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Antonio Cesarani

Showing results (21-30 of 38) with videos related to

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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|February 22, 2012
Public awareness of ear and hearing management as measured using a specific questionnaireFederica Di Berardino, Stella Forti, Elisabetta Iacona, et al.
Brain Research|August 16, 2008
Auditory brainstem responses (ABR) in normal hearing adult subjects with Down's syndromeStella Forti, Chiara Amadeo, Enrico Fagnani, et al.
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|August 16, 2012
Auditory late potentials in normal-hearing adult subjects with Down's syndromeElena Arisi, Stella Forti, Chiara Amadeo, et al.
The International Tinnitus Journal|September 24, 2004
Diagnosis of acute unilateral vestibular deficit by virtual realityRenzo Mora, Antonio Cesarani, Francesco Meloni, et al.
Human Molecular Genetics|November 1, 2011
A novel mutation within the MIR96 gene causes non-syndromic inherited hearing loss in an Italian family by altering pre-miRNA processingGiulia Soldà, Michela Robusto, Paola Primignani, et al.
Hearing Research|October 26, 2010
Cochlear active mechanisms in young normal-hearing subjects affected by Williams syndrome: time-frequency analysis of otoacoustic emissionsAlessia Paglialonga, Stefania Barozzi, Daniele Brambilla, et al.
Human Genetics|February 22, 2003
A novel autosomal dominant non-syndromic deafness locus (DFNA48) maps to 12q13-q14 in a large Italian familyPio D'Adamo, Maura Pinna, Saverio Capobianco, et al.
Phlebology|March 6, 2014
Chronic cerebrospinal venous insufficiency in Ménière diseaseFederica Di Berardino, Dario Carlo Alpini, Pietro Maria Bavera, et al.
European Journal of Medical Genetics|July 27, 2013
Audiological follow-up of 24 patients affected by Williams syndromeStefania Barozzi, Daniela Soi, Emanuela Spreafico, et al.
Gait & Posture|December 11, 2012
Balance function in patients with Williams syndromeStefania Barozzi, Daniela Soi, Chiara Gagliardi, et al.
Pageof 4

Showing results (21-30 of 38) with videos related to

Sort By:
Pageof 4
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|February 22, 2012
Public awareness of ear and hearing management as measured using a specific questionnaireFederica Di Berardino, Stella Forti, Elisabetta Iacona, et al.
Brain Research|August 16, 2008
Auditory brainstem responses (ABR) in normal hearing adult subjects with Down's syndromeStella Forti, Chiara Amadeo, Enrico Fagnani, et al.
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|August 16, 2012
Auditory late potentials in normal-hearing adult subjects with Down's syndromeElena Arisi, Stella Forti, Chiara Amadeo, et al.
The International Tinnitus Journal|September 24, 2004
Diagnosis of acute unilateral vestibular deficit by virtual realityRenzo Mora, Antonio Cesarani, Francesco Meloni, et al.
Human Molecular Genetics|November 1, 2011
A novel mutation within the MIR96 gene causes non-syndromic inherited hearing loss in an Italian family by altering pre-miRNA processingGiulia Soldà, Michela Robusto, Paola Primignani, et al.
Hearing Research|October 26, 2010
Cochlear active mechanisms in young normal-hearing subjects affected by Williams syndrome: time-frequency analysis of otoacoustic emissionsAlessia Paglialonga, Stefania Barozzi, Daniele Brambilla, et al.
Human Genetics|February 22, 2003
A novel autosomal dominant non-syndromic deafness locus (DFNA48) maps to 12q13-q14 in a large Italian familyPio D'Adamo, Maura Pinna, Saverio Capobianco, et al.
Phlebology|March 6, 2014
Chronic cerebrospinal venous insufficiency in Ménière diseaseFederica Di Berardino, Dario Carlo Alpini, Pietro Maria Bavera, et al.
European Journal of Medical Genetics|July 27, 2013
Audiological follow-up of 24 patients affected by Williams syndromeStefania Barozzi, Daniela Soi, Emanuela Spreafico, et al.
Gait & Posture|December 11, 2012
Balance function in patients with Williams syndromeStefania Barozzi, Daniela Soi, Chiara Gagliardi, et al.
Pageof 4