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Modeling the Role of the Glymphatic Pathway and Cerebral Blood Vessel Properties in Alzheimer’s Disease Pathogenesis

https://doi.org/10.1371/journal.pone.0139574
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Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/(sici)1096-9861(19970324)379:4<482::aid-cne2>3.0.co;2-zopenalex-snapshot
Volume and number of neurons of the human hippocampal formation in normal aging and Alzheimer's disease
inferredcites →https://doi.org/10.1002/adem.201080076openalex-snapshot
Image Analysis of Endothelial Microstructure and Endothelial Cell Dimensions of Human Arteries – A Preliminary Study
inferredcites →https://doi.org/10.1002/ana.20503openalex-snapshot
Correlates of hippocampal neuron number in Alzheimer's disease and ischemic vascular dementia
inferredcites →https://doi.org/10.1002/ana.24271openalex-snapshot
Impairment of paravascular clearance pathways in the aging brain
inferredcites →https://doi.org/10.1002/glia.10319openalex-snapshot
Dystrophic microglia in the aging human brain
inferredcites →https://doi.org/10.1002/mrc.2596openalex-snapshot
Aggregation of amyloid Aβ(1–40) peptide in perdeuterated 2,2,2‐trifluoroethanol caused by ultrasound sonication
inferredcites →https://doi.org/10.1002/path.1711360306openalex-snapshot
Endothelial pavement patterns in human arteries
inferredcites →https://doi.org/10.1007/s00401-013-1083-zopenalex-snapshot
Oligomers, fact or artefact? SDS-PAGE induces dimerization of β-amyloid in human brain samples
inferredcites →https://doi.org/10.1007/s10803-012-1513-0openalex-snapshot
Microglia in the Cerebral Cortex in Autism
inferredcites →https://doi.org/10.1007/s11065-009-9118-xopenalex-snapshot
Beta-Amyloid Deposition and the Aging Brain
inferredcites →https://doi.org/10.1016/c2009-0-02551-3openalex-snapshot
Providing Pharmacological Access to the Brain - Alternate Approaches
inferredcites →https://doi.org/10.1016/j.exger.2008.04.002openalex-snapshot
Alzheimer’s disease, cerebrovascular dysfunction and the benefits of exercise: From vessels to neurons
inferredcites →https://doi.org/10.1016/j.neuint.2003.11.006openalex-snapshot
Evidence for bulk flow of brain interstitial fluid: significance for physiology and pathology
inferredcites →https://doi.org/10.1016/j.neurobiolaging.2007.04.013openalex-snapshot
Neocortical glial cell numbers in human brains
inferredcites →https://doi.org/10.1016/j.neuron.2014.01.045openalex-snapshot
ApoE and Aβ in Alzheimer’s Disease: Accidental Encounters or Partners?
inferredcites →https://doi.org/10.1016/j.nicl.2014.01.016openalex-snapshot
LRP-1 polymorphism is associated with global and regional amyloid load in Alzheimer's disease in humans in-vivo
inferredcites →https://doi.org/10.1016/s0006-3495(01)75831-6openalex-snapshot
A Mathematical Model of the Kinetics of β-Amyloid Fibril Growth from the Denatured State
inferredcites →https://doi.org/10.1016/s0092-8240(03)00030-2openalex-snapshot
Chemotactic Signaling, Microglia, and Alzheimer's Disease Senile Plaques: Is There a Connection?
