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Noriko Morimoto

Showing results (41-50 of 60) with videos related to

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Orphanet Journal of Rare Diseases|October 30, 2013
Diverse spectrum of rare deafness genes underlies early-childhood hearing loss in Japanese patients: a cross-sectional, multi-center next-generation sequencing studyHideki Mutai, Naohiro Suzuki, Atsushi Shimizu, et al.
Neuropharmacology|July 21, 2015
Anti-stress effects of ONO-2952, a novel translocator protein 18 kDa antagonist, in ratsKatsukuni Mitsui, Tomohiro Niwa, Yuji Kawahara, et al.
Auris, Nasus, Larynx|September 12, 2024
National epidemiological survey on pharyngeal, laryngeal, and tracheal stenosis in Japan: A national survey on airway stenosisYo Kishimoto, Kayoko Mizuno, Yoshitaka Kawai, et al.
Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc|March 24, 2006
Myocardial apoptosis associated with the expression of proinflammatory cytokines during the course of myocardial infarctionYoshikiyo Akasaka, Noriko Morimoto, Yukio Ishikawa, et al.
The Laryngoscope|March 9, 2017
WFS1 and GJB2 mutations in patients with bilateral low-frequency sensorineural hearing lossNatsuko Kasakura-Kimura, Masatsugu Masuda, Hideki Mutai, et al.
Orphanet Journal of Rare Diseases|May 13, 2015
High prevalence of CDH23 mutations in patients with congenital high-frequency sporadic or recessively inherited hearing lossKunio Mizutari, Hideki Mutai, Kazunori Namba, et al.
Pediatric Radiology|May 14, 2021
Value of parametric indexes to identify tracheal atresia with or without fistula on fetal magnetic resonance imagingHidekazu Aoki, Osamu Miyazaki, Saho Irahara, et al.
International Journal of Pediatric Otorhinolaryngology|May 22, 2014
Cricopharyngeal achalasia treated with myectomy and post-operative high-resolution manometryToshihiko Watanabe, Takahiro Shimizu, Masataka Takahashi, et al.
International Journal of Pediatric Otorhinolaryngology|July 22, 2021
Investigation of the hearing levels of siblings affected by a single GJB2 variant: Possibility of genetic modifiersMakoto Hosoya, Masato Fujioka, Kiyomitsu Nara, et al.
Sleep|April 2, 2017
Sleep Duration, Snoring Prevalence, Obesity, and Behavioral Problems in a Large Cohort of Primary School Students in JapanNaoko Sakamoto, David Gozal, Dale L Smith, et al.
Pageof 6

Showing results (41-50 of 60) with videos related to

Sort By:
Pageof 6
Orphanet Journal of Rare Diseases|October 30, 2013
Diverse spectrum of rare deafness genes underlies early-childhood hearing loss in Japanese patients: a cross-sectional, multi-center next-generation sequencing studyHideki Mutai, Naohiro Suzuki, Atsushi Shimizu, et al.
Neuropharmacology|July 21, 2015
Anti-stress effects of ONO-2952, a novel translocator protein 18 kDa antagonist, in ratsKatsukuni Mitsui, Tomohiro Niwa, Yuji Kawahara, et al.
Auris, Nasus, Larynx|September 12, 2024
National epidemiological survey on pharyngeal, laryngeal, and tracheal stenosis in Japan: A national survey on airway stenosisYo Kishimoto, Kayoko Mizuno, Yoshitaka Kawai, et al.
Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc|March 24, 2006
Myocardial apoptosis associated with the expression of proinflammatory cytokines during the course of myocardial infarctionYoshikiyo Akasaka, Noriko Morimoto, Yukio Ishikawa, et al.
The Laryngoscope|March 9, 2017
WFS1 and GJB2 mutations in patients with bilateral low-frequency sensorineural hearing lossNatsuko Kasakura-Kimura, Masatsugu Masuda, Hideki Mutai, et al.
Orphanet Journal of Rare Diseases|May 13, 2015
High prevalence of CDH23 mutations in patients with congenital high-frequency sporadic or recessively inherited hearing lossKunio Mizutari, Hideki Mutai, Kazunori Namba, et al.
Pediatric Radiology|May 14, 2021
Value of parametric indexes to identify tracheal atresia with or without fistula on fetal magnetic resonance imagingHidekazu Aoki, Osamu Miyazaki, Saho Irahara, et al.
International Journal of Pediatric Otorhinolaryngology|May 22, 2014
Cricopharyngeal achalasia treated with myectomy and post-operative high-resolution manometryToshihiko Watanabe, Takahiro Shimizu, Masataka Takahashi, et al.
International Journal of Pediatric Otorhinolaryngology|July 22, 2021
Investigation of the hearing levels of siblings affected by a single GJB2 variant: Possibility of genetic modifiersMakoto Hosoya, Masato Fujioka, Kiyomitsu Nara, et al.
Sleep|April 2, 2017
Sleep Duration, Snoring Prevalence, Obesity, and Behavioral Problems in a Large Cohort of Primary School Students in JapanNaoko Sakamoto, David Gozal, Dale L Smith, et al.
Pageof 6