Hearing loss (HL) is an etiologically heterogeneous disorder that affects around 5% of the
world's population. There has been an exponential increase in the identification of genes …

As biomolecular approaches for hearing restoration in profound sensorineural hearing loss
evolve, they will be applied in conjunction with or instead of cochlear implants. An …

Usher syndrome (USH) is a rare autosomal recessive disease characterized by the
combination of hearing loss, visual impairment due to retinitis pigmentosa, and in some …

Hearing loss affects more than 430 million people, worldwide, and is the third most common
chronic physical condition in the United States and Europe (GBD Hearing Loss …

The past 30 years have seen an exponential growth concerning the identification of genes
and variants responsible for hereditary hearing loss (HL) worldwide. This has led to a huge …

Usher Syndrome classification takes into account the absence of vestibular function but its
correlation with genotype is not well characterized. We intend to investigate whether video …

The Outcome of Cochlear Implantations in Deaf-Blind Patients... : Otology & Neurotology The
Outcome of Cochlear Implantations in Deaf-Blind Patients: A Multicenter Observational Study …

Auditory neuropathy (AN) is an under-recognized form of hearing loss characterized by
lesions in inner hair cells (IHCs), ribbon synapses and spiral ganglion neurons (SGNs). The …

Usher syndrome (USH) is characterised by degenerative vision loss known as retinitis
pigmentosa (RP), sensorineural hearing loss, and vestibular dysfunction. RP can cause …

Usher syndrome (US) is a clinically and genetically heterogeneous disorder that involves
three main features: sensorineural hearing loss, retinitis pigmentosa (RP), and vestibular …