Zobrazeno 21 - 30
of 554
pro vyhledávání: '"Yoshikazu Inoue"'
Autor:
Yoshinori Hasegawa, Yasuhiko Nishioka, Shinyu Izumi, Sakae Homma, Yoshikazu Inoue, Takumi Kishimoto, Yutaro Nakamura, Takafumi Suda, Kazuya Ichikado, Takeshi Johkoh, Naoki Hamada, Koichi Hagiwara, Akira Hebisawa, Naohiko Inase, Ryoko Egashira, Kinya Abe, Masaki Okamoto, Motoyasu Kato, Yasuhiro Terasaki, Yuko Toyoda, Tomohisa Baba, Yuji Fujikura, Etsuo Fujita, Tomohiro Handa, Koko Hidaka, Takeshi Hisada, Shu Hisata, Chisato Honjo, Keisuke Miki, Masamichi Mineshita, Susumu Sakamoto, Masaaki Sano, Yoshikazu Tsukada, Mari Yamasue, Yoshimi Bando
Publikováno v:
BMJ Open Respiratory Research, Vol 9, Iss 1 (2022)
Background Diffuse pulmonary ossification is a specific lung condition that is accompanied by underlying diseases. However, idiopathic dendriform pulmonary ossification (IDPO) is extremely rare, and the clinical features remain unclear. In this study
Externí odkaz:
https://doaj.org/article/8c58aad29edf4c72b4c8c6193b072fe5
Autor:
Masaki Hirose, Toru Arai, Chikatoshi Sugimoto, Takayuki Takimoto, Reiko Sugawara, Shojiro Minomo, Sayoko Shintani, Naoko Takeuchi, Kanako Katayama, Yasushi Inoue, Tomoko Kagawa, Takahiko Kasai, Masanori Akira, Yoshikazu Inoue
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 16, Iss 1, Pp 1-10 (2021)
Abstract Background Autoimmune pulmonary alveolar proteinosis (APAP) results from the suppression of granulocyte-macrophage colony-stimulating factor (GM-CSF) signaling by a neutralizing autoantibody against GM-CSF. B cell-activating factor (BAFF) an
Externí odkaz:
https://doaj.org/article/bb8074ba53104c0d8efa7e0a63cef45d
Autor:
Saori Sakaue, Etsuro Yamaguchi, Yoshikazu Inoue, Meiko Takahashi, Jun Hirata, Ken Suzuki, Satoru Ito, Toru Arai, Masaki Hirose, Yoshinori Tanino, Takefumi Nikaido, Toshio Ichiwata, Shinya Ohkouchi, Taizou Hirano, Toshinori Takada, Satoru Miyawaki, Shogo Dofuku, Yuichi Maeda, Takuro Nii, Toshihiro Kishikawa, Kotaro Ogawa, Tatsuo Masuda, Kenichi Yamamoto, Kyuto Sonehara, Ryushi Tazawa, Konosuke Morimoto, Masahiro Takaki, Satoshi Konno, Masaru Suzuki, Keisuke Tomii, Atsushi Nakagawa, Tomohiro Handa, Kiminobu Tanizawa, Haruyuki Ishii, Manabu Ishida, Toshiyuki Kato, Naoya Takeda, Koshi Yokomura, Takashi Matsui, Masaki Watanabe, Hiromasa Inoue, Kazuyoshi Imaizumi, Yasuhiro Goto, Hiroshi Kida, Tomoyuki Fujisawa, Takafumi Suda, Takashi Yamada, Yasuomi Satake, Hidenori Ibata, Nobuyuki Hizawa, Hideki Mochizuki, Atsushi Kumanogoh, Fumihiko Matsuda, Koh Nakata, Tomomitsu Hirota, Mayumi Tamari, Yukinori Okada
Publikováno v:
Nature Communications, Vol 12, Iss 1, Pp 1-6 (2021)
Autoimmune pulmonary alveolar proteinosis (aPAP) is a complex lung disease caused by abnormal surfactant homeostasis. Here, the authors carry out a genome-wide association study of aPAP in a Japanese cohort, finding variants in the MHC and suggesting
Externí odkaz:
https://doaj.org/article/d9a62f084a8e4179916af621aeb86739
Autor:
Yoshinobu Matsuda, Tatsuya Morita, Hirotaka Matsumoto, Keita Hosoi, Kayo Kusama, Yasuo Kohashi, Hiroshi Morishita, Sawako Kaku, Keisukie Ariyoshi, Shunsuke Oyamada, Yoshikazu Inoue, Satoru Iwase, Takuhiro Yamaguchi, Mitsunori Nishikawa
Publikováno v:
Palliative Medicine Reports, Vol 2, Iss 1, Pp 15-20 (2021)
Objective: This study aimed to explore the predictors of morphine efficacy in the alleviation of dyspnea in COPD. Background: Dyspnea is prevalent in patients with chronic obstructive pulmonary disease (COPD) and often persists despite conventional t
