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Elona Cama

Showing results (1-10 of 16) with videos related to

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ORL; Journal for Oto-Rhino-Laryngology and Its Related Specialties|November 6, 2002
A rare case of metastases to the maxillary sinus from sigmoid colon adenocarcinomaElona Cama, Stefania Agostino, Riccardo Ricci, et al.
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.
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|December 14, 2011
Primary tumors and tumor-like lesions of the eustachian tube: a systematic review of an emerging entityEnrico Muzzi, Elona Cama, Paolo Boscolo-Rizzo, 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|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.
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.
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.
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.
International Journal of Audiology|January 29, 2009
Hearing loss features in GJB2 biallelic mutations and GJB2/GJB6 digenic inheritance in a large Italian cohortElona Cama, Salvatore Melchionda, Teresa Palladino, et al.
International Journal of Pediatric Otorhinolaryngology|November 8, 2008
A novel missense mutation in the Connexin 26 gene associated with autosomal recessive nonsyndromic sensorineural hearing loss in a consanguineous Tunisian familyMaria Stella Alemanno, Elona Cama, Rosamaria Santarelli, et al.
Pageof 2

Showing results (1-10 of 16) with videos related to

Sort By:
Pageof 2
ORL; Journal for Oto-Rhino-Laryngology and Its Related Specialties|November 6, 2002
A rare case of metastases to the maxillary sinus from sigmoid colon adenocarcinomaElona Cama, Stefania Agostino, Riccardo Ricci, et al.
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.
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|December 14, 2011
Primary tumors and tumor-like lesions of the eustachian tube: a systematic review of an emerging entityEnrico Muzzi, Elona Cama, Paolo Boscolo-Rizzo, 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|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.
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.
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.
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.
International Journal of Audiology|January 29, 2009
Hearing loss features in GJB2 biallelic mutations and GJB2/GJB6 digenic inheritance in a large Italian cohortElona Cama, Salvatore Melchionda, Teresa Palladino, et al.
International Journal of Pediatric Otorhinolaryngology|November 8, 2008
A novel missense mutation in the Connexin 26 gene associated with autosomal recessive nonsyndromic sensorineural hearing loss in a consanguineous Tunisian familyMaria Stella Alemanno, Elona Cama, Rosamaria Santarelli, et al.
Pageof 2