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Ruth Lang-Roth

Showing results (51-60 of 60) with videos related to

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The Laryngoscope|February 4, 2015
Permanent transoral surgery of bilateral vocal fold paralysis: a prospective multi-center trialTadeus Nawka, Christian Sittel, Markus Gugatschka, et al.
European Archives of Oto-Rhino-Laryngology : Official Journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : Affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery|May 21, 2026
Frequency of electrode migration and other device-related complications in a large single-center cochlear implant cohortJulia van de Loo, Ruth Lang-Roth, Verena Müller, et al.
Human Molecular Genetics|October 27, 2022
A mutation in ATP11A causes autosomal-dominant auditory neuropathy type 2Shashank Chepurwar, Sarah M von Loh, Daniela C Wigger, et al.
Audiology & Neuro-Otology|June 12, 2017
AUNA2: A Novel Type of Non-Syndromic Slowly Progressive Auditory Synaptopathy/Auditory Neuropathy with Autosomal-Dominant InheritanceRuth Lang-Roth, Eva Fischer-Krall, Cornelia Kornblum, et al.
Human Mutation|February 16, 2007
Truncating mutation of the DFNB59 gene causes cochlear hearing impairment and central vestibular dysfunctionInga Ebermann, Martin Walger, Hendrik P N Scholl, et al.
The Laryngoscope|August 4, 2015
Voice and respiratory outcomes after permanent transoral surgery of bilateral vocal fold paralysisTadeus Nawka, Christian Sittel, Christoph Arens, et al.
Human Molecular Genetics|October 11, 2017
A TUBB6 mutation is associated with autosomal dominant non-progressive congenital facial palsy, bilateral ptosis and velopharyngeal dysfunctionWalid Fazeli, Peter Herkenrath, Barbara Stiller, et al.
European Archives of Oto-Rhino-Laryngology : Official Journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : Affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery|May 12, 2012
Laryngeal electromyography: a proposal for guidelines of the European Laryngological SocietyGerd Fabian Volk, Rudolf Hagen, Claus Pototschnig, et al.
Journal of Intellectual Disability Research : JIDR|January 16, 2026
Clinical Diagnostics After Failed Hearing Screening in People With Intellectual Disabilities Do Not Often Take PlaceAnna Wiegand, Philipp Mathmann, Susanne Wasmuth, et al.
BMJ Open|May 18, 2023
Effectiveness and costs of a low-threshold hearing screening programme (<i>HörGeist</i>) for individuals with intellectual disabilities: protocol for a screening studyKatharina Schwarze, Philipp Mathmann, Karolin Schäfer, et al.
Pageof 6

Showing results (51-60 of 60) with videos related to

Sort By:
Pageof 6
You have reached the last page of results.This site can display upto 60 results.
The Laryngoscope|February 4, 2015
Permanent transoral surgery of bilateral vocal fold paralysis: a prospective multi-center trialTadeus Nawka, Christian Sittel, Markus Gugatschka, et al.
European Archives of Oto-Rhino-Laryngology : Official Journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : Affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery|May 21, 2026
Frequency of electrode migration and other device-related complications in a large single-center cochlear implant cohortJulia van de Loo, Ruth Lang-Roth, Verena Müller, et al.
Human Molecular Genetics|October 27, 2022
A mutation in ATP11A causes autosomal-dominant auditory neuropathy type 2Shashank Chepurwar, Sarah M von Loh, Daniela C Wigger, et al.
Audiology & Neuro-Otology|June 12, 2017
AUNA2: A Novel Type of Non-Syndromic Slowly Progressive Auditory Synaptopathy/Auditory Neuropathy with Autosomal-Dominant InheritanceRuth Lang-Roth, Eva Fischer-Krall, Cornelia Kornblum, et al.
Human Mutation|February 16, 2007
Truncating mutation of the DFNB59 gene causes cochlear hearing impairment and central vestibular dysfunctionInga Ebermann, Martin Walger, Hendrik P N Scholl, et al.
The Laryngoscope|August 4, 2015
Voice and respiratory outcomes after permanent transoral surgery of bilateral vocal fold paralysisTadeus Nawka, Christian Sittel, Christoph Arens, et al.
Human Molecular Genetics|October 11, 2017
A TUBB6 mutation is associated with autosomal dominant non-progressive congenital facial palsy, bilateral ptosis and velopharyngeal dysfunctionWalid Fazeli, Peter Herkenrath, Barbara Stiller, et al.
European Archives of Oto-Rhino-Laryngology : Official Journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : Affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery|May 12, 2012
Laryngeal electromyography: a proposal for guidelines of the European Laryngological SocietyGerd Fabian Volk, Rudolf Hagen, Claus Pototschnig, et al.
Journal of Intellectual Disability Research : JIDR|January 16, 2026
Clinical Diagnostics After Failed Hearing Screening in People With Intellectual Disabilities Do Not Often Take PlaceAnna Wiegand, Philipp Mathmann, Susanne Wasmuth, et al.
BMJ Open|May 18, 2023
Effectiveness and costs of a low-threshold hearing screening programme (<i>HörGeist</i>) for individuals with intellectual disabilities: protocol for a screening studyKatharina Schwarze, Philipp Mathmann, Karolin Schäfer, et al.
Pageof 6