Zobrazeno 1 - 10
of 32
pro vyhledávání: '"Yuichi, Takami"'
Autor:
Suguru Uemura, Takeshi Mori, Nanako Nino, Nana Sakakibara, Satoru Takafuji, Shota Myojin, Yuichi Takami, Ichiro Morioka, Noriyuki Nishimura, Masaaki Kugo, Kazumoto Iijima
Publikováno v:
Clinical Case Reports, Vol 8, Iss 1, Pp 75-78 (2020)
Abstract The present case underscores the importance of considering the association of severe thrombocytopenia or immune thrombocytopenia with cytomegalovirus (CMV) infection because CMV‐induced thrombocytopenia occasionally requires antiviral ther
Externí odkaz:
https://doaj.org/article/eb064156648b474c8ba8a52e202c0e5c
Autor:
Tomoko Lee, Yuichi Takami, Kenji Yamada, Hironori Kobayashi, Yuki Hasegawa, Hideo Sasai, Hiroki Otsuka, Yasuhiro Takeshima, Toshiyuki Fukao
Publikováno v:
JIMD Reports, Vol 48, Iss 1, Pp 19-25 (2019)
Abstract Mitochondrial 3‐hydroxy‐3‐methylglutaryl‐CoA synthase deficiency (mHS deficiency) is a rare autosomal recessive inborn error of ketogenesis caused by a mutation in the HMGCS2 gene, which is characterized by non‐(hypo)‐ketotic hyp
Externí odkaz:
https://doaj.org/article/e4ee7a8d609845fc96c932e7c13ea715
Autor:
Mari Asaoka, Tetsuhiro Fukuyama, Naohisa Kawamura, Tamami Yano, Takayoshi Kawabata, Kotaro Nakano, Eriko Kikuchi, Tomoyuki Miyamoto, Mika Inoue, Akihisa Okumura, Masato Hiyane, Etsushi Toyofuku, Yuichi Takami, Yusaku Endo, Keiko Tanaka-Taya, Nobuyoshi Sugiyama, Yu Tsuyusaki, Sawa Yasumoto, Keiko Suzuki, Nobuko Moriyama, Takako Fujita, Yasuhiro Suzuki, Eri Takeshita, Hitoshi Mikami, Yuichi Abe, Ryutaro Kira, Chiharu Miyatake, Hiroyuki Torisu, Akira Kumakura, Akane Kanazawa, Tatsuharu Sato, Yuya Takahashi, Hiroshi Terashima, Sonoko Kubota, Genrei Ohta, Mariko Kasai, Yu Ishida, Pin Fee Chong, Noboru Yoshida, Shinichiro Goto, Taira Toki, Ayako Hattori, Wakako Ishii, Kenichi Tanaka, Miho Yamamuro, Sahoko Ono, Yukihiko Konishi, Harushi Mori, Nozomi Koran, Kazuhide Ohta, Kenichi Sakajiri, Michiaki Nagura, Kyoko Ban
Publikováno v:
Pediatric Neurology. 116:14-19
We summarize the long-term motor outcome and disability level in a cluster of pediatric patients with acute flaccid myelitis (AFM) associated with the enterovirus D68 outbreak in 2015.This is a nationwide follow-up questionnaire analysis study. Clini
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e36fde17d9b5b55a851a53dd31a77029
https://doi.org/10.1016/j.pediatrneurol.2020.11.019
https://doi.org/10.1016/j.pediatrneurol.2020.11.019
Autor:
Yohane Miyata, Yonehiro Kanemura, Yuri Uchiyama, Fumihito Nozaki, Fumikatsu Nohara, Satomi Mitsuhashi, Satoshi Hada, Akihito Takeuchi, Fumihiko Ishida, Fumitaka Yoshioka, Hiroshi Terashima, Jiu Okuno-Yuguchi, Hirotomo Saitsu, Tadayuki Kumagai, Hidetoshi Taniguchi, Hiroshi Doi, Atsushi Takata, Atsuko Harada, Shinji Saitoh, Hitoshi Osaka, Eri Imagawa, Yusuke Mitani, Ayako Hattori, Yasuji Kitabatake, Koichi Tanda, Jun-ichi Takanashi, Atsushi Fujita, Hiroshi Arai, Ichiro Kuki, Makoto Kinoshita, Chikako Ogawa, Toshiyuki Itai, Yoshinori Tsurusaki, Yoshihiko Saito, Noriko Togashi, Noriko Miyake, Mazumi Miura, Hiroyuki Higashiyama, Masayasu Ohta, Yoshiichi Abe, Tetsuhiro Fukuyama, Yusuke Yachi, Tomoko Tandou, Etsuko Miyagi, Satoko Kumada, Shoko Shimokawa, Naomichi Matsumoto, Yuko Takei, Keiko Hirano, Satori Hirai, Keiichi Ozono, Yukihiro Kitai, Yuichi Takami, Mitsuo Motobayashi, Ryoko Honda, Masafumi Morimoto, Takaaki Nakano, Yuki Maki, Satoko Miyatake, Akihiko Ishiyama, Tatsuya Fukasawa, Mitsuhiro Kato, Yoshiteru Azuma, Robert Smigiel, Yushi Noguchi, Tsuyoshi Omi, Kohei Hamanaka, Naoki Ando, Masataka Taguri, Takeshi Mizuguchi, Chizuru Seiwa, Mitsuko Nakashima, Eriko Koshimizu, Shin Nabatame, Teruyuki Ishikura
Publikováno v:
Journal of Medical Genetics. 58:505-513
BackgroundVariants in the type IV collagen gene (COL4A1/2) cause early-onset cerebrovascular diseases. Most individuals are diagnosed postnatally, and the prenatal features of individuals with COL4A1/2 variants remain unclear.MethodsWe examined COL4A
