 gene has been described as the second gene involved in most cases of sensorineural non-s...
Results in studies concerning cortical changes in idiopathic sudden sensorineural hearing loss (ISSN...
We recorded cochlear potentials by transtympanic electrocochleography (ECochG) in three hearing-impa...
The common GJB2 (Connexin 26) 35delG mutation might contribute to the development of age-related hea...
Mutations in the GJB2 gene (encoding for Connexin 26 protein) represent a leading cause of genetic h...
We recorded cochlear potentials by transtympanic electrocochleography (ECochG) in three hearing-impa...
<p>CI, cochlear implantation; AgeHL, age at detection of hearing loss; AgeCI, age at implantation; M...
INTRODUCTION: Mutations in GJB2 are the most common cause of non-syndromic autosomal recessive heari...
Contains fulltext : 47828.pdf (publisher's version ) (Closed access)Hearing impair...
Deafness can occur due to damage to the ear, especially the inner ear. In other cases, the cause is ...
In many world populations, mutations in the GJB2 gene (codifyng for Connexin 26) are the most common...