Zobrazeno 1 - 10
of 60
pro vyhledávání: '"Saori Endo"'
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:
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:
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::951d3cd7e27a9d22b60d14f638a0abd1
https://doi.org/10.1097/mph.0000000000002597
https://doi.org/10.1097/mph.0000000000002597
Autor:
Natsuki, Ishikawa, Kenya, Kamimura, Saori, Endo, Soichi, Ishii, Kazuya, Ogawa, Norihiro, Sakai, Hiroyuki, Abe, Masayoshi, Ko, Osamu, Shibata, Youhei, Koseki, Junji, Yokoyama, Akira, Sakamaki, Shuji, Terai
Publikováno v:
Internal Medicine. 61:3233-3237
Regarding the prognosis of cases with advanced-stage hepatocellular carcinoma (HCC), a recent clinical study showed that the immune checkpoint inhibitors atezolizumab plus bevacizumab have superior efficacy to sorafenib. However, only a few reports h
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5d899cf0567bc858f575a3a52aa29b87
https://doi.org/10.2169/internalmedicine.9341-22
https://doi.org/10.2169/internalmedicine.9341-22
Autor:
Toru, Ishikawa, Michitaka, Imai, Saori, Endo, Motoi, Azumi, Yujiro, Nozawa, Akito, Iwanaga, Tomoe, Sano, Terasu, Honma, Toshiaki, Yoshida
Publikováno v:
Annals of Palliative Medicine. 11:1954-1960
Interventional radiology (IVR), including balloon-occluded retrograde transvenous obliteration (BRTO) and percutaneous transhepatic obliteration (PTO), is performed for patients with intractable hepatic encephalopathy (HE). However, information on th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6343873c5a99e83979355ae3920d1d54
https://doi.org/10.21037/apm-21-2594
https://doi.org/10.21037/apm-21-2594
Autor:
Shiho, Yasue, Michio, Ozeki, Saori, Endo, Tomohiro, Kanayama, Natsuko, Suzui, Sayaka, Nakamura, Kenji, Kishimoto, Yoshiyuki, Kosaka, Tatsuhiko, Miyazaki, Yusuke, Demizu, Toshinori, Soejima, Atsufumi, Kawamura, Hidenori, Ohnishi
Publikováno v:
Journal of Pediatric Hematology/Oncology. 44:465-470
Poorly differentiated chordoma (PDC) is a rare, aggressive subtype of chordoma. A two-year-old girl presented with cervical pain, limb paralysis and respiratory failure. Magnetic resonance imaging and positron emission tomography-computed tomography
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::42f7a4c8c7a167d9914a088e45f0fcf7
https://doi.org/10.1097/mph.0000000000002402
https://doi.org/10.1097/mph.0000000000002402