Results 11 to 20 of about 91,538 (160)

Abnormal white matter tracts resembling pencil fibers involving prefrontal cortex (Brodmann area 47) in autism: a case report. [PDF]

open access: yes, 2016
BackgroundAutism is not correlated with any neuropathological hallmark as the brain of autistic individuals lack defined lesions. However, previous investigations have reported cortical heterotopias and local distortion of the cytoarchitecture of the ...
Ariza, Jeanelle   +4 more
core   +1 more source

Loss of Immunohistochemical Reactivity in Association With Handling-Induced Dark Neurons in Mouse Brains. [PDF]

open access: yes, 2020
The handling-induced dark neuron is a histological artifact observed in brain samples handled before fixation with aldehydes. To explore associations between dark neurons and immunohistochemical alterations in mouse brains, we examined protein products ...
Chang, Rachel C   +5 more
core  

Phosphorylation of GFAP is associated with injury in the neonatal pig hypoxic-ischemic brain [PDF]

open access: yes, 2012
Glial fibrillary acidic protein (GFAP) is an intermediate filament protein expressed in the astrocyte cytoskeleton that plays an important role in the structure and function of the cell.
A Lee   +53 more
core   +1 more source

Extracellular vesicle-induced differentiation of neural stem progenitor cells [PDF]

open access: yes, 2019
Neural stem progenitor cells (NSPCs) from E13.5 mouse embryos can be maintained in culture under proliferating conditions. Upon growth-factor removal, they may differentiate toward either neuronal or glial phenotypes or both.
Biagioni, S.   +5 more
core   +1 more source

Maternal embryonic leucine zipper kinase (MELK) regulates multipotent neural progenitor proliferation. [PDF]

open access: yes, 2005
Maternal embryonic leucine zipper kinase (MELK) was previously identified in a screen for genes enriched in neural progenitors. Here, we demonstrate expression of MELK by progenitors in developing and adult brain and that MELK serves as a marker for self-
Bajpai, Ruchi   +17 more
core   +2 more sources

Atypical MRI features in familial adult onset Alexander disease: case report [PDF]

open access: yes, 2016
BACKGROUND: Alexander disease (AxD) is a rare neurological disease, especially in adults. It shows variable clinical and radiological features. CASE PRESENTATION: We diagnosed a female with AxD presenting with paroxysmal numbness of the limbs at the ...
Anna Zhou   +7 more
core   +1 more source

Central Neurocytoma: A Review of Clinical Management and Histopathologic Features. [PDF]

open access: yes, 2016
Central neurocytoma (CN) is a rare, benign brain tumor often located in the lateral ventricles. CN may cause obstructive hydrocephalus and manifest as signs of increased intracranial pressure. The goal of treatment for CN is a gross total resection (GTR),
Bui, Timothy T   +10 more
core   +2 more sources

Teaching NeuroImages: Autoimmune glial fibrillary acidic protein meningoencephalomyelitis [PDF]

open access: yesNeurology, 2019
A 73-year-old woman with myelodysplastic syndrome presented with 2 months of decline in cognition and mobility, accompanied by headache and weight loss. Examination revealed a somnolent woman with symmetric cogwheel rigidity, bradykinesia, arm myoclonus, and hyperreflexia.
Paula K J, Lee   +2 more
openaire   +2 more sources

Combining H-FABP and GFAP increases the capacity to differentiate between CT-positive and CT-negative patients with mild traumatic brain injury [PDF]

open access: yes, 2018
Mild traumatic brain injury (mTBI) patients may have trauma-induced brain lesions detectable using CT scans. However, most patients will be CT-negative. There is thus a need for an additional tool to detect patients at risk. Single blood biomarkers, such
Bustamante, Alejandro   +8 more
core   +1 more source

Parainfectious Anti-Glial Fibrillary Acidic Protein-Associated Meningoencephalitis

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 improvement with empirical treatment. Two weeks after the illness, he suddenly developed orofacial, tongue,
Jae Young Joo, Dallah Yoo, Tae-Beom Ahn
openaire   +3 more sources

Home - About - Disclaimer - Privacy