Zobrazeno 1 - 10
of 112
pro vyhledávání: '"Noriko MORIMOTO"'
Autor:
Masatsugu Masuda, Ayako Kanno, Kiyomitsu Nara, Hideki Mutai, Naoya Morisada, Kazumoto Iijima, Noriko Morimoto, Atsuko Nakano, Tomoko Sugiuchi, Yasuhide Okamoto, Sawako Masuda, Sayaka Katsunuma, Kaoru Ogawa, Tatsuo Matsunaga
Publikováno v:
Scientific Reports, Vol 12, Iss 1, Pp 1-10 (2022)
Abstract Some patients have an atypical form of branchio-oto-renal (BOR) syndrome, which does not satisfy the diagnostic criteria, despite carrying a pathogenic variant (P variant) or a likely pathogenic variant (LP variant) of a causative gene. P/LP
Externí odkaz:
https://doaj.org/article/4493ac24dd0e4f55b506ef65f709bc2f
Autor:
Noriko Morimoto, Takanobu Maekawa, Masaya Kubota, Masayuki Kitamura, Nozomi Takahashi, Mitsuru Kubota
Publikováno v:
Laryngoscope Investigative Otolaryngology, Vol 6, Iss 2, Pp 332-339 (2021)
Abstract Objectives The present study analyzed surgical outcomes of laryngotracheal separation (LTS) in children with neurological disorders. The purpose of this study was to investigate respiratory impairment and severe complications after LTS in ch
Externí odkaz:
https://doaj.org/article/8027132fd0f2491ebfdd40af13e18d39
Autor:
Teizaburo Mori, Yumi Kudo, Yutaka Kanamori, Kazunori Tahara, Yohei Yamada, Mai Kutsukake, Takuro Fujita, Kazue Miyake, Akihiro Fujino, Nozomi Takahashi, Noriko Morimoto, Yohei Kosugi, Yoji Uehara, Yushi Ito, Osamu Miyazaki, Rika Sugibayashi, Katsusuke Ozawa, Seiji Wada, Haruhiko Sago
Publikováno v:
Journal of Pediatric Surgery Case Reports, Vol 57, Iss , Pp - (2020)
We report a case of congenital thyroid teratoma that was diagnosed in fetal life and completely excised after birth. The histopathological diagnosis was immature teratoma. Recurrent nerve palsy was experienced after the complete excision, but hypothy
Externí odkaz:
https://doaj.org/article/9039c97208ca4efe84306b6dfa5e4a14
Autor:
Hideki Mutai, Koichiro Wasano, Yukihide Momozawa, Yoichiro Kamatani, Fuyuki Miya, Sawako Masuda, Noriko Morimoto, Kiyomitsu Nara, Satoe Takahashi, Tatsuhiko Tsunoda, Kazuaki Homma, Michiaki Kubo, Tatsuo Matsunaga
Publikováno v:
PLoS Genetics, Vol 16, Iss 4, p e1008643 (2020)
Hereditary hearing loss is challenging to diagnose because of the heterogeneity of the causative genes. Further, some genes involved in hereditary hearing loss have yet to be identified. Using whole-exome analysis of three families with congenital, s
Externí odkaz:
https://doaj.org/article/a1fd6ee65284460e8b9ac7c9e5a2b959
Autor:
Noriomi Suzuki, Hideki Mutai, Fuyuki Miya, Tatsuhiko Tsunoda, Hiroshi Terashima, Noriko Morimoto, Tatsuo Matsunaga
Publikováno v:
BMC Pediatrics, Vol 18, Iss 1, Pp 1-4 (2018)
Abstract Background Waardenburg syndrome type 1 (WS1) can be distinguished from Waardenburg syndrome type 2 (WS2) by the presence of dystopia canthorum. About 96% of WS1 are due to PAX3 mutations, and SOX10 mutations have been reported in 15% of WS2.
Externí odkaz:
https://doaj.org/article/57b47a4867204a07b1c77ee825d08698
Autor:
Yutaka Kanamori, Toshiko Takezoe, Kazunori Tahara, Toshihiko Watanabe, Michinobu Ohno, Kotaro Tomonaga, Katsuhiro Ogawa, Tomoro Hishiki, Akihiro Fujino, Yuri Ozawa, Shoichiro Amari, Hideshi Fujinaga, Yushi Ito, Osamu Miyazaki, Noriko Morimoto, Rika Sugibayashi, Katsusuke Ozawa, Seiji Wada, Haruhiko Sago
Publikováno v:
Journal of Pediatric Surgery Case Reports, Vol 26, Iss C, Pp 22-25 (2017)
Congenital high airway obstruction syndrome (CHAOS) is a rare congenital anomaly and the most common etiology is laryngeal atresia. Recently, an increasing number of cases have survived due to prenatal diagnosis and pre- and peri-natal care including
Externí odkaz:
https://doaj.org/article/c16640cebfc24f558c8af56edeca476b
Autor:
Michinobu Ohno, Yutaka Kanamori, Kazunori Tahara, Toshihiko Watanabe, Toshiko Takezoe, Kotaro Tomonaga, Katsuhiro Ogawa, Mioko Nomura, Tomoro Hishiki, Akihiro Fujino, Manabu Komori, Noriko Morimoto
Publikováno v:
Journal of Pediatric Surgery Case Reports, Vol 18, Iss C, Pp 39-41 (2017)
Esophageal duplication cyst is the second most common type of duplication cyst in the alimentary tract (10–15%). However, most of these cysts occur in the mediastinal part of the esophagus and cervical esophageal duplication cyst is extremely rare.
Externí odkaz:
https://doaj.org/article/8bf4db79b2684023a6b496c55a01e0bd
Dissertation/ Thesis
Autor:
森本 典子, Noriko Morimoto
本論文は19世紀のデンマーク社会にディアコニッセとディアコニアの働きを広めるために尽力したハラルド・スタインのディアコニア思想に光を当てる。スタインは、産業革命や社会主
Autor:
Ryo Matoba, Noriko Morimoto, Ryo Kawasaki, Miyuki Fujiwara, Keisuke Kanenaga, Hidetoshi Yamashita, Taiji Sakamoto, Yuki Morizane
Publikováno v:
Japanese Journal of Ophthalmology. 67:346-352
Publikováno v:
International Journal of Rheumatic Diseases. 26:480-486
To evaluate the clinical factors associated with the outcome of tonsillectomy in children with periodic fever, aphthous stomatitis, pharyngitis, and cervical adenitis (PFAPA) syndrome, thereby clarifying who would most likely benefit from that surger