Autor Título Original / Colaboración Selecciona una opción Original Colaboración Año Selecciona un año20152016201720182019202020212022202320242025 Cuartil Selecciona un cuartilD1Q1Q2Q3Q4 Tipo Selecciona un tipo#N/DArticleArtículoBook ChapterBook ReviewClinical TrialCommentaryCorrectionData PaperEditorialEditorial MaterialExpression of ConcernLetterProceedings PaperReprintReview Revista Multiomic-based immune response profiling in migraine, vestibular migraine and Meniere’s disease Autores: Cruz-Granados, P; Frejo, L; Perez-Carpena, P; Amor-Dorado, JC; Dominguez-Duran, E; Fernandez-Nava, MJ; Batuecas-Caletrio, A; Haro-Hernandez, E; Martinez-Martinez, M; 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 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 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 A systematic review on the contribution of DNA methylation to hearing loss Autores: Patil, V; Perez-Carpena, P; Lopez-Escamez, JA 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 … 298 299 300 … 1.706 1.707 >
