Results 11 to 20 of about 93,399 (211)

Parainfectious Anti-Glial Fibrillary Acidic Protein-Associated Meningoencephalitis [PDF]

open access: yesJournal of Movement Disorders, 2022
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
doaj   +3 more sources

Autoimmune glial fibrillary acidic protein astrocytopathy [PDF]

open access: yesCurrent Opinion in Neurology, 2019
Purpose of review To describe a recently characterized autoimmune, inflammatory central nervous system (CNS) disorder known as autoimmune glial fibrillary acidic protein (GFAP) astrocytopathy. Recent findings Affected patients present with symptoms of one or more of meningitis ...
Kunchok, Amy   +2 more
openaire   +4 more sources

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

open access: yesHeliyon, 2023
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
doaj   +1 more source

Emergence delirium and postoperative delirium associated with high plasma NfL and GFAP: an observational study

open access: yesFrontiers in Medicine, 2023
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
doaj   +1 more source

MRI findings of autoimmune glial fibrillary acidic protein astrocytopathy involving infratentorial: Case report

open access: yesRadiology Case Reports, 2022
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
doaj   +1 more source

Hippocampal neuron loss and astrogliosis in medial temporal lobe epileptic patients with mental disorders [PDF]

open access: yesJournal of Integrative Neuroscience, 2019
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
doaj   +1 more source

Aberrant Development of Enteric Glial Cells in the Colon of Hirschsprung's Disease

open access: yesFrontiers in Pediatrics, 2021
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
doaj   +1 more source

Autoimmune glial fibrillary acidic protein astrocytosis: one case report

open access: yesChinese Journal of Contemporary Neurology and Neurosurgery, 2021
doi:10.3969/j.issn.1672⁃6731.2021.11 ...
HUANG Gang   +2 more
doaj   +1 more source

Research progress of autoimmune glial fibrillary acidic protein astrocytopathy

open access: yesChinese Journal of Contemporary Neurology and Neurosurgery, 2022
Autoimmune glial fibrillary acidic protein astrocytopathy (GFAP ⁃ A) is a novel autoimmune inflammatory disease of the central nervous system first reported in 2016.
WANG Wen⁃wen, LI Mei
doaj   +1 more source

Diagnostic values of glial fibrillary acidic protein, neuron-specific enolase and protein S100β for sepsis-associated encephalopathy

open access: yesRomanian Journal of Laboratory Medicine, 2023
To investigate the expressions of glial fibrillary acidic protein (GFAP), neuron-specific enolase (NSE) and protein S100β and their diagnostic values for sepsis-associated encephalopathy (SAE).
Cao Zhigang, Huang Xiang, Chen Feixiang
doaj   +1 more source

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