Zobrazeno 1 - 10
of 66
pro vyhledávání: '"Takashi Hibiya"'
Autor:
Takahiro Shibayama, Kaishi Satomi, Ryota Tanaka, Akihiko Yoshida, Kiyotaka Nagahama, Akimasa Hayashi, Takashi Hibiya, Kazuharu Suda, Masachika Fujiwara, Junji Shibahara
Publikováno v:
BMC Pulmonary Medicine, Vol 23, Iss 1, Pp 1-6 (2023)
Abstract Background Pulmonary inflammatory leiomyosarcoma (PILMS) is a rare type of myogenic tumor with prominent lymphohistiocytic infiltration. Despite their histological similarities, PILMS is immunohistochemically and genetically distinct from so
Externí odkaz:
https://doaj.org/article/c7c0181bd16c495ca5ef4cd75fad9fdd
Autor:
Takashi Hibiya, Meiro Tanaka, Mai Matsumura, Ayako Aoki, Tadashi Ikegami, Koji Okudela, Naomi Kawano, Kenichi Ohashi
Publikováno v:
Diagnostic Pathology, Vol 15, Iss 1, Pp 1-6 (2020)
Abstract Background Primary malignant melanoma of the lung (PML) is extremely rare. No precursor lesions of PML have been identified, and little is known about the genetic mutations associated with the disease. Typically, 15–20% of malignant melano
Externí odkaz:
https://doaj.org/article/2a1de85d67b641b3a64799cc358ffbc5
Autor:
Takuya Ikeda, Hideyuki Takeuchi, Keita Takahashi, Haruko Nakamura, Misako Kunii, Atsuko Katsumoto, Mikiko Tada, Yuichi Higashiyama, Takashi Hibiya, Shigeaki Suzuki, Ichizo Nishino, Shigeru Koyano, Hiroshi Doi, Fumiaki Tanaka
Publikováno v:
Frontiers in Immunology, Vol 11 (2020)
Chronic tonsillitis has been attracted attention as a source of abnormal immune responses and a possible trigger of autoimmune diseases such as IgA nephritis, IgA vasculitis, palmoplantar pustulosis, psoriasis, rheumatoid arthritis, Behçet’s disea
Externí odkaz:
https://doaj.org/article/e6c1d0ba2a2e40aea0407f6221789b70
Autor:
Takaomi Kessoku, Noritoshi Kobayashi, Masato Yoneda, Yuki Kasai, Anna Ozaki, Naoki Okubo, Michihiro Iwaki, Takashi Kobayashi, Tsutomu Yoshihara, Yusuke Kurita, Yasushi Honda, Motohiko Tokuhisa, Hiroto Ishiki, Takashi Hibiya, Satoshi Fujii, Atsushi Nakajima, Yasushi Ichikawa
Publikováno v:
Frontiers in Oncology, Vol 10 (2020)
Background: Neuroendocrine tumors (NETs) are rare, but their worldwide incidence is gradually increasing. NETs are generally heterogeneous; however, in rare cases, they have been shown to change their phenotype (i.e., nonfunctional to functional or o
Externí odkaz:
https://doaj.org/article/2eb8a6c882d14ce69f1ebbe3db7a698b
Publikováno v:
Human Pathology: Case Reports, Vol 11, Iss , Pp 79-82 (2018)
Pulmonary tumor thrombotic microangiopathy (PTTM) is a rare complication of cancer. It is histologically characterized by fibrocellular intimal proliferation in small pulmonary arteries and arterioles in patients with metastatic carcinoma. It is most
Externí odkaz:
https://doaj.org/article/e47b85c1d42448c58c69117b2efac005
Autor:
Shinsuke AKIYAMA, Mayumi OZAWA, Kazuya NAKAGAWA, Jun WATANABE, Atsushi ISHIBE, Takashi HIBIYA, Itaru ENDO
Publikováno v:
Nihon Rinsho Geka Gakkai Zasshi (Journal of Japan Surgical Association). 82:2246-2251
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3e4baface0fa1ad8ad03fd936fbeeaf3
https://doi.org/10.3919/jjsa.82.2246
https://doi.org/10.3919/jjsa.82.2246
Autor:
Yuji Ogawa, Eiji Sakai, Noriki Kasuga, Leo Taniguchi, Satoru Saito, Atsushi Nakajima, Yasushi Honda, Kenichi Ohashi, Takashi Hibiya, Hiroyuki Kirikoshi, Kento Imajo, Masato Yoneda
Publikováno v:
Kanzo. 61:504-512
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::454d06ebd03dee3dbdd229c0de40b4cf
https://doi.org/10.2957/kanzo.61.504
https://doi.org/10.2957/kanzo.61.504
Autor:
Shigeru Koyano, Hiroshi Doi, Misako Kunii, Ichizo Nishino, Takashi Hibiya, Keita Takahashi, Mikiko Tada, Takuya Ikeda, Hideyuki Takeuchi, Yuichi Higashiyama, Shigeaki Suzuki, Haruko Nakamura, Atsuko Katsumoto, Fumiaki Tanaka
Publikováno v:
Frontiers in Immunology, Vol 11 (2020)
Frontiers in Immunology
Frontiers in Immunology
Chronic tonsillitis has been attracted attention as a source of abnormal immune responses and a possible trigger of autoimmune diseases such as IgA nephritis, IgA vasculitis, palmoplantar pustulosis, psoriasis, rheumatoid arthritis, Behçet’s disea
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fb3ac0578e9bf6fa007fbe954bed39fe
https://www.frontiersin.org/articles/10.3389/fimmu.2020.595480/full
https://www.frontiersin.org/articles/10.3389/fimmu.2020.595480/full
Autor:
Kenichi Ohashi, Takashi Hibiya, Tadashi Ikegami, Meiro Tanaka, Naomi Kawano, Koji Okudela, Ayako Aoki, Mai Matsumura
Publikováno v:
Diagnostic Pathology
Diagnostic Pathology, Vol 15, Iss 1, Pp 1-6 (2020)
Diagnostic Pathology, Vol 15, Iss 1, Pp 1-6 (2020)
Background Primary malignant melanoma of the lung (PML) is extremely rare. No precursor lesions of PML have been identified, and little is known about the genetic mutations associated with the disease. Typically, 15–20% of malignant melanomas posse
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aa0e322346e9974fb47d030fb72523ec
https://doi.org/10.1186/s13000-020-0928-8
https://doi.org/10.1186/s13000-020-0928-8
Succinate dehydrogenase B-deficient renal cell carcinoma: A case report with novel germline mutation
Autor:
Makiko Enaka, Naoko Udaka, Kenichi Ohashi, Hiromichi Iwashita, Kazuhide Makiyama, Koji Okudela, Akio Miyake, Yoji Nagashima, Mai Matsumura, Naomichi Matsumoto, Takashi Hibiya, Noriko Miyake, Masahiro Yao, Shoji Yamanaka, Tomoe Sawazumi
Publikováno v:
Pathology International. 67:585-589
Succinate dehydrogenase-deficient renal cell carcinoma (SDH-deficient RCC) is a newly introduced histological type of RCC, which is caused by loss of subunit genes of SDH. It is known to frequently demonstrate familial occurrence and be frequently as
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5ccd28117710d54d6da5d3025678d25d
https://doi.org/10.1111/pin.12587
https://doi.org/10.1111/pin.12587