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Hearing disorders

Prevalence and Clinical Features of Hearing Loss Patients with CDH23 Mutations: A Large Cohort Study

Maiko Miyagawa, Shin-ya Nishio, Shin-ichi Usami

Molecular and Clinical Characterization of the Variable Phenotype in Korean Families with Hearing Loss Associated with the Mitochondrial A1555G Mutation

Jae Woong Bae, Dong-Bin Kim, [ ... ], Kyu Yup Lee

Screening of MITF and SOX10 Regulatory Regions in Waardenburg Syndrome Type 2

Viviane Baral, Asma Chaoui, [ ... ], Nadege Bondurand

Diminished Behavioral and Neural Sensitivity to Sound Modulation Is Associated with Moderate Developmental Hearing Loss

Merri J. Rosen, Emma C. Sarro, Jack B. Kelly, Dan H. Sanes

Effect of Hearing Aids on Auditory Function in Infants with Perinatal Brain Injury and Severe Hearing Loss

Alma Janeth Moreno-Aguirre, Efraín Santiago-Rodríguez, Thalía Harmony, Antonio Fernández-Bouzas

Disentangling Depression and Distress Networks in the Tinnitus Brain

Kathleen Joos, Sven Vanneste, Dirk De Ridder

Temporomandibular Joint Disorder Complaints in Tinnitus: Further Hints for a Putative Tinnitus Subtype

Veronika Vielsmeier, Jürgen Strutz, [ ... ], Berthold Langguth

Improving Disease Gene Prioritization by Comparing the Semantic Similarity of Phenotypes in Mice with Those of Human Diseases

Anika Oellrich, Robert Hoehndorf, Georgios V. Gkoutos, Dietrich Rebholz-Schuhmann

Patterns of Retinal Damage Facilitate Differential Diagnosis between Susac Syndrome and MS

Alexander U. Brandt, Hanna Zimmermann, [ ... ], Jan Dörr

Reversible Induction of Phantom Auditory Sensations through Simulated Unilateral Hearing Loss

Roland Schaette, Charlotte Turtle, Kevin J. Munro

Polymorphisms in Toll-Like Receptors 2, 4, and 9 Are Highly Associated with Hearing Loss in Survivors of Bacterial Meningitis

Gijs Th J. van Well, Marieke S. Sanders, [ ... ], Servaas A. Morré

Tinnitus Severity Is Reduced with Reduction of Depressive Mood – a Prospective Population Study in Sweden

Sylvie Hébert, Barbara Canlon, [ ... ], Töres Theorell

The p.V37I Exclusive Genotype Of GJB2: A Genetic Risk-Indicator of Postnatal Permanent Childhood Hearing Impairment

Lei Li, Jingrong Lu, [ ... ], Hao Wu

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