Rapidly progressive dementia: Extending the spectrum of GFAP‐astrocytopathies?

Autoimmune glial fibrillary acidic protein astrocytopathy (GFAP‐A) is a steroid‐responsive meningoencephalomyelitis, sometimes presenting with atypical clinical signs such as movement disorders or psychiatric and autonomic features. Beyond clinical presentation and imaging, diagnosis relies on detec...

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Detalles Bibliográficos
Autores principales: Friedrich, Maximilian, Hartig, Johannes, Prüss, Harald, Ip, Chi Wang, Volkmann, Jens
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 2022
Materias:
Case Study
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8935272/
https://www.ncbi.nlm.nih.gov/pubmed/35130372
http://dx.doi.org/10.1002/acn3.51513

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8935272/
https://www.ncbi.nlm.nih.gov/pubmed/35130372
http://dx.doi.org/10.1002/acn3.51513

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