Showing results (1-10 of 10) with videos related to
Sort By:
Pageof 1
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.European Review of Aging and Physical Activity : Official Journal of the European Group for Research Into Elderly and Physical Activity|February 12, 2016
Effects of BDNF polymorphism and physical activity on episodic memory in the elderly: a cross sectional studyAnne Canivet, Cédric T Albinet, Nathalie André, et al.Frontiers in Human Neuroscience|November 23, 2017
Interaction between <i>BDNF</i> Polymorphism and Physical Activity on Inhibitory Performance in the Elderly without Cognitive ImpairmentAnne Canivet, Cédric T Albinet, Montserrat Rodríguez-Ballesteros, 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.Revista De La Facultad De Ciencias Medicas (Cordoba, Argentina)|September 16, 2004
[Genetic study of hearing loss in families from Argentina]Raúl A Reynoso, Silvia Hendl, Marìa E Barteik, et al.Genes|January 21, 2022
Novel Pathogenic Variants in <i>PJVK</i>, the Gene Encoding Pejvakin, in Subjects with Autosomal Recessive Non-Syndromic Hearing Impairment and Auditory Neuropathy Spectrum DisorderMaría Domínguez-Ruiz, Montserrat Rodríguez-Ballesteros, Marta Gandía, 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.Audiology Research|September 22, 2025
A Novel 1259 bp Intragenic Deletion in the <i>GJB2</i> Gene in a Mexican Family with Congenital Profound Hearing LossDavid Oaxaca-Castillo, Laura Taño-Portuondo, Montserrat Rodríguez-Ballesteros, et al.Human Mutation|April 3, 2008
A multicenter study on the prevalence and spectrum of mutations in the otoferlin gene (OTOF) in subjects with nonsyndromic hearing impairment and auditory neuropathyMontserrat Rodríguez-Ballesteros, Raúl Reynoso, Margarita Olarte, et al.Pageof 1