Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Akira Manki"'
Publikováno v:
Life, Vol 11, Iss 12, p 1433 (2021)
The aim of this study is to describe bilateral optic disc swelling in three consecutive patients with Blau syndrome or cryopyrin-associated periodic syndrome at a single institution. Case 1 was a 30-year-old woman receiving 25 mg etanercept twice wee
Externí odkaz:
https://doaj.org/article/be6532a4ab064fb594e4fbddad662fef
Autor:
Akira Manki, Ryuta Nishikomori, Mami Nakata-Hizume, Taiji Kunitomi, Syuji Takei, Tomoko Urakami, Tsuneo Morishima
Publikováno v:
Allergology International, Vol 55, Iss 3, Pp 337-341 (2006)
Background: We report two cases of tumor necrosis factor receptor-associated periodic syndrome (TRAPS) in patients in whom systemic juvenile idiopathic arthritis (JIA) had initially been diagnosed or suspected. One patient, given a diagnosis of syste
Externí odkaz:
https://doaj.org/article/aa4d88830bfc4b09bf630705209a871c
Autor:
Tsuneo Morishima, Mitsuru Tsuge, Akira Manki, Michiko Yamamoto, Kei Takemoto, Masato Yashiro, Kozo Yasui
Publikováno v:
Arthritis & Rheumatism. 62:250-257
Objective Early-onset sarcoidosis (EOS), which occurs in children younger than 5 years of age, is associated with granulomatous lesions and a sporadic genetic mutation of the nucleotide-binding oligomerization domain 2 that causes constitutive NF-κB
Autor:
Syuji Takei, Ryuta Nishikomori, Mami Nakata-Hizume, Tsuneo Morishima, Taiji Kunitomi, Tomoko Urakami, Akira Manki
Publikováno v:
Allergology International, Vol 55, Iss 3, Pp 337-341 (2006)
Background We report two cases of tumor necrosis factor receptor-associated periodic syndrome (TRAPS) in patients in whom systemic juvenile idiopathic arthritis (JIA) had initially been diagnosed or suspected. One patient, given a diagnosis of system
Autor:
Yasuhiko Yoshinaga, Shinya Miyoshi, T. Aita, Susumu Nishiyama, Michio Toda, Yoshiki Yoshihara, Akira Manki, Hiroki Kishimoto, Shoji Miyawaki
Publikováno v:
Rheumatology International. 32:2569-2571
We proposed a method of regional assessment in patients with rheumatoid arthritis. The utility of this method was demonstrated by assessing drug efficacy in patients who received infliximab (n = 31) or tocilizumab (n = 6). Joints were divided into fo
Autor:
Ritsuo Nishiuchi, Akira Manki, Yoshiki Seino, Megumi Oda, Chie Endo, Nobuko Yamashita, Naohiro Eguchi, Yoshie Tomiyama
Publikováno v:
Cancer. 91:1568-1573
BACKGROUND In the current study, the authors report a 4 year old girl with disseminated retinoblastoma. To find sensitive and specific molecular markers for detection of retinoblastoma cells in blood and marrow, the authors evaluated three photorecep
Autor:
Mitsuru Tsuge, Tsuneo Morishima, Akira Manki, Kozo Yasui, Y. Kondo, Masato Yashiro, Yoshiharu Nagaoka, Tomoaki Wada
Publikováno v:
International journal of immunopathology and pharmacology. 22(3)
Thalidomide is an effective drug for chronic inflammatory diseases, but the mechanism underlying its immunomodulatory action remains uncertain. Thalidomide has been reported to clinically improve chronic inflammatory granulomatous disorders. In such
Autor:
Tomoaki Wada, Akira Manki, Kousuke Chayama, Nobuko Yamashita, Naoto Morishita, Kazunari Yamaguchi, Megumi Oda, Takako Miyamura, Kana Washio, Tsuneo Morishima, Toshiaki Ishida
Publikováno v:
Pediatric transplantation. 12(5)
CAEBV is a high mortality and morbidity disease with life-threatening complications. Nevertheless, the treatment regimens for CAEBV have not yet been established. Although some reports have described CAEBV therapy involving treatments such as antivir
Autor:
Tomoko, Urakami, Akira, Manki, Takuya, Inoue, Megumi, Oda, Hiroyuki, Tanaka, Tsuneo, Morishima
Publikováno v:
The Journal of rheumatology. 33(5)
Serum cartilage oligomeric matrix protein (COMP) concentration is elevated in patients with early osteoarthritis and early rheumatoid arthritis, and may be a biomarker of cartilage turnover. We investigated whether serum COMP concentration could be a
Autor:
Sonoko Nagai, Atsushi Utani, Yoshihiko Sakurai, Akihiko Fuji, Ryuta Nishikomori, Naotomo Kambe, Takenosuke Yuasa, Ikuo Okafuji, Hiroyuki Tsutsumi, Akira Manki, Ikuma Fujiwara, Tatsutoshi Nakahata, Chikako Nishigori, Hiroko Kobayashi, Toshio Heike, Nobuo Kanazawa, Mitsuru Nakajima, Mami Nakata-Hizume, Yoshiki Miyachi
Publikováno v:
Blood. 105(3)
Early-onset sarcoidosis (EOS) and inheritable Blau syndrome (BS) share characteristic clinical features of juvenile-onset systemic granulomatosis syndrome that mainly affects skin, joints, and eyes. However, no direct evidence has been shown for the