Works matching DE "FRONTOTEMPORAL lobar degeneration"
Results: 1372
Characterization of Parkinson's disease using blood-based biomarkers: A multicohort proteomic analysis.
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- PLoS Medicine, 2019, v. 16, n. 10, p. 1, doi. 10.1371/journal.pmed.1002931
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Acute presentation of Chiari 1 malformation in children.
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- Child's Nervous System, 2020, v. 36, n. 5, p. 899, doi. 10.1007/s00381-020-04540-7
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Fluorescein-guided excision of a pediatric intraparenchymal schwannoma presenting with seizure and neurogenic pulmonary edema.
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- Child's Nervous System, 2020, v. 36, n. 5, p. 1075, doi. 10.1007/s00381-019-04438-z
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TDP-43 pathology in the retina of patients with frontotemporal lobar degeneration.
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- Acta Neuropathologica, 2023, v. 146, n. 5, p. 767, doi. 10.1007/s00401-023-02623-8
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Limbic-predominant age-related TDP-43 proteinopathy (LATE-NC) is associated with abundant TMEM106B pathology.
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- Acta Neuropathologica, 2023, v. 146, n. 1, p. 163, doi. 10.1007/s00401-023-02580-2
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Progranulin deficiency results in sex-dependent alterations in microglia in response to demyelination.
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- Acta Neuropathologica, 2023, v. 146, n. 1, p. 97, doi. 10.1007/s00401-023-02578-w
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Tau seeds occur before earliest Alzheimer's changes and are prevalent across neurodegenerative diseases.
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- Acta Neuropathologica, 2023, v. 146, n. 1, p. 31, doi. 10.1007/s00401-023-02574-0
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Brain DNA methylomic analysis of frontotemporal lobar degeneration reveals OTUD4 in shared dysregulated signatures across pathological subtypes.
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- Acta Neuropathologica, 2023, v. 146, n. 1, p. 77, doi. 10.1007/s00401-023-02583-z
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Correction to: Isoform-specific patterns of tau burden and neuronal degeneration in MAPT-associated frontotemporal lobar degeneration.
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- Acta Neuropathologica, 2023, v. 145, n. 5, p. 711, doi. 10.1007/s00401-023-02556-2
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Correction to: Accumulation of TMEM106B C‑terminal fragments in neurodegenerative disease and aging.
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- 2023
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- Correction Notice
Accumulation of TMEM106B C-terminal fragments in neurodegenerative disease and aging.
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- Acta Neuropathologica, 2023, v. 145, n. 3, p. 285, doi. 10.1007/s00401-022-02531-3
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Phosphorylated tau in the retina correlates with tau pathology in the brain in Alzheimer's disease and primary tauopathies.
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- Acta Neuropathologica, 2023, v. 145, n. 2, p. 197, doi. 10.1007/s00401-022-02525-1
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LATE-NC staging in routine neuropathologic diagnosis: an update.
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- Acta Neuropathologica, 2023, v. 145, n. 2, p. 159, doi. 10.1007/s00401-022-02524-2
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The continuing legacy of John.
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- Acta Neuropathologica, 2022, v. 144, n. 6, p. 1063, doi. 10.1007/s00401-022-02514-4
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Isoform-specific patterns of tau burden and neuronal degeneration in MAPT-associated frontotemporal lobar degeneration.
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- Acta Neuropathologica, 2022, v. 144, n. 6, p. 1065, doi. 10.1007/s00401-022-02487-4
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Identification of TMEM106B amyloid fibrils provides an updated view of TMEM106B biology in health and disease.
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- Acta Neuropathologica, 2022, v. 144, n. 5, p. 807, doi. 10.1007/s00401-022-02486-5
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Frequency of LATE neuropathologic change across the spectrum of Alzheimer's disease neuropathology: combined data from 13 community-based or population-based autopsy cohorts.
