Zobrazeno 1 - 10
of 37
pro vyhledávání: '"Satoshi, Egami"'
Autor:
Noriki Okada, Naoya Yamada, Hideo Kawarasaki, Yoshiyuki Ihara, Taizen Urahashi, Shuji Hishikawa, Kentaro Ushijima, Taiichi Wakiya, Koichi Mizuta, Satoshi Egami, Y. Yasuda, Shinya Otomo, Koichi Sakamoto, Yukihiro Sanada
Publikováno v:
Transplantation Proceedings. 44:1341-1345
Background Acute cellular rejection (ACR) is a common cause of morbidity following liver transplantation. Several reports have evaluated the predictive value of peripheral blood eosinophilia as a simple noninvasive diagnostic marker for ACR. This stu
Autor:
Kei Murayama, Noriki Okada, Koichi Sakamoto, Yukihiro Sanada, Naoya Yamada, Taizen Urahashi, Koichi Mizuta, Kenichi Hakamada, Taiichi Wakiya, Yoshikazu Yasuda, Satoshi Egami, Yoshiyuki Ihara
Publikováno v:
Pediatric Transplantation. 16:E196-E200
Liver transplantation (LT) has been adopted as a radical treatment for ornithine transcarbamylase deficiency (OTCD), yielding favorable outcomes. Despite the fact that it is an inheritable disease, a blood relative who is heterozygous for the disorde
Autor:
Yoshiyuki Ihara, Taiichi Wakiya, Noriki Okada, Taizen Urahashi, Satoshi Egami, Koichi Mizuta, Naoya Yamada, Hideo Kawarasaki, Yukihiro Sanada
Publikováno v:
Transplantation Proceedings. 44:780-783
Objectives The aim of this study was to evaluate patients who developed varicella zoster virus (VZV) disease after pediatric living donor liver transplantation (PLDLT). Methods Two hundred fifty-five patients who underwent PLDLT between 1995 and 2010
Autor:
Taizen Urahashi, Yukihiro Sanada, Naoya Yamada, Taiichi Wakiya, Hideo Kawarasaki, Satoshi Egami, Koichi Mizuta, Yoshiyuki Ihara, Noriki Okada, Yoshikazu Yasuda
Publikováno v:
Experimental and Clinical Transplantation. 10:176-179
Background Nonanastomotic biliary stricture is generally considered the most troublesome biliary complication after liver transplant. Nonanastomotic biliary stricture owing to immunologic cholangiopathy (such as acute cellular rejection) has not been
Autor:
Taizen Urahashi, Steven S.S. Poon, Tomio Arai, Kaiyo Takubo, Naoshi Ishikawa, Yoshiyuki Ihara, Naoya Yamada, Satoshi Egami, Takeshi Saito, Noriki Okada, Taiichi Wakiya, Makoto Hayashida, Koichi Mizuta, Kenichi Nakamura, Shuji Hishikawa, Youichi Kawano, Naotaka Shimomura, Yukihiro Sanada, Yoshikazu Yasuda, Hideo Kawarasaki, Junko Aida
Publikováno v:
World Journal of Surgery. 36:908-916
Liver transplantation for biliary atresia is indicated whenever a Kasai portoenterostomy is considered unfeasible. However, the timing of liver transplantation in biliary atresia has not been precisely defined. Excessive shortening of hepatocellular
Autor:
Koichi Sakamoto, Taizen Urahashi, Koichi Mizuta, Yukihiro Sanada, Naoya Yamada, Shuji Hishikawa, Hideo Kawarasaki, Yoshiyuki Ihara, Noriki Okada, Satoshi Egami, Taiichi Wakiya, Shinya Otomo, Kentaro Ushijima, Y. Yasuda
Publikováno v:
Transplantation Proceedings. 43:4019-4024
Background Excessive portal pressure at an early stage after living-donor liver transplantation (LDLT) can damage sinusoidal endothelial cells and hepatocytes through shear stress leading to graft failure, or hepatic arterial complications due to low
Autor:
Hideo Kawarasaki, Yasunaru Sakuma, Kei Murayama, Shuji Hishikawa, Koichi Mizuta, Minoru Umehara, Kenichi Hakamada, T. Urahasi, Masanobu Hyodo, Yukihiro Sanada, Satoshi Egami, Taiichi Wakiya, Yoshikazu Yasuda, T. Fujiwara
Publikováno v:
Pediatric Transplantation. 15:390-395
Ornithine transcarbamylase deficiency, the most common urea cycle disorder, causes hyperammonemic encephalopathy and has a poor prognosis. Recently, LT was introduced as a radical OTCD treatment, yielding favorable outcomes. We retrospectively analyz
Autor:
Noriki Okada, Naoya Yamada, Taiichi Wakiya, Shinya Otomo, Satoshi Egami, Taizen Urahashi, Koichi Sakamoto, Hideo Kawarasaki, Yukihiro Sanada, Koichi Mizuta, Yoshikazu Yasuda, Kentaro Ushijima, Yoshiyuki Ihara
Publikováno v:
Annals of Transplantation. 16:7-11
BACKGROUND At the present time, indications of liver transplantation (LT) for jaundice-free biliary atresia (BA) patients include intractable cholangitis, portal hypertension and pulmonary vascular disorders. However, the timing of LT remains unclear
Autor:
Y. Yasuda, Manabu Nakata, Hideo Kawarasaki, Shuji Hishikawa, Koichi Mizuta, Kenichi Hakamada, Taiichi Wakiya, Satoshi Egami, Yukihiro Sanada
Publikováno v:
Pediatric Transplantation. 16:E81-E85
Early hepatic artery complications after liver transplantation in children, having undergone LDLT, can directly affect graft and recipient outcomes, making early diagnosis and treatment essential. In the past, laparotomy (thrombectomy or reanastomosi
Autor:
Koichi Mizuta, Shuji Hishikawa, Hideo Kawarasaki, Taizen Urahashi, Minoru Umehara, Kenichi Hakamada, Yukihiro Sanada, Satoshi Egami, T. Wakiya, Manabu Nakata, Yoshikazu Yasuda
Publikováno v:
Pediatric Transplantation. 16:E86-E89
Wakiya T, Sanada Y, Mizuta K, Umehara M, Urahashi T, Egami S, Hishikawa S, Nakata M, Hakamada K, Yasuda Y, Kawarasaki H. Hepatic artery reconstruction with the jejunal artery of the Roux-en-Y limb in pediatric living donor liver re-transplantation. A