Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Yasuko Namikawa"'
Publikováno v:
Frontiers in Medical Technology, Vol 6 (2024)
IntroductionThe wearable cyborg Hybrid Assistive Limb (HAL) is a therapeutic exoskeletal device that provides voluntary gait assistance using kinematic/kinetic gait data and bioelectrical signals. By utilizing the gait data automatically measured by
Externí odkaz:
https://doaj.org/article/7470d01af9fe4063bbb91c7338769c27
Publikováno v:
SIGGRAPH Asia 2022 XR.
Publikováno v:
2022 IEEE International Symposium on Mixed and Augmented Reality (ISMAR).
Publikováno v:
Annual International Conference of the IEEE Engineering in Medicine and Biology Society. IEEE Engineering in Medicine and Biology Society. Annual International Conference. 2021
Cybernic treatment with a wearable cyborg Hybrid Assistive Limb for medical use (Medical HAL) improves ambulatory function in patients with progressive neuromuscular diseases. The progress of cybernic treatment is evaluated based on the change in the
Autor:
Akito Tanaka, Yoshihiko Sakata, Jiro Seki, Yukio Motoyama, Hisashi Takasugi, Yasuko Namikawa, Keizo Yoshida, Jiro Fujisaki, Miwako Dohi
Publikováno v:
European Journal of Pharmacology. 243:179-184
The anti-platelet actions of 1-[(4,5-bis(4-methoxyphenyl)-2- thiazoyl)carbonyl]-4-methylpiperazine hydrochloride (FR122047) were investigated in vitro and in vivo. FR122047 was 100 times more potent than aspirin against arachidonic acid- and collagen
Autor:
Takaharu Ono, Miho Sato, Yoshihiko Sakata, Haruo Horiai, Jiro Seki, Yasuko Namikawa, Yukio Motoyama
Publikováno v:
Thrombosis Research. 65:55-63
TFC-612 inhibited thrombus formation on wire coils inserted into the lumen of the inferior vena cava of rats after 5 oral doses of 1.0 and 3.2 mg/kg and subcutaneous doses of 1.0 and 3.2 pg/rat/hr. This compound showed slight inhibition of platelet a
Autor:
Jiro Seki, Yukio Motoyama, Takashi Asada, Yoshihiko Sakata, Haruo Horiai, Yasuko Namikawa, Takaharu Ono
Publikováno v:
Thrombosis Research. 63:29-38
The anti-platelet activities of TFC-612, methyl 6-(((1R, 2S, 3R)-3-hydroxy-2-((1E, 3S, 5R)-3-hydroxy-5-methyl-1-nonenyl)-5- oxocyclopentyl) thio)hexanoate, were compared to prostaglandin E1 (PGE1). TFC-612 inhibited human, guinea-pig and rabbit plate