Adult-onset Alexander disease with unusual inflammatory features and a novel GFAP mutation in two patients
- PMID: 37495513
- DOI: 10.1111/nan.12927
Adult-onset Alexander disease with unusual inflammatory features and a novel GFAP mutation in two patients
Keywords: Alexander disease; GFAP mutation; adult onset; inflammation.
References
REFERENCES
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- Hagemann TL. Alexander disease: models, mechanisms, and medicine. Curr Opin Neurobiol. 2022;72:140-147. doi:10.1016/j.conb.2021.10.002
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- Pajares MA, Hernández-Gerez E, Pekny M, Pérez-Sala D. Alexander disease: the road ahead. Neural Regen Res. 2023;18(10):2156-2160. doi:10.4103/1673-5374.369097
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- Prust M, Wang J, Morizono H, et al. GFAP mutations, age at onset, and clinical subtypes in Alexander disease. Neurology. 2011;77(13):1287-1294. doi:10.1212/WNL.0b013e3182309f72
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- van der Knaap MS, Bugiani M. Leukodystrophies: a proposed classification system based on pathological changes and pathogenetic mechanisms. Acta Neuropathol. 2017;134(3):351-382. doi:10.1007/s00401-017-1739-1
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- Waisman Center. University of Wisconsin-Madison. Alexander disease. GFAP mutations associated with Alexander disease. Available at: http://www.waisman.wisc.edu/alexander-disease
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