Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Yumetaka Shinden"'
Publikováno v:
Clinical Case Reports, Vol 12, Iss 7, Pp n/a-n/a (2024)
Key Clinical Message Polymelia (supernumerary limbs) is an extremely rare congenital condition in humans. Because congenital anorectal malformation is a relatively common complication of polymelia and it may require emergency surgery as in the presen
Externí odkaz:
https://doaj.org/article/267f68ebf8b348dd943f31d2acedbff7
Autor:
Haruki Matsumoto, Hironori Ohashi, Yuya Fujita, Shuhei Yoshida, Kohei Yokose, Jumpei Temmoku, Naoki Matsuoka, Yumetaka Shinden, Keigo Kusano, Tatsuru Sonobe, Yohei Nakamoto, Makiko Yashiro-Furuya, Tomoyuki Asano, Shuzo Sato, Eiji Suzuki, Toru Yago, Hiroshi Watanabe, Kiyoshi Migita
Publikováno v:
The Tohoku Journal of Experimental Medicine. 256:169-174
Familial Mediterranean fever (FMF) is a hereditary autoinflammatory disease characterized by recurrent episodes of fever and serositis. Periodic febrile attack can be managed with biologic medication in colchicine-resistant FMF patients, however, no
Autor:
Masayuki Ito, Michiyuki Hakozaki, Shinichi Konno, Yumetaka Shinden, Yojiro Takahashi, Satoshi Hatashita, Yoichi Kaneuchi
Publikováno v:
In Vivo
Background/aim The number of individuals diagnosed with and requiring medical treatment for osteoporosis continues to increase due to global population aging and the high awareness of osteoporosis. Bone-modifying agents (BMAs) including bisphosphonat
Autor:
YOJIRO TAKAHASHI, SATOSHI HATASHITA, YUMETAKA SHINDEN, MASAYUKI ITO, YOICHI KANEUCHI, MICHIYUKI HAKOZAKI, SHINICHI KONNO
Publikováno v:
In Vivo; May/Jun2021, Vol. 35 Issue 3, p1837-1842, 6p