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Thomas Parzefall

Showing results (31-40 of 36) with videos related to

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Frontiers in Cellular Neuroscience|December 7, 2020
A Novel Variant in the TBC1D24 Lipid-Binding Pocket Causes Autosomal Dominant Hearing Loss: Evidence for a Genotype-Phenotype CorrelationThomas Parzefall, Alexandra Frohne, Martin Koenighofer, et al.
Ear and Hearing|April 23, 2026
Multicenter Natural History Study and Long-Term Cochlear Implant Outcomes in Usher Syndrome SubtypesPaul Emmerich Krumpoeck, Anselm Joseph Gadenstaetter, Natsumi Uehara, et al.
Human Mutation|April 23, 2013
Cytoplasmic mislocalization of POU3F4 due to novel mutations leads to deafness in humans and miceThomas Parzefall, Shaked Shivatzki, Danielle R Lenz, et al.
Human Genetics|November 29, 2022
A homozygous AP3D1 missense variant in patients with sensorineural hearing loss as the leading manifestationAlexandra Frohne, Martin Koenighofer, Hakan Cetin, et al.
Genome Biology|September 16, 2011
Targeted genomic capture and massively parallel sequencing to identify genes for hereditary hearing loss in Middle Eastern familiesZippora Brownstein, Lilach M Friedman, Hashem Shahin, et al.
Acta Oto-Laryngologica|October 25, 2024
Testing for genetic and viral etiologies in congenital hearing loss based on a survey of cochlear implant centers: proposed HEARRING group consensus and future directionsShin-Ichi Usami, Shin-Ya Nishio, Javier Gavilán, et al.
Pageof 4

Showing results (31-40 of 36) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 36 results.
Frontiers in Cellular Neuroscience|December 7, 2020
A Novel Variant in the TBC1D24 Lipid-Binding Pocket Causes Autosomal Dominant Hearing Loss: Evidence for a Genotype-Phenotype CorrelationThomas Parzefall, Alexandra Frohne, Martin Koenighofer, et al.
Ear and Hearing|April 23, 2026
Multicenter Natural History Study and Long-Term Cochlear Implant Outcomes in Usher Syndrome SubtypesPaul Emmerich Krumpoeck, Anselm Joseph Gadenstaetter, Natsumi Uehara, et al.
Human Mutation|April 23, 2013
Cytoplasmic mislocalization of POU3F4 due to novel mutations leads to deafness in humans and miceThomas Parzefall, Shaked Shivatzki, Danielle R Lenz, et al.
Human Genetics|November 29, 2022
A homozygous AP3D1 missense variant in patients with sensorineural hearing loss as the leading manifestationAlexandra Frohne, Martin Koenighofer, Hakan Cetin, et al.
Genome Biology|September 16, 2011
Targeted genomic capture and massively parallel sequencing to identify genes for hereditary hearing loss in Middle Eastern familiesZippora Brownstein, Lilach M Friedman, Hashem Shahin, et al.
Acta Oto-Laryngologica|October 25, 2024
Testing for genetic and viral etiologies in congenital hearing loss based on a survey of cochlear implant centers: proposed HEARRING group consensus and future directionsShin-Ichi Usami, Shin-Ya Nishio, Javier Gavilán, et al.
Pageof 4