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Tau PET patterns mirror clinical and neuroanatomical variability in Alzheimer’s disease

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

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Increased Frequency of Learning Disability in Patients With Primary Progressive Aphasia and Their First-Degree Relatives
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Amyloid-β–Associated Clinical Decline Occurs Only in the Presence of Elevated P-tau
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Use of Florbetapir-PET for Imaging β-Amyloid Pathology
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Prevalence of Cerebral Amyloid Pathology in Persons Without Dementia
inferredcites →https://doi.org/10.1001/jama.2015.4669openalex-snapshot
Prevalence of Amyloid PET Positivity in Dementia Syndromes
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Imaging brain amyloid in Alzheimer's disease with Pittsburgh Compound‐B
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Aβ amyloid and glucose metabolism in three variants of primary progressive aphasia
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18 F‐flutemetamol amyloid imaging in Alzheimer disease and mild cognitive impairment: A phase 2 trial
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Clinicopathological correlations in corticobasal degeneration
inferredcites →https://doi.org/10.1002/ana.24321openalex-snapshot
Tau, amyloid, and hypometabolism in a patient with posterior cortical atrophy
inferredcites →https://doi.org/10.1002/ana.24517openalex-snapshot
Validating novel tau positron emission tomography tracer [F‐18]‐AV‐1451 (T807) on postmortem brain tissue
inferredcites →https://doi.org/10.1002/ana.24546openalex-snapshot
Tau positron emission tomographic imaging in aging and early A lzheimer disease
inferredcites →https://doi.org/10.1002/ana.410380219openalex-snapshot
Apolipoprotein E ϵ4 and cerebral hemorrhage associated with amyloid angiopathy
inferredcites →https://doi.org/10.1002/ana.410410106openalex-snapshot
Neuronal loss correlates with but exceeds neurofibrillary tangles in Alzheimer's disease
inferredcites →https://doi.org/10.1002/hbm.22927openalex-snapshot
Atrophy patterns in early clinical stages across distinct phenotypes of A lzheimer's disease
inferredcites →https://doi.org/10.1007/bf00308809openalex-snapshot
Neuropathological stageing of Alzheimer-related changes
inferredcites →https://doi.org/10.1007/s11940-013-0282-1openalex-snapshot
Diagnosis and Treatment of Corticobasal Degeneration
inferredcites →https://doi.org/10.1007/s12264-013-1414-zopenalex-snapshot
Tau-induced neurodegeneration: mechanisms and targets
inferredcites →https://doi.org/10.1016/j.bandl.2012.12.008openalex-snapshot
Patterns of longitudinal brain atrophy in the logopenic variant of primary progressive aphasia
inferredcites →https://doi.org/10.1016/j.jalz.2011.03.003openalex-snapshot
Toward defining the preclinical stages of Alzheimer's disease: Recommendations from the National Institute on Aging‐Alzheimer's Association workgroups on diagnostic guidelines for Alzheimer's disease
inferredcites →https://doi.org/10.1016/j.jalz.2011.03.005openalex-snapshot
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
inferredcites →https://doi.org/10.1016/j.jalz.2011.03.008openalex-snapshot
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
inferredcites →https://doi.org/10.1016/j.jalz.2011.07.003openalex-snapshot
Amyloid imaging in dementias with atypical presentation
inferredcites →https://doi.org/10.1016/j.jalz.2012.07.003openalex-snapshot
Impact of molecular imaging on the diagnostic process in a memory clinic
inferredcites →https://doi.org/10.1016/j.jalz.2012.11.008openalex-snapshot
[ 18 F]T807, a novel tau positron emission tomography imaging agent for Alzheimer's disease
inferredcites →https://doi.org/10.1016/j.neurobiolaging.2013.02.013openalex-snapshot
Different patterns of gray matter atrophy in early- and late-onset Alzheimer’s disease
inferredcites →https://doi.org/10.1016/j.neurobiolaging.2014.03.009openalex-snapshot
Medial temporal atrophy in early and late-onset Alzheimer's disease
inferredcites →https://doi.org/10.1016/j.neuroimage.2009.01.009openalex-snapshot
Mapping the effect of APOE ε4 on gray matter loss in Alzheimer's disease in vivo
inferredcites →https://doi.org/10.1016/j.neuroimage.2011.07.098openalex-snapshot
Not quite PIB-positive, not quite PIB-negative: Slight PIB elevations in elderly normal control subjects are biologically relevant
inferredcites →https://doi.org/10.1016/j.neuron.2011.11.033openalex-snapshot
Propagation of Tau Pathology in a Model of Early Alzheimer's Disease
inferredcites →https://doi.org/10.1016/j.neuron.2011.12.040openalex-snapshot
A Network Diffusion Model of Disease Progression in Dementia
inferredcites →https://doi.org/10.1016/j.neuron.2012.03.004openalex-snapshot
Predicting Regional Neurodegeneration from the Healthy Brain Functional Connectome
inferredcites →https://doi.org/10.1016/j.neuron.2013.12.003openalex-snapshot
Biomarker Modeling of Alzheimer’s Disease
inferredcites →https://doi.org/10.1016/j.neuron.2014.05.004openalex-snapshot
The Intersection of Amyloid Beta and Tau at Synapses in Alzheimer’s Disease
inferredcites →https://doi.org/10.1016/s0896-6273(02)00569-xopenalex-snapshot
Whole Brain Segmentation
inferredcites →https://doi.org/10.1016/s1474-4422(10)70306-9openalex-snapshot
Early-onset versus late-onset Alzheimer's disease: the case of the missing APOE ɛ4 allele
inferredcites →https://doi.org/10.1016/s1474-4422(11)70077-1openalex-snapshot
Cerebral amyloid-β PET with florbetaben (18F) in patients with Alzheimer's disease and healthy controls: a multicentre phase 2 diagnostic study
inferredcites →https://doi.org/10.1016/s1474-4422(11)70156-9openalex-snapshot
Neuropathologically defined subtypes of Alzheimer's disease with distinct clinical characteristics: a retrospective study
inferredcites →https://doi.org/10.1016/s1474-4422(11)70289-7openalex-snapshot
Posterior cortical atrophy
inferredcites →https://doi.org/10.1016/s1474-4422(14)70090-0openalex-snapshot
Advancing research diagnostic criteria for Alzheimer's disease: the IWG-2 criteria
inferredcites →https://doi.org/10.1016/s1474-4422(14)70194-2openalex-snapshot
Age-specific population frequencies of cerebral β-amyloidosis and neurodegeneration among people with normal cognitive function aged 50–89 years: a cross-sectional study
inferredcites →https://doi.org/10.1016/s1474-4422(14)70252-2openalex-snapshot
Tau imaging: early progress and future directions
inferredcites →https://doi.org/10.1038/ncb1901openalex-snapshot
Transmission and spreading of tauopathy in transgenic mouse brain
inferredcites →https://doi.org/10.1046/j.1365-2990.2002.00385.xopenalex-snapshot
Synapse loss is greater in presenile than senile onset Alzheimer disease: implications for the cognitive reserve hypothesis
inferredcites →https://doi.org/10.1056/nejmoa1304839openalex-snapshot
Two Phase 3 Trials of Bapineuzumab in Mild-to-Moderate Alzheimer's Disease
inferredcites →https://doi.org/10.1073/pnas.1434398100openalex-snapshot
Carboxyl-terminal-truncated apolipoprotein E4 causes Alzheimer's disease-like neurodegeneration and behavioral deficits in transgenic mice
inferredcites →https://doi.org/10.1073/pnas.72.5.1858openalex-snapshot
A protein factor essential for microtubule assembly.
