Zobrazeno 1 - 10
of 180
pro vyhledávání: '"Hiroshi Yagasaki"'
Autor:
Koji Kanezawa, Hiroshi Yagasaki, Ayumu Arakawa, Reina Hoshi, Shuichiro Uehara, Ichiro Morioka
Publikováno v:
Cancer Reports, Vol 7, Iss 5, Pp n/a-n/a (2024)
Abstract Background Melanoma is rare as a secondary malignant neoplasm among childhood cancer survivors. Case We report a case of a 12‐year‐old boy who developed malignant melanoma with systemic metastases 17 months after completing treatment for
Externí odkaz:
https://doaj.org/article/07354cce0d4343c4af206303c10c2d2e
Autor:
Erina Nakahara, Keiko Shimojima Yamamoto, Hiromi Ogura, Takako Aoki, Taiju Utsugisawa, Kenko Azuma, Hiroyuki Akagawa, Kenichiro Watanabe, Michiko Muraoka, Fumihiko Nakamura, Michi Kamei, Koji Tatebayashi, Jun Shinozuka, Takahisa Yamane, Makoto Hibino, Yoshiya Katsura, Sonoko Nakano-Akamatsu, Norimitsu Kadowaki, Yoshiro Maru, Etsuro Ito, Shouichi Ohga, Hiroshi Yagasaki, Ichiro Morioka, Toshiyuki Yamamoto, Hitoshi Kanno
Publikováno v:
Human Genome Variation, Vol 10, Iss 1, Pp 1-6 (2023)
Abstract Hereditary stomatocytosis (HSt) is a type of congenital hemolytic anemia caused by abnormally increased cation permeability of erythrocyte membranes. Dehydrated HSt (DHSt) is the most common subtype of HSt and is diagnosed based on clinical
Externí odkaz:
https://doaj.org/article/f434ba04490942fdab9e164bc91d0e89
Autor:
Masataka Ito, Hiroshi Yagasaki, Koji Kanezawa, Katsuyoshi Shimozawa, Maiko Hirai, Ichiro Morioka
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-6 (2021)
Abstract Treatment of children with refractory immune thrombocytopenic purpura (ITP) is challenging and poorly established. We retrospectively reviewed the clinical data of 87 patients under the age of 16 years who were diagnosed with ITP from April
Externí odkaz:
https://doaj.org/article/533875f135bc4100955466d909261172
Autor:
Shoichi Shimizu, Tamaki Morohashi, Koji Kanezawa, Hiroshi Yagasaki, Shori Takahashi, Ichiro Morioka
Publikováno v:
Frontiers in Pediatrics, Vol 10 (2022)
BackgroundTransplant-associated thrombotic microangiopathy (TA-TMA) is a serious complication of bone marrow transplantation (BMT). Recently, abnormalities in the complement system have been identified in the pathogenesis of TA-TMA, and there are ser
Externí odkaz:
https://doaj.org/article/e05b3b5638e84b13af93ad97248597e0
Autor:
Ko Kudo, Tsutomu Toki, Rika Kanezaki, Tatsuhiko Tanaka, Takuya Kamio, Tomohiko Sato, Shinya Sasaki, Masaru Imamura, Chihaya Imai, Kumiko Ando, Harumi Kakuda, Takehiko Doi, Hiroshi Kawaguchi, Masahiro Irie, Yoji Sasahara, Akihiro Tamura, Daiichiro Hasegawa, Yosuke Itakura, Kenichiro Watanabe, Kenichi Sakamoto, Yoko Shioda, Motohiro Kato, Kazuko Kudo, Reiji Fukano, Atsushi Sato, Hiroshi Yagasaki, Hirokazu Kanegane, Itaru Kato, Katsutsugu Umeda, Souichi Adachi, Tatsuki Kataoka, Akira Kurose, Atsuko Nakazawa, Kiminori Terui, Etsuro Ito
Publikováno v:
Haematologica, Vol 107, Iss 7 (2022)
Externí odkaz:
https://doaj.org/article/0c155267656c45e884c7240dec147ef7
Autor:
