Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Misaki Yamadera"'
Autor:
Misaki Yamadera, Toshio Saito, Masakazu Shinohara, Hisahide Nishio, Shigeo Murayama, Harutoshi Fujimura
Publikováno v:
Neuropathology. 42:141-146
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e6b8d42dd6841a5b7f5179e25e80aa6f
https://doi.org/10.1111/neup.12784
https://doi.org/10.1111/neup.12784
Publikováno v:
Journal of Medical Cases
Encephalitis is very rare, but often fatal immune-related adverse event (irAE) of immune checkpoint inhibitors (ICIs). A 65-year-old Japanese woman was admitted to our hospital because of general fatigue, chillness and high-grade fever for 4 days, 8
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ca0f97dd5f0ae7f123584ac94a0d86d0
https://doi.org/10.14740/jmc3748
https://doi.org/10.14740/jmc3748
Autor:
Misaki Yamadera, Tomoko Okazaki, Takehiko Yanagihara, Kazuo Nakamichi, Kazuo Hashikawa, Hiromi Tsuji, Fukuko Nishida, Yasuko Sugiyama, Yoko Ooka, Daichi Kodama
Publikováno v:
Rinsho Shinkeigaku. 61:833-838
Progressive multifocal leukoencephalopathy (PML) is a rare opportunistic infection caused by JC virus (JCV) activation. We report an 85-years old man who had been diagnosed to have rheumatoid arthritis (RA) 1.5 years prior to diagnosis of PML, and ha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c772b44a716421c2bd86540b646c7932
https://doi.org/10.5692/clinicalneurol.cn-001622
https://doi.org/10.5692/clinicalneurol.cn-001622
Autor:
Misaki Yamadera, Goichi Beck, Makoto Hideshima, Eiichi Morii, Hiroshi Tsuda, Shigeo Murayama, Harutoshi Fujimura, Yuichi Motoyama, Keita Kakuda, Hideki Mochizuki, Seiichi Nagano, Kensuke Ikenaka
Publikováno v:
Neuropathology. 40:191-195
We report an autopsy case of amyotrophic lateral sclerosis with L126S mutation in the superoxide dismutase 1 (SOD1) gene (SOD1). The patient was a 69-year-old Japanese man without relevant family history, who initially presented with slow progressive
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::09be845ebb0c84e43cf5d00c6ea6628d
https://doi.org/10.1111/neup.12620
https://doi.org/10.1111/neup.12620
Autor:
Yuri Shimizu, Saburo Sakoda, Misa Matsui, Misaki Yamadera, Masaru Yokoe, Harutoshi Fujimura, Itsuko Nakamichi
Publikováno v:
Neuropathology. 39:404-410
We investigated two autopsy cases of mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS) using immunohistochemical staining with an anti-mitochondrial antibody against translocase of the outer membrane 20 (TOMM20
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::12a8ed48a4559df3ed5b7d5a66d68f8e
https://doi.org/10.1111/neup.12593
https://doi.org/10.1111/neup.12593
Autor:
Yogik Onky Silvana Wijaya, Hiroyuki Awano, Tomohiro Chiyonobu, Toshio Saito, Kentaro Okamoto, Poh San Lai, Emma Tabe Eko Niba, Yasuhiro Takeshima, Hisahide Nishio, Takenori Tozawa, Misaki Yamadera, Masakazu Shinohara
Publikováno v:
Braindevelopment. 43(2)
Background Spinal muscular atrophy (SMA) is a neuromuscular disease caused by homozygous deletion of SMN1 exons 7 and 8. However, exon 8 is retained in some cases, where SMN2 exon 7 recombines with SMN1 exon 8, forming a hybrid SMN gene. It remains u
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::329888f5a4e88aac7dfd3b1b1e96cc8a
https://pubmed.ncbi.nlm.nih.gov/33036822
https://pubmed.ncbi.nlm.nih.gov/33036822
Autor:
Toshio Saito, Misaki Yamadera, Harutoshi Fujimura, Yasutoshi Koga, Saburo Sakoda, Misa Matsui
Publikováno v:
Neurology and Clinical Neuroscience. 7:344-346
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::31c7514c9affcc2da234b4078d9694f4
https://doi.org/10.1111/ncn3.12325
https://doi.org/10.1111/ncn3.12325
Autor:
Yasushi Oya, Akihiko Ishiyama, Misaki Yamadera, Yoshihiko Saito, Aritoshi Iida, Ichizo Nishino, Satoru Noguchi, Hiroshi Sakiyama, Atsuko Nishikawa, Madoka Mori-Yoshimura, Takashi Kanda, Shinichiro Hayashi, Ikuya Nonaka, Seigo Nakamura, Susumu Fujikawa, Hirofumi Komaki
Publikováno v:
Neurology. 95(11)
ObjectiveTo elucidate the prevalence of Japanese ADSSL1 myopathy and determine the clinicopathologic features of the disease.MethodsWe searched for ADSSL1 variants in myopathic patients from January 1978 to March 2019 in our repository and assessed t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9e12ce634357f1c491527cf51fbf467e
https://pubmed.ncbi.nlm.nih.gov/32646962
https://pubmed.ncbi.nlm.nih.gov/32646962
Autor:
Misa Matsui, Takuyuki Endo, Chiaki Mori, Yuhei Hasuike, Misaki Yamadera, Michiyo Koroyasu, Saburo Sakoda, Harutoshi Fujimura
Publikováno v:
Medical hypotheses. 134
Intestinal dysbiosis refers to an imbalance in the intestinal flora. The concept of small intestinal bacterial overgrowth (SIBO), a condition of abnormal proliferation of the small intestine microbiota, has been proposed as a form of small intestine
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::02347e5acb2df0c2d55a89c43623a3c1
https://pubmed.ncbi.nlm.nih.gov/31678900
https://pubmed.ncbi.nlm.nih.gov/31678900
Autor:
Misaki Yamadera, Harutoshi Fujimura
Publikováno v:
Neuropathology. 40:116-117
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::13659b6a774728d1eeec6180de9cd3f8
https://doi.org/10.1111/neup.12618
https://doi.org/10.1111/neup.12618