Background and Objectives To report the frequency of area postrema syndrome (APS) in
glial fibrillary acidic protein-immunoglobulin G (GFAP-IgG)–positive patients and emphasize …

Background and Objectives To report the clinical, biological, and imaging features and
clinical course of a French cohort of patients with glial fibrillary acidic protein (GFAP) …

Autoimmune glial fibrillary acidic protein (GFAP) astrocytopathy is a recently defined
autoimmune meningoencephalomyelitis, associated with GFAP-IgG antibody. A pooled …

Objective To describe the clinical features of autoimmune glial fibrillary acidic protein
(GFAP) astrocytopathy in children. Method Data from 11 pediatric patients with autoimmune …

Introduction Autoimmune glial fibrillary acidic protein (GFAP) astrocytopathy is scarce and
usually presents as meningoencephalomyelitis. Here, we offer the case of an atypical …

Objective: This paper reports the clinical manifestation and auxiliary examination features of
15 Chinese patients with glial fibrillary acidic protein (GFAP) autoimmunity. Methods: From …

Neuromyelitis optica spectrum disorder (NMOSD) is a rare inflammatory disease of the
central nervous system, characterized by the presence of auto-antibodies directed against …

Methods We searched Medline, Embase, Web of Science, and CNKI from inception to
February 2021 to acquire references on the relationship between neuroimmune diseases …

Background Area postrema syndrome (APS) is recognized as a core feature in neuromyelitis
optica (NMO) diagnosis. Isolated APS can occur at NMO onset and frequently results in a …

Introduction: Autoimmune glial fibrillary acidic protein (GFAP) astrocytopathy is a recently
described steroid-responsive meningoencephalomyelitis positive for cerebrospinal fluid …