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Maartje I. Kester

Researcher at VU University Medical Center

Publications -  21
Citations -  1219

Maartje I. Kester is an academic researcher from VU University Medical Center. The author has contributed to research in topics: Apolipoprotein E & Cognitive decline. The author has an hindex of 16, co-authored 21 publications receiving 1053 citations.

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Neurogranin as a Cerebrospinal Fluid Biomarker for Synaptic Loss in Symptomatic Alzheimer Disease

TL;DR: Neurogranin is a promising biomarker for AD because levels were elevated in patients with AD compared with cognitively normal participants and predicted progression from MCI to AD, and within-person levels of NGRN increased in cognitivelynormal participants but not in Patients with later stage MCI or AD, which suggests that N GRN may reflect presymptomatic synaptic dysfunction or loss.
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Patients With Alzheimer Disease With Multiple Microbleeds Relation With Cerebrospinal Fluid Biomarkers and Cognition

TL;DR: Microbleeds are associated with the clinical manifestation and biochemical hallmarks of Alzheimer disease, suggesting possible involvement of MBs in the pathogenesis of Alzheimer Disease.
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Associations Between Cerebral Small-Vessel Disease and Alzheimer Disease Pathology as Measured by Cerebrospinal Fluid Biomarkers

TL;DR: Deposition of amyloid appears aggravated in patients with cerebral small-vessel disease, especially in apolipoprotein E ε4 carriers, providing evidence for pathophysiological synergy between these 3 biological factors.
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CSF biomarkers predict rate of cognitive decline in Alzheimer disease.

TL;DR: It is hypothesized that high tau, especially in combination with relatively low p-tau-181, is a marker of rapid decline, since it has been associated with fast neuronal degeneration in patients with AD.
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Cerebrospinal fluid VILIP-1 and YKL-40, candidate biomarkers to diagnose, predict and monitor Alzheimer's disease in a memory clinic cohort

TL;DR: CSF levels of YKL-40 may have utility for discriminating between cognitively normal individuals and patients with MCI or AD and increased levels of both YKl-40 and VILIP-1 may be associated with disease progression.