inferredcites →https://doi.org/10.1016/s0166-2236(02)02143-4openalex-snapshot
Exercise: a behavioral intervention to enhance brain health and plasticity
inferredcites →https://doi.org/10.1038/jcbfm.2013.125openalex-snapshot
Contributions of Degradation and Brain-to-blood Elimination Across the Blood—Brain Barrier to Cerebral Clearance of Human Amyloid-β Peptide(1-40) in Mouse Brain
inferredcites →https://doi.org/10.1038/nrd3505openalex-snapshot
The amyloid cascade hypothesis for Alzheimer's disease: an appraisal for the development of therapeutics
inferredcites →https://doi.org/10.1038/nrm2101openalex-snapshot
Soluble protein oligomers in neurodegeneration: lessons from the Alzheimer's amyloid β-peptide
inferredcites →https://doi.org/10.1038/sj.jcbfm.9600419openalex-snapshot
Transport Pathways for Clearance of Human Alzheimer's Amyloid β-Peptide and Apolipoproteins E and J in the Mouse Central Nervous System
inferredcites →https://doi.org/10.1038/srep02942openalex-snapshot
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inferredcites →https://doi.org/10.1038/srep04681openalex-snapshot
Brain microvascular endothelial cells resist elongation due to curvature and shear stress
inferredcites →https://doi.org/10.1056/nejmra0909142openalex-snapshot
Alzheimer's Disease
inferredcites →https://doi.org/10.1073/pnas.1206446109openalex-snapshot
Low-density lipoprotein receptor overexpression enhances the rate of brain-to-blood Aβ clearance in a mouse model of β-amyloidosis
inferredcites →https://doi.org/10.1073/pnas.1220484110openalex-snapshot
ApoE influences amyloid-β (Aβ) clearance despite minimal apoE/Aβ association in physiological conditions
inferredcites →https://doi.org/10.1073/pnas.1502150112openalex-snapshot
Cleavage of amyloid precursor protein by an archaeal presenilin homologue PSH
inferredcites →https://doi.org/10.1073/pnas.93.3.1125openalex-snapshot
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inferredcites →https://doi.org/10.1073/pnas.95.21.12277openalex-snapshot
Temperature dependence of amyloid β-protein fibrillization
inferredcites →https://doi.org/10.1093/brain/awp007openalex-snapshot
MRI of hippocampal volume loss in early Alzheimer's disease in relation to ApoE genotype and biomarkers
inferredcites →https://doi.org/10.1093/brain/aws243openalex-snapshot
Amyloid-β-dependent compromise of microvascular structure and function in a model of Alzheimer’s disease
inferredcites →https://doi.org/10.1093/brain/awu255openalex-snapshot
Highly potent soluble amyloid-β seeds in human Alzheimer brain but not cerebrospinal fluid
inferredcites →https://doi.org/10.1093/cercor/8.8.710openalex-snapshot
Variation in hippocampal neuron number with age and brain volume
inferredcites →https://doi.org/10.1101/cshperspect.a006346openalex-snapshot
Inflammation in Alzheimer Disease--A Brief Review of the Basic Science and Clinical Literature
inferredcites →https://doi.org/10.1111/j.1749-6632.2010.05786.xopenalex-snapshot
Aging and cerebrovascular dysfunction: contribution of hypertension, cerebral amyloid angiopathy, and immunotherapy
inferredcites →https://doi.org/10.1126/science.1240514openalex-snapshot
Garbage Truck of the Brain
inferredcites →https://doi.org/10.1126/science.1241224openalex-snapshot
Sleep Drives Metabolite Clearance from the Adult Brain
inferredcites →https://doi.org/10.1126/scitranslmed.3002156openalex-snapshot
Human apoE Isoforms Differentially Regulate Brain Amyloid-β Peptide Clearance
inferredcites →https://doi.org/10.1126/scitranslmed.3003748openalex-snapshot
A Paravascular Pathway Facilitates CSF Flow Through the Brain Parenchyma and the Clearance of Interstitial Solutes, Including Amyloid β
inferredcites →https://doi.org/10.1137/1.9780898718287openalex-snapshot
Applied Mathematical Models in Human Physiology
inferredcites →https://doi.org/10.1152/ajpheart.00332.2004openalex-snapshot
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inferredcites →https://doi.org/10.1159/000337231openalex-snapshot
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inferredcites →https://doi.org/10.1161/strokeaha.109.559641openalex-snapshot
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inferredcites →https://doi.org/10.1172/jci10498openalex-snapshot
