Found: 28
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CLEC3B p.S106G Mutant in a Caucasian Population of Successful Neurological Aging.
- Published in:
- 2020
- By:
- Publication type:
- journal article
Mitochondrial genomic variation in dementia with Lewy bodies: association with disease risk and neuropathological measures.
- Published in:
- Acta Neuropathologica Communications, 2022, v. 10, n. 1, p. 1, doi. 10.1186/s40478-022-01399-4
- By:
- Publication type:
- Article
MAPT subhaplotypes in corticobasal degeneration: assessing associations with disease risk, severity of tau pathology, and clinical features.
- Published in:
- Acta Neuropathologica Communications, 2020, v. 8, n. 1, p. 1, doi. 10.1186/s40478-020-01097-z
- By:
- Publication type:
- Article
Associations of mitochondrial genomic variation with corticobasal degeneration, progressive supranuclear palsy, and neuropathological tau measures.
- Published in:
- Acta Neuropathologica Communications, 2020, v. 8, n. 1, p. N.PAG, doi. 10.1186/s40478-020-01035-z
- By:
- Publication type:
- Article
Association of ABI3 and PLCG2 missense variants with disease risk and neuropathology in Lewy body disease and progressive supranuclear palsy.
- Published in:
- Acta Neuropathologica Communications, 2020, v. 8, n. 1, p. N.PAG, doi. 10.1186/s40478-020-01050-0
- By:
- Publication type:
- Article
Structural variants in Lewy body dementia and frontotemporal dementia spectrum.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2023, v. 19, p. 1, doi. 10.1002/alz.078497
- By:
- Publication type:
- Article
Structural variants in Lewy body dementia and frontotemporal dementia spectrum.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2023, v. 19, p. 1, doi. 10.1002/alz.078497
- By:
- Publication type:
- Article
Mitophagy alterations in Alzheimer's disease are associated with granulovacuolar degeneration and early tau pathology.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2021, v. 17, n. 3, p. 417, doi. 10.1002/alz.12198
- By:
- Publication type:
- Article
Cathepsin B p.Gly284Val Variant in Parkinson's Disease Pathogenesis.
- Published in:
- International Journal of Molecular Sciences, 2022, v. 23, n. 13, p. 7086, doi. 10.3390/ijms23137086
- By:
- Publication type:
- Article
MAPT haplotype H1G is associated with increased risk of dementia with Lewy bodies.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2016, v. 12, n. 12, p. 1297, doi. 10.1016/j.jalz.2016.05.002
- By:
- Publication type:
- Article
Exonic Re-Sequencing of the Chromosome 2q24.3 Parkinson’s Disease Locus.
- Published in:
- PLoS ONE, 2015, v. 10, n. 6, p. 1, doi. 10.1371/journal.pone.0128586
- By:
- Publication type:
- Article
Frequency of spinocerebellar ataxia mutations in patients with multiple system atrophy.
- Published in:
- Clinical Autonomic Research, 2021, v. 31, n. 1, p. 117, doi. 10.1007/s10286-020-00759-1
- By:
- Publication type:
- Article
PARKIN, PINK1, and DJ1 analysis in early-onset Parkinson's disease in Ireland.
- Published in:
- Irish Journal of Medical Science, 2022, v. 191, n. 2, p. 901, doi. 10.1007/s11845-021-02563-w
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- Publication type:
- Article
Publisher Correction to: Diffuse argyrophilic grain disease with TDP-43 proteinopathy and neuronal intermediate filament inclusion disease: FTLD with mixed tau, TDP-43 and FUS pathologies.
- Published in:
- 2023
- By:
- Publication type:
- Correction Notice
Diffuse argyrophilic grain disease with TDP-43 proteinopathy and neuronal intermediate filament inclusion disease: FTLD with mixed tau, TDP-43 and FUS pathologies.
- Published in:
- Acta Neuropathologica Communications, 2023, v. 11, n. 1, p. 1, doi. 10.1186/s40478-023-01611-z
- By:
- Publication type:
- Article
Association of MAPT subhaplotypes with clinical and demographic features in Parkinson's disease.
- Published in:
- Annals of Clinical & Translational Neurology, 2020, v. 7, n. 9, p. 1557, doi. 10.1002/acn3.51139
- By:
- Publication type:
- Article
Clinicopathologic and genetic features of multiple system atrophy with Lewy body disease.
- Published in:
- Brain Pathology, 2020, v. 30, n. 4, p. 766, doi. 10.1111/bpa.12839
- By:
- Publication type:
- Article
Early-Onset Parkinson Disease Screening in Patients From Nigeria.
- Published in:
- Frontiers in Neurology, 2021, v. 11, p. N.PAG, doi. 10.3389/fneur.2020.594927
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- Publication type:
- Article
Association Between Glucocerebrosidase Mutations and Parkinson's Disease in Ireland.
- Published in:
- Frontiers in Neurology, 2020, p. 1, doi. 10.3389/fneur.2020.00527
- By:
- Publication type:
- Article
Screening of GBA Mutations in Nigerian Patients with Parkinson's Disease.
- Published in:
- Movement Disorders, 2021, v. 36, n. 12, p. 2971, doi. 10.1002/mds.28803
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- Publication type:
- Article
Association of Tripartite Motif Containing 11 rs564309 With Tau Pathology in Progressive Supranuclear Palsy.
- Published in:
- 2020
- By:
- Publication type:
- journal article
Role of GBA variants in Lewy body disease neuropathology.
- Published in:
- Acta Neuropathologica, 2024, v. 147, n. 1, p. 1, doi. 10.1007/s00401-024-02699-w
- By:
- Publication type:
- Article
Corticobasal degeneration with TDP-43 pathology presenting with progressive supranuclear palsy syndrome: a distinct clinicopathologic subtype.
- Published in:
- Acta Neuropathologica, 2018, v. 136, n. 3, p. 389, doi. 10.1007/s00401-018-1878-z
- By:
- Publication type:
- Article
Plasma neurofilament light predicts mortality in patients with stroke.
- Published in:
- Science Translational Medicine, 2020, v. 12, n. 569, p. 1, doi. 10.1126/scitranslmed.aay1913
- By:
- Publication type:
- Article
Multiple system atrophy and apolipoprotein E.
- Published in:
- 2018
- By:
- Publication type:
- journal article
Relationships between lewy and tau pathologies in 375 consecutive non-Alzheimer's olfactory bulbs.
- Published in:
- 2018
- By:
- Publication type:
- Letter
Study of LRRK2 variation in tauopathy: Progressive supranuclear palsy and corticobasal degeneration.
- Published in:
- 2017
- By:
- Publication type:
- journal article
ABI3 and PLCG2 missense variants as risk factors for neurodegenerative diseases in Caucasians and African Americans.
- Published in:
- Molecular Neurodegeneration, 2018, v. 13, n. 1, p. N.PAG, doi. 10.1186/s13024-018-0289-x
- By:
- Publication type:
- Article