Found: 179
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Association of MAPT H1 subhaplotypes with neuropathology of lewy body disease.
- Published in:
- 2019
- 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
Regional analysis and genetic association of nigrostriatal degeneration in Lewy body disease.
- Published in:
- 2017
- By:
- Publication type:
- journal article
Study of LRRK2 variation in tauopathy: Progressive supranuclear palsy and corticobasal degeneration.
- Published in:
- 2017
- By:
- Publication type:
- journal article
Cerebellar ataxia in progressive supranuclear palsy: An autopsy study of PSP-C.
- Published in:
- 2016
- By:
- Publication type:
- journal article
Asymmetrical leg atrophy in levodopa-responsive dystonia due to a novel GTP cyclohydrolase mutation.
- Published in:
- 2014
- By:
- Publication type:
- case study
Asymmetrical leg atrophy in levodopa-responsive dystonia due to a novel GTP cyclohydrolase mutation.
- Published in:
- Movement Disorders, 2014, v. 29, n. 3, p. 425, doi. 10.1002/mds.25813
- By:
- Publication type:
- Article
Patient-control association study of the Leucine-Rich repeat kinase 2 (LRRK2) gene in South African Parkinson's disease patients.
- Published in:
- Movement Disorders, 2013, v. 28, n. 14, p. 2039, doi. 10.1002/mds.25637
- By:
- Publication type:
- 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
LRRK2 haplotype-sharing analysis in Parkinson's disease reveals a novel p.S1761R mutation.
- Published in:
- Movement Disorders, 2012, v. 27, n. 1, p. 146, doi. 10.1002/mds.23968
- By:
- Publication type:
- Article
Genetic variants of α-synuclein are not associated with essential tremor.
- Published in:
- 2011
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- Publication type:
- journal article
Genetic variants of α-synuclein are not associated with essential tremor.
- Published in:
- Movement Disorders, 2011, v. 26, n. 14, p. 2552, doi. 10.1002/mds.23909
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- Publication type:
- Article
Comprehensive sequencing of the LRRK2 gene in patients with familial Parkinson's disease from North Africa.
- Published in:
- Movement Disorders, 2010, v. 25, n. 13, p. 2052, doi. 10.1002/mds.23283
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- Publication type:
- Article
Novel pathogenic LRRK2 p.Asn1437His substitution in familial Parkinson's disease.
- Published in:
- Movement Disorders, 2010, v. 25, n. 13, p. 2156, doi. 10.1002/mds.23265
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- Publication type:
- Article
LRRK2 variation and Parkinson's disease in African Americans.
- Published in:
- Movement Disorders, 2010, v. 25, n. 12, p. 1973, doi. 10.1002/mds.23163
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- Publication type:
- Article
Alpha-synuclein polymorphisms are associated with Parkinson's disease in a Saskatchewan population.
- Published in:
- Movement Disorders, 2009, v. 24, n. 16, p. 2411, doi. 10.1002/mds.22795
- By:
- Publication type:
- Article
GCH1 in early-onset Parkinson's disease.
- Published in:
- Movement Disorders, 2009, v. 24, n. 14, p. 2070, doi. 10.1002/mds.22729
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- Publication type:
- Article
Expanding the clinical phenotype of SNCA duplication carriers.
- Published in:
- Movement Disorders, 2009, v. 24, n. 12, p. 1811, doi. 10.1002/mds.22682
- By:
- Publication type:
- Article
Reply: GIGYF2 variants are not associated with Parkinson's disease in Italy.
- Published in:
- Movement Disorders, 2009, v. 24, n. 12, p. 1868, doi. 10.1002/mds.22614
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- Publication type:
- Article
Reported mutations in GIGYF2 are not a common cause of Parkinson's disease.
- Published in:
- Movement Disorders, 2009, v. 24, n. 4, p. 619, doi. 10.1002/mds.22451
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- Publication type:
- Article
Common variants in Parkinson's disease.
- Published in:
- 2007
- By:
- Publication type:
- letter
ELAVL4, PARK10, and the Celts.
- Published in:
- 2007
- By:
- Publication type:
- journal article
Pathogenicity of the Lrrk2 R1514Q substitution in Parkinson's disease.
- Published in:
- 2007
- By:
- Publication type:
- journal article
The ups and downs of α-synuclein mRNA expression.
- Published in:
- Movement Disorders, 2007, v. 22, n. 2, p. 293, doi. 10.1002/mds.21223
- By:
- Publication type:
- Article
Global distribution and reduced penetrance: Lrrk2 R1441C in an Irish Parkinson's disease kindred.
- Published in:
- 2007
- By:
- Publication type:
- case study
CLEC3B p.S106G Mutant in a Caucasian Population of Successful Neurological Aging.
- Published in:
- 2020
- By:
- Publication type:
- journal 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
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
- By:
- Publication type:
- Article
Adult-onset cerebello-brainstem dominant form of X-linked adrenoleukodystrophy presenting as multiple system atrophy: case report and literature review.
