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Acta Oto-Laryngologica. Supplementum
|
February 18, 2009
3D computerized model of endolymphatic hydrops from specimens of temporal bone
Masaaki Teranishi, Tadao Yoshida, Naomi Katayama, et al.
Geriatrics & Gerontology International
|
May 29, 2015
Cerumen impaction shown by brain magnetic resonance imaging in patients with cognitive impairment
Tsutomu Nakashima, Saiko Sugiura, Shinji Naganawa, et al.
DNA and Cell Biology
|
August 11, 2012
Polymorphisms in genes involved in oxidative stress response in patients with sudden sensorineural hearing loss and Ménière's disease in a Japanese population
Masaaki Teranishi, Yasue Uchida, Naoki Nishio, et al.
Journal of Neurogenetics
|
March 15, 2013
Association between polymorphisms in genes encoding methylenetetrahydrofolate reductase and the risk of Ménière's disease
Yang Huang, Masaaki Teranishi, Yasue Uchida, et al.
Acta Oto-Laryngologica
|
June 23, 2015
Changes in endolymphatic hydrops in patients with Ménière's disease treated conservatively for more than 1 year
Kenji Suga, Masahiro Kato, Tadao Yoshida, et al.
Magnetic Resonance in Medical Sciences : MRMS : an Official Journal of Japan Society of Magnetic Resonance in Medicine
|
April 17, 2020
Intracranial Distribution of Intravenously Administered Gadolinium-based Contrast Agent over a Period of 24 Hours: Evaluation with 3D-real IR Imaging and MR Fingerprinting
Shinji Naganawa, Rintaro Ito, Yutaka Kato, et al.
Auris, Nasus, Larynx
|
July 26, 2025
Robotic and computer-assisted techniques in ear surgery
Takeshi Fujita, Taku Ito, Masaya Uchida, et al.
Acta Oto-Laryngologica
|
October 16, 2014
Idiopathic sudden sensorineural hearing loss in Japan
Tsutomu Nakashima, Hiroaki Sato, Kiyofumi Gyo, et al.
Gene
|
March 20, 2012
Contribution of complement factor H Y402H polymorphism to sudden sensorineural hearing loss risk and possible interaction with diabetes
Naoki Nishio, Masaaki Teranishi, Yasue Uchida, et al.
Life Sciences
|
January 29, 2013
Polymorphisms in genes encoding aquaporins 4 and 5 and estrogen receptor α in patients with Ménière's disease and sudden sensorineural hearing loss
Naoki Nishio, Masaaki Teranishi, Yasue Uchida, et al.
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of 12
Search research articles
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Showing results (91-100 of 113) with videos related to
Sort By:
Page
of 12
Acta Oto-Laryngologica. Supplementum
|
February 18, 2009
3D computerized model of endolymphatic hydrops from specimens of temporal bone
Masaaki Teranishi, Tadao Yoshida, Naomi Katayama, et al.
Geriatrics & Gerontology International
|
May 29, 2015
Cerumen impaction shown by brain magnetic resonance imaging in patients with cognitive impairment
Tsutomu Nakashima, Saiko Sugiura, Shinji Naganawa, et al.
DNA and Cell Biology
|
August 11, 2012
Polymorphisms in genes involved in oxidative stress response in patients with sudden sensorineural hearing loss and Ménière's disease in a Japanese population
Masaaki Teranishi, Yasue Uchida, Naoki Nishio, et al.
Journal of Neurogenetics
|
March 15, 2013
Association between polymorphisms in genes encoding methylenetetrahydrofolate reductase and the risk of Ménière's disease
Yang Huang, Masaaki Teranishi, Yasue Uchida, et al.
Acta Oto-Laryngologica
|
June 23, 2015
Changes in endolymphatic hydrops in patients with Ménière's disease treated conservatively for more than 1 year
Kenji Suga, Masahiro Kato, Tadao Yoshida, et al.
Magnetic Resonance in Medical Sciences : MRMS : an Official Journal of Japan Society of Magnetic Resonance in Medicine
|
April 17, 2020
Intracranial Distribution of Intravenously Administered Gadolinium-based Contrast Agent over a Period of 24 Hours: Evaluation with 3D-real IR Imaging and MR Fingerprinting
Shinji Naganawa, Rintaro Ito, Yutaka Kato, et al.
Auris, Nasus, Larynx
|
July 26, 2025
Robotic and computer-assisted techniques in ear surgery
Takeshi Fujita, Taku Ito, Masaya Uchida, et al.
Acta Oto-Laryngologica
|
October 16, 2014
Idiopathic sudden sensorineural hearing loss in Japan
Tsutomu Nakashima, Hiroaki Sato, Kiyofumi Gyo, et al.
Gene
|
March 20, 2012
Contribution of complement factor H Y402H polymorphism to sudden sensorineural hearing loss risk and possible interaction with diabetes
Naoki Nishio, Masaaki Teranishi, Yasue Uchida, et al.
Life Sciences
|
January 29, 2013
Polymorphisms in genes encoding aquaporins 4 and 5 and estrogen receptor α in patients with Ménière's disease and sudden sensorineural hearing loss
Naoki Nishio, Masaaki Teranishi, Yasue Uchida, et al.
Page
of 12