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Pietro Scimemi

Showing results (1-10 of 19) with videos related to

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Neuro-Degenerative Diseases|March 21, 2015
Abnormal Cochlear Potentials in Friedreich's Ataxia Point to Disordered Synchrony of Auditory Nerve Fiber ActivityRosamaria Santarelli, Elona Cama, Elena Pegoraro, et al.
Hearing Research|July 19, 2015
Audibility, speech perception and processing of temporal cues in ribbon synaptic disorders due to OTOF mutationsRosamaria Santarelli, Ignacio del Castillo, Elona Cama, et al.
European Archives of Oto-Rhino-Laryngology : Official Journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : Affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery|June 10, 2006
Auditory neuropathy in systemic sclerosis: a speech perception and evoked potential study before and after cochlear implantationRosamaria Santarelli, Pietro Scimemi, Erica Dal Monte, et al.
European Archives of Oto-Rhino-Laryngology : Official Journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : Affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery|August 19, 2007
Audiological and electrocochleography findings in hearing-impaired children with connexin 26 mutations and otoacoustic emissionsRosamaria Santarelli, Elona Cama, Pietro Scimemi, et al.
International Journal of Pediatric Otorhinolaryngology|December 31, 2017
A novel mutation of the EYA4 gene associated with post-lingual hearing loss in a proband is co-segregating with a novel PAX3 mutation in two congenitally deaf family membersFederica Cesca, Elisa Bettella, Roberta Polli, et al.
Audiology Research|December 23, 2021
Electrocochleography in Auditory Neuropathy Related to Mutations in the OTOF or OPA1 GeneRosamaria Santarelli, Pietro Scimemi, Chiara La Morgia, 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.
Frontiers in Neuroscience|June 14, 2019
Hearing Dysfunction in a Large Family Affected by Dominant Optic Atrophy (OPA8-Related DOA): A Human Model of Hidden Auditory NeuropathyRosamaria Santarelli, Chiara La Morgia, Maria Lucia Valentino, 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.
Ear and Hearing|September 7, 2023
Preservation of Distortion Product Otoacoustic Emissions in OTOF -Related Hearing ImpairmentRosamaria Santarelli, Pietro Scimemi, Elona Cama, et al.
Pageof 2

Showing results (1-10 of 19) with videos related to

Sort By:
Pageof 2
Neuro-Degenerative Diseases|March 21, 2015
Abnormal Cochlear Potentials in Friedreich's Ataxia Point to Disordered Synchrony of Auditory Nerve Fiber ActivityRosamaria Santarelli, Elona Cama, Elena Pegoraro, et al.
Hearing Research|July 19, 2015
Audibility, speech perception and processing of temporal cues in ribbon synaptic disorders due to OTOF mutationsRosamaria Santarelli, Ignacio del Castillo, Elona Cama, et al.
European Archives of Oto-Rhino-Laryngology : Official Journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : Affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery|June 10, 2006
Auditory neuropathy in systemic sclerosis: a speech perception and evoked potential study before and after cochlear implantationRosamaria Santarelli, Pietro Scimemi, Erica Dal Monte, et al.
European Archives of Oto-Rhino-Laryngology : Official Journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : Affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery|August 19, 2007
Audiological and electrocochleography findings in hearing-impaired children with connexin 26 mutations and otoacoustic emissionsRosamaria Santarelli, Elona Cama, Pietro Scimemi, et al.
International Journal of Pediatric Otorhinolaryngology|December 31, 2017
A novel mutation of the EYA4 gene associated with post-lingual hearing loss in a proband is co-segregating with a novel PAX3 mutation in two congenitally deaf family membersFederica Cesca, Elisa Bettella, Roberta Polli, et al.
Audiology Research|December 23, 2021
Electrocochleography in Auditory Neuropathy Related to Mutations in the OTOF or OPA1 GeneRosamaria Santarelli, Pietro Scimemi, Chiara La Morgia, 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.
Frontiers in Neuroscience|June 14, 2019
Hearing Dysfunction in a Large Family Affected by Dominant Optic Atrophy (OPA8-Related DOA): A Human Model of Hidden Auditory NeuropathyRosamaria Santarelli, Chiara La Morgia, Maria Lucia Valentino, 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.
Ear and Hearing|September 7, 2023
Preservation of Distortion Product Otoacoustic Emissions in OTOF -Related Hearing ImpairmentRosamaria Santarelli, Pietro Scimemi, Elona Cama, et al.
Pageof 2