Results 91 to 100 of about 17,520 (209)

A New Mouse Insertional Mutation That Causes Sensorineural Deafness and Vestibular Defects [PDF]

open access: bronze, 1999
Kumar N. Alagramam   +6 more
openalex   +1 more source

Familial Progressive Sensorineural Deafness Is Mainly Due to the mtDNA A1555G Mutation and Is Enhanced by Treatment with Aminoglycosides [PDF]

open access: bronze, 1998
Xavier Estivill   +10 more
openalex   +1 more source

Usher Syndrome in Two Siblings, A Case Report

open access: yesIJRETINA (International Journal of Retina), 2019
Introduction: Usher Syndrome is a rare genetic disorder involving abnormalities in the retina and hearing, where the patients will experience blindness and hearing loss due to mutations of the gene.
Teddy Kristiyan   +2 more
doaj  

[Tinnitus and depression after cochlear implantation in adult sensorineural deafness]. [PDF]

open access: yesLin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi, 2022
Ming J, Hu J, Wei B.
europepmc   +1 more source

Exploring the Diversity of Music Experiences for Deaf and Hard of Hearing People [PDF]

open access: yesarXiv
Sensory substitution or enhancement techniques have been proposed to enable deaf or hard of hearing (DHH) people to listen to and even compose music. However, little is known about how such techniques enhance DHH people's music experience. Since deafness is a spectrum -- as are DHH people's preferences and perceptions of music -- a more situated ...
arxiv  

"We do use it, but not how hearing people think": How the Deaf and Hard of Hearing Community Uses Large Language Model Tools [PDF]

open access: yesarXiv
Generative AI tools, particularly those utilizing large language models (LLMs), are increasingly used in everyday contexts. While these tools enhance productivity and accessibility, little is known about how Deaf and Hard of Hearing (DHH) individuals engage with them or the challenges they face when using them.
arxiv  

Case of Waardenburg Shah syndrome in a family with review of literature

open access: yesJournal of Otology, 2018
Waardenburg syndrome is a rare disease characterized by sensorineural deafness in association with pigmentary defects. Depending on additional symptoms, WS have been classified into four types. Waardenburg syndrome type 4, also called as Waardenburg Shah
Setty.L.N. Chandra Mohan
doaj  

Tailored Real-time AR Captioning Interface for Enhancing Learning Experience of Deaf and Hard-of-Hearing (DHH) Students [PDF]

open access: yesarXiv
Deaf and hard-of-hearing (DHH) students face significant challenges in specialized educational settings, such as limited exposure to written and spoken language, a lack of tailored educational tools, and restricted access to resources, impacting their language literacy development and overall educational experience.
arxiv  

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