Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Takuro Imamoto"'
Autor:
Kentaro Okamoto, Hajime Yokota, Kazuyuki Matsushita, Takashi Uno, Koichiro Tatsumi, Akira Nishiyama, Yoshihito Ozawa, Takuji Suzuki, Jun Ikari, Megumi Katsumata, Akira Urano, Takuro Imamoto, Yuri Suzuki, Kojiro Ono, Eriko Abe, Tomoko Kamata, Shota Fujii, Kenichiro Okumura, Joji Ota, Eiko Suzuki, Naoko Kawata, Yoshitada Masuda, Seiichiro Sakao
Publikováno v:
BMJ Open Respiratory Research, Vol 11, Iss 1 (2024)
Introduction To date, there is limited evidence on the effects of bronchodilators on respiratory dynamics in chronic obstructive pulmonary disease (COPD). Dynamic chest radiography (DCR) is a novel radiographic modality that provides real-time, objec
Externí odkaz:
https://doaj.org/article/28ef5d6917464cdba85609074c271729
Autor:
Keiichiro Yoshioka, Hironori Sato, Takeshi Kawasaki, Daisuke Ishii, Takuro Imamoto, Mitsuhiro Abe, Yoshinori Hasegawa, Osamu Ohara, Koichiro Tatsumi, Takuji Suzuki
Publikováno v:
Frontiers in Medicine, Vol 9 (2022)
BackgroundSarcoidosis is a granulomatous systemic disease of unknown etiology. Mononuclear cells such as macrophages or lymphocytes in lung tissue and hilar or mediastinal lymph nodes have been recognized to play an essential role in granuloma format
Externí odkaz:
https://doaj.org/article/d98a14b26e7246d68e687de112211411
Autor:
Takahiro Arano, Takuro Imamoto, Rika Suda, Hajime Kasai, Toshihiko Sugiura, Ayako Shigeta, Keiko Yamamoto, Jun Nagata, Seiichiro Sakao, Nobuhiro Tanabe, Koichiro Tatsumi
Publikováno v:
Respiratory Medicine Case Reports, Vol 32, Iss , Pp 101352- (2021)
Heritable pulmonary arterial hypertension (HPAH) is a type of familial pulmonary arterial hypertension, while pulmonary arteriovenous malformations (PAVMs) are abnormal communications between pulmonary arteries and veins that occur frequently in pati
Externí odkaz:
https://doaj.org/article/3ddd430332bb497d900478bc3d5a7b3e
Autor:
Takuro Imamoto, Koichiro Tatsumi, Keiko Yamamoto, Toshihiko Sugiura, Rika Suda, Takahiro Arano, Ayako Shigeta, Hajime Kasai, Seiichiro Sakao, Jun Nagata, Nobuhiro Tanabe
Publikováno v:
Respiratory Medicine Case Reports, Vol 32, Iss, Pp 101352-(2021)
Respiratory Medicine Case Reports
Respiratory Medicine Case Reports
Heritable pulmonary arterial hypertension (HPAH) is a type of familial pulmonary arterial hypertension, while pulmonary arteriovenous malformations (PAVMs) are abnormal communications between pulmonary arteries and veins that occur frequently in pati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2b6594609c0ab81183c6c50fec52cad1
https://doi.org/10.1016/j.rmcr.2021.101352
https://doi.org/10.1016/j.rmcr.2021.101352