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Relationships between lewy and tau pathologies in 375 consecutive non-Alzheimer's olfactory bulbs.
- Published in:
- 2018
- By:
- Publication type:
- letter
Cognitive impairment in progressive supranuclear palsy is associated with tau burden.
- Published in:
- Movement Disorders, 2017, v. 32, n. 12, p. 1772, doi. 10.1002/mds.27198
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- Publication type:
- Article
Distribution and characteristics of transactive response DNA binding protein 43 kDa pathology in progressive supranuclear palsy.
- Published in:
- 2017
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- Publication type:
- journal article
Study of LRRK2 variation in tauopathy: Progressive supranuclear palsy and corticobasal degeneration.
- Published in:
- 2017
- By:
- Publication type:
- journal article
Primary familial brain calcification in the 'IBGC2' kindred: All linkage roads lead to SLC20A2.
- Published in:
- 2016
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- Publication type:
- journal article
Cerebellar ataxia in progressive supranuclear palsy: An autopsy study of PSP-C.
- Published in:
- 2016
- By:
- Publication type:
- journal article
A novel de novo pathogenic mutation in the CACNA1A gene.
- Published in:
- Movement Disorders, 2012, v. 27, n. 12, p. 1578, doi. 10.1002/mds.25198
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- Publication type:
- Article
Progranulin gene mutation with an unusual clinical and neuropathologic presentation.
- Published in:
- Movement Disorders, 2008, v. 23, n. 8, p. 1168, doi. 10.1002/mds.22065
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- Publication type:
- Article
Senile plaque‐associated transactive response DNA‐binding protein 43 in Alzheimer's disease: A case report spanning 16 years of memory loss.
- Published in:
- Neuropathology, 2024, v. 44, n. 2, p. 115, doi. 10.1111/neup.12938
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- Publication type:
- Article
Frontotemporal lobar degeneration with TDP-43 proteinopathy and chromosome 9p repeat expansion in C9ORF72: clinicopathologic correlation.
- Published in:
- Neuropathology, 2013, v. 33, n. 2, p. 122, doi. 10.1111/j.1440-1789.2012.01332.x
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- Publication type:
- Article
Wild-Type Human TDP-43 Expression Causes TDP-43 Phosphorylation, Mitochondrial Aggregation, Motor Deficits, and Early Mortality in Transgenic Mice.
- Published in:
- Journal of Neuroscience, 2010, v. 30, n. 32, p. 10851, doi. 10.1523/JNEUROSCI.1630-10.2010
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- Publication type:
- Article
TMEM106B p.T185S regulates TMEM106B protein levels: implications for frontotemporal dementia.
- Published in:
- Journal of Neurochemistry, 2013, v. 126, n. 6, p. 781, doi. 10.1111/jnc.12329
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- Publication type:
- Article
SLC20A2 and THAP1 deletion in familial basal ganglia calcification with dystonia.
- Published in:
- Neurogenetics, 2014, v. 15, n. 1, p. 23, doi. 10.1007/s10048-013-0378-5
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- Publication type:
- Article
The molecular genetics and neuropathology of frontotemporal lobar degeneration: recent developments.
- Published in:
- Neurogenetics, 2007, v. 8, n. 4, p. 237, doi. 10.1007/s10048-007-0102-4
- By:
- Publication type:
- Article
Mutations in progranulin cause tau-negative frontotemporal dementia linked to chromosome 17.
- Published in:
- Nature, 2006, v. 442, n. 7105, p. 916, doi. 10.1038/nature05016
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- Publication type:
- Article
Null mutations in progranulin cause ubiquitin-positive frontotemporal dementia linked to chromosome 17q21.
- Published in:
- Nature, 2006, v. 442, n. 7105, p. 920, doi. 10.1038/nature05017
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- Publication type:
- Article
Brain MR Spectroscopy Changes Precede Frontotemporal Lobar Degeneration Phenoconversion in Mapt Mutation Carriers.
