MRI features and evolution of autoimmune glial fibrillary acidic protein astrocytopathy: A retrospective cross-sectional and longitudinal study-Reference-Cited by-同舟云学术

MRI features and evolution of autoimmune glial fibrillary acidic protein astrocytopathy: A retrospective cross-sectional and longitudinal study

Published:2022-02 Issue: Volume:58 Page:103512
ISSN:2211-0348
Container-title:Multiple Sclerosis and Related Disorders
language:en
Short-container-title:Multiple Sclerosis and Related Disorders

Author:

Liao Huiting,Chen Qianlan,Zhang Min,Chen Weiwei

Funder

National Natural Science Foundation of China

Natural Science Foundation of Hubei Province

Publisher

Elsevier BV

Subject

Neurology (clinical),Neurology,General Medicine

Reference36 articles.

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1. Case report: Excessive daytime sleepiness as a presenting manifestation of autoimmune glial fibrillary acidic protein astrocytopathy;Frontiers in Immunology;2023-12-20

2. Letter to the Editor: a case of autoimmune glial fibrillary acidic protein astrocytopathy with acute paralytic ileus as initial symptom;Neurological Sciences;2023-11-13

3. Plasma exchange for two patients with autoimmune GFAP astrocytopathy with rapid progression to respiratory failure: a case report;Frontiers in Immunology;2023-10-05

4. Magnetic Resonance Imaging Characteristics of Autoimmune Glial Fibrillary Acidic Protein (GFAP) Astrocytopathy: A Pediatric Series in Southwest China;Neuropsychiatric Disease and Treatment;2023-07

5. Enlarged perivascular spaces in autoimmune glial fibrillary acidic protein astrocytopathy;Neurological Sciences;2023-06-26