- Anesthetic Management of a Patient with Alexander's Disease: Case Report
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Kim BS, Jee DL, Song SO
- KMID: 1462711
- Yeungnam Univ J Med.
- 2010 Jun;27(1):47-51.
- doi: 10.12701/yujm.2010.27.1.47
We present here the case of a 13-year-old male patient with Alexander's disease who underwent surgical correction of a femur fracture. Alexander's disease is a rare and fatal disorder that... -
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- A case of alexander disease
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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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- A Neonatal Form of Alexander Disease Presented with Intractable Seizures and Obstructive Hydrocephalus
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Yoo IH, Hong WG, Kim H, Lim BC, Hwang H, Chae JH, Kim KJ, Hwang YS
- KMID: 1811007
- J Genet Med.
- 2013 Dec;10(2):113-116.
- doi: 10.5734/JGM.2013.10.2.113
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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- A Case of Infantile Alexander Disease
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Park GM, Ko JH, Min KS
- KMID: 2329431
- J Korean Child Neurol Soc.
- 2009 Nov;17(2):215-220.
Alexander disease(AD) is a rare fatal demyelinating disorder, caused by the mutation of glial fibrillary acidic protein(GFAP) gene. It is characterized by progressive demyelination of central nervous system, and the... -
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- A Novel GFAP Mutation in Late-Onset Alexander Disease Showing Diffusion Restriction
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Nam TS, Oh J, Levy M, Kang KW, Choi SY, Kim MK
- KMID: 2392141
- J Clin Neurol.
- 2017 Oct;13(4):426-428.
- doi: 10.3988/jcn.2017.13.4.426
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- Alexander Disease
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Kang JH, Hong SJ, Kim DK
- KMID: 1811002
- J Genet Med.
- 2013 Dec;10(2):88-93.
- doi: 10.5734/JGM.2013.10.2.88
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 Infantile Alexander Disease Accompanied by Infantile Spasms Diagnosed by DNA Analysis
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Lee JM, Kim AS, Lee SJ, Cho SM, Lee DS, Choi SM, Kim DK, Ki CS, Kim JW
- KMID: 1781924
- J Korean Med Sci.
- 2006 Oct;21(5):954-957.
- doi: 10.3346/jkms.2006.21.5.954
Alexander disease (AD) is a rare leukodystrophy of the central nervous system of unknown etiology. AD is characterized by progressive failure of central myelination and the accumulation of Rosenthal fibers... -
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