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inferredcites →https://doi.org/10.1182/blood-2004-08-3026openalex-snapshot
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inferredcites →https://doi.org/10.1182/blood-2005-03-1185openalex-snapshot
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inferredcites →https://doi.org/10.1182/blood.v91.10.3527openalex-snapshot
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inferredcites →https://doi.org/10.1186/2045-8118-11-10openalex-snapshot
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inferredcites →https://doi.org/10.1186/2045-824x-4-12openalex-snapshot
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inferredcites →https://doi.org/10.1186/alzrt187openalex-snapshot
Evidence for impaired amyloid β clearance in Alzheimer's disease
inferredcites →https://doi.org/10.1186/alzrt6openalex-snapshot
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inferredcites →https://doi.org/10.1186/s12979-015-0029-9openalex-snapshot
Blood–brain barrier dysfunction developed during normal aging is associated with inflammation and loss of tight junctions but not with leukocyte recruitment
inferredcites →https://doi.org/10.1194/jlr.r800069-jlr200openalex-snapshot
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inferredcites →https://doi.org/10.1371/journal.pone.0015176openalex-snapshot
Mathematical Modeling for the Pathogenesis of Alzheimer's Disease
inferredcites →https://doi.org/10.1371/journal.pone.0041636openalex-snapshot
Disruption of Arterial Perivascular Drainage of Amyloid-β from the Brains of Mice Expressing the Human APOE ε4 Allele
inferredcites →https://doi.org/10.1523/jneurosci.0496-05.2005openalex-snapshot
Voluntary Exercise Decreases Amyloid Load in a Transgenic Model of Alzheimer's Disease
inferredcites →https://doi.org/10.1523/jneurosci.1592-13.2013openalex-snapshot
Cerebral Arterial Pulsation Drives Paravascular CSF–Interstitial Fluid Exchange in the Murine Brain
inferredcites →https://doi.org/10.1523/jneurosci.23-26-08844.2003openalex-snapshot
In vivo assessment of brain interstitial fluid with microdialysis reveals plaque-associated changes in amyloid-beta metabolism and half-life.
inferredcites →https://doi.org/10.2174/138161208784705487openalex-snapshot
The Role of the Cell Surface LRP and Soluble LRP in Blood-Brain Barrier Aβ Clearance in Alzheimers Disease
inferredcites →https://doi.org/10.2174/138161210790883723openalex-snapshot
β -Amyloid: A Disease Target or a Synaptic Regulator Affecting Age-Related Neurotransmitter Changes?
inferredcites →https://doi.org/10.3109/13550289909021285openalex-snapshot
Blood-brain barrier biology and methodology
inferredcites →https://doi.org/10.3171/2008.9.jns08584openalex-snapshot
Monitoring of brain interstitial total tau and beta amyloid proteins by microdialysis in patients with traumatic brain injury
inferredcites →https://doi.org/10.3389/fnagi.2014.00251openalex-snapshot
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inferredcites →https://doi.org/10.3389/fneng.2013.00007openalex-snapshot
The blood-brain barrier: an engineering perspective
inferredcites →https://doi.org/10.4062/biomolther.2012.20.3.245openalex-snapshot
Mechanisms of Amyloid-β Peptide Clearance: Potential Therapeutic Targets for Alzheimer's Disease

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.2139/ssrn.3031579openalex-extracted
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inferred← citeshttps://doi.org/10.2139/ssrn.3041744openalex-extracted
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inferred← citeshttps://doi.org/10.1002/nbm.5132openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/psp4.12155openalex-snapshot
The Impact of Mathematical Modeling in Understanding the Mechanisms Underlying Neurodegeneration: Evolving Dimensions and Future Directions
