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Martin Koenighofer

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Experimental Eye Research|February 17, 2021
A novel proline substitution (Arg201Pro) in alpha helix 8 of TMEM98 causes autosomal dominant nanophthalmos-4, closed angle glaucoma and attenuated visual acuityMartin Koenighofer, Thomas Parzefall, Alexandra Frohne, et al.
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|March 12, 2021
High Prevalence of MYO6 Variants in an Austrian Patient Cohort With Autosomal Dominant Hereditary Hearing LossAlexandra Frohne, Martin Koenighofer, David Tianxiang Liu, et al.
Journal of Clinical Medicine|February 5, 2020
Body-Mass-Index Associated Differences in Ortho- and Retronasal Olfactory Function and the Individual Significance of Olfaction in Health and DiseaseGerold Besser, Brigitte Erlacher, Kadriye Aydinkoc-Tuzcu, et al.
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.
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.
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Showing results (11-20 of 15) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 15 results.
Experimental Eye Research|February 17, 2021
A novel proline substitution (Arg201Pro) in alpha helix 8 of TMEM98 causes autosomal dominant nanophthalmos-4, closed angle glaucoma and attenuated visual acuityMartin Koenighofer, Thomas Parzefall, Alexandra Frohne, et al.
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|March 12, 2021
High Prevalence of MYO6 Variants in an Austrian Patient Cohort With Autosomal Dominant Hereditary Hearing LossAlexandra Frohne, Martin Koenighofer, David Tianxiang Liu, et al.
Journal of Clinical Medicine|February 5, 2020
Body-Mass-Index Associated Differences in Ortho- and Retronasal Olfactory Function and the Individual Significance of Olfaction in Health and DiseaseGerold Besser, Brigitte Erlacher, Kadriye Aydinkoc-Tuzcu, et al.
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.
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.
Pageof 2