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Tatsuo Matsunaga

Showing results (1-10 of 126) with videos related to

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Auris, Nasus, Larynx|August 30, 2020
Clinical genetics, practice, and research of deafblindness: From uncollected experiences to the national registry in JapanTatsuo Matsunaga
The Keio Journal of Medicine|December 29, 2009
Value of genetic testing in the otological approach for sensorineural hearing lossTatsuo Matsunaga
Advances in Oto-Rhino-Laryngology|October 19, 2013
Etiology and genesTatsuo Matsunaga
Acta Oto-Laryngologica|January 30, 2016
The auditory phenotype of children harboring mutations in the prestin geneTatsuo Matsunaga, Noriko Morimoto
American Journal of Medical Genetics. Part A|January 11, 2003
Familial lateral semicircular canal malformation with external and middle ear abnormalitiesTatsuo Matsunaga, Eiko Hirota
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|March 2, 2013
Cochlear nerve deficiency and associated clinical features in patients with bilateral and unilateral hearing lossAtsuko Nakano, Yukiko Arimoto, Tatsuo Matsunaga
International Journal of Pediatric Otorhinolaryngology|December 4, 2012
High prevalence of inner-ear and/or internal auditory canal malformations in children with unilateral sensorineural hearing lossSawako Masuda, Satoko Usui, Tatsuo Matsunaga
Acta Oto-Laryngologica|July 27, 2012
Unilateral cochlear nerve hypoplasia in children with mild to moderate hearing lossHidenobu Taiji, Noriko Morimoto, Tatsuo Matsunaga
Nihon Rinsho. Japanese Journal of Clinical Medicine|January 21, 2014
[Current status and perspectives of the research in Pendred syndrome]Tatsuo Matsunaga, Masato Fujioka, Makoto Hosoya
International Journal of Pediatric Otorhinolaryngology|June 24, 2018
Response to "infantile-onset deafness in m.7445A>G carriers may be multicausal"Tatsuo Matsunaga, Kana Matsushima, Kei Murayama
Pageof 13

Showing results (1-10 of 126) with videos related to

Sort By:
Pageof 13
Auris, Nasus, Larynx|August 30, 2020
Clinical genetics, practice, and research of deafblindness: From uncollected experiences to the national registry in JapanTatsuo Matsunaga
The Keio Journal of Medicine|December 29, 2009
Value of genetic testing in the otological approach for sensorineural hearing lossTatsuo Matsunaga
Advances in Oto-Rhino-Laryngology|October 19, 2013
Etiology and genesTatsuo Matsunaga
Acta Oto-Laryngologica|January 30, 2016
The auditory phenotype of children harboring mutations in the prestin geneTatsuo Matsunaga, Noriko Morimoto
American Journal of Medical Genetics. Part A|January 11, 2003
Familial lateral semicircular canal malformation with external and middle ear abnormalitiesTatsuo Matsunaga, Eiko Hirota
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|March 2, 2013
Cochlear nerve deficiency and associated clinical features in patients with bilateral and unilateral hearing lossAtsuko Nakano, Yukiko Arimoto, Tatsuo Matsunaga
International Journal of Pediatric Otorhinolaryngology|December 4, 2012
High prevalence of inner-ear and/or internal auditory canal malformations in children with unilateral sensorineural hearing lossSawako Masuda, Satoko Usui, Tatsuo Matsunaga
Acta Oto-Laryngologica|July 27, 2012
Unilateral cochlear nerve hypoplasia in children with mild to moderate hearing lossHidenobu Taiji, Noriko Morimoto, Tatsuo Matsunaga
Nihon Rinsho. Japanese Journal of Clinical Medicine|January 21, 2014
[Current status and perspectives of the research in Pendred syndrome]Tatsuo Matsunaga, Masato Fujioka, Makoto Hosoya
International Journal of Pediatric Otorhinolaryngology|June 24, 2018
Response to "infantile-onset deafness in m.7445A>G carriers may be multicausal"Tatsuo Matsunaga, Kana Matsushima, Kei Murayama
Pageof 13