inferredcites →https://doi.org/10.1073/pnas.90.20.9649openalex-snapshot
Increased amyloid beta-peptide deposition in cerebral cortex as a consequence of apolipoprotein E genotype in late-onset Alzheimer disease.
inferredcites →https://doi.org/10.1093/brain/awp326openalex-snapshot
Increased metabolic vulnerability in early-onset Alzheimer’s disease is not related to amyloid burden
inferredcites →https://doi.org/10.1093/brain/aws076openalex-snapshot
Clinically concordant variations of Alzheimer pathology in aphasic versus amnestic dementia
inferredcites →https://doi.org/10.1093/brain/aws113openalex-snapshot
Amyloid burden and metabolic function in early-onset Alzheimer's disease: parietal lobe involvement
inferredcites →https://doi.org/10.1093/brain/aws327openalex-snapshot
Diverging patterns of amyloid deposition and hypometabolism in clinical variants of probable Alzheimer’s disease
inferredcites →https://doi.org/10.1093/brain/awt242openalex-snapshot
Handedness and language learning disability differentially distribute in progressive aphasia variants
inferredcites →https://doi.org/10.1093/brain/awt266openalex-snapshot
Deciphering logopenic primary progressive aphasia: a clinical, imaging and biomarker investigation
inferredcites →https://doi.org/10.1093/brain/awv191openalex-snapshot
The behavioural/dysexecutive variant of Alzheimer’s disease: clinical, neuroimaging and pathological features
inferredcites →https://doi.org/10.1093/brain/awv229openalex-snapshot
Asymmetries of amyloid-β burden and neuronal dysfunction are positively correlated in Alzheimer’s disease
inferredcites →https://doi.org/10.1093/cercor/bht076openalex-snapshot
Is Verbal Episodic Memory in Elderly with Amyloid Deposits Preserved Through Altered Neuronal Function?
inferredcites →https://doi.org/10.1093/hmg/dds161openalex-snapshot
Evidence for a role of the rare p.A152T variant in MAPT in increasing the risk for FTD-spectrum and Alzheimer's diseases
inferredcites →https://doi.org/10.1093/jnen/61.11.935openalex-snapshot
Office of Rare Diseases Neuropathologic Criteria for Corticobasal Degeneration
inferredcites →https://doi.org/10.1097/00004647-199609000-00008openalex-snapshot
Distribution Volume Ratios without Blood Sampling from Graphical Analysis of PET Data
inferredcites →https://doi.org/10.1097/00004728-199507000-00006openalex-snapshot
Preserved Pontine Glucose Metabolism in Alzheimer Disease
inferredcites →https://doi.org/10.1097/00146965-200312000-00002openalex-snapshot
Distinctive Neuropsychological Patterns in Frontotemporal Dementia, Semantic Dementia, And Alzheimer Disease
inferredcites →https://doi.org/10.1097/nen.0b013e31825018f7openalex-snapshot
Correlation of Alzheimer Disease Neuropathologic Changes With Cognitive Status: A Review of the Literature
inferredcites →https://doi.org/10.1097/wad.0b013e318279d02aopenalex-snapshot
Potential Impact of Amyloid Imaging on Diagnosis and Intended Management in Patients With Progressive Cognitive Decline
inferredcites →https://doi.org/10.1111/ene.12761openalex-snapshot
Regional β‐amyloid burden does not correlate with cognitive or language deficits in Alzheimer's disease presenting as aphasia
inferredcites →https://doi.org/10.1111/j.1471-4159.2009.06181.xopenalex-snapshot
The amyloid hypothesis for Alzheimer’s disease: a critical reappraisal
inferredcites →https://doi.org/10.1111/j.1749-6632.1996.tb34415.xopenalex-snapshot
Apolipoprotein E, Plaques, Tangles and Cholinergic Dysfunction in Alzheimer's Diseasea
inferredcites →https://doi.org/10.1136/jnnp-2013-305858openalex-snapshot
Greater medial temporal hypometabolism and lower cortical amyloid burden in ApoE4-positive AD patients
inferredcites →https://doi.org/10.1159/000058331openalex-snapshot
Posterior Cortical Atrophy: Clinical Characteristics and Differences Compared to Alzheimer’s Disease
inferredcites →https://doi.org/10.1159/000339367openalex-snapshot
Impact of Beta-Amyloid-Specific Florbetaben PET Imaging on Confidence in Early Diagnosis of Alzheimer’s Disease
inferredcites →https://doi.org/10.1159/000477538openalex-snapshot
Qualitative Assessment of Verbal Fluency Performance in Frontotemporal Dementia
inferredcites →https://doi.org/10.1176/appi.focus.11.1.96openalex-snapshot
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
inferredcites →https://doi.org/10.1177/0891988706297086openalex-snapshot
Early-Onset Alzheimer’s Disease Is Associated With Greater Pathologic Burden
inferredcites →https://doi.org/10.1177/1533317512454711openalex-snapshot
Nonamnestic Presentations of Early-Onset Alzheimer’s Disease
inferredcites →https://doi.org/10.1186/s13195-014-0093-yopenalex-snapshot
Predicting amyloid status in corticobasal syndrome using modified clinical criteria, magnetic resonance imaging and fluorodeoxyglucose positron emission tomography
inferredcites →https://doi.org/10.1212/01.wnl.0000128091.92139.0fopenalex-snapshot
Impact of APOE genotype on neuropathologic and neurochemical markers of Alzheimer disease
inferredcites →https://doi.org/10.1212/wnl.0000000000000032openalex-snapshot
Practical utility of amyloid and FDG-PET in an academic dementia center
inferredcites →https://doi.org/10.1212/wnl.0000000000000550openalex-snapshot
Vascular risk and Aβ interact to reduce cortical thickness in AD vulnerable brain regions
inferredcites →https://doi.org/10.1212/wnl.0000000000000824openalex-snapshot
Asymmetry of cortical decline in subtypes of primary progressive aphasia
inferredcites →https://doi.org/10.1212/wnl.0000000000001877openalex-snapshot
