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Med (New York, N.Y.)|April 13, 2024
A cure for deafness?Nicola Strenzke
Med (New York, N.Y.)|August 9, 2025
Gradual recovery of auditory brainstem responses in the first DFNB9 patients with successful virus-mediated gene therapyBarbara Vona, Nicola Strenzke
Medcomm|September 10, 2025
Is CABP2-Associated Hearing Loss (DFNB93) a Gene Therapy Target? Preclinical Progress and Patient RegistryBarbara Vona, Bernd Wollnik, Nicola Strenzke, et al.
Laryngo- Rhino- Otologie|April 23, 2026
[Botulinum toxin reduces sweat-related problems for hearing aid users - a clinical study]Shabnam Shahpasand, Rainer Laskawi, Jenny Blum, et al.
BMC Neuroscience|April 27, 2012
Mice do not require auditory input for the normal development of their ultrasonic vocalizationsKurt Hammerschmidt, Ellen Reisinger, Katharina Westekemper, et al.
Frontiers in Neuroscience|February 9, 2023
Patient perspectives on the need for improved hearing rehabilitation: A qualitative survey study of German cochlear implant usersVictoria Hunniford, Robert Kühler, Bettina Wolf, et al.
Laryngoscope Investigative Otolaryngology|February 14, 2022
Performance and self-perceived hearing impairment after cochlear implantation in Menière's diseaseChristian Wrobel, Nicholas F Bevis, Astrid Klinge-Strahl, et al.
Frontiers in Cellular Neuroscience|August 2, 2021
Otoferlin Is Required for Proper Synapse Maturation and for Maintenance of Inner and Outer Hair Cells in Mouse Models for DFNB9Ursula Stalmann, Albert Justin Franke, Hanan Al-Moyed, et al.
FEBS Letters|April 2, 2014
The Clouston syndrome mutation connexin30 A88V leads to hyperproliferation of sebaceous glands and hearing impairments in miceFelicitas Bosen, Melanie Schütz, Anna Beinhauer, et al.
Nature Communications|February 22, 2017
A connexin30 mutation rescues hearing and reveals roles for gap junctions in cochlear amplification and micromechanicsVictoria A Lukashkina, Snezana Levic, Andrei N Lukashkin, et al.
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