M. Moleon

A Predictive Model of Bilateral Sensorineural Hearing Loss in Meniere Disease Using Clinical Data

J. Lopez-Escamez, F. Di Berardino, M. Rossi, 2021, Ear and hearing.

Burden of Rare Variants in the OTOG Gene in Familial Meniere's Disease.

A. Gallego-Martinez, J. Lopez-Escamez, A. Soto-Varela, 2020, Ear and hearing.

Rare Variants in the OTOG Gene Are a Frequent Cause of Familial Meniere’s Disease

A. Gallego-Martinez, J. Lopez-Escamez, A. Soto-Varela, 2019 .

Rare coding variants involving MYO7A and other genes encoding stereocilia link proteins in familial meniere disease

J. Lopez-Escamez, A. Soto-Varela, D. Bächinger, 2021, Hearing Research.

Clinical and Cytokine Profile in Patients with Early and Late Onset Meniere Disease

J. Lopez-Escamez, A. Soto-Varela, M. Flook, 2021, Journal of clinical medicine.