Zobrazeno 1 - 10
of 29
pro vyhledávání: '"Katsuhide Eguchi"'
Autor:
Hikaru Kanemasa, Masataka Ishimura, Katsuhide Eguchi, Tamami Tanaka, Etsuro Nanishi, Akira Shiraishi, Motohiro Goto, Yoshitomo Motomura, Shouichi Ohga
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-14 (2021)
Abstract CD71+ erythroid cells (CECs) are recognized to have an immunoregulatory function via direct cell–cell interaction and soluble mediators. Circulating CECs appear in newborns or patients with hemolytic and cardiopulmonary disorders. To asses
Externí odkaz:
https://doaj.org/article/73f180ddbff14b20b1f8c96d9c4dece0
Autor:
Kay Tanita, Yoshiki Kawamura, Hiroki Miura, Noriko Mitsuiki, Takahiro Tomoda, Kento Inoue, Akihiro Iguchi, Masafumi Yamada, Taro Yoshida, Hideki Muramatsu, Norimasa Tada, Toshihiro Matsui, Motohiro Kato, Katsuhide Eguchi, Masataka Ishimura, Shouichi Ohga, Kohsuke Imai, Tomohiro Morio, Tetsushi Yoshikawa, Hirokazu Kanegane
Publikováno v:
Frontiers in Immunology, Vol 13 (2022)
Severe combined immunodeficiency (SCID) is an inborn error of immunity that occurs in approximately 1 in 50,000 births, mainly due to impaired lymphocyte differentiation. Without curative treatment, such as hematopoietic cell transplantation (HCT) or
Externí odkaz:
https://doaj.org/article/cd3ac7b517e9466b8c2a235bea9c91ff
Autor:
Yutaro Yada, Michiko Torio, Yuhki Koga, Fumiya Yamashita, Takuya Ichimura, Katsuhide Eguchi, Masataka Ishimura, Yuichi Mushimoto, Akio Hiwatashi, Momoko Sasazuki, Ryutaro Kira, Yasunari Sakai, Shouichi Ohga
Publikováno v:
Molecular Genetics and Metabolism Reports, Vol 28, Iss , Pp 100778- (2021)
Background: Adrenoleukodystrophy (ALD) is an X-linked disorder characterized by rapidly progressive deterioration of neurocognitive functions and premature death. In addition to the difficulty in identifying the earliest signs of ALD, treatment-assoc
Externí odkaz:
https://doaj.org/article/a76616030bce4d86a18e0553af9e0ead
Autor:
Masataka Ishimura, Katsuhide Eguchi, Akira Shiraishi, Motoshi Sonoda, Yoshihiro Azuma, Hiroyuki Yamamoto, Ken-ichi Imadome, Shouichi Ohga
Publikováno v:
Frontiers in Pediatrics, Vol 7 (2019)
X-linked lymphoproliferative disease (XLP) is one of the X-linked primary immunodeficiency diseases (PIDs) with defective immune response to Epstein–Barr virus (EBV) infection. Chronic active EBV infection (CAEBV) and EBV-hemophagocytic lymphohisti
Externí odkaz:
https://doaj.org/article/e452f5090e1f412d8ca02403e56f9df7
Autor:
Yutaro Yada, Akira Shiraishi, Masataka Ishimura, Katsuhide Eguchi, Yoshitomo Motomura, Yasushi Kibe, Katsuhiko Kamei, Shouichi Ohga
Publikováno v:
Journal of Infection and Chemotherapy. 29:219-222
Autor:
Tamami Tanaka, Masataka Ishimura, Shouichi Ohga, Etsuro Nanishi, Akira Shiraishi, Katsuhide Eguchi, Motohiro Goto, Yoshitomo Motomura, Hikaru Kanemasa
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-14 (2021)
Scientific Reports
Scientific Reports
CD71+ erythroid cells (CECs) are recognized to have an immunoregulatory function via direct cell–cell interaction and soluble mediators. Circulating CECs appear in newborns or patients with hemolytic and cardiopulmonary disorders. To assess the bio
Autor:
Masatoshi Takagi, Tomohiro Morio, Masataka Ishimura, Junichi Sugita, Katsuhide Eguchi, Asami Shimbo, Hirokazu Kanegane, Masaki Shimizu
Publikováno v:
Rheumatology. 61:e1-e3
Autor:
Shouichi Ohga, Kei Nishiyama, Mari Kurokawa, Akira Shiraishi, Hazumu Nagata, Utako Oba, Noriyuki Kaku, Yuhki Koga, Takashi Imai, Satoshi Honjo, Masataka Ishimura, Katsuhide Eguchi
Publikováno v:
Pediatric Nephrology. 35:1977-1984
Acute kidney injury (AKI) often occurs in pediatric patients who received allogeneic hematopoietic cell transplantation (HCT). We evaluated the risk and effect of HCT-related AKI in pediatric patients. We retrospectively studied the survival and rena
Autor:
Wataru Takemori, Kenichiro Yamamura, Yoshitaka Tomita, Naoki Egami, Katsuhide Eguchi, Hazumu Nagata, Hiromitsu Shirouzu, Yuichi Ishikawa, Daisuke Nakajima, Akihiko Yoshizawa, Hiroshi Date, Shouichi Ohga
Publikováno v:
Pediatric pulmonologyREFERENCES. 57(5)
Pulmonary veno-occlusive disease (PVOD) and idiopathic/heritable pulmonary arterial hypertension (I/HPAH) cause progressive PH on the distinct genetic impact. A 29-month-old boy presented with a loss of consciousness. He had severe PH refractory to p
Autor:
Toshihiko Kakiuchi, Katsuhide Eguchi, Daisuke Koga, Hiroi Eguchi, Masanori Nishi, Motoshi Sonoda, Masataka Ishimura, Muneaki Matsuo
Publikováno v:
Medicine. 101(8)
Hepatitis-associated aplastic anemia (HAAA) is a rare illness that results in bone marrow failure following hepatitis development. The etiological agent remains unknown in most HAAA cases. However, clinical features of the disease and immunotherapy r