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Thierry Morlet

Showing results (31-40 of 42) with videos related to

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SAGE Open Medical Case Reports|September 14, 2019
Cochlear implantation in a patient with mucopolysaccharidosis IVAKyoko Nagao, Cassidy Walter, William J Parkes, et al.
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|March 31, 2025
Auditory Characteristics in Children With Enlarged Vestibular AqueductPunam Patel, William Parkes, Cedric Pritchett, et al.
Archives of Otolaryngology--Head & Neck Surgery|March 17, 2010
Ophthalmologic disorders in children with syndromic and nonsyndromic hearing lossDouglas R Johnston, Joseph M Curry, Brian Newborough, et al.
Telemedicine Journal and E-Health : the Official Journal of the American Telemedicine Association|October 26, 2018
Tablet-Based Hearing Test Among Child Clinical Populations: Performance and PreferenceKyoko Nagao, Alexa S Bullard, Lauren E Pasko, et al.
Human Molecular Genetics|February 6, 2015
Ganglioside GM3 is essential for the structural integrity and function of cochlear hair cellsMisato Yoshikawa, Shinji Go, Shun-ichi Suzuki, et al.
Otolaryngology--Head and Neck Surgery : Official Journal of American Academy of Otolaryngology-Head and Neck Surgery|April 16, 2011
Comprehensive vestibular and balance testing in the dizzy pediatric populationRobert C O'Reilly, Jewell Greywoode, Thierry Morlet, et al.
Cochlear Implants International|March 13, 2026
Cochlear implantation in pediatric and young adult oncologic population: institutional experience and case-control analysisAran Sullivan, Johnnie K Bass, Sarah E Warren, et al.
International Journal of Audiology|January 8, 2010
Multi-site diagnosis and management of 260 patients with auditory neuropathy/dys-synchrony (auditory neuropathy spectrum disorder)Charles I Berlin, Linda J Hood, Thierry Morlet, et al.
The Laryngoscope|August 16, 2013
A homozygous SLITRK6 nonsense mutation is associated with progressive auditory neuropathy in humansThierry Morlet, Mindy R Rabinowitz, Liesl R Looney, et al.
Molecular Genetics and Metabolism|January 30, 2019
Recessive GM3 synthase deficiency: Natural history, biochemistry, and therapeutic frontierLauren E Bowser, Millie Young, Olivia K Wenger, et al.
Pageof 5

Showing results (31-40 of 42) with videos related to

Sort By:
Pageof 5
SAGE Open Medical Case Reports|September 14, 2019
Cochlear implantation in a patient with mucopolysaccharidosis IVAKyoko Nagao, Cassidy Walter, William J Parkes, et al.
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|March 31, 2025
Auditory Characteristics in Children With Enlarged Vestibular AqueductPunam Patel, William Parkes, Cedric Pritchett, et al.
Archives of Otolaryngology--Head & Neck Surgery|March 17, 2010
Ophthalmologic disorders in children with syndromic and nonsyndromic hearing lossDouglas R Johnston, Joseph M Curry, Brian Newborough, et al.
Telemedicine Journal and E-Health : the Official Journal of the American Telemedicine Association|October 26, 2018
Tablet-Based Hearing Test Among Child Clinical Populations: Performance and PreferenceKyoko Nagao, Alexa S Bullard, Lauren E Pasko, et al.
Human Molecular Genetics|February 6, 2015
Ganglioside GM3 is essential for the structural integrity and function of cochlear hair cellsMisato Yoshikawa, Shinji Go, Shun-ichi Suzuki, et al.
Otolaryngology--Head and Neck Surgery : Official Journal of American Academy of Otolaryngology-Head and Neck Surgery|April 16, 2011
Comprehensive vestibular and balance testing in the dizzy pediatric populationRobert C O'Reilly, Jewell Greywoode, Thierry Morlet, et al.
Cochlear Implants International|March 13, 2026
Cochlear implantation in pediatric and young adult oncologic population: institutional experience and case-control analysisAran Sullivan, Johnnie K Bass, Sarah E Warren, et al.
International Journal of Audiology|January 8, 2010
Multi-site diagnosis and management of 260 patients with auditory neuropathy/dys-synchrony (auditory neuropathy spectrum disorder)Charles I Berlin, Linda J Hood, Thierry Morlet, et al.
The Laryngoscope|August 16, 2013
A homozygous SLITRK6 nonsense mutation is associated with progressive auditory neuropathy in humansThierry Morlet, Mindy R Rabinowitz, Liesl R Looney, et al.
Molecular Genetics and Metabolism|January 30, 2019
Recessive GM3 synthase deficiency: Natural history, biochemistry, and therapeutic frontierLauren E Bowser, Millie Young, Olivia K Wenger, et al.
Pageof 5