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FTLD‐TDP assemblies seed neoaggregates with subtype‐specific features via a prion‐like cascade.
- Published in:
- EMBO Reports, 2021, v. 22, n. 12, p. 1, doi. 10.15252/embr.202153877
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- Publication type:
- Article
Neuroligin-1 in brain and CSF of neurodegenerative disorders: investigation for synaptic biomarkers.
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- Acta Neuropathologica Communications, 2021, v. 9, n. 1, p. 1, doi. 10.1186/s40478-021-01119-4
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- Publication type:
- Article
Soluble and insoluble dipeptide repeat protein measurements in C9orf72-frontotemporal dementia brains show regional differential solubility and correlation of poly-GR with clinical severity.
- Published in:
- Acta Neuropathologica Communications, 2020, v. 8, n. 1, p. N.PAG, doi. 10.1186/s40478-020-01036-y
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- Publication type:
- Article
Epigenomics and transcriptomics analyses of multiple system atrophy brain tissue supports a role for inflammatory processes in disease pathogenesis.
- Published in:
- 2020
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- Publication type:
- Letter
Analysis of neurodegenerative disease-causing genes in dementia with Lewy bodies.
- Published in:
- Acta Neuropathologica Communications, 2020, v. 8, n. 1, p. 1, doi. 10.1186/s40478-020-0879-z
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- Publication type:
- Article
Investigation of somatic CNVs in brains of synucleinopathy cases using targeted SNCA analysis and single cell sequencing.
- Published in:
- Acta Neuropathologica Communications, 2019, v. 7, n. 1, p. 1, doi. 10.1186/s40478-019-0873-5
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- Publication type:
- Article
Variant Alzheimer's disease with spastic paraparesis and cotton wool plaques is caused by PS-1 mutations that lead to exceptionally high amyloid-β concentrations.
- Published in:
- Annals of Neurology, 2000, v. 48, n. 5, p. 806, doi. 10.1002/1531-8249(200011)48:5<806::AID-ANA18>3.0.CO;2-F
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- Publication type:
- Article
A Clinicopathologic Study of Movement Disorders in Frontotemporal Lobar Degeneration.
- Published in:
- Movement Disorders, 2021, v. 36, n. 3, p. 632, doi. 10.1002/mds.28356
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- Publication type:
- Article
Apomorphine: A potential modifier of amyloid deposition in Parkinson's disease?
- Published in:
- 2016
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- Publication type:
- journal article
Genetic Analysis of Inherited Leukodystrophies Genotype-Phenotype Correlations in the CSF1R Gene.
- Published in:
- JAMA Neurology, 2013, v. 70, n. 7, p. 875, doi. 10.1001/jamaneurol.2013.698
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- Publication type:
- Article
The presenilin 1 mutation P436S causes familial Alzheimer's disease with elevated Aβ43 and atypical clinical manifestations.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2024, v. 20, n. 7, p. 4717, doi. 10.1002/alz.13904
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- Publication type:
- Article
Neuronal intranuclear inclusion disease is genetically heterogeneous.
- Published in:
- Annals of Clinical & Translational Neurology, 2020, v. 7, n. 9, p. 1716, doi. 10.1002/acn3.51151
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- Publication type:
- Article
Heterogeneous nuclear ribonucleoproteins R and Q accumulate in pathological inclusions in FTLD-FUS.
- Published in:
- Acta Neuropathologica Communications, 2019, v. 7, n. 1, p. N.PAG, doi. 10.1186/s40478-019-0673-y
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- Publication type:
- Article
The presubiculum is preserved from neurodegenerative changes in Alzheimer's disease.
- Published in:
- Acta Neuropathologica Communications, 2018, v. 6, n. 1, p. N.PAG, doi. 10.1186/s40478-018-0563-8
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- Publication type:
- Article
Large inter- and intra-case variability of first generation tau PET ligand binding in neurodegenerative dementias.
- Published in:
- Acta Neuropathologica Communications, 2018, v. 6, n. 1, p. N.PAG, doi. 10.1186/s40478-018-0535-z
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- Publication type:
- Article
Heterogeneous ribonuclear protein E2 (hnRNP E2) is associated with TDP-43-immunoreactive neurites in Semantic Dementia but not with other TDP-43 pathological subtypes of Frontotemporal Lobar Degeneration.
