Zobrazeno 1 - 10
of 169
pro vyhledávání: '"Masanori AKIRA"'
Autor:
Masanori Akira, Narufumi Suganuma
Publikováno v:
Health Sciences Review, Vol 11, Iss , Pp 100167- (2024)
The inhalation of hard metal may produce various respiratory manifestations including upper respiratory tract irritation, asthma, hypersensitivity pneumonia (HP), and a particular form of interstitial lung disease. Co is the main cause of the adverse
Externí odkaz:
https://doaj.org/article/5495960d67a943bca901ef435c9db52f
Autor:
Masanori Akira, Narufumi Suganuma
Publikováno v:
Canadian Respiratory Journal, Vol 2024 (2024)
Objectives. The purpose of this study was to retrospectively assess cystic changes in findings on follow-up CT scans of patients with fibrotic nonspecific interstitial pneumonia (NSIP). Methods. The initial and last high-resolution CT scans of 58 pat
Externí odkaz:
https://doaj.org/article/5a197e68f5ba490ca0b8886abe4a8486
Autor:
Kazunobu Tachibana, Masanori Akira, Toru Arai, Chikatoshi Sugimoto, Seiji Hayashi, Yoshikazu Inoue
Publikováno v:
Canadian Respiratory Journal, Vol 2023 (2023)
Background. Pulmonary sarcoidosis predominantly affects the upper lung zones but sometimes affects the lower lung zones. We hypothesised that patients with lower lung zone-dominant sarcoidosis had lower baseline forced vital capacity, progressive res
Externí odkaz:
https://doaj.org/article/f21878b961ed4e5e866a5cad146f6bc2
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:
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:
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:
Yoshikazu Inoue, Satoshi Marumo, Toru Arai, Hiroshi Kida, Yoshitaka Ogata, Hiroto Matsuoka, Iwao Gohma, Suguru Yamamoto, Masahide Mori, Chikatoshi Sugimoto, Kazunobu Tachibana, Masanori Akira
Publikováno v:
BMJ Open Respiratory Research, Vol 7, Iss 1 (2020)
Background Acute exacerbation (AE) in idiopathic pulmonary fibrosis and other idiopathic interstitial pneumonias (IIPs) are poor prognostic events although they are usually treated with conventional therapy with corticosteroids and immunosuppressants
Externí odkaz:
https://doaj.org/article/2dfdc477e62d4eb29b84817d944cbcf1
Autor:
Shinji Futami, Toru Arai, Masaki Hirose, Chikatoshi Sugimoto, Naoya Ikegami, Masanori Akira, Takahiko Kasai, Masanori Kitaichi, Seiji Hayashi, Yoshikazu Inoue
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 13, Iss 1, Pp 1-9 (2018)
Abstract Background Lymphangioleiomyomatosis (LAM) and connective tissue diseases (CTDs) occur more frequently among women than men. We investigated the frequency of comorbid CTD and positive serum autoantibody findings in patients with LAM. Methods
Externí odkaz:
https://doaj.org/article/2f849e71a3074949b67fd7d245e09554
Autor:
Masaki Hirose, Akiko Matsumuro, Toru Arai, Chikatoshi Sugimoto, Masanori Akira, Masanori Kitaichi, Lisa R Young, Francis X McCormack, Yoshikazu Inoue
Publikováno v:
PLoS ONE, Vol 14, Iss 2, p e0212776 (2019)
BackgroundIn lymphangioleiomyomatosis (LAM), tuberous sclerosis gene mutations activate the mechanistic target of the rapamycin pathway, resulting in vascular endothelial growth factor-D (VEGF-D) overproduction. While the utility of serum VEGF-D test
Externí odkaz:
https://doaj.org/article/6db2a1fd9f1a469ba22ca984cf73584d
Autor:
Masanori Akira, Narufumi Suganuma
Publikováno v:
Clinical Imaging. 97:28-33
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f7d25f660c78bf2d99ad07abc6020808
https://doi.org/10.1016/j.clinimag.2023.02.010
https://doi.org/10.1016/j.clinimag.2023.02.010