- Published in:
- 2019
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- Publication type:
- journal article
MRS in Early and Presymptomatic Carriers of a Novel Octapeptide Repeat Insertion in the Prion Protein Gene.
- Published in:
- Journal of Neuroimaging, 2013, v. 23, n. 3, p. 409, doi. 10.1111/j.1552-6569.2012.00717.x
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- Publication type:
- Article
Targeted manipulation of the sortilin–progranulin axis rescues progranulin haploinsufficiency.
- Published in:
- Human Molecular Genetics, 2014, v. 23, n. 6, p. 1467, doi. 10.1093/hmg/ddt534
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- Publication type:
- Article
Common variation in the miR-659 binding-site of GRN is a major risk factor for TDP43-positive frontotemporal dementia.
- Published in:
- Human Molecular Genetics, 2008, v. 17, n. 23, p. 3631, doi. 10.1093/hmg/ddn257
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- Publication type:
- Article
High-density SNP haplotyping suggests altered regulation of tau gene expression in progressive supranuclear palsy.
- Published in:
- Human Molecular Genetics, 2005, v. 14, n. 21, p. 3281, doi. 10.1093/hmg/ddi361
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- Publication type:
- Article
Genomic architecture of human 17q21 linked to frontotemporal dementia uncovers a highly homologous family of low-copy repeats in the tau region.
- Published in:
- Human Molecular Genetics, 2005, v. 14, n. 13, p. 1753, doi. 10.1093/hmg/ddi182
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- Publication type:
- Article
Psychometric evaluation of personality in a patient with FTDP-17.
- Published in:
- 2010
- By:
- Publication type:
- Letter
The genetics of frontotemporal lobar degeneration.
- Published in:
- Current Neurology & Neuroscience Reports, 2007, v. 7, n. 5, p. 434, doi. 10.1007/s11910-007-0067-6
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- Publication type:
- Article
Genome-wide association study of brain biochemical phenotypes reveals distinct genetic architecture of Alzheimer's disease related proteins.
- Published in:
- Molecular Neurodegeneration, 2023, v. 18, n. 1, p. 1, doi. 10.1186/s13024-022-00592-2
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- Publication type:
- Article
Uncovering the distinct macro-scale anatomy of dysexecutive and behavioural degenerative diseases.
- Published in:
- Brain: A Journal of Neurology, 2024, v. 147, n. 4, p. 1483, doi. 10.1093/brain/awad356
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- Publication type:
- Article
C-terminal TMEM106B fragments in human brain correlate with disease-associated TMEM106B haplotypes.
- Published in:
- Brain: A Journal of Neurology, 2023, v. 146, n. 10, p. 4055, doi. 10.1093/brain/awad133
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- Publication type:
- Article
Shared brain transcriptomic signature in TDP-43 type A FTLD patients with or without GRN mutations.
- Published in:
- 2022
- By:
- Publication type:
- journal article
Cortical and subcortical pathological burden and neuronal loss in an autopsy series of FTLD-TDP-type C.
- Published in:
- 2022
- By:
- Publication type:
- journal article
Long-read targeted sequencing uncovers clinicopathological associations for C9orf72-linked diseases.
- Published in:
- 2021
- By:
- Publication type:
- journal article
Reply: LATE to the PART-y.
- Published in:
- 2019
- By:
- Publication type:
- letter
Limbic-predominant age-related TDP-43 encephalopathy (LATE): consensus working group report.
- Published in:
- 2019
- By:
- Publication type:
- journal article
Ossified blood vessels in primary familial brain calcification elicit a neurotoxic astrocyte response.
- Published in:
- 2019
- By:
- Publication type:
- journal article
A C6orf10/LOC101929163 locus is associated with age of onset in C9orf72 carriers.
- Published in:
- 2018
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- Publication type:
- journal article
TMEM106B and myelination: rare leukodystrophy families reveal unexpected connections.
- Published in:
- 2017
- By:
- Publication type:
- journal article
Lewy Body Disease is a Contributor to Logopenic Progressive Aphasia Phenotype.