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f2dd2760375d155949c433d65a592c68
https://doi.org/10.1136/jmedgenet-2020-106896
https://doi.org/10.1136/jmedgenet-2020-106896
Autor:
Masaaki Kugo, Nanako Nino, Suguru Uemura, Noriyuki Nishimura, Kazumoto Iijima, Nana Sakakibara, Ichiro Morioka, Shota Myojin, Satoru Takafuji, Yuichi Takami, Takeshi Mori
Publikováno v:
Clinical Case Reports
Clinical Case Reports, Vol 8, Iss 1, Pp 75-78 (2020)
Clinical Case Reports, Vol 8, Iss 1, Pp 75-78 (2020)
The present case underscores the importance of considering the association of severe thrombocytopenia or immune thrombocytopenia with cytomegalovirus (CMV) infection because CMV‐induced thrombocytopenia occasionally requires antiviral therapy.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9b7d5264120e615eeb2e2fce0cd25ff4
https://hdl.handle.net/20.500.14094/90006702
https://hdl.handle.net/20.500.14094/90006702
Autor:
Masahiro Nishiyama, Tsukasa Tanaka, Azusa Maruyama, Kazumi Tomioka, Taku Nakagawa, Kazumoto Iijima, Yoshinobu Oyazato, Hiroshi Yamaguchi, Daisaku Toyoshima, Noriyuki Nishimura, Yusuke Ishida, Kaori Sasaki, Kandai Nozu, Ichiro Nakashima, Yuichi Takami, Hiroaki Nagase, Kyoko Fujita
Publikováno v:
Brain and Development. 41:531-537
The detailed clinical time course in acute disseminated encephalomyelitis (ADEM) from initial symptoms, through exacerbation, to remission has not been widely reported. Hence, this study aimed to investigate the clinical time course of pediatric ADEM
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::efa2cf4a25855cc9f295ae280fdd0ad2
https://doi.org/10.1016/j.braindev.2019.02.011
https://doi.org/10.1016/j.braindev.2019.02.011
Autor:
Toshiyuki Fukao, Hideo Sasai, Hiroki Otsuka, Yuki Hasegawa, Hironori Kobayashi, Yasuhiro Takeshima, Kenji Yamada, Yuichi Takami, Tomoko Lee
Publikováno v:
JIMD Reports
JIMD Reports, Vol 48, Iss 1, Pp 19-25 (2019)
JIMD Reports, Vol 48, Iss 1, Pp 19-25 (2019)
Mitochondrial 3‐hydroxy‐3‐methylglutaryl‐CoA synthase deficiency (mHS deficiency) is a rare autosomal recessive inborn error of ketogenesis caused by a mutation in the HMGCS2 gene, which is characterized by non‐(hypo)‐ketotic hypoglycemia
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::94b8018bf9fbb6d4c88856d04266fee6
http://europepmc.org/articles/PMC6606983
http://europepmc.org/articles/PMC6606983
Autor:
Hiroshi Yamaguchi, Noriyuki Nishimura, Kazumi Tomioka, Masahiro Nishiyama, Daisaku Toyoshima, Azusa Maruyama, Yusuke Ishida, Kandai Nozu, Tsukasa Tanaka, Taku Nakagawa, Kazumoto Iijima, Yuichi Takami, Shoichi Tokumoto, Hiroaki Nagase
Publikováno v:
Epilepsy & Behavior. 90:15-19
Although previous studies have investigated the influence of antiepileptic drugs (AEDs) on lipid profiles and thyroid hormone levels, there is little evidence regarding the effects of levetiracetam (LEV). Therefore, we conducted a prospective longitu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8f223abc7e0a247fa76f094de4a51b41
https://hdl.handle.net/20.500.14094/90005739
https://hdl.handle.net/20.500.14094/90005739
Autor:
Yuichi Takami, Taku Nakagawa
Publikováno v:
Braindevelopment. 43(8)
Objective The aim of this study was to assess the risk of recurrence after a first unprovoked seizure in childhood and to explore the correlation between the first and second seizures in recurrent patients. Methods In a prospective study, we included
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::82f925d1470847d1078c0bd5bca6ddfa
https://pubmed.ncbi.nlm.nih.gov/34001397
https://pubmed.ncbi.nlm.nih.gov/34001397
Autor:
Toshiyuki Itai, Satoko Miyatake, Masataka Taguri, Fumihito Nozaki, Masayasu Ohta, Hitoshi Osaka, Masafumi Morimoto, Tomoko Tandou, Fumikatsu Nohara, Yuichi Takami, Fumitaka Yoshioka, Shoko Shimokawa, Jiu Okuno-Yuguchi, Mitsuo Motobayashi, Yuko Takei, Tetsuhiro Fukuyama, Satoko Kumada, Yohane Miyata, Chikako Ogawa, Yuki Maki
Publikováno v:
Journal of Medical Genetics; Aug2021, Vol. 58 Issue 8, p505-513, 9p