Art

J-GLOBAL ID：201002298318852717   Reference number：10A0254704

Bilateral occipital cortical dysplasia and white matter T2 hyperintensity with mild non-specific myopathy: Two sibling cases

軽度非特異的ミオパチを伴う両側後頭皮質形成異常および白質T2高強度: 二人の兄弟症例

Author (9)： OKANISHI Tohru (Dep. of Neonatology and Pediatrics, Nagoya City Univ. Graduate School of Medical Sciences, Nagoya, Aichi, JPN) ,  OKANISHI Tohru (Dep. of Pediatrics, Seirei-Hamamatsu General Hospital, Hamamatsu, Shizuoka, JPN) ,  ISHIKAWA Tatsuya (Dep. of Neonatology and Pediatrics, Nagoya City Univ. Graduate School of Medical Sciences, Nagoya, Aichi, JPN) ,  ISHIKAWA Tatsuya (Dep. of Clinical Psychology, Fac. of Child Dev., Nihon Fukushi Univ., Chita, Aichi, JPN) ,  KOBAYASHI Satoru (Dep. of Neonatology and Pediatrics, Nagoya City Univ. Graduate School of Medical Sciences, Nagoya, Aichi, JPN) ,  ANDO Naoki (Dep. of Neonatology and Pediatrics, Nagoya City Univ. Graduate School of Medical Sciences, Nagoya, Aichi, JPN) ,  NISHINO Ichizo (Dep. of Neuromuscular Res., National Inst. of Neuroscience, National Center of Neurology and Psychiatry, Kodaira ...) ,  TOGARI Hajime (Dep. of Neonatology and Pediatrics, Nagoya City Univ. Graduate School of Medical Sciences, Nagoya, Aichi, JPN) ,  NONAKA Ikuya (Dep. of Neuromuscular Res., National Inst. of Neuroscience, National Center of Neurology and Psychiatry, Kodaira ...)
Material： Brain & Development  (Brain & Dev)
Volume： 32  Issue： 4  Page： 342-346  Publication year： Apr. 2010 
JST Material Number： W0814A  ISSN： 0387-7604  Document type： Article
Article type： 原著論文  Country of issue： Netherlands (NLD)  Language： ENGLISH (EN)

Thesaurus term： human(primates) ,...
Semi thesaurus term： *両側後頭皮質形成異常 ,...

Register(free) or Log In to access     To see more with JDream III (charged).   {{ this.onShowAbsJLink("http://jdream3.com/lp/jglobal/index.html?docNo=10A0254704&from=J-GLOBAL&jstjournalNo=W0814A") }}

JST classification (1)： Nervous system diseases  (GN03000O)

Reference (13)：

• Toda T, Kobayashi K, Kondo-Iida E, Sasaki J, Nakamura Y. The Fukuyama congenital muscular dystrophy story. Neuromuscul Disord 2000;10:153-9.
• Barkovich AJ, Kuzniecky RI, Jackson GD, Guerrini R, Dobyns WB. A developmental and genetic classification for malformations of cortical development. Neurology 2005;65:1873-87.
• Aida N, Tamagawa K, Takada K, Yagishita A, Kobayashi N, Chikumaru K, et al. Brain MR in Fukuyama congenital muscular dystrophy. AJNR Am J Neuroradiol 1996;17:605-13.
• Philpot J, Cowan F, Pennock J, Sewry C, Dubowitz V, Bydder G, et al. Merosin-deficient congenital muscular dystrophy: the spectrum of brain involvement on magnetic resonance imaging. Neuromuscul Disord 1999;9:81-5.
• Yamamoto T, Kato Y, Kawaguchi-Niida M, Shibata N, Osawa M, Saito K, et al. Characteristics of neurons and glia in the brain of Fukuyama type congenital muscular dystrophy. Acta Myol 2008;27:9-13.

Terms in the title (6)： 軽度 ,  後頭皮質 ,  白質 ,  高強度 ,  兄弟 ,  症例