Zobrazeno 1 - 10
of 57
pro vyhledávání: '"Tadashi Matsubayashi"'
Autor:
Takayuki Miyamoto, Yoshitaka Honda, Kazushi Izawa, Nobuo Kanazawa, Saori Kadowaki, Hidenori Ohnishi, Masakazu Fujimoto, Naotomo Kambe, Naoya Kase, Takeshi Shiba, Yasuo Nakagishi, Shuji Akizuki, Kosaku Murakami, Masahiro Bamba, Yutaka Nishida, Ayano Inui, Tomoo Fujisawa, Daisuke Nishida, Naomi Iwata, Yoshikazu Otsubo, Shingo Ishimori, Momoko Nishikori, Kiminobu Tanizawa, Tomoyuki Nakamura, Takeshi Ueda, Yoko Ohwada, Yu Tsuyusaki, Masaki Shimizu, Takasuke Ebato, Kousho Iwao, Akiharu Kubo, Toshinao Kawai, Tadashi Matsubayashi, Tatsuhiko Miyazaki, Tomohiro Kanayama, Masahiko Nishitani-Isa, Hiroshi Nihira, Junya Abe, Takayuki Tanaka, Eitaro Hiejima, Satoshi Okada, Osamu Ohara, Megumu K. Saito, Junko Takita, Ryuta Nishikomori, Takahiro Yasumi
Publikováno v:
Frontiers in Immunology, Vol 13 (2022)
PurposeUpregulation of type I interferon (IFN) signaling has been increasingly detected in inflammatory diseases. Recently, upregulation of the IFN signature has been suggested as a potential biomarker of IFN-driven inflammatory diseases. Yet, it rem
Externí odkaz:
https://doaj.org/article/5700023cf0774dc68dac5c83825a3a61
Publikováno v:
Modern Rheumatology Case Reports; Jul2024, Vol. 8 Issue 2, p357-360, 4p
Autor:
Hidehiko Narazaki, Shinji Akioka, Yuko Akutsu, Mariko Araki, Mikiya Fujieda, Daisuke Fukuhara, Ryoki Hara, Kunio HashimotoDepartment of Pediatrics,Nagasaki University Graduate School of Biomedical Sciences,Nagasaki, Japan, Seira Hattori, Ren Hayashibe, Tomoyuki Imagawa, Yuzaburo Inoue, Hiroyuki Ishida, Shuici Ito, Yasuhiko Itoh, Tomohiro Kawabe, Toshiyuki Kitoh, Ichiro Kobayashi, Tadashi Matsubayashi, Takako Miyamae
Publikováno v:
Modern Rheumatology; Sep2023, Vol. 33 Issue 5, p1021-1029, 9p
Augmentation of Stimulator of Interferon Genes–Induced Type I Interferon Production in COPA Syndrome
Autor:
Takashi Orimo, Junko Takita, Hidenori Nakamura, Masaki Yamamoto, Kyoichi Isono, Toshiaki Miyamoto, Takashi Kato, Kohei Murakami, Tsuneyasu Kaisho, Tadashi Matsubayashi, Yuri Fukuda-Ohta, Hiroaki Hemmi, Yoshiro Otsuki, Yoshitaka Honda, Saki Takayama, Kazushi Izawa, Izumi Sasaki, Takahiro Yasumi, Ryuta Nishikomori
Publikováno v:
Arthritis & Rheumatology. 73:2105-2115
OBJECTIVE Coatomer subunit alpha (COPA) syndrome, also known as autoinflammatory interstitial lung, joint, and kidney disease, is caused by heterozygous mutations in COPA. We identified a novel COPA variant in 4 patients in one family. We undertook t
Publikováno v:
Cureus.
Autor:
Hidehiko Narazaki, Shinji Akioka, Yuko Akutsu, Mariko Araki, Mikiya Fujieda, Daisuke Fukuhara, Ryoki Hara, Kunio Hashimoto, Seira Hattori, Ren Hayashibe, Tomoyuki Imagawa, Yuzaburo Inoue, Hiroyuki Ishida, Shuici Ito, Yasuhiko Itoh, Tomohiro Kawabe, Toshiyuki Kitoh, Ichiro Kobayashi, Tadashi Matsubayashi, Takako Miyamae, Mao Mizuta, Masaaki Mori, Ayako Murase, Yasuo Nakagishi, Koji Nagatani, Naoko Nakano, Toyoki Nishimura, Tomo Nozawa, Nami Okamoto, Yuka Okura, Hiromi Sawada, Emi Sawanobori, Yuko Sugita, Yujiro Tanabe, Minako Tomiita, Ken-ichi Yamaguchi, Ryuhei Yasuoka, Koji Yokoyama
Publikováno v:
Modern Rheumatology.
Objectives Although epidemiological surveys of paediatric rheumatic diseases in Japan have been conducted, they were single surveys with no continuity. This is the first report of the Pediatric Rheumatology Association of Japan registry database, whi
Successful Hematopoietic Stem Cell Transplantation for Autosomal Recessive STAT1 Complete Deficiency
Publikováno v:
Journal of Clinical Immunology
Autor:
Jacinta Bustamante, Tomohiro Morio, Masao Kobayashi, Tom Le Voyer, Tsubasa Okano, Reiko Kagawa, Jean-Laurent Casanova, Tadashi Matsubayashi, Moe Tamaura, Takuya Naruto, Sonoko Sakata, Shiho Nishimura, Satoshi Okada, Yoko Mizoguchi, Miyuki Tsumura, Osamu Ohara, Shunsuke Kimura, Shuhei Karakawa, Kohsuke Imai
Publikováno v:
International Immunology. 32:663-671
Autosomal recessive (AR) complete signal transducer and activator of transcription 1 (STAT1) deficiency is an extremely rare primary immunodeficiency that causes life-threatening mycobacterial and viral infections. Only seven patients from five unrel
Autor:
Nao Wakuta, Tadashi Matsubayashi, Keiko Oba, Hiromi Nakashima, Ken Suzuki, Toshika Okumiya, Midori Ishibashi, Masafumi Koga
Publikováno v:
Annals of Clinical & Laboratory Science; Jan/Feb2023, Vol. 53 Issue 1, p134-139, 6p
Publikováno v:
Journal of Infection and Chemotherapy. 26:1070-1072
Mycobacterium malmoense is a nontuberculous mycobacteria (NTM), that is uncommon in areas other than Northern Europe. We describe the case of mediastinal lymphadenitis caused by M. malmoense in a 4-year-old boy who has a past medical history of disse