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Sporadic Creutzfeldt-Jakob disease VM1: phenotypic and molecular characterization of a novel subtype of human prion disease.
- Published in:
- Acta Neuropathologica Communications, 2022, v. 10, n. 1, p. 1, doi. 10.1186/s40478-022-01415-7
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- Publication type:
- Article
Clinicopathological correlates in the frontotemporal lobar degeneration–motor neuron disease spectrum.
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- Brain: A Journal of Neurology, 2024, v. 147, n. 7, p. 2357, doi. 10.1093/brain/awae011
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- Publication type:
- Article
SLITRK2, an X-linked modifier of the age at onset in C9orf72 frontotemporal lobar degeneration.
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- Brain: A Journal of Neurology, 2021, v. 144, n. 9, p. 2798, doi. 10.1093/brain/awab171
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- Publication type:
- Article
Down Syndrome Biobank Consortium: A perspective.
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- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2024, v. 20, n. 3, p. 2262, doi. 10.1002/alz.13692
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- Publication type:
- Article
Galectin‐3 is upregulated in frontotemporal dementia patients with subtype specificity.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2024, v. 20, n. 3, p. 1515, doi. 10.1002/alz.13536
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- Publication type:
- Article
Transcriptome‐wide characterization of the frontal cortex in FTLD.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2021, v. 17, n. 3, p. 1, doi. 10.1002/alz.049569
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- Publication type:
- Article
Transcriptome characterization of the motor cortex suggests microglial‐related key events due to TDP‐43 aberrant inclusions: Genetics: Molecular genetics of AD and ADRD.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2020, v. 16, n. 11, p. 1, doi. 10.1002/alz.042953
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- Publication type:
- Article
Wasteosomes (corpora amylacea) of human brain can be phagocytosed and digested by macrophages.
- Published in:
- Cell & Bioscience, 2022, v. 12, n. 1, p. 1, doi. 10.1186/s13578-022-00915-2
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- Publication type:
- Article
A megalin polymorphism associated with increased Alzheimer's disease risk
- Published in:
- 2009
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- Publication type:
- Abstract
Pathologic tau conformer ensembles induce dynamic, liquid-liquid phase separation events at the nuclear envelope.
- Published in:
- BMC Biology, 2021, v. 19, n. 1, p. 1, doi. 10.1186/s12915-021-01132-y
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- Publication type:
- Article
Myelin loss in C9orf72 hexanucleotide expansion carriers.
- Published in:
- Journal of Neuroscience Research, 2022, v. 100, n. 10, p. 1862, doi. 10.1002/jnr.25100
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- Publication type:
- Article
Homocysteine and Cognitive Impairment.
- Published in:
- Dementia & Geriatric Cognitive Disorders, 2008, v. 26, n. 6, p. 506, doi. 10.1159/000173710
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- Publication type:
- Article
Interrupted CAG expansions in <italic>ATXN2</italic> gene expand the genetic spectrum of frontotemporal dementias.
- Published in:
- 2018
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- Publication type:
- Letter
Uncovering tau in wasteosomes (corpora amylacea) of Alzheimer's disease patients.
- Published in:
- Frontiers in Aging Neuroscience, 2023, v. 15, p. 1, doi. 10.3389/fnagi.2023.1110425
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- Publication type:
- Article
Increase in wasteosomes (corpora amylacea) in frontotemporal lobar degeneration with specific detection of tau, TDP-43 and FUS pathology.
- Published in:
- Acta Neuropathologica Communications, 2024, v. 12, n. 1, p. 1, doi. 10.1186/s40478-024-01812-0
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- Publication type:
- Article
IgLON5 deficiency produces behavioral alterations in a knockout mouse model.
- Published in:
- Frontiers in Immunology, 2024, p. 1, doi. 10.3389/fimmu.2024.1347948
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- Publication type:
- Article
Amyloid precursor protein 훽CTF accumulates in synapses in sporadic and genetic forms of Alzheimer's disease.
- Published in:
- Neuropathology & Applied Neurobiology, 2023, v. 49, n. 1, p. 1, doi. 10.1111/nan.12879
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- Publication type:
- Article
Neuropathology of a patient with Alzheimer disease treated with low doses of verubecestat.
- Published in:
- Neuropathology & Applied Neurobiology, 2022, v. 48, n. 3, p. 1, doi. 10.1111/nan.12781
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- Publication type:
- Article
Atypical astroglial pTDP‐43 pathology in astroglial predominant tauopathy.
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- Neuropathology & Applied Neurobiology, 2021, v. 47, n. 7, p. 1109, doi. 10.1111/nan.12707
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- Publication type:
- Article
Heterozygous APOE Christchurch in familial Alzheimer's disease without mutations in other Mendelian genes.
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- Neuropathology & Applied Neurobiology, 2021, v. 47, n. 4, p. 579, doi. 10.1111/nan.12670
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- Publication type:
- Article
Perforant path synaptic loss correlates with cognitive impairment and Alzheimer's disease in the oldest-old.
- Published in:
- Brain: A Journal of Neurology, 2014, v. 137, n. 9, p. 2578, doi. 10.1093/brain/awu190
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- Publication type:
- Article
Corpora Amylacea in the Human Brain Exhibit Neoepitopes of a Carbohydrate Nature.
- Published in:
- Frontiers in Immunology, 2021, v. 12, p. 1, doi. 10.3389/fimmu.2021.618193
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- Publication type:
- Article
Cognitive decline in amyotrophic lateral sclerosis: Neuropathological substrate and genetic determinants.
