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Noriko Morimoto

Showing results (31-40 of 60) with videos related to

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The Journal of Pediatrics|November 11, 2006
Hearing loss in Turner syndromeNoriko Morimoto, Toshiaki Tanaka, Hidenobu Taiji, et al.
Japanese Journal of Ophthalmology|September 27, 2018
Incidence and causes of visual impairment in Japan: the first nation-wide complete enumeration survey of newly certified visually impaired individualsYuki Morizane, Noriko Morimoto, Atsushi Fujiwara, et al.
BMC Pediatrics|May 25, 2018
A case report of reversible generalized seizures in a patient with Waardenburg syndrome associated with a novel nonsense mutation in the penultimate exon of SOX10Noriomi Suzuki, Hideki Mutai, Fuyuki Miya, et al.
Photochemistry and Photobiology|December 11, 2008
Amelioration of airway stenosis in rabbit models by photodynamic therapy with talaporfin sodium (NPe6)Yoshinori Nakagishi, Noriko Morimoto, Masanori Fujita, et al.
Journal of Human Genetics|March 16, 2021
A novel missense variant of the GNAI3 gene and recognisable morphological characteristics of the mandibula in ARCND1Kumiko Yanagi, Noriko Morimoto, Manami Iso, et al.
International Journal of Pediatric Otorhinolaryngology|July 6, 2013
Gorham-Stout syndrome affecting the temporal bone with cerebrospinal fluid leakageNoriko Morimoto, Hideki Ogiwara, Osamu Miyazaki, et al.
Japanese Journal of Ophthalmology|April 17, 2023
A nationwide survey of newly certified visually impaired individuals in Japan for the fiscal year 2019: impact of the revision of criteria for visual impairment certificationRyo Matoba, Noriko Morimoto, Ryo Kawasaki, et al.
Gene|April 13, 2019
A clinical and genetic study of 16 Japanese families with Waardenburg syndromeShujiro B Minami, Kiyomitsu Nara, Hideki Mutai, et al.
The Journal of Craniofacial Surgery|September 18, 2025
Type of Primary Surgery and Postoperative Velopharyngeal Function in Patients With Submucous Cleft Palate at 3 years and OlderMasafumi Kamata, Makoto Hikosaka, Tsuyoshi Kaneko, et al.
Pediatric Nephrology (Berlin, Germany)|February 24, 2006
EYA1 and SIX1 gene mutations in Japanese patients with branchio-oto-renal (BOR) syndrome and related conditionsMichiyo Okada, Rika Fujimaru, Noriko Morimoto, et al.
Pageof 6

Showing results (31-40 of 60) with videos related to

Sort By:
Pageof 6
The Journal of Pediatrics|November 11, 2006
Hearing loss in Turner syndromeNoriko Morimoto, Toshiaki Tanaka, Hidenobu Taiji, et al.
Japanese Journal of Ophthalmology|September 27, 2018
Incidence and causes of visual impairment in Japan: the first nation-wide complete enumeration survey of newly certified visually impaired individualsYuki Morizane, Noriko Morimoto, Atsushi Fujiwara, et al.
BMC Pediatrics|May 25, 2018
A case report of reversible generalized seizures in a patient with Waardenburg syndrome associated with a novel nonsense mutation in the penultimate exon of SOX10Noriomi Suzuki, Hideki Mutai, Fuyuki Miya, et al.
Photochemistry and Photobiology|December 11, 2008
Amelioration of airway stenosis in rabbit models by photodynamic therapy with talaporfin sodium (NPe6)Yoshinori Nakagishi, Noriko Morimoto, Masanori Fujita, et al.
Journal of Human Genetics|March 16, 2021
A novel missense variant of the GNAI3 gene and recognisable morphological characteristics of the mandibula in ARCND1Kumiko Yanagi, Noriko Morimoto, Manami Iso, et al.
International Journal of Pediatric Otorhinolaryngology|July 6, 2013
Gorham-Stout syndrome affecting the temporal bone with cerebrospinal fluid leakageNoriko Morimoto, Hideki Ogiwara, Osamu Miyazaki, et al.
Japanese Journal of Ophthalmology|April 17, 2023
A nationwide survey of newly certified visually impaired individuals in Japan for the fiscal year 2019: impact of the revision of criteria for visual impairment certificationRyo Matoba, Noriko Morimoto, Ryo Kawasaki, et al.
Gene|April 13, 2019
A clinical and genetic study of 16 Japanese families with Waardenburg syndromeShujiro B Minami, Kiyomitsu Nara, Hideki Mutai, et al.
The Journal of Craniofacial Surgery|September 18, 2025
Type of Primary Surgery and Postoperative Velopharyngeal Function in Patients With Submucous Cleft Palate at 3 years and OlderMasafumi Kamata, Makoto Hikosaka, Tsuyoshi Kaneko, et al.
Pediatric Nephrology (Berlin, Germany)|February 24, 2006
EYA1 and SIX1 gene mutations in Japanese patients with branchio-oto-renal (BOR) syndrome and related conditionsMichiyo Okada, Rika Fujimaru, Noriko Morimoto, et al.
Pageof 6