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tau-deposition
12 studies tagged tau-deposition, dated 2018-03-24 to 2024-02-17. Bibliography: BibTeX (.bib) · RIS (.ris)
Newest in this topic
- Plasma N-terminal containing tau fragments (NTA-tau): a biomarker of tau deposition in Alzheimer's Disease 2024-02-17
- White Matter Degeneration Pathways Associated With Tau Deposition in Alzheimer Disease 2023-04-17
- The association between white matter hyperintensities and amyloid and tau deposition 2023-03-20
Studies
12 studies carry this tag.
Date range
2018 to 2024
Top journals
- Alzheimer's & dementia (Amsterdam, Netherlands) 2
- Brain communications 2
- Neurobiology of aging 2
- Alzheimer's research & therapy 1
- Brain : a journal of neurology 1
9 journals in all.
Newest first, then by address. Each study has a usefulness score out of 100 (rubric version 4.0); tap a score to see what makes it up. Tags were assigned automatically from each study's title and summary. The same studies as a filter in the library.
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However, because these biomarkers are strongly associated with the emergence of Aβ pathology, it is difficult to determine the contribution of insoluble tau aggregates to the plasma p-tau signal in blood.
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We found spatially dependent WM degeneration associated with regional flortaucipir SUVRs in Braak stages, suggesting a spatial pattern in WM damage.
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As secondary analyses, we observed effects of age and sex differences, atrophy, cognitive scores, and APOE genotype.
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These findings offer novel perspectives to the design of AD clinical trials and aid in understanding the tau accumulation inside and outside MTL in AD.
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Similar to late-onset and autosomal dominant Alzheimer's disease (AD), high tau was an indicator of early prodromal AD in DS.
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Sites of early neuropathologic change provide important clues regarding the initial clinical features of Alzheimer's disease (AD).
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Recent studies in cognitively unimpaired elderly individuals suggest that the APOE ε4 allele exerts a dosage-dependent effect on brain tau deposition.
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71/100
The apolipoprotein E gene ( APOE ) is the most important genetic risk factor for sporadic Alzheimer disease, with the ε4 allele being associated with increased cerebral amyloid-β and tau pathologies.
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The relationship between magnetic resonance imaging (MRI)-visible enlarged perivascular spaces (EPVS) and Aβ and tau deposition is poorly investigated in cognitively normal older population.
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52/100
Visual deficits are common in neurodegenerative diseases including Alzheimer's disease.
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After applying PVC and controlling for age, education level and global cortical 18 F-AV-45 SUVR, we found that the entorhinal cortex, amygdala, parahippocampal gyrus, posterior cingulate, and occipital ROIs exhibited a significant ApoE ε4 by sex interaction effect (false discovery rate P < 0.1) among MCI individuals.
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48/100
Quantitative assessment of perceived memory functioning may be useful for screening older adults at risk for Alzheimer's disease.