- Published in:
- Brain Pathology, 2021, v. 31, n. 3, p. 1, doi. 10.1111/bpa.12942
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- Publication type:
- Article
Does Thrombolysis Benefit Patients with Lacunar Syndrome?
- Published in:
- European Neurology, 2006, v. 55, n. 2, p. 70, doi. 10.1159/000091982
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- Publication type:
- Article
Intermediate and Expanded HTT Alleles and the Risk for α-Synucleinopathies.
- Published in:
- 2022
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- Publication type:
- journal article
Neuropathological spectrum of anti-IgLON5 disease and stages of brainstem tau pathology: updated neuropathological research criteria of the disease-related tauopathy.
- Published in:
- Acta Neuropathologica, 2024, v. 148, n. 1, p. 1, doi. 10.1007/s00401-024-02805-y
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- Publication type:
- Article
Galectin-3 is elevated in CSF and is associated with Aβ deposits and tau aggregates in brain tissue in Alzheimer's disease.
- Published in:
- Acta Neuropathologica, 2022, v. 144, n. 5, p. 843, doi. 10.1007/s00401-022-02469-6
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- Publication type:
- Article
Correction to: Diverse, evolving conformer populations drive distinct phenotypes in frontotemporal lobar degeneration caused by the same MAPT‑P301L mutation.
- Published in:
- 2021
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- Publication type:
- Correction Notice
Diverse, evolving conformer populations drive distinct phenotypes in frontotemporal lobar degeneration caused by the same MAPT-P301L mutation.
- Published in:
- Acta Neuropathologica, 2020, v. 139, n. 6, p. 1045, doi. 10.1007/s00401-020-02148-4
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- Publication type:
- Article
TDP-43 pathology in a case of hereditary spastic paraplegia with a NIPA1/SPG6 mutation.
- Published in:
- 2012
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- Publication type:
- Report
Pattern of ubiquilin pathology in ALS and FTLD indicates presence of C9ORF72 hexanucleotide expansion.
- Published in:
- Acta Neuropathologica, 2012, v. 123, n. 6, p. 825, doi. 10.1007/s00401-012-0970-z
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- Publication type:
- Article
Exploration of SUMO2/3 Expression Levels and Autophagy Process in Fragile X-Associated Tremor/Ataxia Syndrome: Addressing Study Limitations and Insights for Future Research.
- Published in:
- Cells (2073-4409), 2023, v. 12, n. 19, p. 2364, doi. 10.3390/cells12192364
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- Publication type:
- Article
Pilot Study of the Effects of Chronic Intracerebroventricular Infusion of Human Anti-IgLON5 Disease Antibodies in Mice.
- Published in:
- Cells (2073-4409), 2022, v. 11, n. 6, p. 1024, doi. 10.3390/cells11061024
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- Publication type:
- Article
RTP801 interacts with the tRNA ligase complex and dysregulates its RNA ligase activity in Alzheimer's disease.
- Published in:
- Nucleic Acids Research, 2024, v. 52, n. 18, p. 11158, doi. 10.1093/nar/gkae776
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- Publication type:
- Article
Mitochondrial complex I deficiency stratifies idiopathic Parkinson’s disease.
- Published in:
- Nature Communications, 2024, v. 15, n. 1, p. 1, doi. 10.1038/s41467-024-47867-4
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- Publication type:
- Article
Homozygous R136S mutation in PRNP gene causes inherited early onset prion disease.
- Published in:
- Alzheimer's Research & Therapy, 2021, v. 13, n. 1, p. 1, doi. 10.1186/s13195-021-00912-6
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- Publication type:
- Article
Whole-genome sequencing analysis reveals new susceptibility loci and structural variants associated with progressive supranuclear palsy.
- Published in:
- Molecular Neurodegeneration, 2024, v. 19, n. 1, p. 1, doi. 10.1186/s13024-024-00763-3
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- Publication type:
- Article
Whole-genome sequencing analysis reveals new susceptibility loci and structural variants associated with progressive supranuclear palsy.
- Published in:
- Molecular Neurodegeneration, 2024, v. 19, n. 1, p. 1, doi. 10.1186/s13024-024-00747-3
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- Publication type:
- Article
Mild cholesterol depletion reduces amyloid-β production by impairing APP trafficking to the cell surface.
- Published in:
- Journal of Neurochemistry, 2009, v. 110, n. 1, p. 220, doi. 10.1111/j.1471-4159.2009.06126.x
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- Publication type:
- Article
Genome-Wide DNA Methylation in Early-Onset-Dementia Patients Brain Tissue and Lymphoblastoid Cell Lines.
- Published in:
- International Journal of Molecular Sciences, 2024, v. 25, n. 10, p. 5445, doi. 10.3390/ijms25105445
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- Publication type:
- Article
Differential Gene Expression in Sporadic and Genetic Forms of Alzheimer's Disease and Frontotemporal Dementia in Brain Tissue and Lymphoblastoid Cell Lines.
- Published in:
- Molecular Neurobiology, 2022, v. 59, n. 10, p. 6411, doi. 10.1007/s12035-022-02969-2
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- Publication type:
- Article
Reduced mtDNA Copy Number in the Prefrontal Cortex of C9ORF72 Patients.
- Published in:
- Molecular Neurobiology, 2022, v. 59, n. 2, p. 1230, doi. 10.1007/s12035-021-02673-7
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- Publication type:
- Article
Selectively Silencing GSK-3 Isoforms Reduces Plaques and Tangles in Mouse Models of Alzheimer's Disease.
- Published in:
- Journal of Neuroscience, 2012, v. 32, n. 21, p. 7392, doi. 10.1523/JNEUROSCI.0889-12.2012
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- Publication type:
- Article