- Published in:
- 2021
- By:
- Publication type:
- journal article
Sensitivity–Specificity of Tau and Amyloid β Positron Emission Tomography in Frontotemporal Lobar Degeneration.
- Published in:
- Annals of Neurology, 2020, v. 88, n. 5, p. 1009, doi. 10.1002/ana.25893
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- Publication type:
- Article
Abundant transcriptomic alterations in the human cerebellum of patients with a C9orf72 repeat expansion.
- Published in:
- Acta Neuropathologica, 2024, v. 147, n. 1, p. 1, doi. 10.1007/s00401-024-02720-2
- By:
- Publication type:
- Article
Limbic-predominant age-related TDP-43 proteinopathy (LATE-NC) is associated with abundant TMEM106B pathology.
- Published in:
- Acta Neuropathologica, 2023, v. 146, n. 1, p. 163, doi. 10.1007/s00401-023-02580-2
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- Publication type:
- Article
Correction to: Accumulation of TMEM106B C‑terminal fragments in neurodegenerative disease and aging.
- Published in:
- 2023
- By:
- Publication type:
- Correction Notice
Accumulation of TMEM106B C-terminal fragments in neurodegenerative disease and aging.
- Published in:
- Acta Neuropathologica, 2023, v. 145, n. 3, p. 285, doi. 10.1007/s00401-022-02531-3
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- Publication type:
- Article
Identification of TMEM106B amyloid fibrils provides an updated view of TMEM106B biology in health and disease.
- Published in:
- Acta Neuropathologica, 2022, v. 144, n. 5, p. 807, doi. 10.1007/s00401-022-02486-5
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- Publication type:
- Article
Latent trait modeling of tau neuropathology in progressive supranuclear palsy.
- Published in:
- Acta Neuropathologica, 2021, v. 141, n. 5, p. 667, doi. 10.1007/s00401-021-02289-0
- By:
- Publication type:
- Article
Revisiting the utility of TDP-43 immunoreactive (TDP-43-ir) pathology to classify FTLD-TDP subtypes.
- Published in:
- Acta Neuropathologica, 2019, v. 138, n. 1, p. 167, doi. 10.1007/s00401-019-02024-w
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- Publication type:
- Article
Genome-wide analyses as part of the international FTLD-TDP whole-genome sequencing consortium reveals novel disease risk factors and increases support for immune dysfunction in FTLD.
- Published in:
- Acta Neuropathologica, 2019, v. 137, n. 6, p. 879, doi. 10.1007/s00401-019-01962-9
- By:
- Publication type:
- Article
Pathological, imaging and genetic characteristics support the existence of distinct TDP-43 types in non-FTLD brains.
- Published in:
- Acta Neuropathologica, 2019, v. 137, n. 2, p. 227, doi. 10.1007/s00401-018-1951-7
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- Publication type:
- Article
Conserved DNA methylation combined with differential frontal cortex and cerebellar expression distinguishes C9orf72-associated and sporadic ALS, and implicates SERPINA1 in disease.
- Published in:
- Acta Neuropathologica, 2017, v. 134, n. 5, p. 715, doi. 10.1007/s00401-017-1760-4
- By:
- Publication type:
- Article
Shared genetic risk between corticobasal degeneration, progressive supranuclear palsy, and frontotemporal dementia.
- Published in:
- Acta Neuropathologica, 2017, v. 133, n. 5, p. 825, doi. 10.1007/s00401-017-1693-y
- By:
- Publication type:
- Article
What we know about TMEM106B in neurodegeneration.
- Published in:
- Acta Neuropathologica, 2016, v. 132, n. 5, p. 639, doi. 10.1007/s00401-016-1610-9
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- Publication type:
- Article
Chronic traumatic encephalopathy pathology in a neurodegenerative disorders brain bank.
- Published in:
- Acta Neuropathologica, 2015, v. 130, n. 6, p. 877, doi. 10.1007/s00401-015-1502-4
- By:
- Publication type:
- Article