Zobrazeno 1 - 10
of 28
pro vyhledávání: '"Naomi Fujimoto"'
Autor:
Tomoya Kinouchi, Yasuyuki Morishima, Shinichi Uyama, Tadashi Miyamoto, Hidehisa Horiguchi, Naomi Fujimoto, Hiromi Ueta
Publikováno v:
BMC Infectious Diseases, Vol 21, Iss 1, Pp 1-6 (2021)
Abstract Background Taenia solium, present in most developing countries, infects many individuals and may result in their death. Neurocysticercosis (NCC) develops after invasion of the brain by parasitic larvae. It is the most common parasitic diseas
Externí odkaz:
https://doaj.org/article/e9e07dcf0e0f4b95b21f95cdf2806e29
Autor:
Tomoya Kinouchi, Keisuke Ishitani, Shinichi Uyama, Tadashi Miyamoto, Naomi Fujimoto, Hiromi Ueta
Publikováno v:
Journal of Medical Case Reports, Vol 15, Iss 1, Pp 1-5 (2021)
Abstract Background Most sudden-onset hearing loss is due to otolaryngologic- and very rarely to cerebrovascular disease. We report a woman with sudden bilateral sensorineural hearing loss. This case suggests that even in the absence of brainstem or
Externí odkaz:
https://doaj.org/article/9edd3cb5f8b54bb2a102535fb121f94f
Autor:
Tadashi Miyamoto, Tomoya Kinouchi, Yasuyuki Morishima, Shinichi Uyama, Hidehisa Horiguchi, Hiromi Ueta, Naomi Fujimoto
Publikováno v:
BMC Infectious Diseases
BMC Infectious Diseases, Vol 21, Iss 1, Pp 1-6 (2021)
BMC Infectious Diseases, Vol 21, Iss 1, Pp 1-6 (2021)
Background Taenia solium, present in most developing countries, infects many individuals and may result in their death. Neurocysticercosis (NCC) develops after invasion of the brain by parasitic larvae. It is the most common parasitic disease of the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9a9c16df1d3d927e11013755fcb5b370
http://europepmc.org/articles/PMC8524942
http://europepmc.org/articles/PMC8524942
Autor:
Hiromi Ueta, Tadashi Miyamoto, Naomi Fujimoto, Keisuke Ishitani, Tomoya Kinouchi, Shinichi Uyama
Publikováno v:
Journal of Medical Case Reports, Vol 15, Iss 1, Pp 1-5 (2021)
Journal of Medical Case Reports
Journal of Medical Case Reports
Background Most sudden-onset hearing loss is due to otolaryngologic- and very rarely to cerebrovascular disease. We report a woman with sudden bilateral sensorineural hearing loss. This case suggests that even in the absence of brainstem or cerebella
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::61b499634bf801b5236772557edadca0
https://doi.org/10.1186/s13256-020-02574-8
https://doi.org/10.1186/s13256-020-02574-8
Autor:
Tadashi Miyamoto, Shinichi Uyama, Sumihito Nobusawa, Naomi Fujimoto, Hideaki Yokoo, Hidehisa Horiguchi, Satoshi Nakata, Hiromi Ueta
Publikováno v:
Neuropathology. 37:52-57
Atypical teratoid/rhabdoid tumors (AT/RTs) are rare malignant neoplasms of the CNS that preferentially affect young children. We herein report an adult case of AT/RT surviving for more than 5 years with the residual tumor. The patient, a 24-year-old
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::18a331d2c714065905339175ba15542d
https://doi.org/10.1111/neup.12317
https://doi.org/10.1111/neup.12317
Autor:
Naomi Fujimoto, Sumihito Nobusawa, Vishwa Jeet Amatya, Akiyoshi Kakita, Yoshiki Mikami, Kazuhiko Sugiyama, Shinya Tanaka, Hideaki Yokoo, Takanori Hirose, Atsushi Sasaki
Publikováno v:
Brain Pathol
Astroblastoma is a rare, enigmatic tumor of the central nervous system (CNS) which shares some clinicopathologic aspects with other CNS tumors, especially ependymoma. To further clarify the nature of astroblastoma, we performed clinicopathologic and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4480fff26bd5a23a0c0fbe136c1ff271
https://pubmed.ncbi.nlm.nih.gov/28990708
