Abstract
Zongpai Zhang, Jingpu Wu, Isabel M. Rios Pulgar, Elizabeth H. T. Chang, Keyi Chai, Puyang Wang, Shanshan Jiang, Kenichi Oishi, Gwenn S. Smith, Carrie Wagandt, Gregory M. Pontone, Abhay Moghekar, Arnold Bakker
Abstract
Authors
Institutions
Provenance
crossref
Confidence 100%
ror
Confidence 99%
pubmed
Confidence 98%
europepmc
Confidence 96%
openalex
Confidence 95%
doaj
Confidence 92%
datacite
Confidence 0%
No local reference links have been materialized yet.
No local citing links have been materialized yet.
Early detection of mild cognitive impairment (MCI) in primary care
10.14283/jpad.2020.21 · 2020
Practical recommendations for timely, accurate diagnosis of symptomatic Alzheimer’s disease (MCI and dementia) in primary care: A review and synthesis
10.1111/joim.13244 · 2021
Research criteria for the diagnosis of prodromal dementia with Lewy bodies
10.1212/wnl.0000000000009323 · 2020
10.1001/jamaneurol.2025.3242
10.1001/jamaneurol.2025.3242
Revised criteria for diagnosis and staging of Alzheimer’s disease: Alzheimer’s Association Workgroup
10.1002/alz.13859 · 2024
10.3390/neurolint18070139
10.3390/neurolint18070139
10.7759/cureus.73353
10.7759/cureus.73353
Importance of hypoglycemia episodes and glycemic variability in parkinsonian syndromes
10.5603/pjnns.109238 · 2025
10.36922/an025270077
10.36922/an025270077
Mapping scores onto stages: Mini-mental state examination and clinical dementia rating
10.1097/01.jgp.0000192478.82189.a8 · 2006
Updated appropriate use criteria for amyloid and tau PET: A report from the Alzheimer’s Association and Society for Nuclear Medicine and Molecular Imaging Workgroup
10.2967/jnumed.124.268756 · 2025
The clinical use of structural MRI in Alzheimer disease
10.1038/nrneurol.2009.215 · 2010
Structural MRI changes detectable up to ten years before clinical Alzheimer’s disease
10.1016/j.neurobiolaging.2011.05.018 · 2012
Magnetization transfer in MRI: A review
10.1002/nbm.683 · 2001
Susceptibility-weighted imaging and quantitative susceptibility mapping in the brain
10.1002/jmri.24768 · 2015
10.1371/journal.pone.0049072
10.1371/journal.pone.0049072
10.3389/fneur.2021.640239
10.3389/fneur.2021.640239
10.1148/radiol.250513
10.1148/radiol.250513
Neuroimaging and other biomarkers for Alzheimer’s disease: The changing landscape of early detection
10.1146/annurev-clinpsy-050212-185535 · 2013
10.1177/25424823251394399
10.1177/25424823251394399
Neuroimaging biomarkers for Alzheimer’s disease
10.1186/s13024-019-0325-5 · 2019
A new class of contrast agents for MRI based on proton chemical exchange dependent saturation transfer (CEST)
10.1006/jmre.1999.1956 · 2000
Chemical exchange saturation transfer imaging and spectroscopy
10.1016/j.pnmrs.2006.01.001 · 2006
Differentiation between glioma and radiation necrosis using molecular magnetic resonance imaging of endogenous proteins and peptides
10.1038/nm.2268 · 2011
10.3390/ijms222111559
10.3390/ijms222111559
10.1002/nbm.4731
10.1002/nbm.4731
10.1002/nbm.4906
10.1002/nbm.4906
Magnetic resonance imaging of glutamate
10.1038/nm.2615 · 2012
10.3390/brainsci12010053
10.3390/brainsci12010053
Amide proton transfer imaging of Alzheimer’s disease and Parkinson’s disease
10.1016/j.mrl.2022.10.002 · 2023
10.1002/nbm.4780
10.1002/nbm.4780
Chemical exchange saturation transfer MRI for neurodegenerative diseases: An update on clinical and preclinical studies
10.4103/nrr.nrr-d-24-01246 · 2026
Soluble fibrillar oligomer levels are elevated in Alzheimer’s disease brain and correlate with cognitive dysfunction
10.1016/j.nbd.2009.05.024 · 2009
The amyloid-beta oligomer hypothesis: Beginning of the third decade
10.3233/jad-179941 · 2018
10.3390/neurolint18030048
10.3390/neurolint18030048
Amide proton transfer magnetic resonance imaging of Alzheimer’s disease at 3.0 Tesla: A preliminary study
10.4103/0366-6999.151658 · 2015
10.1016/j.nicl.2019.102153
10.1016/j.nicl.2019.102153
10.3389/fneur.2021.707030
10.3389/fneur.2021.707030
Robust Extrapolated Semi-Solid Magnetization Transfer Reference Fitting for Quantitative Amide Proton Transfer Imaging at 3 T: Application to Patients with Mild Cognitive Impairment and Mild Dementia
10.1002/mrm.70122 · 2026
The diagnosis of mild cognitive impairment due to Alzheimer’s disease: Recommendations from the National Institute on Aging-Alzheimer’s Association workgroups on diagnostic guidelines for Alzheimer’s disease
10.1016/j.jalz.2011.03.008 · 2011
10.1002/nbm.3934
10.1002/nbm.3934 · doi-reference
Numerical solution of the Bloch equations provides insights into the optimum design of PARACEST agents for MRI
10.1002/mrm.20408 · doi-reference
Review and consensus recommendations on clinical APT-weighted imaging approaches at 3T: Application to brain tumors
10.1002/mrm.29241 · doi-reference
10.1371/journal.pone.0076203
10.1371/journal.pone.0076203 · doi-reference
10.1016/j.ejrad.2020.109243
10.1016/j.ejrad.2020.109243 · doi-reference
