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Acta Otorrinolaringologica Espanola|March 22, 2025
Cochleo-vestibular phenotype in patients with pathogenic variations in the ACTG1 geneRocío González-Aguado, Jaime Gallo-Terán, Eshter Onecha, et al.The Annals of Otology, Rhinology, and Laryngology|February 5, 2025
Hearing Loss Secondary to TECTA Gene MutationsRocío González-Aguado, Esther Onecha, Jaime Gallo-Terán, et al.International Journal of Pediatric Otorhinolaryngology|September 12, 2024
Hearing loss secondary to variants in the OTOF geneCarmelo Morales-Angulo, Jaime Gallo-Terán, Rocío González-Aguado, et al.Medicina Clinica|July 29, 2003
[Familial susceptibility to aminoglycoside ototoxicity due to the A1555G mutation in the mitochondrial DNA]Jaime Gallo-Terán, Carmelo Morales-Angulo, Ignacio del Castillo, et al.Acta Otorrinolaringologica Espanola|December 7, 2010
[Prevalence of the A1555G MTDNA mutation in sporadic hearing-impaired patients without known history of aminoglycoside treatment]Carmelo Morales Angulo, Jaime Gallo-Terán, Blanca Señaris, et al.Medicina Oral, Patologia Oral Y Cirugia Bucal|June 8, 2010
Unilateral submandibular gland aplasia with ipsilateral sublingual gland hypertrophy presenting as a neck massGonzalo Herrera-Calvo, Belén García-Montesinos-Perea, Ramón Saiz-Bustillo, et al.The Laryngoscope|September 26, 2024
Sensorineural Hearing Loss in Patients With the m.1555A>G Mutation in the MTRNR1 GeneJaime Gallo-Terán, Cristina Salomón-Felechosa, Rocío González-Aguado, et al.Human Mutation|November 25, 2003
Auditory neuropathy in patients carrying mutations in the otoferlin gene (OTOF)Montserrat Rodríguez-Ballesteros, Francisco J del Castillo, Yolanda Martín, et al.Pageof 1