Zobrazeno 1 - 10
of 145
pro vyhledávání: '"Michio, Ozeki"'
Autor:
Ayaka Yagasaki, Taishi Miyase, Shota Sakai, Kiyofumi Mochizuki, Hirokazu Sakaguchi, Teiji Yagasaki, Naoyuki Ohe, Shiho Yasue, Saori Endo, Michio Ozeki
Publikováno v:
Case Reports in Ophthalmology, Vol 14, Iss 1, Pp 613-619 (2023)
Introduction: Acute acquired comitant esotropia (AACE) is an acquired strabismus with uncrossed sudden-onset diplopia due to esodeviation, comitant esotropia without accommodation factor, or paretic eye movement. The diagnosis of AACE entails differe
Externí odkaz:
https://doaj.org/article/f96efbae2aa641fda56a1aa407b23bf7
Autor:
Michio Ozeki, Saori Endo, Shiho Yasue, Akifumi Nozawa, Ryuta Asada, Akiko M. Saito, Hiroya Hashimoto, Takumi Fujimura, Yohei Yamada, Tatsuo Kuroda, Shigeru Ueno, Shoji Watanabe, Shunsuke Nosaka, Mikiko Miyasaka, Akihiro Umezawa, Kentaro Matsuoka, Takanobu Maekawa, Satoshi Hirakawa, Taizo Furukawa, Shigehisa Fumino, Tatsuro Tajiri, Junkichi Takemoto, Ryota Souzaki, Yoshiaki Kinoshita, Akihiro Fujino
Publikováno v:
Frontiers in Medicine, Vol 11 (2024)
IntroductionIntractable lymphatic anomalies (LAs) include cystic lymphatic malformation (LM; macrocystic, microcystic, or mixed), generalized lymphatic anomaly, and Gorham–Stout disease. LAs can present with severe symptoms and poor prognosis. Thus
Externí odkaz:
https://doaj.org/article/75d954cef4394ed4b3e0cce1df803598
Publikováno v:
PLoS ONE, Vol 19, Iss 5, p e0289187 (2024)
Recently, a low-level somatic mutation in the NRAS gene (c.182 A > G, Q61R) was identified in various specimens from patients with kaposiform lymphangiomatosis. However, it is unknown how these low-frequency mutated cells can affect the characterizat
Externí odkaz:
https://doaj.org/article/d31c1228fc8548449b7d24956c69a887
Autor:
Azusa Haba, Yuko Imaizumi, Daichi Hayashi, Shiho Yasue, Hiroki Otsuka, Saori Endo, Michio Ozeki, Kazuhiro Kobayashi, Tatsuhiko Miyazaki, Akira Hara, Hidenori Ohnishi
Publikováno v:
Hematology, Vol 28, Iss 1 (2023)
ABSTRACTBackground Transient abnormal myelopoiesis (TAM) is characterized by leukocytosis with increased circulating megakaryoblasts that harbor N-terminal truncating mutations in the GATA1 gene. Approximately 10% of affected patients experience earl
Externí odkaz:
https://doaj.org/article/d41750bc1a3346248b64fb0dc059783b
Autor:
Yumiko Hori, Katsutoshi Hirose, Michio Ozeki, Kenji Hata, Daisuke Motooka, Shinichiro Tahara, Takahiro Matsui, Masaharu Kohara, Hiroki Higashihara, Yusuke Ono, Kaishu Tanaka, Satoru Toyosawa, Eiichi Morii
Publikováno v:
Diagnostic Pathology, Vol 17, Iss 1, Pp 1-7 (2022)
Abstract Background Fibro-adipose vascular anomaly (FAVA) is a rare and new entity of vascular anomaly. Activating mutations in the phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha (PIK3CA) gene were identified at a frequency of
Externí odkaz:
https://doaj.org/article/b3aeca8a4e6c408cb4fa27d6fd3e1461
Autor:
Michio Ozeki, Yoko Aoki, Akifumi Nozawa, Shiho Yasue, Saori Endo, Yumiko Hori, Kentaro Matsuoka, Tetsuya Niihori, Ryo Funayama, Matsuyuki Shirota, Keiko Nakayama, Toshiyuki Fukao
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 14, Iss 1, Pp 1-9 (2019)
Abstract Background Kaposiform lymphangiomatosis (KLA) has recently been distinguished as a novel subtype of generalized lymphatic anomaly (GLA) with foci of spindle endothelial cells. All cases of KLA involve multiple organs and have an unfavorable
Externí odkaz:
https://doaj.org/article/b6246cfbeb3548eaa352aee6bbce0d20
Autor:
Michio Ozeki, Akifumi Nozawa, Shiho Yasue, Saori Endo, Ryuta Asada, Hiroya Hashimoto, Toshiyuki Fukao
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 14, Iss 1, Pp 1-11 (2019)
Abstract Background Lymphatic anomalies (LAs) include several disorders in which abnormal lymphatic tissue invades the neck, chest, and various organs. Progressive cases may result in lethal outcomes and have proven difficult to treat. Sirolimus is s
Externí odkaz:
https://doaj.org/article/9f0ff69589884d61b4c689b73199a608
Autor:
Michio Ozeki, Ryuta Asada, Akiko M. Saito, Hiroya Hashimoto, Takumi Fujimura, Tatsuo Kuroda, Shigeru Ueno, Shoji Watanabe, Shunsuke Nosaka, Mikiko Miyasaka, Akihiro Umezawa, Kentaro Matsuoka, Takanobu Maekawa, Yohei Yamada, Akihiro Fujino, Satoshi Hirakawa, Taizo Furukawa, Tatsuro Tajiri, Yoshiaki Kinoshita, Ryota Souzaki, Toshiyuki Fukao
Publikováno v:
Regenerative Therapy, Vol 10, Iss , Pp 84-91 (2019)
Introduction: Lymphatic anomalies (LAs) refer to a group of diseases involving systemic dysplasia of lymphatic vessels. These lesions are classified as cystic lymphatic malformation (macrocystic, microcystic or mixed), generalized lymphatic anomaly,
Externí odkaz:
https://doaj.org/article/aa99aea173204b3ea66d135e1f78b560
Autor:
Yumiko Hori, Katsutoshi Hirose, Michio Ozeki, Kenji Hata, Daisuke Motooka, Shinichiro Tahara, Takahiro Matsui, Masaharu Kohara, Hiroki Higashihara, Yusuke Ono, Kaishu Tanaka, Satoru Toyosawa, Eiichi Morii
Publikováno v:
Diagnostic Pathology, Vol 17, Iss 1, Pp 1-1 (2022)
Externí odkaz:
https://doaj.org/article/240b78e67d6b429ca0bb864a6c053290
Autor:
Daiki Nagao, Michio Ozeki, Akifumi Nozawa, Shiho Yasue, Hideo Sasai, Saori Endo, Takazumi Kato, Yumiko Hori, Hidenori Ohnishi
Publikováno v:
Journal of Pediatric Hematology/Oncology. 45:e384-e388