Zobrazeno 1 - 10
of 299
pro vyhledávání: '"Hiromasa YABE"'
Autor:
Yoshiyuki Takahashi, Hisashi Noma, Akiko Saito, Keizo Horibe, Hirotoshi Sakaguchi, Katsustugu Umeda, Itaru Kato, Kimiyoshi Sakaguchi, Hidefumi Hiramatsu, Hiroyuki Ishida, Hiromasa Yabe, Hiroaki Goto, Yuta Kawahara, Yuka Iijima Yamashita, Masashi Sanada, Takao Deguchi, Takashi Taga, Souichi Adachi
Publikováno v:
BMJ Open, Vol 13, Iss 4 (2023)
Introduction Relapsed and refractory B-cell acute lymphoblastic leukaemia (R/R-B-ALL) is linked to a significant relapse rate after allogeneic haematopoietic cell transplantation (allo-HCT) in children, adolescents and young adults (CAYA). No standar
Externí odkaz:
https://doaj.org/article/4e2a3190c22c4e4381335bdb12f4486c
Autor:
Rintaro Ono, Takashi Watanabe, Eiryo Kawakami, Makoto Iwasaki, Mariko Tomizawa-Murasawa, Masashi Matsuda, Yuho Najima, Shinsuke Takagi, Saera Fujiki, Rumi Sato, Yoshiki Mochizuki, Hisahiro Yoshida, Kaoru Sato, Hiromasa Yabe, Shunichi Kato, Yoriko Saito, Shuichi Taniguchi, Leonard D. Shultz, Osamu Ohara, Masayuki Amagai, Haruhiko Koseki, Fumihiko Ishikawa
Publikováno v:
EBioMedicine, Vol 41, Iss , Pp 584-596 (2019)
Background: Graft-versus host disease (GVHD) is a complication of stem cell transplantation associated with significant morbidity and mortality. Non-specific immune-suppression, the mainstay of treatment, may result in immune-surveillance dysfunction
Externí odkaz:
https://doaj.org/article/280692afcb6f4d14804164565b679c85
Autor:
Minako Mori, Asuka Hira, Kenichi Yoshida, Hideki Muramatsu, Yusuke Okuno, Yuichi Shiraishi, Michiko Anmae, Jun Yasuda, Shu Tadaka, Kengo Kinoshita, Tomoo Osumi, Yasushi Noguchi, Souichi Adachi, Ryoji Kobayashi, Hiroshi Kawabata, Kohsuke Imai, Tomohiro Morio, Kazuo Tamura, Akifumi Takaori-Kondo, Masayuki Yamamoto, Satoru Miyano, Seiji Kojima, Etsuro Ito, Seishi Ogawa, Keitaro Matsuo, Hiromasa Yabe, Miharu Yabe, Minoru Takata
Publikováno v:
Haematologica, Vol 105, Iss 4 (2020)
Externí odkaz:
https://doaj.org/article/1e27fb0a8ca04310ab6bda480ec5592e
Autor:
Yoshihiro Inamoto, Tomohiro Matsuda, Ken Tabuchi, Saiko Kurosawa, Hideki Nakasone, Hisakazu Nishimori, Satoshi Yamasaki, Noriko Doki, Koji Iwato, Takehiko Mori, Satoshi Takahashi, Hiromasa Yabe, Akio Kohno, Hirohisa Nakamae, Toru Sakura, Hisako Hashimoto, Junichi Sugita, Hiroatsu Ago, Takahiro Fukuda, Tatsuo Ichinohe, Yoshiko Atsuta, Takuya Yamashita
Publikováno v:
Blood Advances, Vol 2, Iss 15, Pp 1901-1913 (2018)
Abstract: To characterize the outcomes of patients who developed a particular subsequent solid cancer after hematopoietic cell transplantation (HCT), age at cancer diagnosis, survival, and causes of death were compared with the respective primary can
Externí odkaz:
https://doaj.org/article/3f1cb01d5574458a97be8edda72a47f9
Autor:
Minako Mori, Asuka Hira, Kenichi Yoshida, Hideki Muramatsu, Yusuke Okuno, Yuichi Shiraishi, Michiko Anmae, Jun Yasuda, Shu Tadaka, Kengo Kinoshita, Tomoo Osumi, Yasushi Noguchi, Souichi Adachi, Ryoji Kobayashi, Hiroshi Kawabata, Kohsuke Imai, Tomohiro Morio, Kazuo Tamura, Akifumi Takaori-Kondo, Masayuki Yamamoto, Satoru Miyano, Seiji Kojima, Etsuro Ito, Seishi Ogawa, Keitaro Matsuo, Hiromasa Yabe, Miharu Yabe, Minoru Takata
