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A Novel GFAP Mutation in Late-Onset Alexander Disease Showing Diffusion Restriction

Nam TS, Oh J, Levy M, Kang KW, Choi SY, Kim MK

No abstract available.
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A Neonatal Form of Alexander Disease Presented with Intractable Seizures and Obstructive Hydrocephalus

Yoo IH, Hong WG, Kim H, Lim BC, Hwang H, Chae JH, Kim KJ, Hwang YS

Alexander disease is a rare degenerative leukodystrophy caused by dominant mutations in glial fibrillary acidic protein (GFAP). The neonatal form of Alexander disease may manifest as frequent and intractable seizures...
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Alexander Disease

Kang JH, Hong SJ, Kim DK

Alexander disease (ALXD) is a rare demyelinating disease of the white matter of the brain that is caused by a mutation in the glial fibrillary acidic protein (GFAP) gene. The...
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A case of alexander disease

Jeon HJ, Lee BH, Hwang SH, Hwang YS, Chi JG

  • KMID: 1684847
  • J Korean Child Neurol Soc.
  • 1993 Sep;1(1):173-178.
No abstract available.
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