Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Shuji Hisikawa"'
Autor:
Takeshi Saito, Hideo Kawarasaki, Masami Ohmori, Weidong Liu, Toshikazu Hada, Koichi Mizuta, Koichi Sakamoto, T. Fujiwara, Yoshikazu Yasuda, Yukihiro Sanada, Shuhei Nishiguchi, Youichi Kawano, Satoshi Egami, Yuka Takatsuka, Shuji Hisikawa
Publikováno v:
Pediatric Transplantation. 11:694-697
Hypocholinesterasemia is often observed clinically, especially in various liver diseases. Not well known, however, is the fact that some patients have a hereditary BChE variant. Little has been reported on liver transplants associated with this hered
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6454f3dc76b7a1c471eec6f7e591e35e
https://doi.org/10.1111/j.1399-3046.2007.00750.x
https://doi.org/10.1111/j.1399-3046.2007.00750.x
Autor:
Yoshiyuki Yoshida, T. Fujiwara, Koichi Mizuta, Satoshi Egami, Yukihiro Sanada, Youichi Kawano, Yoshikazu Yasuda, Hideo Kawarasaki, Shuji Hisikawa, Masanobu Hyodo, Yasuhiko Sugawara, Yasunaru Sakuma, Eiji Sugimoto
Publikováno v:
Transplant international : official journal of the European Society for Organ Transplantation. 22(12)
Summary Portal vein stenosis (PVS) after living donor liver transplantation (LDLT) is a serious complication that can lead to graft failure. Few studies of the diagnosis and treatment of late-onset (≥3 months after liver transplantation) PVS have b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9139e73fbbfcb463e9397ad4d195acd7
https://pubmed.ncbi.nlm.nih.gov/19663938
https://pubmed.ncbi.nlm.nih.gov/19663938
Autor:
Youichi, Kawano, Koichi, Mizuta, Shuji, Hisikawa, Takeshi, Saito, Satoshi, Egami, Yuka, Takatsuka, Yukihiro, Sanada, Takehito, Fujiwara, Yoshikazu, Yasuda, Masami, Ohmori, Koichi, Sakamoto, Weidong, Liu, Shuhei, Nishiguchi, Toshikazu, Hada, Hideo, Kawarasaki
Publikováno v:
Pediatric transplantation. 11(6)
Hypocholinesterasemia is often observed clinically, especially in various liver diseases. Not well known, however, is the fact that some patients have a hereditary BChE variant. Little has been reported on liver transplants associated with this hered
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::36196b1989c1a6e58448a4750e8eb640
https://pubmed.ncbi.nlm.nih.gov/17663697
https://pubmed.ncbi.nlm.nih.gov/17663697