Katsunori Shijo, Nobuhiro Moro, Mari Sasano, Mitsuru Watanabe, Hiroshi Yagasaki, Shori Takahashi, Taku Homma, Atsuo Yoshino
Publikováno v:
BMC Neurology, Vol 18, Iss 1, Pp 1-6 (2018)
Abstract Background Sarcoidosis is a multi-organ disease of unknown etiology characterised by the presence of epithelioid granulomas, without caseous necrosis. Systemic sarcoidosis is rare among children, while neurosarcoidosis in children is even ra
Externí odkaz:
https://doaj.org/article/6dd9be1ead184a2684d88644c23a7952
Autor:
Nao Yoshida, Ryoji Kobayashi, Hiromasa Yabe, Yoshiyuki Kosaka, Hiroshi Yagasaki, Ken-ichiro Watanabe, Kazuko Kudo, Akira Morimoto, Shouichi Ohga, Hideki Muramatsu, Yoshiyuki Takahashi, Koji Kato, Ritsuro Suzuki, Akira Ohara, Seiji Kojima
Publikováno v:
Haematologica, Vol 99, Iss 12 (2014)
The current treatment approach for severe aplastic anemia in children is based on studies performed in the 1980s, and updated evidence is required. We retrospectively compared the outcomes of children with acquired severe aplastic anemia who received
Externí odkaz:
https://doaj.org/article/1cef4d847e774b4dacfa436d0a204c5b
Autor:
Takuya Kamio, Etsuro Ito, Akira Ohara, Yoshiyuki Kosaka, Masahiro Tsuchida, Hiroshi Yagasaki, Hideo Mugishima, Hiromasa Yabe, Akira Morimoto, Shouichi Ohga, Hideki Muramatsu, Asahito Hama, Takashi Kaneko, Masayuki Nagasawa, Atsushi Kikuta, Yuko Osugi, Fumio Bessho, Tatsutoshi Nakahata, Ichiro Tsukimoto, Seiji Kojima
Publikováno v:
Haematologica, Vol 96, Iss 6 (2011)
Background Although the therapeutic outcome of acquired aplastic anemia has improved markedly with the introduction of immunosuppressive therapy using antithymocyte globulin and cyclosporine, a significant proportion of patients subsequently relapse
Externí odkaz:
https://doaj.org/article/d32a0c4963804b63bd0742183c6d2c1f
Autor:
Nao Yoshida, Hiroshi Yagasaki, Asahito Hama, Yoshiyuki Takahashi, Yoshiyuki Kosaka, Ryoji Kobayashi, Hiromasa Yabe, Takashi Kaneko, Masahiro Tsuchida, Akira Ohara, Tatsutoshi Nakahata, Seiji Kojima
Publikováno v:
Haematologica, Vol 96, Iss 5 (2011)
In aplastic anemia, predictive markers of response to immunosuppressive therapy have not been well defined. We retrospectively evaluated whether clinical and laboratory findings before treatment could predict response in a pediatric cohort from the m
Externí odkaz:
https://doaj.org/article/cca7611aa4f24ec2bd829c0b5a56f9c3
Autor:
Yuko Osugi, Hiroshi Yagasaki, Masahiro Sako, Yoshiyuki Kosaka, Takashi Taga, Tsuyoshi Ito, Masuji Yamamoto, Akira Ohara, Takeyuki Sato, Junichi Mimaya, Ichiro Tsukimoto, Seiji Kojima, the Japan Childhood Aplastic Anemia Study Group
Publikováno v:
Haematologica, Vol 92, Iss 12 (2007)
We analyzed the outcomes of 44 children with hepatitis associated aplastic anemia (HAA) who received immunosuppressive therapy (IST) with antithymocyte globulin (ATG) and cyclosporine (CsA). Fourteen (31.8%) patients achieved complete response and 17
Externí odkaz:
https://doaj.org/article/df163af19479436fb1764e8e97593108