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1
Tractography of supplementary motor area projections in progressive speech apraxia and aphasia
In: Neuroimage Clin (2022)
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2
Posterior cortical atrophy phenotypic heterogeneity revealed by decoding (18)F-FDG-PET
In: Brain Commun (2021)
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3
Changing the face of neuroimaging research: Comparing a new MRI de-facing technique with popular alternatives
In: Neuroimage (2021)
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4
A molecular pathology, neurobiology, biochemical, genetic and neuroimaging study of progressive apraxia of speech
In: Nat Commun (2021)
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5
Longitudinal neuroimaging biomarkers differ across Alzheimer’s disease phenotypes
In: Brain (2020)
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6
Association of amyloid angiopathy with microbleeds in logopenic progressive aphasia: an imaging-pathology study
In: Eur J Neurol (2020)
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7
Longitudinal anatomic, functional, and molecular characterization of Pick disease phenotypes
In: Neurology (2020)
Abstract: OBJECTIVE: To characterize longitudinal MRI and PET abnormalities in autopsy-confirmed Pick disease (PiD) and determine how patterns of neurodegeneration differ with respect to clinical syndrome. METHODS: Seventeen patients with PiD were identified who had antemortem MRI (8 with behavioral variant frontotemporal dementia [bvFTD-PiD], 6 with nonfluent/agrammatic primary progressive aphasia [naPPA-PiD], 1 with semantic primary progressive aphasia, 1 with unclassified primary progressive aphasia, and 1 with corticobasal syndrome). Thirteen patients had serial MRI for a total of 56 MRIs, 7 had [(18)F]fluorodeoxyglucose PET, 4 had Pittsburgh compound B (PiB) PET, and 1 patient had [(18)F]flortaucipir PET. Cross-sectional and longitudinal comparisons of gray matter volume and metabolism were performed between bvFTD-PiD, naPPA-PiD, and controls. Cortical PiB summaries were calculated to determine β-amyloid positivity. RESULTS: The bvFTD-PiD and naPPA-PiD groups showed different foci of volume loss and hypometabolism early in the disease, with bvFTD-PiD involving bilateral prefrontal and anterior temporal cortices and naPPA-PiD involving left inferior frontal gyrus, insula, and orbitofrontal cortex. However, patterns merged over time, with progressive spread into prefrontal and anterior temporal lobe in naPPA-PiD, and eventual involvement of posterior temporal lobe, motor cortex, and parietal lobe in both groups. Rates of frontotemporal atrophy were faster in bvFTD-PiD than naPPA-PiD. One patient was β-amyloid–positive on PET with low Alzheimer neuropathologic changes at autopsy. Flortaucipir PET showed elevated uptake in frontotemporal white matter. CONCLUSION: Patterns of atrophy and hypometabolism differ in PiD according to presenting syndrome, although patterns of neurodegeneration appear to converge over time.
Keyword: Article
URL: https://doi.org/10.1212/WNL.0000000000010948
http://www.ncbi.nlm.nih.gov/pubmed/32989107
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7836669/
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8
An Evaluation of the Progressive Supranuclear Palsy Speech/Language Variant
In: Mov Disord Clin Pract (2019)
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9
Clinical and Neuroimaging Characteristics of Clinically Unclassifiable Primary Progressive Aphasia
In: Brain Lang (2019)
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10
The influence of β-amyloid on [(18)F]AV-1451 in semantic variant of primary progressive aphasia
Whitwell, Jennifer L.; Martin, Peter R.; Duffy, Joseph R.. - : Lippincott Williams & Wilkins, 2019
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11
Patterns of Neuropsychological Dysfunction and Cortical Volume Changes in Logopenic Aphasia
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12
[18F]AV-1451 tau-PET and primary progressive aphasia
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13
Tau Uptake in Agrammatic Primary Progressive Aphasia with and without Apraxia of Speech
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14
Disrupted functional connectivity in primary progressive apraxia of speech
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15
Tau-PET imaging with [18F]AV-1451 in Primary Progressive Apraxia of Speech
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16
Prosodic and Phonetic Subtypes of Primary Progressive Apraxia of Speech
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17
Predicting clinical decline in progressive agrammatic aphasia and apraxia of speech
Whitwell, Jennifer L.; Weigand, Stephen D.; Duffy, Joseph R.. - : Lippincott Williams & Wilkins, 2017
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18
Varying degrees of temporoparietal hypometabolism on FDG-PET reveal amyloid-positive logopenic primary progressive aphasia is not a homogeneous clinical entity
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19
Association Between Anticholinergic Medication Use and Cognition, Brain Metabolism, and Brain Atrophy in Cognitively Normal Older Adults
In: PMC (2016)
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20
Tracking the Development of Agrammatic Aphasia: a Tensor-Based Morphometry Study
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