Increased iron deposition in putamen and substantia nigra correlates with cognitive function in cerebral small vessel disease: A quantitative susceptibility mapping study
10.1177/0271678x251377569 · doi-reference
Correlating quantitative susceptibility mapping with cognitive decline in Alzheimer’s disease
10.1093/brain/awx167 · doi-reference
10.1016/j.neuroimage.2020.117433
10.1016/j.neuroimage.2020.117433 · doi-reference
Analysis of the posterior cingulate cortex with [18 F] FDG-PET and Naa/mI in mild cognitive impairment and Alzheimer’s disease: Correlations and differences between the two methods
10.1590/1980-57642015dn94000385 · doi-reference
Posterior cingulate cortex atrophy across the Alzheimer’s disease spectrum: A cross-sectional MRI study linking volumetrics to cognitive decline
10.1177/13872877251401612 · doi-reference
Magnetic resonance imaging of the entorhinal cortex and hippocampus in mild cognitive impairment and Alzheimer’s disease
10.1136/jnnp.71.4.441 · doi-reference
Imaging correlations of tau, amyloid, metabolism, and atrophy in typical and atypical Alzheimer’s disease
10.1016/j.jalz.2018.02.020 · doi-reference
10.21037/qims-24-1602
10.21037/qims-24-1602 · doi-reference
Magnetization transfer measurements of the hippocampus in the early diagnosis of Alzheimer’s disease
10.1016/s0022-510x(01)00553-6 · doi-reference
10.1186/s12888-020-02910-8
10.1186/s12888-020-02910-8 · doi-reference
The mini-mental state examination: A comprehensive review
10.1111/j.1532-5415.1992.tb01992.x · doi-reference
“Mini-mental state”: A practical method for grading the cognitive state of patients for the clinician
10.1016/0022-3956(75)90026-6 · doi-reference
The Clinical Dementia Rating (CDR) current version and scoring rules
10.1212/wnl.43.11.2412-a · doi-reference
Cognitive tests to detect dementia: A systematic review and meta-analysis
10.1001/jamainternmed.2015.2152 · doi-reference
Convergent and distinct neural structural and functional patterns of mild cognitive impairment: A multimodal meta-analysis
10.1093/cercor/bhad167 · doi-reference
Neuroanatomic changes and their association with cognitive decline in mild cognitive impairment: A meta-analysis
10.1007/s00429-011-0333-x · doi-reference
Neural correlates of Alzheimer’s disease and mild cognitive impairment: A systematic and quantitative meta-analysis involving 1351 patients
10.1016/j.neuroimage.2009.05.037 · doi-reference
User-guided 3D active contour segmentation of anatomical structures: Significantly improved efficiency and reliability
10.1016/j.neuroimage.2006.01.015 · doi-reference
APT-weighted MRI: Techniques, current neuro applications, and challenging issues
10.1002/jmri.26645 · doi-reference
Quantitative susceptibility mapping of brain iron and β-amyloid in MRI and PET relating to cognitive performance in cognitively normal older adults
10.1148/radiol.2020201603 · doi-reference
Multi-atlas tool for automated segmentation of brain gray matter nuclei and quantification of their magnetic susceptibility
10.1016/j.neuroimage.2019.02.016 · doi-reference
Quantitative Susceptibility Mapping Using Structural Feature Based Collaborative Reconstruction (SFCR) in the Human Brain
10.1109/tmi.2016.2544958 · doi-reference
Optimization of the ultrafast Look-Looker echo-plannar imaging T1 mapping sequence
10.1016/s0730-725x(98)00011-3 · doi-reference
Water saturation shift referencing (WASSR) for chemical exchange saturation transfer (CEST) experiments
10.1002/mrm.21873 · doi-reference
The diagnosis of dementia due to Alzheimer’s disease: Recommendations from the National Institute on Aging-Alzheimer’s Association workgroups on diagnostic guidelines for Alzheimer’s disease
10.1016/j.jalz.2011.03.005 · doi-reference
The diagnosis of mild cognitive impairment due to Alzheimer’s disease: Recommendations from the National Institute on Aging-Alzheimer’s Association workgroups on diagnostic guidelines for Alzheimer’s disease
10.1016/j.jalz.2011.03.008 · doi-reference
Robust Extrapolated Semi-Solid Magnetization Transfer Reference Fitting for Quantitative Amide Proton Transfer Imaging at 3 T: Application to Patients with Mild Cognitive Impairment and Mild Dementia
10.1002/mrm.70122 · doi-reference
10.3389/fneur.2021.707030
10.3389/fneur.2021.707030 · doi-reference
10.1016/j.nicl.2019.102153
10.1016/j.nicl.2019.102153 · doi-reference
Amide proton transfer magnetic resonance imaging of Alzheimer’s disease at 3.0 Tesla: A preliminary study
10.4103/0366-6999.151658 · doi-reference
10.3390/neurolint18030048
10.3390/neurolint18030048 · doi-reference
The amyloid-beta oligomer hypothesis: Beginning of the third decade
10.3233/jad-179941 · doi-reference
Soluble fibrillar oligomer levels are elevated in Alzheimer’s disease brain and correlate with cognitive dysfunction
10.1016/j.nbd.2009.05.024 · doi-reference
Chemical exchange saturation transfer MRI for neurodegenerative diseases: An update on clinical and preclinical studies
10.4103/nrr.nrr-d-24-01246 · doi-reference
10.1002/nbm.4780
10.1002/nbm.4780 · doi-reference