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Elona Cama

Showing results (11-20 of 16) with videos related to

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Ear and Hearing|September 7, 2023
Preservation of Distortion Product Otoacoustic Emissions in OTOF -Related Hearing ImpairmentRosamaria Santarelli, Pietro Scimemi, Elona Cama, et al.
ORL; Journal for Oto-Rhino-Laryngology and Its Related Specialties|February 23, 2012
Temporal bone high-resolution computed tomography in non-syndromic unilateral hearing loss in childrenElona Cama, Ingrid Inches, Enrico Muzzi, et al.
International Journal of Pediatric Otorhinolaryngology|July 21, 2009
Identification of a novel mutation in the SLC26A4 gene in an Italian with fluctuating sensorineural hearing lossElona Cama, Maria Stella Alemanno, Emanuele Bellacchio, et al.
Human Molecular Genetics|July 20, 2006
Pathogenetic role of the deafness-related M34T mutation of Cx26Massimiliano Bicego, Martina Beltramello, Salvatore Melchionda, et al.
Brain : a Journal of Neurology|January 8, 2015
OPA1-related auditory neuropathy: site of lesion and outcome of cochlear implantationRosamaria Santarelli, Roberta Rossi, Pietro Scimemi, et al.
Journal of Human Genetics|May 30, 2020
Frequency of Usher gene mutations in non-syndromic hearing loss: higher variability of the Usher phenotypeFederica Cesca, Elisa Bettella, Roberta Polli, et al.
Pageof 2

Showing results (11-20 of 16) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 16 results.
Ear and Hearing|September 7, 2023
Preservation of Distortion Product Otoacoustic Emissions in OTOF -Related Hearing ImpairmentRosamaria Santarelli, Pietro Scimemi, Elona Cama, et al.
ORL; Journal for Oto-Rhino-Laryngology and Its Related Specialties|February 23, 2012
Temporal bone high-resolution computed tomography in non-syndromic unilateral hearing loss in childrenElona Cama, Ingrid Inches, Enrico Muzzi, et al.
International Journal of Pediatric Otorhinolaryngology|July 21, 2009
Identification of a novel mutation in the SLC26A4 gene in an Italian with fluctuating sensorineural hearing lossElona Cama, Maria Stella Alemanno, Emanuele Bellacchio, et al.
Human Molecular Genetics|July 20, 2006
Pathogenetic role of the deafness-related M34T mutation of Cx26Massimiliano Bicego, Martina Beltramello, Salvatore Melchionda, et al.
Brain : a Journal of Neurology|January 8, 2015
OPA1-related auditory neuropathy: site of lesion and outcome of cochlear implantationRosamaria Santarelli, Roberta Rossi, Pietro Scimemi, et al.
Journal of Human Genetics|May 30, 2020
Frequency of Usher gene mutations in non-syndromic hearing loss: higher variability of the Usher phenotypeFederica Cesca, Elisa Bettella, Roberta Polli, et al.
Pageof 2