Decreased expression of aquaporin 4 at the muscle plasma membrane of children with Fukuyama-type congenital muscular dystrophy

被引:0
|
作者
Wakayama, Y
Jimi, T
Kojima, H
Inoue, M
Yamashita, S
Kumagai, T
Murahashi, M
Hara, H
Shibuya, S
机构
关键词
D O I
暂无
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
引用
收藏
页码:S93 / S94
页数:2
相关论文
共 50 条
  • [31] ABNORMAL EXPRESSION OF DYSTROPHIN-ASSOCIATED PROTEINS IN FUKUYAMA-TYPE CONGENITAL MUSCULAR-DYSTROPHY
    MATSUMURA, K
    NONAKA, I
    CAMPBELL, KP
    LANCET, 1993, 341 (8844): : 521 - 522
  • [32] Expression profiling of muscles from Fukuyama-type congenital muscular dystrophy and laminin-α2 deficient congenital muscular dystrophy;: is congenital muscular dystrophy a primary fibrotic disease?
    Taniguchi, M
    Kurahashi, H
    Noguchi, S
    Sese, J
    Okinaga, T
    Tsukahara, T
    Guicheney, P
    Ozono, K
    Nishino, I
    Morishita, S
    Toda, T
    BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2006, 342 (02) : 489 - 502
  • [33] Molecular genetic evidence of clinical heterogeneity in Fukuyama-type congenital muscular dystrophy
    KondoIida, E
    Saito, K
    Tanaka, H
    Tsuji, S
    Ishihara, T
    Osawa, M
    Fukuyama, Y
    Toda, T
    HUMAN GENETICS, 1997, 99 (04) : 427 - 432
  • [34] 2-DUTCH SIBLINGS WITH CONGENITAL MUSCULAR-DYSTROPHY (FUKUYAMA-TYPE)
    VLES, JSH
    DEKROM, MCTFM
    VISSER, R
    HOWELER, CJ
    CLINICAL NEUROLOGY AND NEUROSURGERY, 1983, 85 (03) : 175 - 180
  • [35] CLINICAL VARIATION WITHIN SIBSHIPS IN FUKUYAMA-TYPE CONGENITAL MUSCULAR-DYSTROPHY
    YOSHIOKA, M
    KUROKI, S
    NIGAMI, H
    KAWAI, T
    NAKAMURA, H
    BRAIN & DEVELOPMENT, 1992, 14 (05): : 334 - 337
  • [36] Molecular genetic evidence of clinical heterogeneity in Fukuyama-type congenital muscular dystrophy
    E. Kondo-Iida
    Kayoko Saito
    Hajime Tanaka
    Shoji Tsuji
    Tadayuki Ishihara
    Makiko Osawa
    Yukio Fukuyama
    Tatsushi Toda
    Human Genetics, 1997, 99 : 427 - 432
  • [37] Founder-haplotype analysis in Fukuyama-type congenital muscular dystrophy (FCMD)
    Kazuhiro Kobayashi
    Yutaka Nakahori
    Kunihiko Mizuno
    Masashi Miyake
    Toshiyuki Kumagai
    Akira Honma
    Ikuya Nonaka
    Yusuke Nakamura
    Katsushi Tokunaga
    T. Toda
    Human Genetics, 1998, 103 : 323 - 327
  • [38] FUKUYAMA-TYPE CONGENITAL MUSCULAR-DYSTROPHY AND THE WALKER-WARBURG SYNDROME
    KIMURA, S
    SASAKI, Y
    KOBAYASHI, T
    OHTSUKI, N
    TANAKA, Y
    HARA, M
    MIYAKE, S
    YAMADA, M
    IWAMOTO, H
    MISUGI, N
    BRAIN & DEVELOPMENT, 1993, 15 (03): : 182 - 191
  • [39] A case of Fukuyama-type congenital muscular dystrophy with a very mild mental deficit
    Hino-Fukuyo, N
    Haginoya, K
    Hayashi, YK
    Nishino, I
    Murakami, T
    Nonaka, I
    Togashi, K
    Tanaka, S
    Takayanagi, M
    Yokoyama, H
    Sakamoto, O
    Abe, T
    Toda, T
    Iinuma, K
    NEUROMUSCULAR DISORDERS, 2006, 16 (04) : 274 - 276
  • [40] Founder-haplotype analysis in Fukuyama-type congenital muscular dystrophy (FCMD)
    Kobayashi, K
    Nakahori, Y
    Mizuno, K
    Miyake, M
    Kumagai, T
    Honma, A
    Nonaka, I
    Nakamura, Y
    Tokunaga, K
    Toda, T
    HUMAN GENETICS, 1998, 103 (03) : 323 - 327