Molecular genetic study in Japanese patients with Alexander disease: a novel mutation, R79L

[1]  H. Hoshi,et al.  MR imaging and 1H-MR spectroscopy in a case of juvenile Alexander disease , 2002, Brain and Development.

[2]  G. Takada,et al.  Juvenile Alexander disease with a novel mutation in glial fibrillary acidic protein gene. , 2002, Neurology.

[3]  E. Hoffman,et al.  Molecular findings in symptomatic and pre-symptomatic Alexander disease patients , 2002, Neurology.

[4]  K. Arimura,et al.  Autosomal dominant palatal myoclonus and spinal cord atrophy , 2002, Journal of the Neurological Sciences.

[5]  T. Shiihara,et al.  Fluctuation of Computed Tomographic Findings in White Matter in Alexander's Disease , 2002, Journal of child neurology.

[6]  E. Bertini,et al.  Infantile Alexander disease: spectrum of GFAP mutations and genotype-phenotype correlation. , 2001, American journal of human genetics.

[7]  Y. Matsubara,et al.  A novel mutation in glial fibrillary acidic protein gene in a patient with Alexander disease , 2001, Neuroscience Letters.

[8]  S. Tsujino,et al.  Diagnosis of Alexander disease in a Japanese patient by molecular genetic analysis , 2001, Journal of Human Genetics.

[9]  D. Rodriguez,et al.  Mutations in GFAP, encoding glial fibrillary acidic protein, are associated with Alexander disease , 2001, Nature Genetics.

[10]  W. Grodd,et al.  Alexander disease--classification revisited and isolation of a neonatal form. , 2000, Neuropediatrics.

[11]  W. S. Alexander.  Progressive fibrinoid degeneration of fibrillary astrocytes associated with mental retardation in a hydrocephalic infant. , 1949, Brain : a journal of neurology.