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A Incesulu

Showing results (1-10 of 8) with videos related to

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The Annals of Otology, Rhinology, and Laryngology|November 21, 1998
Correlation of acoustic threshold measures and spiral ganglion cell survival in severe to profound sensorineural hearing loss: implications for cochlear implantationA Incesulu, J B Nadol
The Journal of Laryngology and Otology|February 26, 2004
Cochlear implantation in chronic otitis mediaA Incesulu, S Kocaturk, M Vural
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|May 12, 2001
Histologic studies of the posterior stapediovestibular joint in otosclerosisS N Merchant, A Incesulu, R J Glynn, et al.
Genetic Counseling (Geneva, Switzerland)|January 24, 2004
Moderate hearing loss and pseudodominant inheritance due to L90P/35delG mutations in the GJB2 (connexin 26) geneM Tekin, T Duman, G Boğoçlu, et al.
The Laryngoscope|September 18, 1997
Revision stapedectomy: intraoperative findings, results, and review of the literatureW W Han, A Incesulu, M J McKenna, et al.
Clinical Genetics|May 15, 2009
A founder TMIE mutation is a frequent cause of hearing loss in southeastern AnatoliaA Sirmaci, H Oztürkmen-Akay, S Erbek, et al.
European Journal of Pediatrics|March 26, 2003
Frequency of mtDNA A1555G and A7445G mutations among children with prelingual deafness in TurkeyM Tekin, T Duman, G Boğoçlu, et al.
Clinical Genetics|April 26, 2008
Homozygous FGF3 mutations result in congenital deafness with inner ear agenesis, microtia, and microdontiaM Tekin, H Oztürkmen Akay, S Fitoz, et al.
Pageof 1

Showing results (1-10 of 8) with videos related to

Sort By:
Pageof 1
The Annals of Otology, Rhinology, and Laryngology|November 21, 1998
Correlation of acoustic threshold measures and spiral ganglion cell survival in severe to profound sensorineural hearing loss: implications for cochlear implantationA Incesulu, J B Nadol
The Journal of Laryngology and Otology|February 26, 2004
Cochlear implantation in chronic otitis mediaA Incesulu, S Kocaturk, M Vural
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|May 12, 2001
Histologic studies of the posterior stapediovestibular joint in otosclerosisS N Merchant, A Incesulu, R J Glynn, et al.
Genetic Counseling (Geneva, Switzerland)|January 24, 2004
Moderate hearing loss and pseudodominant inheritance due to L90P/35delG mutations in the GJB2 (connexin 26) geneM Tekin, T Duman, G Boğoçlu, et al.
The Laryngoscope|September 18, 1997
Revision stapedectomy: intraoperative findings, results, and review of the literatureW W Han, A Incesulu, M J McKenna, et al.
Clinical Genetics|May 15, 2009
A founder TMIE mutation is a frequent cause of hearing loss in southeastern AnatoliaA Sirmaci, H Oztürkmen-Akay, S Erbek, et al.
European Journal of Pediatrics|March 26, 2003
Frequency of mtDNA A1555G and A7445G mutations among children with prelingual deafness in TurkeyM Tekin, T Duman, G Boğoçlu, et al.
Clinical Genetics|April 26, 2008
Homozygous FGF3 mutations result in congenital deafness with inner ear agenesis, microtia, and microdontiaM Tekin, H Oztürkmen Akay, S Fitoz, et al.
Pageof 1