Amyloid-β 11 C-PiB-PET imaging results from 2 randomized bapineuzumab phase 3 AD trials
inferredcites →https://doi.org/10.1212/wnl.0b013e31821103e6openalex-snapshot
Classification of primary progressive aphasia and its variants
inferredcites →https://doi.org/10.1212/wnl.0b013e31825dce28openalex-snapshot
Early-onset Alzheimer disease clinical variants
inferredcites →https://doi.org/10.1212/wnl.0b013e31827f0889openalex-snapshot
Differential effect of APOE genotype on amyloid load and glucose metabolism in AD dementia
inferredcites →https://doi.org/10.1212/wnl.42.3.631openalex-snapshot
Neurofibrillary tangles but not senile plaques parallel duration and severity of Alzheimer's disease
inferredcites →https://doi.org/10.1371/journal.pone.0062471openalex-snapshot
FDG PET and MRI in Logopenic Primary Progressive Aphasia versus Dementia of the Alzheimer’s Type
inferredcites →https://doi.org/10.3233/jad-121960openalex-snapshot
Cerebrospinal Fluid Biomarkers Mirror Rate of Cognitive Decline
inferredcites →https://doi.org/10.3233/jad-122059openalex-snapshot
Early Clinical PET Imaging Results with the Novel PHF-Tau Radioligand [F-18]-T807
inferredcites →https://doi.org/10.3233/jad-130098openalex-snapshot
Early Clinical PET Imaging Results with the Novel PHF-Tau Radioligand [F18]-T808
inferredcites →https://doi.org/10.3233/jad-2011-111694openalex-snapshot
Injury Markers but not Amyloid Markers are Associated with Rapid Progression from Mild Cognitive Impairment to Dementia in Alzheimer's Disease
inferredcites →https://doi.org/10.3233/jad-2012-111934openalex-snapshot
Early Onset Alzheimer's Disease is Associated with a Distinct Neuropsychological Profile

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.3716976openalex-extracted
Neurotoxic Astrocytes Secreted Glypican-4 Drives Alzheimer's Tau Pathology
inferred← citeshttps://doi.org/10.1001/jama.2018.12917openalex-snapshot
Discriminative Accuracy of [ 18 F]flortaucipir Positron Emission Tomography for Alzheimer Disease vs Other Neurodegenerative Disorders
inferred← citeshttps://doi.org/10.1001/jamanetworkopen.2019.13909openalex-snapshot
Association of Apolipoprotein E ɛ4, Educational Level, and Sex With Tau Deposition and Tau-Mediated Metabolic Dysfunction in Older Adults
inferred← citeshttps://doi.org/10.1001/jamaneurol.2016.2481openalex-snapshot
Tau and β-Amyloid—The Malignant Duo
inferred← citeshttps://doi.org/10.1001/jamaneurol.2016.3338openalex-snapshot
Tau Positron Emission Tomographic Imaging in the Lewy Body Diseases
inferred← citeshttps://doi.org/10.1001/jamaneurol.2016.5349openalex-snapshot
Alzheimer Disease Signature Neurodegeneration and APOE Genotype in Mild Cognitive Impairment With Suspected Non–Alzheimer Disease Pathophysiology
inferred← citeshttps://doi.org/10.1001/jamaneurol.2016.5701openalex-snapshot
Tau and Cortical Thickness in Alzheimer Disease
inferred← citeshttps://doi.org/10.1001/jamaneurol.2016.5755openalex-snapshot
Association of In Vivo [ 18 F]AV-1451 Tau PET Imaging Results With Cortical Atrophy and Symptoms in Typical and Atypical Alzheimer Disease
inferred← citeshttps://doi.org/10.1001/jamaneurol.2017.0323openalex-snapshot
Linking Amyloid-β and Tau Deposition in Alzheimer Disease
inferred← citeshttps://doi.org/10.1001/jamaneurol.2017.2216openalex-snapshot
Region-Specific Association of Subjective Cognitive Decline With Tauopathy Independent of Global β-Amyloid Burden
inferred← citeshttps://doi.org/10.1001/jamaneurol.2017.3713openalex-snapshot
Associations Between Tau, β-Amyloid, and Cognition in Parkinson Disease
inferred← citeshttps://doi.org/10.1001/jamaneurol.2017.4026openalex-snapshot
Tau Positron Emission Tomography in Autosomal Dominant Alzheimer Disease
inferred← citeshttps://doi.org/10.1001/jamaneurol.2018.3692openalex-snapshot
Correlation of In Vivo [18F]Flortaucipir With Postmortem Alzheimer Disease Tau Pathology
inferred← citeshttps://doi.org/10.1001/jamaneurol.2019.1424openalex-snapshot
Association of Amyloid and Tau With Cognition in Preclinical Alzheimer Disease
inferred← citeshttps://doi.org/10.1001/jamaneurol.2019.1971openalex-snapshot
Prevalence of Biologically vs Clinically Defined Alzheimer Spectrum Entities Using the National Institute on Aging–Alzheimer’s Association Research Framework
inferred← citeshttps://doi.org/10.1001/jamaneurol.2019.3606openalex-snapshot
Selective Vulnerability of the Nucleus Basalis of Meynert Among Neuropathologic Subtypes of Alzheimer Disease
inferred← citeshttps://doi.org/10.1001/jamaneurol.2019.4421openalex-snapshot
Association of Apolipoprotein E ε4 With Medial Temporal Tau Independent of Amyloid-β
inferred← citeshttps://doi.org/10.1001/jamaneurol.2019.4509openalex-snapshot
Tau Positron Emission Tomographic Findings in a Former US Football Player With Pathologically Confirmed Chronic Traumatic Encephalopathy
inferred← citeshttps://doi.org/10.1001/jamaneurol.2019.5154openalex-snapshot
Assessment of Demographic, Genetic, and Imaging Variables Associated With Brain Resilience and Cognitive Resilience to Pathological Tau in Patients With Alzheimer Disease
inferred← citeshttps://doi.org/10.1001/jamaneurol.2020.0989openalex-snapshot
Diagnostic Performance of RO948 F 18 Tau Positron Emission Tomography in the Differentiation of Alzheimer Disease From Other Neurodegenerative Disorders
inferred← citeshttps://doi.org/10.1001/jamaneurol.2020.1741openalex-snapshot
Prevalence and Clinical Phenotype of Quadruple Misfolded Proteins in Older Adults
