Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Koyuru Kurane"'
Publikováno v:
Pediatrics International
Autor:
Takanori Yamagata, Hitoshi Osaka, Narumi Omika, Kenji Kurosawa, Makiko Tajika, Masaru Shimura, Kazuhiro Muramatsu, Mari Kuwajima, Eriko F. Jimbo, Hiroko Shimbo, Kei Murayama, Koyuru Kurane, Masahide Goto
Publikováno v:
Brain and Development. 41:465-469
Mutations in the mitochondrial tRNAMet gene have been reported in only five patients to date, all of whom presented with muscle weakness and exercise intolerance as signs of myopathy. We herein report the case of a 12-year-old girl with focal epileps
Autor:
Toshiyuki Takahashi, Koyuru Kurane, Akihiko Miyauchi, Takanori Yamagata, Takahiro Ikeda, Hitoshi Osaka, Yuji Gunji, Yukifumi Monden, Daisuke Tanaka
Publikováno v:
Multiple Sclerosis and Related Disorders. 45:102320
Intravenous corticosteroids have been regarded as the first-line therapy of anti-myelin-oligodendrocyte glycoprotein antibody (MOG-Ab)-positive acute disseminated encephalomyelitis (ADEM). While steroids are the first-choice therapy, MOG-Ab-positive
Autor:
Mari, Kuwajima, Masahide, Goto, Koyuru, Kurane, Hiroko, Shimbo, Narumi, Omika, Eriko F, Jimbo, Kazuhiro, Muramatsu, Makiko, Tajika, Masaru, Shimura, Kei, Murayama, Kenji, Kurosawa, Takanori, Yamagata, Hitoshi, Osaka
Publikováno v:
Braindevelopment. 41(5)
Mutations in the mitochondrial tRNA
Publikováno v:
Internal Medicine
A 76-year-old man complicated with end-stage renal disease had latent tuberculosis infection (LTBI), and isoniazid (INH) 300 mg daily was started to prevent reactivation of LTBI before using biologic agents for rheumatoid arthritis. On the 8th day af