Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Kyota Akasaki"'
Autor:
Hiroki Asakura, Masataka Horita, Koutaro Yokote, Yoshiro Maezawa, Makoto Yonezawa, Takehiro Kanamori, Reina Yamamoto, Masaya Koshizaka, Kyota Akasaki, Seiichiro Kurita
Publikováno v:
Endocrine journal. 67(12)
Werner syndrome (WS), a type of progeria, is a hereditary condition caused by a mutation in the WRN gene. A 62-year-old Japanese woman was diagnosed with WS at the age of 32 and has been visiting the hospital for follow-up since the last 30 years. Th
Autor:
Takashi Sone, Kyota Akasaki, Yuichi Tambo, Miki Abo, Takafumi Kobayashi, Kazuo Kasahara, Mizuki Yuasa, Keigo Saeki, Kenta Yamamura, Hiroki Matsuoka, Shingo Nishikawa, Hideharu Kimura, Johsuke Hara, Noriyuki Ohkura, Nanao Terada, Syunichi Nomura
Publikováno v:
The journal of medical investigation : JMI. 66(1.2)
Background Asthma-COPD overlap (ACO) is a disease that shares clinical features of both asthma and COPD. The purpose of this study is to investigate the prevalence and clinical features of ACO. Methods We retrospectively reviewed data for 170 patient
Autor:
Reina Yamamoto, Kyota Akasaki, Masataka Horita, Makoto Yonezawa, Hiroki Asakura, Takehiro Kanamori, Yoshiro Maezawa, Masaya Koshizaka, Koutaro Yokote, Seiichiro Kurita
Publikováno v:
Endocrine Journal; 2020, Vol. 67 Issue 12, p1239-1246, 8p