inferred← citeshttps://doi.org/10.1001/jamaneurol.2020.3921openalex-snapshot
Association of Initial β-Amyloid Levels With Subsequent Flortaucipir Positron Emission Tomography Changes in Persons Without Cognitive Impairment
inferred← citeshttps://doi.org/10.1001/jamaneurol.2020.5505openalex-snapshot
Aggregated Tau Measured by Visual Interpretation of Flortaucipir Positron Emission Tomography and the Associated Risk of Clinical Progression of Mild Cognitive Impairment and Alzheimer Disease
inferred← citeshttps://doi.org/10.1001/jamaneurol.2021.1858openalex-snapshot
Accuracy of Tau Positron Emission Tomography as a Prognostic Marker in Preclinical and Prodromal Alzheimer Disease
inferred← citeshttps://doi.org/10.1001/jamaneurol.2021.4417openalex-snapshot
Research Criteria for the Behavioral Variant of Alzheimer Disease
inferred← citeshttps://doi.org/10.1001/jamaneurol.2021.4654openalex-snapshot
Biomarker-Based Prediction of Longitudinal Tau Positron Emission Tomography in Alzheimer Disease
inferred← citeshttps://doi.org/10.1001/jamaneurol.2022.0676openalex-snapshot
Divergent Cortical Tau Positron Emission Tomography Patterns Among Patients With Preclinical Alzheimer Disease
inferred← citeshttps://doi.org/10.1001/jamaneurol.2023.1067openalex-snapshot
Comparison of Group-Level and Individualized Brain Regions for Measuring Change in Longitudinal Tau Positron Emission Tomography in Alzheimer Disease
inferred← citeshttps://doi.org/10.1001/jamaneurol.2024.0784openalex-snapshot
Clinicopathologic Heterogeneity and Glial Activation Patterns in Alzheimer Disease
inferred← citeshttps://doi.org/10.1001/jamaneurol.2025.0013openalex-snapshot
Sex Differences in Longitudinal Tau-PET in Preclinical Alzheimer Disease
inferred← citeshttps://doi.org/10.1002/9781118661895.ch11openalex-snapshot
Alzheimer's Disease
inferred← citeshttps://doi.org/10.1002/9783527845583.oth1openalex-snapshot
Declaration of Competing Interest
inferred← citeshttps://doi.org/10.1002/acn3.51038openalex-snapshot
MRI and flortaucipir relationships in Alzheimer's phenotypes are heterogeneous
inferred← citeshttps://doi.org/10.1002/acn3.51237openalex-snapshot
Ante‐ and postmortem tau in autosomal dominant and late‐onset Alzheimer’s disease
inferred← citeshttps://doi.org/10.1002/acn3.51297openalex-snapshot
Flortaucipir (tau) PET in LGI1 antibody encephalitis
inferred← citeshttps://doi.org/10.1002/acn3.51457openalex-snapshot
Amyloid‐dependent and amyloid‐independent effects of Tau in individuals without dementia
inferred← citeshttps://doi.org/10.1002/acn3.631openalex-snapshot
[ 18 F]AV‐1451 binding is increased in frontotemporal dementia due to C9orf72 expansion
inferred← citeshttps://doi.org/10.1002/adtp.202400008openalex-snapshot
Effect of APOE ɛ4 Status on Brain Amyloid‐β and Cognitive Function in Amnestic and Nonamnestic Mild Cognitive Impairment: A [18F] Florbetapir PET‐CT Study
inferred← citeshttps://doi.org/10.1002/alz.12124openalex-snapshot
An agnostic reevaluation of the amyloid cascade hypothesis of Alzheimer's disease pathogenesis: The role of APP homeostasis
inferred← citeshttps://doi.org/10.1002/alz.12173openalex-snapshot
APOE interacts with tau PET to influence memory independently of amyloid PET in older adults without dementia
inferred← citeshttps://doi.org/10.1002/alz.12245openalex-snapshot
Cerebral amyloid‐β load is associated with neurodegeneration and gliosis: Mediation by p‐tau and interactions with risk factors early in the Alzheimer's continuum
inferred← citeshttps://doi.org/10.1002/alz.12249openalex-snapshot
Distinct effects of beta‐amyloid and tau on cortical thickness in cognitively healthy older adults
inferred← citeshttps://doi.org/10.1002/alz.12349openalex-snapshot
Reduced synchrony in alpha oscillations during life predicts post mortem neurofibrillary tangle density in early‐onset and atypical Alzheimer's disease
inferred← citeshttps://doi.org/10.1002/alz.12356openalex-snapshot
Towards clinical application of tau PET tracers for diagnosing dementia due to Alzheimer's disease
inferred← citeshttps://doi.org/10.1002/alz.12445openalex-snapshot
Relationships among tau burden, atrophy, age, and naming in the aphasic variant of Alzheimer's disease
inferred← citeshttps://doi.org/10.1002/alz.12487openalex-snapshot
The protective gene dose effect of the APOEε2 allele on gray matter volume in cognitively unimpaired individuals
inferred← citeshttps://doi.org/10.1002/alz.12518openalex-snapshot
Differential expression of tau species and the association with cognitive decline and synaptic loss in Alzheimer's disease
inferred← citeshttps://doi.org/10.1002/alz.12749openalex-snapshot
Phosphorylated tau sites that are elevated in Alzheimer's disease fluid biomarkers are visualized in early neurofibrillary tangle maturity levels in the post mortem brain
inferred← citeshttps://doi.org/10.1002/alz.12867openalex-snapshot
Functional network segregation is associated with attenuated tau spreading in Alzheimer's disease
inferred← citeshttps://doi.org/10.1002/alz.12875openalex-snapshot
Tau‐PET is superior to phospho‐tau when predicting cognitive decline in symptomatic AD patients
inferred← citeshttps://doi.org/10.1002/alz.12922openalex-snapshot
Initial non‐amnestic symptoms relate to faster rate of functional and cognitive decline compared to amnestic symptoms in neuropathologically confirmed dementias
inferred← citeshttps://doi.org/10.1002/alz.12943openalex-snapshot
Does Alzheimer's disease with mesial temporal lobe epilepsy represent a distinct disease subtype?