https://pubmed.ncbi.nlm.nih.gov/28990708
Autor:
Yuriko Tomita, Yukihiko Sugita, Dongming Zhao, Masato Hatta, Shinya Yamada, Tomokazu Tamura, Eileen A. Maher, Takato Odagiri, Noriko Nakajima, Masatoshi Okamatsu, Mutsumi Ito, Masayuki Shirakura, Amie J. Eisfeld, Masaki Imai, Eiryo Kawakami, Seiya Yamayoshi, Yoshihiro Kawaoka, Shinji Watanabe, Kiyoko Iwatsuki-Horimoto, Ryan McBride, Takeshi Noda, Hiroshi Kida, Ryuta Uraki, Hiroaki Katsura, Gongxun Zhong, Noriko Kishida, Anthony Hanson, Hideki Hasegawa, Robert P. de Vries, Hirotaka Imai, Naomi Fujimoto, Satoshi Fukuyama, Takehiko Saito, Shintaro Shichinohe, Makoto Ozawa, Reina Yamaji, Izumi Ishikawa, Yuko Sakai-Tagawa, Gabriele Neumann, Shufang Fan, Jihui Ping, Yuko Uchida, Masato Tashiro, James C. Paulson, Maki Kiso, Tokiko Watanabe, Shin Murakami, Emi Takashita, Kazue Goto, Yoshihiro Sakoda
Publikováno v:
Nature
Avian influenza A viruses rarely infect humans; however, when human infection and subsequent human-to-human transmission occurs, worldwide outbreaks (pandemics) can result. The recent sporadic infections of humans in China with a previously unrecogni
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2d586f28b7afcec7f3e12609de542e43
http://europepmc.org/articles/PMC3891892
http://europepmc.org/articles/PMC3891892
Autor:
Etsuko Ikeda, Naomi Fujimoto, Kazumi Ito, Tohru Ogihara, Hiroko Abe, Satoru Ogawa, Emi Fujiwara, Tomomi Hachiya, Satsuki Nakayama, Mutsumi Nakano, Hiroshi Tamai, Satoko Ban
Publikováno v:
Archives of Disease in Childhood - Fetal and Neonatal Edition. 90:F432-F436
The analgesic effect of oral sucrose in newborn infants undergoing painful procedures is generally accepted. For blood sampling, some studies have shown that venepuncture (VP) is less painful than heel lance (HL).To determine the least painful and mo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::65f05c98758aafc2a190f1fb1a090048
https://doi.org/10.1136/adc.2004.069328
https://doi.org/10.1136/adc.2004.069328
Autor:
Toshihiko Shiroishi, Hideki Kaneda, Junko Ishijima, Tetsuo Noda, Junko Nagano, Shigeharu Wakana, Kunihiko Shimizu, Yoshiyuki Sakuraba, Kimio Kobayashi, Yoichi Gondo, Hiroshi Masuya, Ikuo Miura, Naomi Fujimoto, Hideki Sezutsu, Aya Shimizu, Akiko Kawai, Takahide Maeda
Publikováno v:
Human Molecular Genetics. 14:575-583
Amelogenesis imperfecta (AI) is a group of commonly inherited defects of dental enamel formation, which exhibits marked genetic and clinical heterogeneity. The genetic basis of this heterogeneity is still poorly understood. Enamelin, the affected gen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fab8907717424eb6b7030fda0e1e843d
https://doi.org/10.1093/hmg/ddi054
https://doi.org/10.1093/hmg/ddi054
Autor:
Yoshiyuki Sakuraba, Yoichi Gondo, Toshihiko Shiroishi, Ayako Inoue, Takashi Kadowaki, Hiromi Motegi, Rie Matsumoto, Junko Ishijima, Hiroshi Masuya, Tomohiro Suzuki, Shigeharu Wakana, Maki Inoue, Yasuo Terauchi, Naoto Kubota, Hideki Kaneda, Tetsuo Noda, Ichitomo Miwa, Keiko Tsuchihashi, Masato Kasuga, Tomoko Kagami, Yutaka Shigeyama, Yukiyasu Toyoda, Hideaki Toki, Junko Matsui, Osamu Minowa, Naomi Fujimoto, Takashi Adachi
Publikováno v:
Human Molecular Genetics. 13:1147-1157
Mutant mouse models are indispensable tools for clarifying the functions of genes and for elucidating the underlying pathogenic mechanisms of human diseases. Currently, several large-scale mutagenesis projects that employ the chemical mutagen N-ethyl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4dc01a6ee91a531d2e3895313ebec7c0
https://doi.org/10.1093/hmg/ddh133
https://doi.org/10.1093/hmg/ddh133