Autor Título Original / Colaboración Selecciona una opción Original Colaboración Año Selecciona un año2015201620172018201920202021202220232024 Cuartil Selecciona un cuartilD1Q1Q2Q3Q4 Tipo Selecciona un tipo#N/DArticleArtículoBook ChapterBook ReviewClinical TrialCommentaryCorrectionData PaperEditorialEditorial MaterialLetterProceedings PaperReprintReview Revista Update on the pathophysiology, diagnosis and management of Ménière’s disease Autores: Lopez-Escamez, JA; Perez-Carpena, P 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 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 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 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 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 < 1 2 … 96 97 98 … 1.504 1.505 >