inferred← citeshttps://doi.org/10.1002/alz.12963openalex-snapshot
Alzheimer's disease phenotypes show different sleep architecture
inferred← citeshttps://doi.org/10.1002/alz.12978openalex-snapshot
Protein disulfide isomerases as CSF biomarkers for the neuronal response to tau pathology
inferred← citeshttps://doi.org/10.1002/alz.13011openalex-snapshot
Cortical tau is associated with microstructural imaging biomarkers of neurite density and dendritic complexity in Alzheimer's disease
inferred← citeshttps://doi.org/10.1002/alz.13355openalex-snapshot
The impact of tau deposition and hypometabolism on cognitive impairment and longitudinal cognitive decline
inferred← citeshttps://doi.org/10.1002/alz.13438openalex-snapshot
Successful cognitive aging is associated with thicker anterior cingulate cortex and lower tau deposition compared to typical aging
inferred← citeshttps://doi.org/10.1002/alz.13444openalex-snapshot
Characterizing the emergence of amyloid and tau burden in Down syndrome
inferred← citeshttps://doi.org/10.1002/alz.13533openalex-snapshot
Novel avenues of tau research
inferred← citeshttps://doi.org/10.1002/alz.13769openalex-snapshot
Data‐driven decomposition and staging of flortaucipir uptake in Alzheimer's disease
inferred← citeshttps://doi.org/10.1002/alz.13859openalex-snapshot
Revised criteria for diagnosis and staging of Alzheimer's disease: Alzheimer's Association Workgroup
inferred← citeshttps://doi.org/10.1002/alz.13908openalex-snapshot
Harmonizing tau positron emission tomography in Alzheimer's disease: The CenTauR scale and the joint propagation model
inferred← citeshttps://doi.org/10.1002/alz.13914openalex-snapshot
Relationships between PET and blood plasma biomarkers in corticobasal syndrome
inferred← citeshttps://doi.org/10.1002/alz.14060openalex-snapshot
Associations of cerebral amyloid beta and tau with cognition from midlife
inferred← citeshttps://doi.org/10.1002/alz.14338openalex-snapshot
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
inferred← citeshttps://doi.org/10.1002/alz.14411openalex-snapshot
Plasma pTau217 ratio predicts continuous regional brain tau accumulation in amyloid‐positive early Alzheimer's disease
inferred← citeshttps://doi.org/10.1002/alz.14423openalex-snapshot
Characterizing visual read tau‐PET‐negative participants with Alzheimer's disease dementia
inferred← citeshttps://doi.org/10.1002/alz.14489openalex-snapshot
Dissociable spatial topography of cortical atrophy in early‐onset and late‐onset Alzheimer's disease: A head‐to‐head comparison of the LEADS and ADNI cohorts
inferred← citeshttps://doi.org/10.1002/alz.14515openalex-snapshot
Cognitive aging outcomes are related to both tau pathology and maintenance of cingulate cortex structure
inferred← citeshttps://doi.org/10.1002/alz.14600openalex-snapshot
Machine learning prediction of tau‐PET in Alzheimer's disease using plasma, MRI, and clinical data
inferred← citeshttps://doi.org/10.1002/alz.14625openalex-snapshot
Tau‐related reduction of glucose metabolism in mild cognitive impairment occurs independently of APOE ε4 genotype and is influenced by Aβ
inferred← citeshttps://doi.org/10.1002/alz.70003openalex-snapshot
Impact of the polygenic risk scores for attention‐deficit/hyperactivity disorder in Alzheimer's disease
inferred← citeshttps://doi.org/10.1002/alz.70061openalex-snapshot
Connectome‐based predictive modeling of brain pathology and cognition in autosomal dominant Alzheimer's disease
inferred← citeshttps://doi.org/10.1002/alz.70075openalex-snapshot
Amyloid PET predicts longitudinal functional and cognitive trajectories in a heterogeneous cohort
inferred← citeshttps://doi.org/10.1002/alz.70153openalex-snapshot
Heterogeneous tau deposition patterns in the preclinical stage link to domain‐specific cognitive deficits
inferred← citeshttps://doi.org/10.1002/alz.70346openalex-snapshot
Tau burden is best captured by magnitude and extent: Tau‐MaX as a measure of global tau
inferred← citeshttps://doi.org/10.1002/alz.70352openalex-snapshot
Integrating visual assessments and quantification methods for tau PET staging
inferred← citeshttps://doi.org/10.1002/alz.70511openalex-snapshot
Tau, atrophy, and domain‐specific cognitive impairment in typical Alzheimer's disease
inferred← citeshttps://doi.org/10.1002/alz.70520openalex-snapshot
Comparison of visual and analytic methods of Alzheimer's disease pathologic staging
inferred← citeshttps://doi.org/10.1002/alz.70689openalex-snapshot
The relationship of soluble tau species with Alzheimer's disease amyloid plaque removal and tau pathology
inferred← citeshttps://doi.org/10.1002/alz.70725openalex-snapshot
Expanding the horizon of sex‐specific proteomic insights in Alzheimer's disease
inferred← citeshttps://doi.org/10.1002/alz.70749openalex-snapshot
Catecholaminergic nucleus integrity and Alzheimer's pathology, symptoms, and progression
inferred← citeshttps://doi.org/10.1002/alz.70881openalex-snapshot
Combining CSF MTBR‐tau243 and plasma pTau217 ratio enhances the prediction of continuous regional tau PET burden in early Alzheimer's disease
inferred← citeshttps://doi.org/10.1002/alz.71017openalex-snapshot
Characterizing amyloid and tau positron emission tomography‐based stages across the clinical continuum
inferred← citeshttps://doi.org/10.1002/alz.71319openalex-snapshot
Florzolotau (18F) retention is linked to neuropsychological performance in tauopathy
inferred← citeshttps://doi.org/10.1002/alz.71427openalex-snapshot
Locus coeruleus degeneration is associated with cortical tau deposition and cognitive decline in older adults at familial risk of Alzheimer's disease
inferred← citeshttps://doi.org/10.1002/alz.71431openalex-snapshot
Emerging directions in tauopathy research
inferred← citeshttps://doi.org/10.1002/alz.71483openalex-snapshot
Evaluation of an in vivo biomarker of arteriolosclerosis (ARTS) and its associations with cognition and multimodal ATN(V) biomarkers in a cardiometabolic‐risk enriched community cohort
inferred← citeshttps://doi.org/10.1002/alz.71491openalex-snapshot
Sex differences in brain glucose metabolism and Alzheimer's disease risk and progression
inferred← citeshttps://doi.org/10.1002/alz.71571openalex-snapshot