Externí odkaz:
https://doaj.org/article/2ff61b0907f44b20a4a12aae5a1258dc
Autor:
Shiomi Yoshida, Tomotada Iwamoto, Takehiko Kobayashi, Ryohei Nomoto, Yoshikazu Inoue, Kazunari Tsuyuguchi, Katsuhiro Suzuki
Publikováno v:
Emerging Infectious Diseases, Vol 26, Iss 11, Pp 2728-2732 (2020)
We report 2 case-patients in Japan with Mycobacterium shigaense pulmonary infections. One patient was given aggressive treatment and the other conservative treatment, according to distinctive radiologic evidence. A close phylogenetic relationship bas
Externí odkaz:
https://doaj.org/article/8d8b0900fa294a8f946287e32fb7b8ef
Autor:
Kanako Katayama, Masaki Hirose, Toru Arai, Kazuyoshi Hatsuda, Kazunobu Tachibana, Reiko Sugawara, Chikatoshi Sugimoto, Takahiko Kasai, Masanori Akira, Yoshikazu Inoue
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 15, Iss 1, Pp 1-10 (2020)
Abstract Background Anti-granulocyte–macrophage colony-stimulating factor autoantibody (GMAb) has been recognized as a diagnostic biomarker for autoimmune pulmonary alveolar proteinosis (aPAP). The aims of this study were to know the incidence of i
Externí odkaz:
https://doaj.org/article/19e90e6dc2a34a78bbb4261c085374ff
Autor:
Toru Arai, Masaki Hirose, Yoshimasa Hamano, Tomoko Kagawa, Akihiro Murakami, Hiroshi Kida, Atsushi Kumanogoh, Yoshikazu Inoue
Publikováno v:
Canadian Respiratory Journal, Vol 2022 (2022)
Background. We have previously analysed serum autoantibody levels in patients with idiopathic pulmonary fibrosis (IPF), idiopathic nonspecific interstitial pneumonia (iNSIP), and healthy controls and identified the autoantibody against anti-myxovirus
Externí odkaz:
https://doaj.org/article/399ed16bea414b94b3e41a22fda9dec8
Autor:
Takehiko Kobayashi, Kazunari Tsuyuguchi, Shiomi Yoshida, Yu Kurahara, Shojiro Minomo, Yoshikazu Inoue, Katsuhiro Suzuki
Publikováno v:
International Journal of Mycobacteriology, Vol 9, Iss 1, Pp 76-82 (2020)
Background: Mycobacteroides abscessus complex (MABC) exhibits smooth morphotypes, expressing glycopeptidolipid (GPL), and rough morphotypes, expressing diminished GPL, on the MABC cell wall. Few reports have focused on the relationship between anti-G
Externí odkaz:
https://doaj.org/article/110a69442b614bdbbb815c6dac1f6dd5
Autor:
Yoshikazu Inoue, Toru Arai, Hiroshi Kida, Yoshitaka Ogata, Hiroto Matsuoka, Suguru Yamamoto, Masahide Mori, Chikatoshi Sugimoto, Kazunobu Tachibana, Masanori Akira, Masaki Hirose, Kazuyoshi Hatsuda
Publikováno v:
BMJ Open Respiratory Research, Vol 8, Iss 1 (2021)
Background Acute exacerbation (AE) has been reported to herald a poor prognosis in idiopathic pulmonary fibrosis and is now thought to do so in idiopathic interstitial pneumonias (IIPs). However, the pathophysiology of AE-IIPs is not sufficiently und
Externí odkaz:
https://doaj.org/article/f7e316e6ea8a4eb4858e64d4a35c0955
Autor:
Fuminori Mizukoshi, Nobuyuki Kobayashi, Fumiko Kirikae, Ken Ohta, Kazunari Tsuyuguchi, Noritaka Yamada, Yoshikazu Inoue, Masahide Horiba, Noriko Kawata, Akiko Ichinose, Tohru Miyoshi-Akiyama, Reiko Kiritani, Keiji Funatogawa, Teruo Kirikae
Publikováno v:
mSphere, Vol 6, Iss 4 (2021)
The incidence rate of tuberculosis (TB) in Japan was 11.5 per 100,000 of the population in 2019. Of TB patients in Japan, 61.1% were aged >70 years, and 10.7% were born outside Japan, mostly in Asian countries with a high burden of tuberculosis.
Externí odkaz:
https://doaj.org/article/7c105a6b9e094f028e6d69aec0d99a65