inferred← citeshttps://doi.org/10.1007/978-3-032-22008-0_3openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s00213-016-4473-9openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s00281-020-00816-xopenalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s10237-019-01253-yopenalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s11357-026-02133-xopenalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s13721-022-00366-2openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/b978-0-12-819603-8.00004-3openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/b978-0-323-95702-1.00243-8openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.amjcard.2020.09.008openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.arr.2020.101067openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.brainres.2016.06.040openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.cell.2019.02.014openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.cis.2017.12.002openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.ejphar.2017.05.062openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.expneurol.2024.114702openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2025.142887openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.neubiorev.2017.08.016openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.neubiorev.2018.03.028openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.neubiorev.2019.05.016openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.neuroimage.2018.12.039openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.pharmr.2025.100052openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.tins.2016.05.002openalex-snapshot
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inferred← citeshttps://doi.org/10.1038/s41598-020-77787-4openalex-snapshot
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inferred← citeshttps://doi.org/10.1038/s41598-025-02054-3openalex-snapshot
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inferred← citeshttps://doi.org/10.1063/1.5039854openalex-snapshot
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inferred← citeshttps://doi.org/10.1101/2025.03.28.645905openalex-snapshot
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inferred← citeshttps://doi.org/10.14336/ad.2023.0426openalex-snapshot
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inferred← citeshttps://doi.org/10.2463/mrms.mp.2016-0039openalex-snapshot
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inferred← citeshttps://doi.org/10.26481/dis.20210601ivopenalex-snapshot
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inferred← citeshttps://doi.org/10.30707/spora3.1kinneyopenalex-snapshot
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inferred← citeshttps://doi.org/10.3233/bpl-180069openalex-snapshot
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inferred← citeshttps://doi.org/10.3233/jad-215680openalex-snapshot
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inferred← citeshttps://doi.org/10.3233/jad-230933openalex-snapshot
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inferred← citeshttps://doi.org/10.3233/jad-240212openalex-snapshot
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inferred← citeshttps://doi.org/10.3325/cmj.2016.57.223openalex-snapshot
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inferred← citeshttps://doi.org/10.3389/fnagi.2020.00136openalex-snapshot
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inferred← citeshttps://doi.org/10.3389/fnagi.2021.599724openalex-snapshot
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inferred← citeshttps://doi.org/10.3389/fnagi.2021.659457openalex-snapshot
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inferred← citeshttps://doi.org/10.3389/fnagi.2022.841798openalex-snapshot
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inferred← citeshttps://doi.org/10.3389/fnagi.2022.873697openalex-snapshot
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inferred← citeshttps://doi.org/10.3389/fnagi.2025.1671741openalex-snapshot
Unvalidated efficacy and significant risks hinder clinical use of deep cervical lymphatic-venous anastomosis for Alzheimer’s disease
inferred← citeshttps://doi.org/10.3389/fnagi.2026.1788077openalex-snapshot
Imaging the therapeutic effects of cerebral endothelial cell derived exosome treatment of a preclinical model of Alzheimer’s disease
inferred← citeshttps://doi.org/10.3389/fnana.2021.665803openalex-snapshot
Waste Clearance in the Brain