Vulnerability of anterior medial temporal lobe subregions to early tau‐related neurodegeneration in Alzheimer's disease: Converging evidence from tau‐PET and plasma p‐tau217
inferred← citeshttps://doi.org/10.1002/alz.71617openalex-snapshot
Modular brain networks shape amyloid‐driven tau spread and cognitive decline
inferred← citeshttps://doi.org/10.1002/alz.71718openalex-snapshot
Group‐level versus individualized approaches for capturing tau PET changes and clinical progression in Alzheimer's disease
inferred← citeshttps://doi.org/10.1002/alz.71829openalex-snapshot
Operationalizing Alzheimer's disease trials in the era of targeted therapies
inferred← citeshttps://doi.org/10.1002/alz.71898openalex-snapshot
Plasma eMTBR‐tau243 as a disease biomarker across Alzheimer's disease clinical phenotypes
inferred← citeshttps://doi.org/10.1002/alz.71899openalex-snapshot
Brain microstructure mediates the relationship between Alzheimer's proteinopathies and memory
inferred← citeshttps://doi.org/10.1002/alz.71914openalex-snapshot
Network‐dependent remote effects and local tau burden jointly shape neuronal dysfunction in Alzheimer's disease
inferred← citeshttps://doi.org/10.1002/ana.24711openalex-snapshot
In vivo cortical spreading pattern of tau and amyloid in the Alzheimer disease spectrum
inferred← citeshttps://doi.org/10.1002/ana.24825openalex-snapshot
AV‐1451 tau and β‐amyloid positron emission tomography imaging in dementia with Lewy bodies
inferred← citeshttps://doi.org/10.1002/ana.24910openalex-snapshot
Fluorodeoxyglucose metabolism associated with tau‐amyloid interaction predicts memory decline
inferred← citeshttps://doi.org/10.1002/ana.25060openalex-snapshot
18F‐flortaucipir tau positron emission tomography distinguishes established progressive supranuclear palsy from controls and Parkinson disease: A multicenter study
inferred← citeshttps://doi.org/10.1002/ana.25183openalex-snapshot
[18F]AV‐1451 tau‐PET and primary progressive aphasia
inferred← citeshttps://doi.org/10.1002/ana.25406openalex-snapshot
Longitudinal tau accumulation and atrophy in aging and alzheimer disease
inferred← citeshttps://doi.org/10.1002/ana.25968openalex-snapshot
Diagnostic Accuracy of Amyloid versus18F‐Fluorodeoxyglucose Positron Emission Tomography in Autopsy‐Confirmed Dementia
inferred← citeshttps://doi.org/10.1002/ana.26620openalex-snapshot
Change in Cerebrospinal Fluid Tau Microtubule Binding Region Detects Symptom Onset, Cognitive Decline, Tangles, and Atrophy in Dominantly Inherited Alzheimer's Disease
inferred← citeshttps://doi.org/10.1002/ana.78300openalex-snapshot
Distribution of Big Tau Isoforms in the Human Central and Peripheral Nervous System
inferred← citeshttps://doi.org/10.1002/brb3.1548openalex-snapshot
Frontal variant of Alzheimer's disease with asymmetric presentation mimicking frontotemporal dementia: Case report and literature review
inferred← citeshttps://doi.org/10.1002/brh2.70008openalex-snapshot
Transforming Brain Health With Neurotechnological Convergence (Part I): Precision Diagnostics and Targeted Interventions
inferred← citeshttps://doi.org/10.1002/cns.71125openalex-snapshot
GWAS of Tau‐Neurodegeneration Mismatch Identifies New Risk Loci for Susceptibility to Tau
inferred← citeshttps://doi.org/10.1002/dad2.12125openalex-snapshot
Association between neurite metrics and tau/inflammatory pathology in Alzheimer's disease
inferred← citeshttps://doi.org/10.1002/dad2.12200openalex-snapshot
Spatio‐spectral relationships between pathological neural dynamics and cognitive impairment along the Alzheimer's disease spectrum
inferred← citeshttps://doi.org/10.1002/dad2.12217openalex-snapshot
Current advances in digital cognitive assessment for preclinical Alzheimer's disease
inferred← citeshttps://doi.org/10.1002/dad2.12218openalex-snapshot
Hippocampal subfield imaging and fractional anisotropy show parallel changes in Alzheimer's disease tau progression using simultaneous tau‐PET/MRI at 3T
inferred← citeshttps://doi.org/10.1002/dad2.12284openalex-snapshot
The neuroinflammatory marker sTNFR2 relates to worse cognition and tau in women across the Alzheimer's disease spectrum
inferred← citeshttps://doi.org/10.1002/dad2.12454openalex-snapshot
CenTauR: Toward a universal scale and masks for standardizing tau imaging studies
inferred← citeshttps://doi.org/10.1002/dad2.12550openalex-snapshot
APOE ε4 allele status modulates the spatial patterns of progressive atrophy in the temporal lobes after mild traumatic brain injury
inferred← citeshttps://doi.org/10.1002/dad2.70033openalex-snapshot
Survey among experts on the future role of tau‐PET in clinical practice and trials
inferred← citeshttps://doi.org/10.1002/dad2.70264openalex-snapshot
Hallucinations and delusions are associated with elevated tau PET signal independent of age, clinical severity, and amyloid burden
inferred← citeshttps://doi.org/10.1002/dad2.70365openalex-snapshot
From clinical trial to clinical experience: Lecanemab therapy in a real‐world case series
inferred← citeshttps://doi.org/10.1002/dad2.70442openalex-snapshot
Decreased cerebral metabolic rate of oxygen (CMRO 2 ) is associated with increased tau deposition in Alzheimer's disease
inferred← citeshttps://doi.org/10.1002/dad2.70475openalex-snapshot
Plasma GFAP and language‐network tau mediate the effect of amyloid burden on semantic fluency: A mediation analysis
inferred← citeshttps://doi.org/10.1002/eji.70250openalex-snapshot
Active Vaccination Strategies for Alzheimer's Disease: An Expanded Review
inferred← citeshttps://doi.org/10.1002/gps.4926openalex-snapshot
Chronic depressive symptomatology and CSF amyloid beta and tau levels in mild cognitive impairment
inferred← citeshttps://doi.org/10.1002/gps.5310openalex-snapshot
Joint trajectories of cognition and gait speed in Mexican American and European American older adults: The San Antonio longitudinal study of aging
inferred← citeshttps://doi.org/10.1002/hbm.23772openalex-snapshot
Gray matter asymmetries in aging and neurodegeneration: A review and meta‐analysis
inferred← citeshttps://doi.org/10.1002/hbm.23874openalex-snapshot
Tau PET imaging predicts cognition in atypical variants of Alzheimer's disease
