Zobrazeno 1 - 10
of 75
pro vyhledávání: '"Hideaki Imamura"'
Autor:
Kazuhiro Higuchi, Koji Furukawa, Eisaku Nakamura, Hideaki Imamura, Toshihiro Gi, Kunihide Nakamura
Publikováno v:
EJVES Vascular Forum, Vol 48, Iss , Pp 12-18 (2020)
Introduction: Abdominal aortic aneurysm (AAA) in neonates, infants, and children is uncommon, usually occurring as a result of infections, connective tissue disorders, vasculitis, or iatrogenic trauma. A case of idiopathic congenital AAA, an extremel
Externí odkaz:
https://doaj.org/article/e7519ee5aa5d4bde814400b4e2cc280e
Publikováno v:
信州大学経済学論集. 49:163-164
Other
信州大学経済学論集 49:163-164(2003)
信州大学経済学論集 49:163-164(2003)
Autor:
Shin Morizane, Takenobu Yamamoto, Yoji Hirai, Toshihisa Hamada, Tomoko Miyake, Keiji Iwatsuki, Hideaki Imamura, Kazuyasu Fujii
Publikováno v:
Journal of Medical Virology. 92:3689-3696
Epstein-Barr virus (EBV) DNA load in the blood increases in posttransplant lymphoproliferative disorders and chronic active EBV infection. In this report, we analyzed the EBV DNA load in the peripheral blood mononuclear cells (PBMCs) and plasma of pa
Autor:
Eisaku Nakamura, Kunihide Nakamura, Koji Furukawa, Hideaki Imamura, Kazuhiro Higuchi, Toshihiro Gi
Publikováno v:
EJVES Vascular Forum
EJVES Vascular Forum, Vol 48, Iss, Pp 12-18 (2020)
EJVES Vascular Forum, Vol 48, Iss, Pp 12-18 (2020)
Introduction Abdominal aortic aneurysm (AAA) in neonates, infants, and children is uncommon, usually occurring as a result of infections, connective tissue disorders, vasculitis, or iatrogenic trauma. A case of idiopathic congenital AAA, an extremely
Autor:
Takaya Abe, Hidenori Matsuo, Ryuzo Abe, Shinji Abe, Hiroaki Asada, Akira Ashida, Akiyasu Baba, Kei Eguchi, Yutaka Eguchi, Yoshihiro Endo, Yoshihiro Fujimori, Kengo Furuichi, Yutaka Furukawa, Mayumi Furuya, Tomoki Furuya, Norio Hanafusa, Wataru Hara, Mariko Harada‐Shiba, Midori Hasegawa, Noriyuki Hattori, Motoshi Hattori, Sumi Hidaka, Toshihiko Hidaka, Chika Hirayama, Shigaku Ikeda, Hideaki Imamura, Kazuaki Inoue, Keita Ishizuka, Kiyonobu Ishizuka, Takafumi Ito, Hitomi Iwamoto, Syoko Izaki, Maki Kagitani, Shuzo Kaneko, Naoto Kaneko, Takuro Kanekura, Kiyoki Kitagawa, Makio Kusaoi, Youwei Lin, Takeshi Maeda, Hisashi Makino, Shigeki Makino, Kenichi Matsuda, Takao Matsugane, Yusuke Minematsu, Michio Mineshima, Kenichiro Miura, Katsuichi Miyamoto, Takeshi Moriguchi, Mayumi Murata, Makoto Naganuma, Hajime Nakae, Shinya Narukawa, Atsushi Nohara, Kyoichi Nomura, Hirofumi Ochi, Atsushi Ohkubo, Takayasu Ohtake, Kazuya Okada, Tomokazu Okado, Yoshiki Okuyama, Susumu Omokawa, Satoru Oji, Norihiko Sakai, Yuichiro Sakamoto, Shigeru Sasaki, Motoyoshi Sato, Mariko Seishima, Hidetoshi Shiga, Homare Shimohata, Noriko Sugawara, Kohei Sugimoto, Yasushi Suzuki, Masato Suzuki, Takashi Tajima, Yasuhiro Takikawa, Satoru Tanaka, Kenjiro Taniguchi, Satoko Tsuchida, Tatsuo Tsukamoto, Kenji Tsushima, Yasunori Ueda, Takashi Wada, Hiromichi Yamada, Hiroyuki Yamada, Toshihiko Yamaka, Ken'ichiro Yamamoto, Yoko Yokoyama, Norihito Yoshida, Toyokazu Yoshioka, Ken Yamaji
Publikováno v:
Therapeutic apheresis and dialysis : official peer-reviewed journal of the International Society for Apheresis, the Japanese Society for Apheresis, the Japanese Society for Dialysis TherapyREFERENCE. 25(6)
Most of the diseases for which apheresis therapy is indicated are intractable and rare, and each patient has a different background and treatment course prior to apheresis therapy initiation. Therefore, it is difficult to conduct large-scale randomiz
Autor:
Yasuyuki Sato, Hideki Ishida, Masataka Hisano, Hiroko Chikamoto, Hideaki Imamura, Shohei Fuchinoue, Tomoo Yabuuchi, Kazunari Tanabe, Seisuke Sakamoto, Naoto Kaneko, Takayuki Miyai, Motoshi Hattori, Yuri Nawashiro, Yuko Akioka, Masayoshi Okumi, Kiyonobu Ishizuka, Kenichiro Miura, Mureo Kasahara
Publikováno v:
Pediatric Transplantation. 24
Management of children with autosomal recessive polycystic kidney disease (ARPKD) who develop end-stage renal disease (ESRD) remains challenging because of concomitant liver disease. Patients with recurrent cholangitis are candidates for liver-kidney
Autor:
Yasuhiro Kimoto, Hideaki Imamura, Hiroshi Moritake, Kayo Ochiai, Makoto Matsukubo, Toshio Ikeda, Ai Yamada, Satoshi Ieiri
Publikováno v:
Pediatric bloodcancer. 66(8)
We report a 38-month-old Japanese male with premature chromatid separation/mosaic variegated aneuploidy syndrome bearing biallelic BUB1B germline mutations who suffered from bilateral Wilms tumor. After right nephrectomy, dactinomycin monotherapy was
Autor:
Hiromi Sakaguchi, Akihiko Nakahara, Hiroyuki Nunoi, Takao Konomoto, Hideaki Imamura, Etsuko Tanaka, Mayuko Orita
Publikováno v:
Nihon Shoni Jinzobyo Gakkai Zasshi. 28:68-74
Autor:
Hideaki Imamura, Etsuko Tanaka, Mayuko Orita, Hirotake Sawada, Takao Konomoto, Hiroyuki Nunoi
Publikováno v:
Pediatric Nephrology. 29:927-930
Background There is ongoing discussion regarding the mechanisms underlying edema formation in nephrotic syndrome (NS). Many studies published in the last decade reported that primary renal sodium retention was a major factor in edema formation. Howev
Autor:
Satoshi Hisano, Hideaki Imamura, Etsuko Tanaka, Yoshihiro Fujimura, Toshiyuki Miyata, Yoko Yoshida, Hiroyuki Nunoi, Takao Konomoto
Publikováno v:
Nephrology Dialysis Transplantation. 30:862-864
We report the first case of familial C3 glomerulonephritis (C3GN) associated with mutations in the gene for complement factor B (CFB). A 12-year-old girl was diagnosed with biopsy-proven C3GN. Her mother had a history of treatment for membranoprolife