- Published in:
- Neuropathology, 2016, v. 36, n. 1, p. 64, doi. 10.1111/neup.12230
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- Publication type:
- Article
Systematic Functional Analysis of PINK1 and PRKN Coding Variants.
- Published in:
- Cells (2073-4409), 2022, v. 11, n. 15, p. 2426, doi. 10.3390/cells11152426
- By:
- Publication type:
- Article
A commentary on fine mapping and resequencing of the PARK16 locus in Parkinson's disease.
- Published in:
- Journal of Human Genetics, 2015, v. 60, n. 8, p. 405, doi. 10.1038/jhg.2015.76
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- Publication type:
- Article
Accountable Care for the Poor and Underserved: Minnesota's Hennepin Health Model.
- Published in:
- American Journal of Public Health, 2015, v. 105, n. 4, p. 622, doi. 10.2105/AJPH.2014.302432
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- Publication type:
- Article
40 Per Cent of Fatal Accidents in Norway Involve People at Work.
- Published in:
- Nordic Road & Transport Research, 2012, n. 2, p. 3
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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
LINGO1 and LINGO2 variants are associated with essential tremor and Parkinson disease.
- Published in:
- Neurogenetics, 2010, v. 11, n. 4, p. 401, doi. 10.1007/s10048-010-0241-x
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- Publication type:
- Article
Ataxin-2 repeat-length variation and neurodegeneration.
- Published in:
- Human Molecular Genetics, 2011, v. 20, n. 16, p. 3207, doi. 10.1093/hmg/ddr227
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- Publication type:
- Article
Functional alteration of PARL contributes to mitochondrial dysregulation in Parkinson's disease.
- Published in:
- Human Molecular Genetics, 2011, v. 20, n. 10, p. 1966, doi. 10.1093/hmg/ddr077
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- Publication type:
- Article
Genome-wide association study of corticobasal degeneration identifies risk variants shared with progressive supranuclear palsy.
- Published in:
- Nature Communications, 2015, v. 6, n. 6, p. 7247, doi. 10.1038/ncomms8247
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- 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
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- Publication type:
- Article
VPS35 and DNAJC13 disease-causing variants in essential tremor.
- Published in:
- European Journal of Human Genetics, 2015, v. 23, n. 6, p. 887, doi. 10.1038/ejhg.2014.164
- By:
- Publication type:
- Article
Poly (ADP-Ribose) and α–synuclein extracellular vesicles in patients with Parkinson disease: A possible biomarker of disease severity.
- Published in:
- PLoS ONE, 2022, v. 17, n. 4, p. 1, doi. 10.1371/journal.pone.0264446
- By:
- Publication type:
- Article
Genetics of Parkinson's Disease: state-of-the-art and role in clinical settings.
- Published in:
- Polish Journal of Neurology & Neurosurgery / Neurologia i Neurochirurgia Polska, 2024, v. 58, n. 1, p. 38, doi. 10.5603/pjnns.97806
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- Publication type:
- Article
Effects of sex and APOE on Parkinson’s Disease-related cognitive decline.
- Published in:
- Polish Journal of Neurology & Neurosurgery / Neurologia i Neurochirurgia Polska, 2021, v. 55, n. 6, p. 559, doi. 10.5603/PJNNS.a2021.0071
- By:
- Publication type:
- Article
Genetics of Parkinson's disease in the Polish population.
- Published in:
- Polish Journal of Neurology & Neurosurgery / Neurologia i Neurochirurgia Polska, 2021, v. 55, n. 3, p. 241, doi. 10.5603/PJNNS.a2021.0013
- By:
- Publication type:
- Article
Genetics of ischemic stroke: Inheritance of a sporadic disorder.
- Published in:
- Current Neurology & Neuroscience Reports, 2009, v. 9, n. 1, p. 19, doi. 10.1007/s11910-009-0004-y
- By:
- Publication type:
- Article
PTPA variants are rare in early-onset and familial Parkinson's disease.
- Published in:
- Brain: A Journal of Neurology, 2023, v. 146, n. 12, p. e125, doi. 10.1093/brain/awad244
- By:
- Publication type:
- Article
Genetic risk scores enhance the diagnostic value of plasma biomarkers of brain amyloidosis.
- Published in:
- Brain: A Journal of Neurology, 2023, v. 146, n. 11, p. 4508, doi. 10.1093/brain/awad196
- By:
- Publication type:
- Article
Lysosomal polygenic risk is associated with the severity of neuropathology in Lewy body disease.
- Published in:
- Brain: A Journal of Neurology, 2023, v. 146, n. 10, p. 4077, doi. 10.1093/brain/awad183
- By:
- Publication type:
- Article
Risk Compensation and Bicycle Helmets.
- Published in:
- Risk Analysis: An International Journal, 2011, v. 31, n. 8, p. 1187, doi. 10.1111/j.1539-6924.2011.01589.x
- By:
- Publication type:
- Article
Lewy Body Disease is a Contributor to Logopenic Progressive Aphasia Phenotype.
- Published in:
- 2021
- By:
- Publication type:
- journal article