inferred← citeshttps://doi.org/10.1002/hbm.23897openalex-snapshot
Regionally specific changes in the hippocampal circuitry accompany progression of cerebrospinal fluid biomarkers in preclinical Alzheimer's disease
inferred← citeshttps://doi.org/10.1002/hbm.24056openalex-snapshot
Cortical microstructure in young onset Alzheimer's disease using neurite orientation dispersion and density imaging
inferred← citeshttps://doi.org/10.1002/hbm.24401openalex-snapshot
Data‐driven approaches for tau‐PET imaging biomarkers in Alzheimer's disease
inferred← citeshttps://doi.org/10.1002/hbm.24473openalex-snapshot
Regional multimodal relationships between tau, hypometabolism, atrophy, and fractional anisotropy in atypical Alzheimer's disease
inferred← citeshttps://doi.org/10.1002/hbm.24782openalex-snapshot
Applications of amyloid, tau, and neuroinflammation PET imaging to Alzheimer's disease and mild cognitive impairment
inferred← citeshttps://doi.org/10.1002/hbm.25105openalex-snapshot
Finding specificity in structural brain alterations through Bayesian reverse inference
inferred← citeshttps://doi.org/10.1002/hbm.26043openalex-snapshot
Tau as a biomarker of cognitive impairment and neuropsychiatric symptom in Alzheimer's disease
inferred← citeshttps://doi.org/10.1002/hbm.26388openalex-snapshot
Network anatomy in logopenic variant of primary progressive aphasia
inferred← citeshttps://doi.org/10.1002/hbm.26689openalex-snapshot
Characterization of tau propagation pattern and cascading hypometabolism from functional connectivity in Alzheimer's disease
inferred← citeshttps://doi.org/10.1002/mds.27252openalex-snapshot
Distinct patterns of amyloid‐dependent tau accumulation in Lewy body diseases
inferred← citeshttps://doi.org/10.1002/mds.27356openalex-snapshot
[18F]AV‐1451 binding and postmortem pathology of CBD
inferred← citeshttps://doi.org/10.1002/mds.27603openalex-snapshot
18F‐AV‐1451 uptake differs between dementia with lewy bodies and posterior cortical atrophy
inferred← citeshttps://doi.org/10.1002/mds.27677openalex-snapshot
Reply to letter: Basis of cingulate island sign may differ in dementia with lewy bodies and posterior cortical atrophy
inferred← citeshttps://doi.org/10.1002/mp.17902openalex-snapshot
Physical phantom validation of clustering‐initiated factorization in dynamic PET
inferred← citeshttps://doi.org/10.1002/nbm.70383openalex-snapshot
Quantifying the Diamagnetic and Paramagnetic Components of Beta‐Amyloid Plaques Using Decomposed Quantitative Susceptibility Mapping in Mouse Models of Alzheimer's Disease
inferred← citeshttps://doi.org/10.1002/npr2.12281openalex-snapshot
Findings of 18F‐PI ‐2620 tau PET imaging in patients with Alzheimer’s disease and healthy controls in relation to the plasma P‐tau181 levels in a Japanese sample
inferred← citeshttps://doi.org/10.1002/ptr.7387openalex-snapshot
A novel DPP ‐4 inhibitor Gramcyclin A attenuates cognitive deficits in APP / PS1 /tau triple transgenic mice via enhancing brain GLP ‐1‐dependent glucose uptake
inferred← citeshttps://doi.org/10.1002/trc2.12096openalex-snapshot
Relationship of amyloid beta and neurofibrillary tau deposition in Neurodegeneration in Aging Down Syndrome (NiAD) study at baseline
inferred← citeshttps://doi.org/10.1002/trc2.12154openalex-snapshot
Association between regional tau pathology and neuropsychiatric symptoms in aging and dementia due to Alzheimer's disease
inferred← citeshttps://doi.org/10.1002/trc2.12356openalex-snapshot
Free water derived by multi‐shell diffusion MRI reflects tau/neuroinflammatory pathology in Alzheimer's disease
inferred← citeshttps://doi.org/10.1002/trc2.12372openalex-snapshot
Development, initial validation, and application of a visual read method for [ 18 F]MK‐6240 tau PET
inferred← citeshttps://doi.org/10.1002/trc2.12490openalex-snapshot
Relationships between plasma biomarkers, tau PET, FDG PET, and volumetric MRI in mild to moderate Alzheimer's disease patients
inferred← citeshttps://doi.org/10.1002/trc2.70101openalex-snapshot
Creatine monohydrate pilot in Alzheimer's: Feasibility, brain creatine, and cognition
inferred← citeshttps://doi.org/10.1002/wnan.1946openalex-snapshot
Advances in nanoprobes for molecular MRI of Alzheimer's disease
inferred← citeshttps://doi.org/10.1007/7854_2021_267openalex-snapshot
Psychedelics as Novel Therapeutics in Alzheimer’s Disease: Rationale and Potential Mechanisms
inferred← citeshttps://doi.org/10.1007/978-1-0716-3195-9_25openalex-snapshot
Machine Learning for Alzheimer’s Disease and Related Dementias
inferred← citeshttps://doi.org/10.1007/978-1-4939-7704-8_15openalex-snapshot
Quantification of Tau Load in Alzheimer’s Disease Clinical Trials Using Positron Emission Tomography
inferred← citeshttps://doi.org/10.1007/978-1-4939-7704-8_3openalex-snapshot
Systems Biology Methods for Alzheimer’s Disease Research Toward Molecular Signatures, Subtypes, and Stages and Precision Medicine: Application in Cohort Studies and Trials
inferred← citeshttps://doi.org/10.1007/978-3-030-01523-7_5openalex-snapshot
18F-FDG-PET/CT (FDG-PET) in Neurodegenerative Disease
inferred← citeshttps://doi.org/10.1007/978-3-030-20351-1_29openalex-snapshot
A Longitudinal Model for Tau Aggregation in Alzheimer’s Disease Based on Structural Connectivity
inferred← citeshttps://doi.org/10.1007/978-3-030-41878-6_14openalex-snapshot
The Limbic System
inferred← citeshttps://doi.org/10.1007/978-3-030-48419-4_20openalex-snapshot
Positron Emission Tomography
inferred← citeshttps://doi.org/10.1007/978-3-030-51140-1_11openalex-snapshot
Progressive Supranuclear Palsy and Corticobasal Degeneration
inferred← citeshttps://doi.org/10.1007/978-3-030-53168-3_12openalex-snapshot
Neuroimaging Findings in Mild Cognitive Impairment
inferred← citeshttps://doi.org/10.1007/978-3-030-53168-3_9openalex-snapshot
PET Neuroimaging in Dementia Conditions
inferred← citeshttps://doi.org/10.1007/978-3-030-66773-3_1openalex-snapshot
Alzheimer’s Disease
inferred← citeshttps://doi.org/10.1007/978-3-030-82367-2_12openalex-snapshot
Tau Imaging in Neurodegenerative Dementia
inferred← citeshttps://doi.org/10.1007/978-3-031-10909-6_30openalex-snapshot
Functional MRI Studies of Memory in Aging, Mild Cognitive Impairment, and Alzheimer’s Disease