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- Acta Neuropathologica, 2022, v. 144, n. 1, p. 27, doi. 10.1007/s00401-022-02444-1
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Heteroplasmic mitochondrial DNA mutations in frontotemporal lobar degeneration.
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- Acta Neuropathologica, 2022, v. 143, n. 6, p. 687, doi. 10.1007/s00401-022-02423-6
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Signature laminar distributions of pathology in frontotemporal lobar degeneration.
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- Acta Neuropathologica, 2022, v. 143, n. 3, p. 363, doi. 10.1007/s00401-021-02402-3
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Transcriptomic analysis of frontotemporal lobar degeneration with TDP-43 pathology reveals cellular alterations across multiple brain regions.
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- Acta Neuropathologica, 2022, v. 143, n. 3, p. 383, doi. 10.1007/s00401-021-02399-9
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HnRNP K mislocalisation is a novel protein pathology of frontotemporal lobar degeneration and ageing and leads to cryptic splicing.
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- Acta Neuropathologica, 2021, v. 142, n. 4, p. 609, doi. 10.1007/s00401-021-02340-0
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TMEM106B modifies TDP-43 pathology in human ALS brain and cell-based models of TDP-43 proteinopathy.
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- Acta Neuropathologica, 2021, v. 142, n. 4, p. 629, doi. 10.1007/s00401-021-02330-2
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Tau immunotherapy is associated with glial responses in FTLD-tau.
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- Acta Neuropathologica, 2021, v. 142, n. 2, p. 243, doi. 10.1007/s00401-021-02318-y
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TBK1 haploinsufficiency in ALS and FTD compromises membrane trafficking.
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- Acta Neuropathologica, 2021, v. 142, n. 1, p. 217, doi. 10.1007/s00401-021-02331-1
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A new non-aggregative splicing isoform of human Tau is decreased in Alzheimer's disease.
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- Acta Neuropathologica, 2021, v. 142, n. 1, p. 159, doi. 10.1007/s00401-021-02317-z
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TDP-43 interacts with pathological τ protein in Alzheimer's disease.
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- Acta Neuropathologica, 2021, v. 141, n. 5, p. 795, doi. 10.1007/s00401-021-02295-2
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Correction to: Diverse, evolving conformer populations drive distinct phenotypes in frontotemporal lobar degeneration caused by the same MAPT‑P301L mutation.
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- 2021
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- Correction Notice
Physiological and pathological functions of TMEM106B: a gene associated with brain aging and multiple brain disorders.
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- Acta Neuropathologica, 2021, v. 141, n. 3, p. 327, doi. 10.1007/s00401-020-02246-3
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Dipeptide repeat protein and TDP-43 pathology along the hypothalamic–pituitary axis in C9orf72 and non-C9orf72 ALS and FTLD-TDP cases.
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- Acta Neuropathologica, 2020, v. 140, n. 5, p. 777, doi. 10.1007/s00401-020-02216-9
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Distinct clinicopathologic clusters of persons with TDP-43 proteinopathy.
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- Acta Neuropathologica, 2020, v. 140, n. 5, p. 659, doi. 10.1007/s00401-020-02211-0
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Degeneration of the locus coeruleus is a common feature of tauopathies and distinct from TDP-43 proteinopathies in the frontotemporal lobar degeneration spectrum.
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- Acta Neuropathologica, 2020, v. 140, n. 5, p. 675, doi. 10.1007/s00401-020-02210-1
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Antibody against TDP-43 phosphorylated at serine 375 suggests conformational differences of TDP-43 aggregates among FTLD–TDP subtypes.
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- Acta Neuropathologica, 2020, v. 140, n. 5, p. 645, doi. 10.1007/s00401-020-02207-w
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TDP-43 transports ribosomal protein mRNA to regulate axonal local translation in neuronal axons.
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- Acta Neuropathologica, 2020, v. 140, n. 5, p. 695, doi. 10.1007/s00401-020-02205-y
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PTEN activation contributes to neuronal and synaptic engulfment by microglia in tauopathy.
