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Children (Basel, Switzerland)|May 27, 2023
Severe Juvenile-Onset Systemic Lupus Erythematosus: A Case Series-Based Review and UpdateSergi Huerta-Calpe, Ignacio Del Castillo-Velilla, Aida Felipe-Villalobos, et al.Ear and Hearing|April 28, 2021
Cochlear Synaptopathy due to Mutations in OTOF Gene May Result in Stable Mild Hearing Loss and Severe Impairment of Speech PerceptionRosamaria Santarelli, Pietro Scimemi, Marco Costantini, et al.Journal of the Association for Research in Otolaryngology : JARO|July 29, 2009
Abnormal cochlear potentials from deaf patients with mutations in the otoferlin geneRosamaria Santarelli, Ignacio Del Castillo, Montserrat Rodríguez-Ballesteros, 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.American Journal of Human Genetics|May 16, 2007
A mutation in CCDC50, a gene encoding an effector of epidermal growth factor-mediated cell signaling, causes progressive hearing lossSilvia Modamio-Hoybjor, Angeles Mencia, Richard Goodyear, et al.Ear and Hearing|September 7, 2023
Preservation of Distortion Product Otoacoustic Emissions in OTOF -Related Hearing ImpairmentRosamaria Santarelli, Pietro Scimemi, Elona Cama, 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.Neurobiology of Disease|August 27, 2022
Postnatal Foxp2 regulates early psychiatric-like phenotypes and associated molecular alterations in the R6/1 transgenic mouse model of Huntington's diseaseEned Rodríguez-Urgellés, Irene Rodríguez-Navarro, Iván Ballasch, et al.Brain, Behavior, and Immunity|July 31, 2025
Microglia depletion in a mouse model of prenatal and postnatal immune activationNaomi Ciano Albanese, Ignacio Del Castillo, Giulia Ragaglia, et al.The New England Journal of Medicine|January 25, 2002
A deletion involving the connexin 30 gene in nonsyndromic hearing impairmentIgnacio del Castillo, Manuela Villamar, Miguel A Moreno-Pelayo, et al.Pageof 7