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Journal of Neurophysiology|May 31, 2013
Mechanisms of adaptation in human auditory cortexCornelis P Lanting, Paul M Briley, Christian J Sumner, et al.Plos One|October 21, 2014
Unilateral tinnitus: changes in connectivity and response lateralization measured with FMRICornelis P Lanting, Emile de Kleine, Dave R M Langers, et al.Journal of Medical Genetics|May 10, 2023
Analysis of Rotterdam Study cohorts confirms a previously identified RIPOR2 in-frame deletion as a prevalent genetic factor in phenotypically variable adult-onset hearing loss (DFNA21) in the NetherlandsHedwig M Velde, Nienke C Homans, André Goedegebure, et al.Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|June 8, 2026
Performance Results and Timing of Cochlear Implantation in Patients With DFNA9 (p.Pro51Ser)Sybren M M Robijn, Josephine W I van Nierop, Wendy J Huinck, et al.Biomolecules|February 25, 2022
Genotype-Phenotype Correlations of Pathogenic COCH Variants in DFNA9: A HuGE Systematic Review and Audiometric Meta-AnalysisSybren M M Robijn, Jeroen J Smits, Kadriye Sezer, 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.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.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 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.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.Pageof 2