Zobrazeno 1 - 10
of 143
pro vyhledávání: '"Yoshiyuki, Ogawa"'
Autor:
Tsuyoshi Tajika, Takuro Kuboi, Hideo Sakane, Yuhei Hatori, Ryuta Saida, Satoshi Shinagawa, Hitoshi Shitara, Yoshiyuki Ogawa, Hirotaka Chikuda
Publikováno v:
SAGE Open Medical Case Reports, Vol 11 (2023)
Total elbow arthroplasty is effective for pain relief and the functional improvement of severe symptomatic hemophilic osteoproliferative arthropathy. Nevertheless, high complication rates have been reported. This report describes clinical results obt
Externí odkaz:
https://doaj.org/article/ce8ab541e35f47358f8f50dcbb9eee83
Autor:
Takaomi Seki, Mariko Tsukagoshi, Norifumi Harimoto, Kenichiro Araki, Akira Watanabe, Norihiro Ishii, Kei Hagiwara, Kouki Hoshino, Ryo Muranushi, Satoru Kakizaki, Yoshiyuki Ogawa, Hiroshi Handa, Ken Shirabe
Publikováno v:
Surgical Case Reports, Vol 8, Iss 1, Pp 1-7 (2022)
Abstract Background Factor V (FV) deficiency is an extremely rare disease, with an incidence of 1 in 1 million. The bleeding symptoms are mild, and the prognosis is good; however, the safety of surgical treatment is unclear, because there are few ava
Externí odkaz:
https://doaj.org/article/141096e3f393462daab3c8d5f537c8e1
Autor:
Yoko Takagi, Yasuko Kobayashi, Ayako Hirakata, Mariko Takei, Satoshi Ogasawara, Chikage Yajima, Yuka Ikeuchi, Akira Matsumoto, Yoshiyuki Ogawa, Hiroshi Handa, Masanori Matsumoto, Hirokazu Arakawa, Takumi Takizawa
Publikováno v:
Frontiers in Pediatrics, Vol 10 (2022)
BackgroundThrombotic microangiopathy (TMA) is a syndrome associated with hemolytic anemia, thrombocytopenia, and various organ disorders. Thrombotic thrombocytopenic purpura (TTP) is a disease that develops when a disintegrin-like and metalloproteina
Externí odkaz:
https://doaj.org/article/442560d8e3e3422c9550853cfcf08b60
Autor:
Midori Shima, Kagehiro Amano, Yoshiyuki Ogawa, Koichiro Yoneyama, Ryoto Ozaki, Ryota Kobayashi, Emiko Sakaida, Makoto Saito, Takashi Okamura, Toshihiro Ito, Norimichi Hattori, Satoshi Higasa, Nobuaki Suzuki, Yoshinobu Seki, Keiji Nogami
Publikováno v:
Journal of Thrombosis and Haemostasis. 21:534-545
Autor:
Masayoshi, Souri, Tsukasa, Osaki, Yuji, Shimura, Satoshi, Ichikawa, Makiko, Mori, Yoshiyuki, Ogawa, Akitada, Ichinose
Publikováno v:
Haemophilia. 29:555-563
Autoimmune factor X (FX or F10) deficiency (AiF10D) is an extremely rare acquired haemorrhagic disorder characterized by a severe reduction in FX activity due to autoantibodies against FX.Anti-FX autoantibodies were investigated in four patients with
Autor:
Yoshiyuki Ogawa, Kagehiro Amano, Yukari Matsuo-Tezuka, Norihiro Okada, Yoichi Murakami, Takao Nakamura, Haruko Yamaguchi-Suita, Keiji Nogami
Publikováno v:
International Journal of Hematology. 117:44-55
Background Acquired hemophilia A (AHA) is a rare disorder, and clinical practices for treating AHA have not been fully clarified in Japan. Objectives This study aims to investigate the epidemiology of AHA and real-world treatment practices in Japan.
Autor:
Kunio Yanagisawa, Nuanjun Wichukchinda, Naho Tsuchiya, Michio Yasunami, Archawin Rojanawiwat, Hidenori Tanaka, Hiroh Saji, Yoshiyuki Ogawa, Hiroshi Handa, Panita Pathipvanich, Koya Ariyoshi, Pathom Sawanpanyalert
Publikováno v:
PLoS ONE, Vol 15, Iss 12, p e0242438 (2020)
BackgroundMannose-binding lectin (MBL) plays a pivotal role in innate immunity; however, its impact on susceptibility to opportunistic infections (OIs) has not yet been examined in a natural history cohort of people living with HIV/AIDS.MethodsWe use
Externí odkaz:
https://doaj.org/article/75036dfcc3d34a0dbbafbe40c3c5cfdd
Autor:
Toshimitsu Kato, Norimichi Koitabashi, Yukie Sano, Kunio Yanagisawa, Yoshiyuki Ogawa, Takayuki Saitoh, Hideki Ishii
Publikováno v:
Journal of Medical Ultrasonics. 50:255-257
Autor:
Yoshiyuki OGAWA
Publikováno v:
Japanese Journal of Thrombosis and Hemostasis. 33:433-436
Autor:
Akira, Matsumoto, Yoshiyuki, Ogawa, Yuri, Uchiyama, Tetsuya, Ishikawa, Chiaki, Naito, Nobuhiko, Kobayashi, Yuri, Miyazawa, Takuma, Ishizaki, Madoka, Inoue, Yuichi, Moteki, Saki, Kitazawa, Masami, Murakami, Naomichi, Matsumoto, Hiroshi, Handa
Publikováno v:
[Rinsho ketsueki] The Japanese journal of clinical hematology. 63(10)
From a young age, a 63-year-old Japanese man had experienced difficulties with hemostasis during tooth extraction and epistaxis and swelling of bruised areas. He had previously been diagnosed with mild hemophilia (FVIII:C 8.5%) at age of 60 due to sw