Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Ryoji Ida"'
Autor:
Nobukazu Fuwa, Daisaku Suga, Ryoji Ida, Tosiaki Miyati, Kazuki Terashima, Kei Katahira, Masayuki Kanamoto
Publikováno v:
Radiological Physics and Technology. 10:234-239
The purpose of this study was to compare between superparamagnetic iron oxide (SPIO)-enhanced three-dimensional balanced turbo field-echo (B-TFE) sequence with T2 preparation pulse (T2 prep) and T2*-weighted imaging (T2*WI) for the simultaneous detec
Autor:
Kazuki Terashima, Takahiro Sato, Yoshihide Sawa, Masakazu Shimizu, Toshihiro Yanou, Ryoji Ida
Publikováno v:
Japanese Journal of Radiological Technology. 72:1074-1083
BACKGROUND Though the dosimetric criteria for the gastrointestinal tract were met, late gastrointestinal toxicity was seen in several cases. Therefore, we thought that it was caused by the positional variation of gastrointestine surrounding pancreati
Autor:
Masayuki, Kanamoto, Tosiaki, Miyati, Kazuki, Terashima, Kei, Katahira, Ryoji, Ida, Daisaku, Suga, Nobukazu, Fuwa
Publikováno v:
Radiological physics and technology. 10(2)
The purpose of this study was to compare between superparamagnetic iron oxide (SPIO)-enhanced three-dimensional balanced turbo field-echo (B-TFE) sequence with T
Autor:
Ryoji Ida, Masahisa Nakada
Publikováno v:
Tetrahedron Letters. 48:4855-4859
The enantioselective preparation of the tricyclo[4.4.0.05,7]dec-2-ene derivatives via the catalytic asymmetric intramolecular cyclopropanation (CAIMCP) reactions of α-diazo-β-keto esters with excellent ee (95–98% ee) is described. The chiral buil
Publikováno v:
Synlett. 2007:0579-0582
This manuscript describes studies on the catalytic asymmetric intramolecular cyclopropanation (IMCP) of 2-diazo-3-oxo-6-heptenoic acid esters. The enantioselectivity depends on the bulkiness of the ester moiety, and the 2,6-di-tert-butyl-4-methylphen
Autor:
Yasuhiko Inoue, Ryuji Takahashi, Toshihiko Oda, Daisaku Suga, Kikuko Mitsuki, Koji Kimura, Toyozo Komiyama, Ryoji Ida
Publikováno v:
Japanese Journal of Radiological Technology. 53:226