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Andy J Beynon

Showing results (21-30 of 35) with videos related to

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The Annals of Otology, Rhinology, and Laryngology|January 28, 2012
Prediction of vestibular schwannoma growth: a novel rule based on clinical symptomatologyFerdinand C A Timmer, Janneke C J M Artz, Andy J Beynon, et al.
Genetics|June 21, 2005
Identification of a rat model for usher syndrome type 1B by N-ethyl-N-nitrosourea mutagenesis-driven forward geneticsBart M G Smits, Theo A Peters, Joram D Mul, et al.
The Laryngoscope|April 29, 2009
Gamma knife radiosurgery for vestibular schwannomas: results of hearing preservation in relation to the cochlear radiation doseFerdinand C A Timmer, Patrick E J Hanssens, Anniek E P van Haren, et al.
Genes|February 25, 2023
Genotype and Phenotype Analyses of a Novel <i>WFS1</i> Variant (c.2512C>T p.(Pro838Ser)) Associated with DFNA6/14/38Hedwig M Velde, Xanne J J Huizenga, Helger G Yntema, et al.
Biomolecules|February 25, 2022
Genotype-Phenotype Correlations of Pathogenic <i>COCH</i> 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.
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.
Ear and Hearing|January 1, 2014
Similar phenotypes caused by mutations in OTOG and OTOGLAnne M M Oonk, Joop M Leijendeckers, Patrick L M Huygen, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 30, 2009
ATP8B1 is essential for maintaining normal hearingJanneke M Stapelbroek, Theo A Peters, Denis H A van Beurden, et al.
Journal of Medical Genetics|July 8, 2020
A <i>RIPOR2</i> 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.
Pageof 4

Showing results (21-30 of 35) with videos related to

Sort By:
Pageof 4
The Annals of Otology, Rhinology, and Laryngology|January 28, 2012
Prediction of vestibular schwannoma growth: a novel rule based on clinical symptomatologyFerdinand C A Timmer, Janneke C J M Artz, Andy J Beynon, et al.
Genetics|June 21, 2005
Identification of a rat model for usher syndrome type 1B by N-ethyl-N-nitrosourea mutagenesis-driven forward geneticsBart M G Smits, Theo A Peters, Joram D Mul, et al.
The Laryngoscope|April 29, 2009
Gamma knife radiosurgery for vestibular schwannomas: results of hearing preservation in relation to the cochlear radiation doseFerdinand C A Timmer, Patrick E J Hanssens, Anniek E P van Haren, et al.
Genes|February 25, 2023
Genotype and Phenotype Analyses of a Novel <i>WFS1</i> Variant (c.2512C>T p.(Pro838Ser)) Associated with DFNA6/14/38Hedwig M Velde, Xanne J J Huizenga, Helger G Yntema, et al.
Biomolecules|February 25, 2022
Genotype-Phenotype Correlations of Pathogenic <i>COCH</i> 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.
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.
Ear and Hearing|January 1, 2014
Similar phenotypes caused by mutations in OTOG and OTOGLAnne M M Oonk, Joop M Leijendeckers, Patrick L M Huygen, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 30, 2009
ATP8B1 is essential for maintaining normal hearingJanneke M Stapelbroek, Theo A Peters, Denis H A van Beurden, et al.
Journal of Medical Genetics|July 8, 2020
A <i>RIPOR2</i> 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.
Pageof 4