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- Acta Neuropathologica, 2020, v. 140, n. 1, p. 7, doi. 10.1007/s00401-020-02151-9
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Diverse, evolving conformer populations drive distinct phenotypes in frontotemporal lobar degeneration caused by the same MAPT-P301L mutation.
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- Acta Neuropathologica, 2020, v. 139, n. 6, p. 1045, doi. 10.1007/s00401-020-02148-4
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Picalm reduction exacerbates tau pathology in a murine tauopathy model.
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- Acta Neuropathologica, 2020, v. 139, n. 4, p. 773, doi. 10.1007/s00401-020-02125-x
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Correction to: 4-Repeat tau seeds and templating subtypes as brain and CSF biomarkers of frontotemporal lobar degeneration.
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- 2020
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- Correction Notice
Subcortical TDP-43 pathology patterns validate cortical FTLD-TDP subtypes and demonstrate unique aspects of C9orf72 mutation cases.
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- Acta Neuropathologica, 2020, v. 139, n. 1, p. 83, doi. 10.1007/s00401-019-02070-4
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Evidence of corticofugal tau spreading in patients with frontotemporal dementia.
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- Acta Neuropathologica, 2020, v. 139, n. 1, p. 27, doi. 10.1007/s00401-019-02075-z
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The TMEM106B FTLD-protective variant, rs1990621, is also associated with increased neuronal proportion.
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- Acta Neuropathologica, 2020, v. 139, n. 1, p. 45, doi. 10.1007/s00401-019-02066-0
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Poly-glycine–alanine exacerbates C9orf72 repeat expansion-mediated DNA damage via sequestration of phosphorylated ATM and loss of nuclear hnRNPA3.
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- Acta Neuropathologica, 2020, v. 139, n. 1, p. 99, doi. 10.1007/s00401-019-02082-0
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4-Repeat tau seeds and templating subtypes as brain and CSF biomarkers of frontotemporal lobar degeneration.
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- Acta Neuropathologica, 2020, v. 139, n. 1, p. 63, doi. 10.1007/s00401-019-02080-2
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The basis of clinicopathological heterogeneity in TDP-43 proteinopathy.
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- Acta Neuropathologica, 2019, v. 138, n. 5, p. 751, doi. 10.1007/s00401-019-02077-x
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Increased prevalence of granulovacuolar degeneration in C9orf72 mutation.
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- Acta Neuropathologica, 2019, v. 138, n. 5, p. 783, doi. 10.1007/s00401-019-02028-6
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Revisiting the utility of TDP-43 immunoreactive (TDP-43-ir) pathology to classify FTLD-TDP subtypes.
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- Acta Neuropathologica, 2019, v. 138, n. 1, p. 167, doi. 10.1007/s00401-019-02024-w
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Pathological, imaging and genetic characteristics support the existence of distinct TDP-43 types in non-FTLD brains.
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- Acta Neuropathologica, 2019, v. 137, n. 2, p. 227, doi. 10.1007/s00401-018-1951-7
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The lysosomal function of progranulin, a guardian against neurodegeneration.
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- Acta Neuropathologica, 2018, v. 136, n. 1, p. 1, doi. 10.1007/s00401-018-1861-8
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Interactions of pathological proteins in neurodegenerative diseases.
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- Acta Neuropathologica, 2017, v. 134, n. 2, p. 187, doi. 10.1007/s00401-017-1709-7
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Reappraisal of TDP-43 pathology in FTLD-U subtypes.
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- Acta Neuropathologica, 2017, v. 134, n. 1, p. 79, doi. 10.1007/s00401-017-1716-8
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Expansion of the classification of FTLD-TDP: distinct pathology associated with rapidly progressive frontotemporal degeneration.
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- Acta Neuropathologica, 2017, v. 134, n. 1, p. 65, doi. 10.1007/s00401-017-1679-9
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