Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Kazuro KOTODA"'
Autor:
Hirotaka MUSHA, Yukio NAKAJIMA, Koji SUZUKI, Kenichi TAKAYASU, Hideki OHKUBO, Hirohumi KOHEN, Kunihiko KOHNO, Naondo SUZUKI, Kazuro KOTODA, Kunio OKUDA
Publikováno v:
Kanzo. 19:871-879
Autor:
Shosuke IWAMA, Kunihiko OHNISHI, Yukio NAKAJIMA, Masao OMATA, Toshiko SUZUKI, Kunio OKUDA, Keiko IMAZEKI, Kazuro KOTODA
Publikováno v:
Kanzo. 23:1292-1298
Autor:
Kunio Okuda, Naoyoshi Tsuchiya, Akira Ichinohe, Masahiko Igarashi, Takemi Sasaki, Kazuro Kotoda
Publikováno v:
Kanzo. 16:100-107
Autor:
Hideki Ohkubo, Kenichi Takayasu, Hirotaka Musha, Takeshi Yamazaki, Koji Suzuki, Kunihiko Kohno, Yukio Nakajima, Kunio Okuda, Hirohumi Kohen, Kazuro Kotoda
Publikováno v:
Kanzo. 20:1048-1055
経皮経肝的門脈造影(PTP)像による肝外門脈短絡路を肝硬変症を中心とした83例において検討した.短絡路として左胃静脈,短胃静脈,傍〓静脈,脾静脈末梢より後腹膜へ到る短絡路,脾腎短絡路,
Autor:
Shigenobu Jinnouchi, Eisuke Nagata, Yasuhiko Kubo, Naoaki Hayashi, Makoto Tamiya, Hiroshi Obata, Yutaka Shimokawa, F. Yakushiji, Kunio Okuda, Toju Hisamitsu, Kazuro Kotoda
Publikováno v:
Gastroenterology. 69:226-234
Five cases of hepatocellular carcinoma in whom diagnosis was made when the tumor was relatively small, are described. In 2 cases, serum alpha-fetoprotein (AFP) strted to rise sharply, which enabled early detection and surgical removal of the tumor. S
Publikováno v:
Kanzo. 22:1009-1015
Publikováno v:
Kanzo. 21:1322-1329
肝硬変患者の末梢エンドトキシン血症出現の機序を知る為に,肝硬変20例,非硬変7例に経皮経肝カテーテル法を用い門脈系(門脈本幹,上腸間膜静脈,脾静脈)と末梢の血液を同時に採血しエン
Publikováno v:
Kanzo. 21:275-281
ラットにbrombenzene (90mg/100g bw)を投与すると2日目に小葉中心部の広範壊死像を主体とする肝病変がみられた.bromobenzene投与前にpolymyxin B (0.167mg/100g bw, 0.083mg/100g bw)を前投与するとpolymyxin B未処
Publikováno v:
SEIBUTSU BUTSURI KAGAKU. 11:335-343
A method is described for the determination of the fatty acid composition of serum cholesterol esters by gas liquid chromatography, after their separation by thin layer chromatography.Serum extracts were prepared and washed by the method of Folch et
Five patients showing a normal to near-normal BSP test and a marked delay in ICG plasma clearance, and two families with clustering of the same abnormality, are described. Two had Gilbert's syndrome, one was convalescing from acute hepatitis, and the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::074d9100eca140f02b9da0c942fd0362
https://europepmc.org/articles/PMC1411325/
https://europepmc.org/articles/PMC1411325/