inferred← citeshttps://doi.org/10.1007/978-3-031-35098-6_6openalex-snapshot
Traits and Trammels of Tau Tracer Imaging
inferred← citeshttps://doi.org/10.1007/978-3-031-43356-6_11openalex-snapshot
Neuroimaging Biomarkers in Alzheimer’s Disease and Related Disorders
inferred← citeshttps://doi.org/10.1007/978-3-031-52641-1_69-1openalex-snapshot
APOE Polymorphism and Brain Imaging
inferred← citeshttps://doi.org/10.1007/978-3-031-68237-7_51openalex-snapshot
Immunotherapy of Alzheimer’s Disease
inferred← citeshttps://doi.org/10.1007/978-3-031-80849-4_20openalex-snapshot
Imaging Markers of Amyloid and Tau in Alzheimer Disease
inferred← citeshttps://doi.org/10.1007/978-3-032-38470-6_59openalex-snapshot
Stage-Aware Adaptive Reaction–Diffusion Framework for Modeling Alzheimer’s Disease Progression with Tau and Amyloid-$$\beta $$ PET Scans
inferred← citeshttps://doi.org/10.1007/978-981-16-7977-3_19openalex-snapshot
PET Imaging of Amyloid and Tau in Alzheimer’s Disease
inferred← citeshttps://doi.org/10.1007/978-981-32-9358-8_11openalex-snapshot
Tau Secretion
inferred← citeshttps://doi.org/10.1007/978-981-32-9358-8_15openalex-snapshot
Associations Between APOE Variants, Tau and α-Synuclein
inferred← citeshttps://doi.org/10.1007/978-981-32-9628-2_2openalex-snapshot
Therapeutic Vaccines Targeting Alzheimer’s Disease
inferred← citeshttps://doi.org/10.1007/978-981-95-7121-5_1openalex-snapshot
Introduction: Stages and Progression of Alzheimer’s Disease
inferred← citeshttps://doi.org/10.1007/s00115-019-0697-3openalex-snapshot
Posteriore kortikale Atrophie – ein heterogenes Syndrom
inferred← citeshttps://doi.org/10.1007/s00115-019-0773-8openalex-snapshot
Innovation in der Diagnostik – mobile Technologien
inferred← citeshttps://doi.org/10.1007/s00234-025-03781-0openalex-snapshot
Spatiotemporal patterns of amyloid deposition as prognostic markers of Alzheimer’s disease
inferred← citeshttps://doi.org/10.1007/s00259-017-3790-5openalex-snapshot
18F–FDG PET diagnostic and prognostic patterns do not overlap in Alzheimer’s disease (AD) patients at the mild cognitive impairment (MCI) stage
inferred← citeshttps://doi.org/10.1007/s00259-017-3840-zopenalex-snapshot
Multimodal correlation of dynamic [18F]-AV-1451 perfusion PET and neuronal hypometabolism in [18F]-FDG PET
inferred← citeshttps://doi.org/10.1007/s00259-018-4012-5openalex-snapshot
Dual tracer tau PET imaging reveals different molecular targets for 11C-THK5351 and 11C-PBB3 in the Alzheimer brain
inferred← citeshttps://doi.org/10.1007/s00259-018-4075-3openalex-snapshot
Distinct [18F]THK5351 binding patterns in primary progressive aphasia variants
inferred← citeshttps://doi.org/10.1007/s00259-018-4113-1openalex-snapshot
The relationship between CSF biomarkers and cerebral metabolism in early-onset Alzheimer’s disease
inferred← citeshttps://doi.org/10.1007/s00259-018-4125-xopenalex-snapshot
Differences in gray and white matter 18F-THK5351 uptake between behavioral-variant frontotemporal dementia and other dementias
inferred← citeshttps://doi.org/10.1007/s00259-019-04342-3openalex-snapshot
Level of education mitigates the impact of tau pathology on neuronal function
inferred← citeshttps://doi.org/10.1007/s00259-019-04488-0openalex-snapshot
Advances in CNS PET: the state-of-the-art for new imaging targets for pathophysiology and drug development
inferred← citeshttps://doi.org/10.1007/s00259-019-04496-0openalex-snapshot
Head-to-head comparison of tau positron emission tomography tracers [18F]flortaucipir and [18F]RO948
inferred← citeshttps://doi.org/10.1007/s00259-019-04519-wopenalex-snapshot
Three-year changes of cortical 18F-FDG in amnestic vs. non-amnestic sporadic early-onset Alzheimer’s disease
inferred← citeshttps://doi.org/10.1007/s00259-019-04640-wopenalex-snapshot
A future for PET imaging in Alzheimer’s disease
inferred← citeshttps://doi.org/10.1007/s00259-019-4273-7openalex-snapshot
Imaging of tau deposits in adults with Niemann-Pick type C disease: a case-control study
inferred← citeshttps://doi.org/10.1007/s00259-020-04758-2openalex-snapshot
Regional [18F]flortaucipir PET is more closely associated with disease severity than CSF p-tau in Alzheimer’s disease
inferred← citeshttps://doi.org/10.1007/s00259-020-04831-wopenalex-snapshot
Tau pathology and relative cerebral blood flow are independently associated with cognition in Alzheimer’s disease
inferred← citeshttps://doi.org/10.1007/s00259-020-04923-7openalex-snapshot
Tau PET imaging with 18F-PI-2620 in aging and neurodegenerative diseases
inferred← citeshttps://doi.org/10.1007/s00259-020-05099-wopenalex-snapshot
The impact of demographic, clinical, genetic, and imaging variables on tau PET status
inferred← citeshttps://doi.org/10.1007/s00259-020-05118-wopenalex-snapshot
Clinical validity of increased cortical uptake of [18F]flortaucipir on PET as a biomarker for Alzheimer’s disease in the context of a structured 5-phase biomarker development framework
inferred← citeshttps://doi.org/10.1007/s00259-020-05152-8openalex-snapshot
Comparing ATN-T designation by tau PET visual reads, tau PET quantification, and CSF PTau181 across three cohorts
inferred← citeshttps://doi.org/10.1007/s00259-020-05183-1openalex-snapshot
Indication of retrograde tau spreading along Braak stages and functional connectivity pathways
inferred← citeshttps://doi.org/10.1007/s00259-021-05192-8openalex-snapshot
Differential associations of APOE-ε2 and APOE-ε4 alleles with PET-measured amyloid-β and tau deposition in older individuals without dementia
inferred← citeshttps://doi.org/10.1007/s00259-021-05401-4openalex-snapshot
A multicenter comparison of [18F]flortaucipir, [18F]RO948, and [18F]MK6240 tau PET tracers to detect a common target ROI for differential diagnosis
inferred← citeshttps://doi.org/10.1007/s00259-021-05662-zopenalex-snapshot
Image-level trajectory inference of tau pathology using variational autoencoder for Flortaucipir PET
inferred← citeshttps://doi.org/10.1007/s00259-021-05669-6openalex-snapshot
Differential associations between neocortical tau pathology and blood flow with cognitive deficits in early-onset vs late-onset Alzheimer’s disease
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