Clinical characteristics and diagnostic criteria on Alexander disease
Author:
Affiliation:
1. Department of Neurology, Graduate School of Medical Science, Kyoto Prefectural University of Medicine
Publisher
Societas Neurologica Japonica
Subject
Clinical Neurology
Link
https://www.jstage.jst.go.jp/article/clinicalneurol/60/9/60_cn-001442/_pdf
Reference53 articles.
1. 1) Alexander WS. Progressive fibrinoid degeneration of fibrillary astrocytes associated with mental retardation in a hydrocephalic infant. Brain 1949;72:373-381.
2. 2) Rosenthal W. Über eine eigenthϋmliche, mit Sylingomyelie complicirte Geschwulst des Ruckenmarks. Beitrage zur pathologischen Anatomie und zur allgemeinen Pathologie 1898;23:111-143.
3. 3) Brenner M, Johnson AB, Boespflug-Tanguy O, et al. Mutations in GFAP, encoding glial fibrillary acidic protein, are associated with Alexander disease. Nat Genet 2001;27:117-120.
4. 4) Okamoto Y, Mitsuyama H, Jonosono M, et al. Autosomal dominant palatal myoclonus and spinal cord atrophy. J Neurol Sci 2002;19:71-76.
5. 5) Namekawa M, Takiyama Y, Aoki Y, et al. Identification of GFAP gene mutation in hereditary adult-onset Alexander’s disease. Ann Neurol 2002;52:779-785.
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