Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Hidekazu Saitoh"'
Autor:
Masaaki Ichiki, Ryuichi Naganawa, Yasuo Kanazawa, Muneyasu Suzuki, Shouhei Mine, Hidekazu Saitoh, Ko-Ichi Sugawara
Publikováno v:
IIAI-AAI
With the aim of developing doctral talent that can perform across a broad range of fields in society, AIST hosts Innovation School for postdoctral researchers and PhD students with a curriculum to encourage broader perspective and reforming of awaren
Autor:
Y. Okuno, Yoshikazu Satoh, Katsumi Hayakawa, Tatsuo Torizuka, Takashi Misaki, Hidekazu Saitoh, Kazuhisa Fujiwara, Michihide Mitsumori, Fumiko Tanaka
Publikováno v:
Investigative Radiology. 28:434-438
RATIONALE AND OBJECTIVES The purpose of the study was to evaluate the venous drainage pathways of the bronchial circulation during bronchial embolotheraphy or infusion therapy. METHODS The subjects consisted of 21 patients with lung disorders. All of
Publikováno v:
Fertility and sterility. 95(6)
Objective To evaluate the effect of frozen-thawed blastocyst transfer on ectopic pregnancy (EP) rate. Design Retrospective analysis. Setting Japanese registry of assisted reproductive medicine. Patient(s) Women who were registered during 2008. Interv
Autor:
A Ogura, Y Satoh, Y Nakayama, Junji Konishi, T Torizuka, F Tanaka, Okuno Y, Hidekazu Saitoh, Katsumi Hayakawa
Publikováno v:
Radiology. 184(1)
High-resolution computed tomography (CT) of the temporal bone, particularly axial scanning on a baseline parallel to the orbitomeatal line, produces radiation exposure to the patient's lenses. The authors evaluated the radiation dose to the lens and
Publikováno v:
HETEROCYCLES. 38:769
Thermal reaction of cyclobuta [b] pyrroles, which derived by photochemical cyclization of methyl 2,5- and 3,6-di-t-butyl-1H-azepine-1-carboxylate gave di-t-butyl substituted 3H-azepines. The kinetics of the reaction were measured and the activation e
Publikováno v:
Journal of the Chemical Society, Chemical Communications. :1121
Di-t-butyl derivatives of 3a,5a-dihydro-3H-cyclobuta[b]pyrroles, synthesized from photoisomers of 1H-azepine derivatives (Dewar azepines), isomerized thermally to 3H-azepines.