Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Naoya Kohda"'
Autor:
Kenji Matsuura, Naka Gotoda, Shu Yano, Naoya Kohda, Stephen Karungaru, Hiroki Tanioka, Tomohito Wada
Publikováno v:
IMCOM
Basketball is one of the most popular team-sports played on a shared court. It is important to shoot a basket based on a predominant strategy. In terms of individual movement along with the strategy, it is necessary for an offense player to understan
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d2b860af734c52ccfe1713a904b76847
https://doi.org/10.1109/imcom48794.2020.9001784
https://doi.org/10.1109/imcom48794.2020.9001784
Publikováno v:
TALE
Integrated movement, which is comprised of several motor-skills requires appropriate arrangement of motions at each body part. Most of team sports follow such integrated movements. This study focuses on learning and training the feint motion in one-o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cee734ce8c55edd9bf68fa4938cef7b7
https://doi.org/10.1109/tale.2018.8615318
https://doi.org/10.1109/tale.2018.8615318
Autor:
Hiroo Niimi, Kanshi Minamitani, Naoya Kohda, Toshiyuki Yasuda, Masanori Minagawa, Hiroshi Mochizuki, Tomoyuki Watanabe
Publikováno v:
European journal of endocrinology. 139(6)
Objective: A family is described which has a unique combination of autosomal dominant hypoparathyroidism and sensorineural deafness without renal dysplasia. Case report: The proband was a male infant aged 1 month with episodes of seizures for 20 days
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b1510c6032ac6615db51876ee0fe9ecf
https://pubmed.ncbi.nlm.nih.gov/9916869
https://pubmed.ncbi.nlm.nih.gov/9916869
Autor:
Shigeru Minowada, Yutaka Nakahori, Takashi Tamura, Yutaka Matsuzaki, Yasuo Nakagome, Shigeo Nagafuchi, Masahiko Yoshida, Hideki Fuse, Naoya Kohda, Yoshimitsu Fukushima, Hironao Numabe, Hiromichi Kiuchi, Motoyasu Kusano, Mikio Namiki, Tatsuro Ikeuchi, Takayuki Arai, Yoshikazu Kuroki, Koichiro Isurugi, Keiko Fukutani
Publikováno v:
Human genetics. 90(3)
Fourteen 46,XX “males” were analyzed by Southern blot hybridization with seventeen different Y chromosome-derived DNA probes and by the polymerase chain reaction for an additional two sites on the short arm of Y. Eight 46,XX males possessed vario
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cf53f63704929613c8dc76f369c3a74b
https://pubmed.ncbi.nlm.nih.gov/1487232
https://pubmed.ncbi.nlm.nih.gov/1487232
Publikováno v:
The Journal of Dermatology. 12:174-182
Disseminated angiokeratoma were seen in a 14-year-old Japanese boy with an inherited deficiency for alpha-L-fucosidase. He had gargoylian features, psychomotor retardation, small stature, vertebral changes, pale nail beds, recurrent infections and hy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::81d2be5dd02df46088032c54f2c61124
https://doi.org/10.1111/j.1346-8138.1985.tb01556.x
https://doi.org/10.1111/j.1346-8138.1985.tb01556.x