シマダ シノ
  島田 姿野
   所属   医学部 医学科(東京女子医科大学病院)
   職種   助教
論文種別 原著
言語種別 英語
査読の有無 査読あり
表題 Mutations in the genes encoding eukaryotic translation initiation factor 2B in Japanese patients with vanishing white matter disease.
掲載誌名 正式名:Brain & development
略  称:Brain Dev
ISSNコード:(1872-7131)0387-7604(Linking)
掲載区分国外
巻・号・頁 37(10),960-6頁
著者・共著者 Shimada S, Shimojima K, Sangu N, Hoshino A, Hachiya Y, Ohto T, Hashi Y, Nishida K, Mitani M, Kinjo S, Tsurusaki Y, Matsumoto N, Morimoto M, Yamamoto T
発行年月 2015/11
概要 All patients showed white matter abnormalities with various degrees. One patient showed manifestations of end-stage VWM disease. Some patients showed late onset and slow progression associated with brain magnetic resonance imaging displaying T2 high intensity only in the deep white matter. There was clinical heterogeneity among patients with VWM.
DOI 10.1016/j.braindev.2015.03.003
PMID 25843247