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Grupo Autor Título Original / Colaboración Año Cuartil Tipo Revista

Update on the pathophysiology, diagnosis and management of Ménière’s disease

Autores: Lopez-Escamez, JA; Perez-Carpena, P

An overload of missense variants in the OTOG gene may drive a higher prevalence of familial Meniere disease in the European population

Autores: Parra-Perez, AM; Gallego-Martinez, A; Lopez-Escamez, JA

Phenotypic spectrum of tinnitus patients bearing rare ANK2 gene variants

Autores: Martin-Lagos, J; Bernal-Robledano, A; Perez-Carpena, P; Lamolda, M; Escalera-Balsera, A; Frejo, L; Lopez-Escamez, JA

Rare Deletions or Large Duplications Contribute to Genetic Variation in Patients with Severe Tinnitus and Meniere Disease

Autores: Escalera-Balsera, A; Parra-Perez, AM; Gallego-Martinez, A; Frejo, L; Martin-Lagos, J; de Jesus, VR; Pérez-Vázquez, P; Perez-Carpena, P; Lopez-Escamez, JA

Treatment of Meniere’s disease with simultaneous triple semicircular canal occlusion and cochlear implantation

Autores: Xiao, QW; Wu, Q; Zhang, Q; He, JC; Liu, YP; Shen, JL; Lv, JR; Duan, M; Lopez-Escamez, JA; Yang, J; Zhang, Q

Cajal’s contributions to vestibular research

Autores: Espinosa-Sanchez, JM; Perez-Fernandez, N; de Castro, F; Batuecas-Caletrio, A

A systematic review on the contribution of DNA methylation to hearing loss (vol 16, 88, 2024)

Autores: Patil, V; Perez-Carpena, P; Lopez-Escamez, JA

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