Publikováno v:
Haematologica, Vol 104, Iss 10 (2019)
Fanconi anemia is a rare recessive disease characterized by multiple congenital abnormalities, progressive bone marrow failure, and a predisposition to malignancies. It results from mutations in one of the 22 known FANC genes. The number of Japanese
Externí odkaz:
https://doaj.org/article/d3c2fd958fd54b47ac29c05a214c04da
Autor:
Pravin Patel, Yasuyuki Suzuki, Akemi Tanaka, Hiromasa Yabe, Shunichi Kato, Tsutomu Shimada, Robert W. Mason, Kenji E. Orii, Toshiyuki Fukao, Tadao Orii, Shunji Tomatsu
Publikováno v:
Molecular Genetics and Metabolism Reports, Vol 1, Iss C, Pp 184-196 (2014)
Patients with Hunter syndrome (mucopolysaccharidosis II) present with skeletal dysplasia including short stature as well as CNS and visceral organ involvement. A previous study on Hunter syndrome indicated an impact on brain and heart involvement aft
Externí odkaz:
https://doaj.org/article/7d916b6eaded44bb923773e2df8db8cd
Autor:
Atsushi Narita, Hideki Muramatsu, Yuko Sekiya, Yusuke Okuno, Hirotoshi Sakaguchi, Nobuhiro Nishio, Nao Yoshida, Xinan Wang, Yinyan Xu, Nozomu Kawashima, Sayoko Doisaki, Asahito Hama, Yoshiyuki Takahashi, Kazuko Kudo, Hiroshi Moritake, Masao Kobayashi, Ryoji Kobayashi, Etsuro Ito, Hiromasa Yabe, Shouichi Ohga, Akira Ohara, Seiji Kojima
Publikováno v:
Haematologica, Vol 100, Iss 12 (2015)
Acquired aplastic anemia is an immune-mediated disease characterized by severe defects in stem cell number resulting in hypocellular marrow and peripheral blood cytopenias. Minor paroxysmal nocturnal hemoglobinuria populations and a short telomere le
Externí odkaz:
https://doaj.org/article/7a63235ff28f483187109a6ac3d30ef6
Autor:
Asahito Hama, Yoshiyuki Takahashi, Hideki Muramatsu, Masafumi Ito, Atsushi Narita, Yoshiyuki Kosaka, Masahiro Tsuchida, Ryoji Kobayashi, Etsuro Ito, Hiromasa Yabe, Shouichi Ohga, Akira Ohara, Seiji Kojima
Publikováno v:
Haematologica, Vol 100, Iss 11 (2015)
The 2008 World Health Organization classification proposed a new entity in childhood myelodysplastic syndrome, refractory cytopenia of childhood. However, it is unclear whether this morphological classification reflects clinical outcomes. We retrospe
Externí odkaz:
https://doaj.org/article/176a0a717b3f4332acf31b7e660454cd
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:
Hirotoshi Sakaguchi, Nobuhiro Nishio, Asahito Hama, Nozomu Kawashima, Xinan Wang, Atsushi Narita, Sayoko Doisaki, Yinyan Xu, Hideki Muramatsu, Nao Yoshida, Yoshiyuki Takahashi, Kazuko Kudo, Hiroshi Moritake, Kazuhiro Nakamura, Ryoji Kobayashi, Etsuro Ito, Hiromasa Yabe, Shouichi Ohga, Akira Ohara, Seiji Kojima
Publikováno v:
Haematologica, Vol 99, Iss 8 (2014)
Predicting the response to immunosuppressive therapy could provide useful information to help the clinician define treatment strategies for patients with aplastic anemia. In our current study, we evaluated the relationship between telomere length of
Externí odkaz:
https://doaj.org/article/696c3d16a35e4d21bfe1d263911c8b6d