Autoimmune glial fibrillary acidic protein astrocytopathy: case report of a treatable cause of rapidly progressive dementia
Author:
Publisher
Springer Science and Business Media LLC
Subject
Clinical Neurology,Neurology
Link
https://link.springer.com/content/pdf/10.1007/s00415-021-10484-y.pdf
Reference9 articles.
1. Rosales JJ, Toledano C, Riverol M, Arbizu J (2020) [18F]-FDG PET imaging in autoimmune GFAP meningoencephalomyelitis. Eur J Nucl Med Mol Imaging. https://doi.org/10.1007/s00259-020-05001-8
2. Josephs KA, Ahlskog JE, Parisi JE et al (2009) Rapidly progressive neurodegenerative dementias. Arch Neurol 66:201–207. https://doi.org/10.1001/archneurol.2008.534
3. Fang B, McKeon A, Hinson SR et al (2016) Autoimmune glial fibrillary acidic protein astrocytopathy: a novel meningoencephalomyelitis. JAMA Neurol 73:1297–1307. https://doi.org/10.1001/jamaneurol.2016.2549
4. Flanagan EP, Hinson SR, Lennon VA et al (2017) GFAP-IgG as biomarker of autoimmune astrocytopathy: analysis of 102 patients. Ann Neurol 7:1–34. https://doi.org/10.1002/ana.24881
5. Sasaki K, Bean A, Shah S et al (2014) Relapsing-remitting central nervous system autoimmunity mediated by GFAP-specific CD8 T cells. J Immunol 192:3029–3042. https://doi.org/10.4049/jimmunol.1302911
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