Results 1 to 10 of about 3,631,478 (254)
Glial fibrillary acidic protein in fibromyalgia: its serum levels and antibodies [PDF]
Background Fibromyalgia is a stress-related disorder in which dorsal root ganglia (DRG) may play an important pathogenic role. DRG exhibit unique stress-induced, pro-algesic physio-anatomy, where each pain-sensing nerve fiber soma is encased and ...
Felipe Massó +5 more
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Autoimmune Glial Fibrillary Acidic Protein Astrocytopathy: A Review of the Literature
Autoimmune glial fibrillary acidic protein (GFAP) astrocytopathy is an autoimmune disease of the nervous system first defined in 2016. GFAP autoantibody, especially IgG that binds to GFAPα, has been reported in the cerebrospinal fluid (CSF) and serum of ...
Fulan Shan +3 more
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Overlapping Autoimmune Syndromes in Patients With Glial Fibrillary Acidic Protein Antibodies
BackgroundGlial fibrillary acidic protein (GFAP) astrocytopathy, an autoimmune central nervous system disorder with a specific GFAP-IgG, often coexists with other antibodies.ObjectiveThe aim of this article was to study overlapping syndromes in ...
Xinguang Yang +16 more
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Parainfectious Anti-Glial Fibrillary Acidic Protein-Associated Meningoencephalitis [PDF]
Movement disorders associated with glial fibrillary acidic protein (GFAP) autoantibodies have rarely been reported as ataxia or tremors. A 32-year-old man with headache and fever, initially diagnosed with viral meningoencephalitis, showed gradual ...
Jae Young Joo, Dallah Yoo, Tae-Beom Ahn
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Glial fibrillary acidic protein astrocytopathy is a form of autoimmune meningoencephalomyelitis. The presence of antibodies in spinal fluid against glial fibrillary acidic protein is necessary to diagnose the disease.
Mihiro Kaga +2 more
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BackgroundNeuroinflammation and neuronal injury have been reported to be associated with the development of postoperative delirium in both preclinical and clinical settings.
Xingyang Liu +7 more
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Autoimmune glial fibrillary acidic protein astrocytopathy (GFAP-A) is a new type of autoimmune astrocytopathy first defined in 2016. Lack of clinical understanding, often misdiagnosed as optic neuromyelitis or multiple sclerosis.
Wenhui Ma, BA +3 more
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Hippocampal neuron loss and astrogliosis in medial temporal lobe epileptic patients with mental disorders [PDF]
Hippocampal neuron loss and reactive astrogliosis are pathological features of medial temporal lobe epilepsy. Here, the expression of hippocampal astrogliosis-associated genes are studied in subjects with medial temporal lobe epilepsy and mental ...
Jun Lu, Hongxing Huang, Qichang Zeng, Xinmei Zhang, Min Xu, Yi Cai, Qin Wang, Yahui Huang, Qiong Peng, Lanqiuzi Deng
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Aberrant Development of Enteric Glial Cells in the Colon of Hirschsprung's Disease
Objective: The aim of this study was to explore the development of enteric glial cells (EGCs) in different segments of Hirschsprung's disease (HSCR).Methods: Colonic specimens from 35 children with HSCR were selected to analyze the relative expression of
Tingting Zhou +8 more
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Autoimmune glial fibrillary acidic protein astrocytosis: one case report
doi:10.3969/j.issn.1672⁃6731.2021.11 ...
HUANG Gang +2 more
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