- Published in:
- Acta Neuropathologica Communications, 2017, v. 5, p. 1, doi. 10.1186/s40478-017-0454-4
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- Publication type:
- Article
Heterogeneous ribonuclear protein A3 (hnRNP A3) is present in dipeptide repeat protein containing inclusions in Frontotemporal Lobar Degeneration and Motor Neurone disease associated with expansions in C9orf72 gene.
- Published in:
- Acta Neuropathologica Communications, 2017, v. 5, p. 12, doi. 10.1186/s40478-017-0437-5
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- Publication type:
- Article
Bidirectional nucleolar dysfunction in C9orf72 frontotemporal lobar degeneration.
- Published in:
- Acta Neuropathologica Communications, 2017, v. 5, p. 1, doi. 10.1186/s40478-017-0432-x
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- Publication type:
- Article
Neuropathological features of genetically confirmed DYT1 dystonia: investigating disease-specific inclusions.
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- Acta Neuropathologica Communications, 2014, v. 2, n. 1, p. 1, doi. 10.1186/s40478-014-0159-x
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- Publication type:
- Article
Epigenetic Age Acceleration in Frontotemporal Lobar Degeneration: A Comprehensive Analysis in the Blood and Brain.
- Published in:
- Cells (2073-4409), 2023, v. 12, n. 14, p. 1922, doi. 10.3390/cells12141922
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- Publication type:
- Article
HnRNP Pathologies in Frontotemporal Lobar Degeneration.
- Published in:
- Cells (2073-4409), 2023, v. 12, n. 12, p. 1633, doi. 10.3390/cells12121633
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- Publication type:
- Article
Advances in the Understanding of Frontotemporal Dementia.
- Published in:
- Cells (2073-4409), 2023, v. 12, n. 5, p. 781, doi. 10.3390/cells12050781
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- Publication type:
- Article
Chemical traits of cerebral amyloid angiopathy in familial British‐, Danish‐, and non‐Alzheimerʼs dementias.
- Published in:
- Journal of Neurochemistry, 2022, v. 163, n. 3, p. 233, doi. 10.1111/jnc.15694
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- Publication type:
- Article
Amyloid pathology and synaptic loss in pathological aging.
- Published in:
- Journal of Neurochemistry, 2021, v. 159, n. 2, p. 258, doi. 10.1111/jnc.15487
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- Publication type:
- Article
Molecular forms of neurogranin in cerebrospinal fluid.
- Published in:
- Journal of Neurochemistry, 2021, v. 157, n. 3, p. 816, doi. 10.1111/jnc.15252
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- Publication type:
- Article
Novel tau fragments in cerebrospinal fluid: relation to tangle pathology and cognitive decline in Alzheimer's disease.
- Published in:
- Acta Neuropathologica, 2019, v. 137, n. 2, p. 279, doi. 10.1007/s00401-018-1948-2
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- Publication type:
- Article
The intact postsynaptic protein neurogranin is reduced in brain tissue from patients with familial and sporadic Alzheimer's disease.
- Published in:
- Acta Neuropathologica, 2019, v. 137, n. 1, p. 89, doi. 10.1007/s00401-018-1910-3
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- Publication type:
- Article
Histological evidence of chronic traumatic encephalopathy in a large series of neurodegenerative diseases.
- Published in:
- 2015
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- Publication type:
- Letter
A 30-unit hexanucleotide repeat expansion in C9orf72 induces pathological lesions with dipeptide-repeat proteins and RNA foci, but not TDP-43 inclusions and clinical disease.
- Published in:
- 2015
- By:
- Publication type:
- Letter
The novel MAPT mutation K298E: mechanisms of mutant tau toxicity, brain pathology and tau expression in induced fibroblast-derived neurons.
- Published in:
- 2014
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- Publication type:
- Report
<i>C9orf72</i> frontotemporal lobar degeneration is characterised by frequent neuronal sense and antisense RNA foci.
- Published in:
- Acta Neuropathologica, 2013, v. 126, n. 6, p. 845, doi. 10.1007/s00401-013-1200-z
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- Publication type:
- Article
Homozygosity for the C9orf72 GGGGCC repeat expansion in frontotemporal dementia.
- Published in:
- Acta Neuropathologica, 2013, v. 126, n. 3, p. 401, doi. 10.1007/s00401-013-1147-0
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- Publication type:
- Article
Transportin1: a marker of FTLD-FUS.
- Published in:
- Acta Neuropathologica, 2011, v. 122, n. 5, p. 591, doi. 10.1007/s00401-011-0863-6
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- Publication type:
- Article
Globular glial tauopathies (GGT) presenting with motor neuron disease or frontotemporal dementia: an emerging group of 4-repeat tauopathies.
