A case of infantile Alexander disease diagnosed by magnetic resonance imaging and genetic analysis-Reference-Cited by-同舟云学术

A case of infantile Alexander disease diagnosed by magnetic resonance imaging and genetic analysis

Published:2007-09 Issue:8 Volume:29 Page:525-528
ISSN:0387-7604
Container-title:Brain and Development
language:en
Short-container-title:Brain and Development

Author:

Sakakibara Takafumi,Takahashi Yukihiro,Fukuda Kazuyoshi,Inoue Tomomi,Kurosawa Tomoko,Nishikubo Toshiya,Shima Midori,Taoka Toshiaki,Aida Noriko,Tsujino Seiichi,Kanazawa Naomi,Yoshioka Akira

Publisher

Elsevier BV

Subject

Clinical Neurology,Developmental Neuroscience,General Medicine,Pediatrics, Perinatology, and Child Health

Reference10 articles.

1. GFAP mutations in Alexander disease;Li;Int J Dev Neurosci,2002

2. Alexander-disease mutation of GFAP causes filament disorganization and decreased solubility of GFAP;Hsiao;J Cell Sci,2005

3. Alexander disease: diagnosis with MR imaging;van der Knaap;AJNR Am J Neuroradiol,2001

4. Diagnosis of Alexander disease in a Japanese patient by molecular genetic analysis;Shiroma;J Hum Genet,2001

5. Progressive fibrinoid degeneration of fibrillary astrocytes associated with mental retardation in a hydrocephalic infant;Alexander;Brain,1949

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