A rare case of glial fibrillary acidic protein astrocytopathy that resolved spontaneously within a self-limited course-Reference-Cited by-同舟云学术

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A rare case of glial fibrillary acidic protein astrocytopathy that resolved spontaneously within a self-limited course

Published:2023-10 Issue:10 Volume:9 Page:e20912
ISSN:2405-8440
Container-title:Heliyon
language:en
Short-container-title:Heliyon

Author:

Kaga Mihiro^ORCID,Ueda Takeshi^ORCID,Yoshikawa Satoshi^ORCID

Publisher

Elsevier BV

Subject

Multidisciplinary

Reference13 articles.

1. Autoimmune glial fibrillary acidic protein astrocytopathy: a novel meningoencephalomyelitis;B., Fang;JAMA Neurol.,2016

2. Glial fibrillary acidic protein in blood as a disease biomarker of neuromyelitis optica spectrum disorders;H., Kim;Front. Neurol.,2022

3. Characteristics of Movement Disorders in patients with autoimmune GFAP astrocytopathy;A., Kimura;Brain Sci.,2022

4. Autoimmune glial fibrillary acidic protein astrocytopathy;A., Kunchok;Curr. Opin. Neurol.,2019

5. Autoimmune GFAP astrocytopathy: prospective evaluation of 90 patients in 1 year;D., Dubey;J. Neuroimmunol.,2018

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