- Published in:
- Acta Neuropathologica, 2011, v. 122, n. 4, p. 415, doi. 10.1007/s00401-011-0857-4
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- Publication type:
- Article
TDP-43 pathology may occur in the BRI2 gene-related dementias.
- Published in:
- 2011
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- Publication type:
- Letter
TDP-43 in ubiquitinated inclusions in the inferior olives in frontotemporal lobar degeneration and in other neurodegenerative diseases: a degenerative process distinct from normal ageing.
- Published in:
- Acta Neuropathologica, 2009, v. 118, n. 3, p. 359, doi. 10.1007/s00401-009-0526-z
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- Publication type:
- Article
Genetics and molecular pathogenesis of sporadic and hereditary cerebral amyloid angiopathies.
- Published in:
- 2009
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- Publication type:
- Correction notice
Genetics and molecular pathogenesis of sporadic and hereditary cerebral amyloid angiopathies.
- Published in:
- Acta Neuropathologica, 2009, v. 118, n. 1, p. 115, doi. 10.1007/s00401-009-0501-8
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- Publication type:
- Article
LRRK2 and parkin immunoreactivity in multiple system atrophy inclusions.
- Published in:
- Acta Neuropathologica, 2008, v. 116, n. 6, p. 639, doi. 10.1007/s00401-008-0446-3
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- Publication type:
- Article
Cortical α-synuclein load is associated with amyloid-β plaque burden in a subset of Parkinson’s disease patients.
- Published in:
- Acta Neuropathologica, 2008, v. 115, n. 4, p. 417, doi. 10.1007/s00401-007-0336-0
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- Publication type:
- Article
An immunohistochemical study of cases of sporadic and inherited frontotemporal lobar degeneration using 3R- and 4R-specific tau monoclonal antibodies.
- Published in:
- Acta Neuropathologica, 2006, v. 111, n. 4, p. 329, doi. 10.1007/s00401-006-0048-x
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- Publication type:
- Article
Sporadic four-repeat tauopathy with frontotemporal degeneration, parkinsonism and motor neuron disease.
- Published in:
- Acta Neuropathologica, 2005, v. 110, n. 6, p. 600, doi. 10.1007/s00401-005-1086-5
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- Publication type:
- Article
Detecting tau isoforms in archival cases.
- Published in:
- Acta Neuropathologica, 2004, v. 107, n. 2, p. 181, doi. 10.1007/s00401-003-0795-x
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- Publication type:
- Article
Epigenetic age acceleration is associated with oligodendrocyte proportions in MSA and control brain tissue.
- Published in:
- Neuropathology & Applied Neurobiology, 2023, v. 49, n. 1, p. 1, doi. 10.1111/nan.12872
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- Publication type:
- Article
HnRNP K mislocalisation in neurons of the dentate nucleus is a novel neuropathological feature of neurodegenerative disease and ageing.
- Published in:
- Neuropathology & Applied Neurobiology, 2022, v. 48, n. 4, p. 1, doi. 10.1111/nan.12793
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- Publication type:
- Article
MOBP and HIP1 in multiple system atrophy: New α‐synuclein partners in glial cytoplasmic inclusions implicated in the disease pathogenesis.
- Published in:
- Neuropathology & Applied Neurobiology, 2021, v. 47, n. 5, p. 640, doi. 10.1111/nan.12688
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- Publication type:
- Article
Review: An update on clinical, genetic and pathological aspects of frontotemporal lobar degenerations.
- Published in:
- Neuropathology & Applied Neurobiology, 2015, v. 41, n. 7, p. 858, doi. 10.1111/nan.12250
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- Publication type:
- Article
Alterations in global DNA methylation and hydroxymethylation are not detected in Alzheimer's disease.
- Published in:
- Neuropathology & Applied Neurobiology, 2015, v. 41, n. 4, p. 497, doi. 10.1111/nan.12183
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- Publication type:
- Article
A pathogenic progranulin mutation and C9orf72 repeat expansion in a family with frontotemporal dementia.
- Published in:
- Neuropathology & Applied Neurobiology, 2014, v. 40, n. 4, p. 502, doi. 10.1111/nan.12100
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- Publication type:
- Article
Variability in the type and layer distribution of cortical Aβ pathology in familial Alzheimer's disease.
- Published in:
- Brain Pathology, 2022, v. 32, n. 3, p. 1, doi. 10.1111/bpa.13009
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- Publication type:
- Article