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Kozo Kumakawa

Showing results (1-10 of 27) with videos related to

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The Annals of Otology, Rhinology, and Laryngology|May 23, 2015
Massively parallel DNA sequencing successfully identified seven families with deafness-associated MYO6 mutations: the mutational spectrum and clinical characteristicsMaiko Miyagawa, Shin-Ya Nishio, Kozo Kumakawa, et al.
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|April 29, 2014
High-frequency involved hearing loss caused by novel mitochondrial DNA mutation in 16S ribosomal RNA geneSatoko Abe, Makoto Nagano, Shin-Ya Nishio, et al.
Journal of Human Genetics|January 22, 2016
Frequency of Usher syndrome type 1 in deaf children by massively parallel DNA sequencingHidekane Yoshimura, Maiko Miyagawa, Kozo Kumakawa, et al.
Clinical Case Reports|November 21, 2018
Diagnostic pitfalls for <i>GJB2</i>-related hearing loss: A novel deletion detected by Array-CGH analysis in a Japanese patient with congenital profound hearing lossSatoko Abe, Shin-Ya Nishio, Yoh Yokota, et al.
Auris, Nasus, Larynx|September 27, 2020
Successful cochlear implantation in a patient with Epstein syndrome during long-term follow-upAnjin Mori, Hidehiko Takeda, Marina Kobayashi, et al.
BMC Medical Genetics|September 24, 2013
OTOF mutation screening in Japanese severe to profound recessive hearing loss patientsYoh-ichiro Iwasa, Shin-ya Nishio, Hidekane Yoshimura, et al.
International Journal of Pediatric Otorhinolaryngology|November 20, 2016
Facial nerve stimulation following cochlear implantation for X-linked stapes gusher syndrome leading to identification of a novel POU3F4 mutationJacob L Wester, Catherine Merna, Kevin A Peng, et al.
Acta Oto-Laryngologica|September 14, 2007
Clinical characteristics and genotype-phenotype correlation of hearing loss patients with SLC26A4 mutationsHiroaki Suzuki, Aki Oshima, Koji Tsukamoto, et al.
Genes|February 26, 2025
Prevalence and Clinical Characteristics of <i>OTOGL</i>-Associated Hearing Loss Identified in a Cohort of 7065 Japanese Patients with Hearing LossKaruna Maekawa, Shin-Ya Nishio, Kotaro Ishikawa, et al.
ORL; Journal for Oto-Rhino-Laryngology and Its Related Specialties|September 18, 2013
Auditory brainstem implantation improves speech recognition in neurofibromatosis type II patientsCordula Matthies, Stefan Brill, Kimitaka Kaga, et al.
Pageof 3

Showing results (1-10 of 27) with videos related to

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The Annals of Otology, Rhinology, and Laryngology|May 23, 2015
Massively parallel DNA sequencing successfully identified seven families with deafness-associated MYO6 mutations: the mutational spectrum and clinical characteristicsMaiko Miyagawa, Shin-Ya Nishio, Kozo Kumakawa, et al.
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|April 29, 2014
High-frequency involved hearing loss caused by novel mitochondrial DNA mutation in 16S ribosomal RNA geneSatoko Abe, Makoto Nagano, Shin-Ya Nishio, et al.
Journal of Human Genetics|January 22, 2016
Frequency of Usher syndrome type 1 in deaf children by massively parallel DNA sequencingHidekane Yoshimura, Maiko Miyagawa, Kozo Kumakawa, et al.
Clinical Case Reports|November 21, 2018
Diagnostic pitfalls for <i>GJB2</i>-related hearing loss: A novel deletion detected by Array-CGH analysis in a Japanese patient with congenital profound hearing lossSatoko Abe, Shin-Ya Nishio, Yoh Yokota, et al.
Auris, Nasus, Larynx|September 27, 2020
Successful cochlear implantation in a patient with Epstein syndrome during long-term follow-upAnjin Mori, Hidehiko Takeda, Marina Kobayashi, et al.
BMC Medical Genetics|September 24, 2013
OTOF mutation screening in Japanese severe to profound recessive hearing loss patientsYoh-ichiro Iwasa, Shin-ya Nishio, Hidekane Yoshimura, et al.
International Journal of Pediatric Otorhinolaryngology|November 20, 2016
Facial nerve stimulation following cochlear implantation for X-linked stapes gusher syndrome leading to identification of a novel POU3F4 mutationJacob L Wester, Catherine Merna, Kevin A Peng, et al.
Acta Oto-Laryngologica|September 14, 2007
Clinical characteristics and genotype-phenotype correlation of hearing loss patients with SLC26A4 mutationsHiroaki Suzuki, Aki Oshima, Koji Tsukamoto, et al.
Genes|February 26, 2025
Prevalence and Clinical Characteristics of <i>OTOGL</i>-Associated Hearing Loss Identified in a Cohort of 7065 Japanese Patients with Hearing LossKaruna Maekawa, Shin-Ya Nishio, Kotaro Ishikawa, et al.
ORL; Journal for Oto-Rhino-Laryngology and Its Related Specialties|September 18, 2013
Auditory brainstem implantation improves speech recognition in neurofibromatosis type II patientsCordula Matthies, Stefan Brill, Kimitaka Kaga, et al.
Pageof 3