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Ear and Hearing|March 6, 2021
Computational Audiology: New Approaches to Advance Hearing Health Care in the Digital AgeJan-Willem A Wasmann, Cris P Lanting, Wendy J Huinck, et al.Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|March 12, 2021
A Novel COCH Mutation Affects the vWFA2 Domain and Leads to a Relatively Mild DFNA9 PhenotypeJeroen J Smits, Eline van Beelen, Nicole J D Weegerink, et al.Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|February 23, 2026
From Sound to Stability: Lessons Learned From the CRUSH Study on Hearing Loss Progression and Vestibular Phenotype in Usher Syndrome Type 2ADirk H Wijn, Mirthe L A Fehrmann, Sybren M M Robijn, et al.Human Genetics|October 15, 2024
Exome variant prioritization in a large cohort of hearing-impaired individuals indicates IKZF2 to be associated with non-syndromic hearing loss and guides future research of unsolved casesHedwig M Velde, Maryam Vaseghi-Shanjani, Jeroen J Smits, et al.Human Genetics|August 19, 2021
Exploring the missing heritability in subjects with hearing loss, enlarged vestibular aqueducts, and a single or no pathogenic SLC26A4 variantJeroen J Smits, Suzanne E de Bruijn, Cornelis P Lanting, et al.Journal of Medical Genetics|July 8, 2020
A RIPOR2 in-frame deletion is a frequent and highly penetrant cause of adult-onset hearing lossSuzanne E de Bruijn, Jeroen J Smits, Chang Liu, et al.Developmental Cell|May 8, 2021
Cochlear supporting cells require GAS2 for cytoskeletal architecture and hearingTingfang Chen, Alex M Rohacek, Matthew Caporizzo, et al.Journal of Otolaryngology - Head & Neck Surgery = Le Journal D'Oto-Rhino-Laryngologie Et De Chirurgie Cervico-Faciale|December 16, 2023
Stable long-term outcomes after cochlear implantation in subjects with TMPRSS3 associated hearing loss: a retrospective multicentre studyM L A Fehrmann, W J Huinck, M E G Thijssen, et al.Human Genetics|February 28, 2022
Usher syndrome type IV: clinically and molecularly confirmed by novel ARSG variantsHedwig M Velde, Janine Reurink, Sebastian Held, et al.Human Genetics|December 12, 2018
De novo and inherited loss-of-function variants of ATP2B2 are associated with rapidly progressive hearing impairmentJeroen J Smits, Jaap Oostrik, Andy J Beynon, et al.Pageof 4