inferred← citeshttps://doi.org/10.3389/fncel.2020.618986openalex-snapshot
Microvascular Alterations in Alzheimer's Disease
inferred← citeshttps://doi.org/10.3389/fneur.2017.00734openalex-snapshot
Pseudotumor Cerebri and Glymphatic Dysfunction
inferred← citeshttps://doi.org/10.3389/fneur.2018.00867openalex-snapshot
The Glymphatic System in Diabetes-Induced Dementia
inferred← citeshttps://doi.org/10.3389/fninf.2025.1590968openalex-snapshot
Sensitivity analysis of a mathematical model of Alzheimer's disease progression unveils important causal pathways
inferred← citeshttps://doi.org/10.3389/fnins.2018.00330openalex-snapshot
Sleep Disorders Associated With Alzheimer's Disease: A Perspective
inferred← citeshttps://doi.org/10.3389/fnins.2020.566428openalex-snapshot
Neurodegenerative Disorders of the Eye and of the Brain: A Perspective on Their Fluid-Dynamical Connections and the Potential of Mechanism-Driven Modeling
inferred← citeshttps://doi.org/10.3389/fnins.2021.605586openalex-snapshot
Research on the Glial–Lymphatic System and Its Relationship With Alzheimer’s Disease
inferred← citeshttps://doi.org/10.3389/fnins.2024.1428085openalex-snapshot
Influencing factors of glymphatic system during perioperative period
inferred← citeshttps://doi.org/10.3390/biomimetics3010004openalex-snapshot
Targeting Early Dementia: Using Lipid Cubic Phase Nanocarriers to Cross the Blood–Brain Barrier
inferred← citeshttps://doi.org/10.3390/biomimetics5010011openalex-snapshot
Biomimetic Nanocarrier Targeting Drug(s) to Upstream-Receptor Mechanisms in Dementia: Focusing on Linking Pathogenic Cascades
inferred← citeshttps://doi.org/10.3390/brainsci12060742openalex-snapshot
Effects of Sound Interventions on the Permeability of the Blood–Brain Barrier and Meningeal Lymphatic Clearance
inferred← citeshttps://doi.org/10.3390/cells9122581openalex-snapshot
Novel PET Biomarkers to Disentangle Molecular Pathways across Age-Related Neurodegenerative Diseases
inferred← citeshttps://doi.org/10.3390/diagnostics10060344openalex-snapshot
Magnetic Resonance Imaging and Modeling of the Glymphatic System
inferred← citeshttps://doi.org/10.3390/diagnostics15081019openalex-snapshot
Vascular Contribution to Cerebral Waste Clearance Affected by Aging or Diabetes
inferred← citeshttps://doi.org/10.3390/genes15121509openalex-snapshot
Is the Relationship Between Cardiovascular Disease and Alzheimer’s Disease Genetic? A Scoping Review
inferred← citeshttps://doi.org/10.3390/medsci5040029openalex-snapshot
Alzheimer’s Disease, Brain Injury, and C.N.S. Nanotherapy in Humans: Sonoporation Augmenting Drug Targeting
inferred← citeshttps://doi.org/10.36959/734/381openalex-snapshot
Drug Nanotargeting for Treating Vascular Dementia and Alzheimer's Disease
inferred← citeshttps://doi.org/10.3945/an.115.011775openalex-snapshot
Associations between Sleep, Cortisol Regulation, and Diet: Possible Implications for the Risk of Alzheimer Disease
inferred← citeshttps://doi.org/10.6084/m9.figshare.13115544openalex-snapshot
Additional file 1 of The effects of six months Persicaria minor extract supplement among older adults with mild cognitive impairment: a double-blinded, randomized, and placebo-controlled trial
inferred← citeshttps://doi.org/10.6084/m9.figshare.13115547openalex-snapshot
Additional file 2 of The effects of six months Persicaria minor extract supplement among older adults with mild cognitive impairment: a double-blinded, randomized, and placebo-controlled trial
inferred← citeshttps://doi.org/10.6084/m9.figshare.13115550openalex-snapshot
Additional file 3 of The effects of six months Persicaria minor extract supplement among older adults with mild cognitive impairment: a double-blinded, randomized, and placebo-controlled trial
inferred← citeshttps://doi.org/10.6084/m9.figshare.13115553openalex-snapshot
Additional file 4 of The effects of six months Persicaria minor extract supplement among older adults with mild cognitive impairment: a double-blinded, randomized, and placebo-controlled trial
inferred← citeshttps://doi.org/10.64898/2026.01.22.701195openalex-snapshot
Probing the Glymphatic System Using Optical Imaging and Mathematical Modeling
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