Search research articles
Contact Us
Filters
Showing results (31-40 of 60) with videos related to
Page
of 6
Sort By:
The Journal of Pediatrics
|
November 11, 2006
Hearing loss in Turner syndrome
Noriko 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 individuals
Yuki 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 SOX10
Noriomi 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 ARCND1
Kumiko 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 leakage
Noriko 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 certification
Ryo Matoba, Noriko Morimoto, Ryo Kawasaki, et al.
Gene
|
April 13, 2019
A clinical and genetic study of 16 Japanese families with Waardenburg syndrome
Shujiro 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 Older
Masafumi 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 conditions
Michiyo Okada, Rika Fujimaru, Noriko Morimoto, et al.
Page
of 6
Search research articles
Search
Showing results (31-40 of 60) with videos related to
Sort By:
Page
of 6
The Journal of Pediatrics
|
November 11, 2006
Hearing loss in Turner syndrome
Noriko 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 individuals
Yuki 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 SOX10
Noriomi 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 ARCND1
Kumiko 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 leakage
Noriko 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 certification
Ryo Matoba, Noriko Morimoto, Ryo Kawasaki, et al.
Gene
|
April 13, 2019
A clinical and genetic study of 16 Japanese families with Waardenburg syndrome
Shujiro 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 Older
Masafumi 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 conditions
Michiyo Okada, Rika Fujimaru, Noriko Morimoto, et al.
Page
of 6