Found: 11
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Study of the collagen type VI alpha 3 (COL6A3) gene in Parkinson's disease.
- Published in:
- 2021
- By:
- Publication type:
- journal article
Association of Concurrent Olfactory Dysfunction and Probable Rapid Eye Movement Sleep Behavior Disorder with Early Parkinson's Disease Progression.
- Published in:
- Movement Disorders Clinical Practice, 2022, v. 9, n. 7, p. 909, doi. 10.1002/mdc3.13511
- By:
- Publication type:
- Article
Parkinson's Disease in Teneurin Transmembrane Protein 4 (TENM4) Mutation Carriers.
- Published in:
- Frontiers in Genetics, 2020, v. 11, p. N.PAG, doi. 10.3389/fgene.2020.598064
- By:
- Publication type:
- Article
Asymmetric, multifocal musculoskeletal pain preceding the onset of progressive supranuclear palsy: A case report.
- Published in:
- CNS Neuroscience & Therapeutics, 2021, v. 27, n. 2, p. 256, doi. 10.1111/cns.13527
- By:
- Publication type:
- Article
The lack of association between ubiquinol‐cytochrome c reductase core protein I (UQCRC1) variants and Parkinson's disease in an eastern Chinese population.
- Published in:
- CNS Neuroscience & Therapeutics, 2020, v. 26, n. 9, p. 990, doi. 10.1111/cns.13436
- By:
- Publication type:
- Article
Assessment of three essential tremor genetic loci in sporadic Parkinson's disease in Eastern China.
- Published in:
- CNS Neuroscience & Therapeutics, 2020, v. 26, n. 4, p. 448, doi. 10.1111/cns.13272
- By:
- Publication type:
- Article
Associations of Body Mass Index-Metabolic Phenotypes with Cognitive Decline in Parkinson's Disease.
- Published in:
- European Neurology, 2022, v. 85, n. 1, p. 24, doi. 10.1159/000517538
- By:
- Publication type:
- Article
Different Perivascular Space Burdens in Idiopathic Rapid Eye Movement Sleep Behavior Disorder and Parkinson's Disease.
- Published in:
- Frontiers in Aging Neuroscience, 2020, v. 12, p. N.PAG, doi. 10.3389/fnagi.2020.580853
- By:
- Publication type:
- Article
Apolipoprotein E Genotype Contributes to Motor Progression in Parkinson's Disease.
- Published in:
- Movement Disorders, 2022, v. 37, n. 1, p. 196, doi. 10.1002/mds.28805
- By:
- Publication type:
- Article
Analysis of rare variants of autosomal‐dominant genes in a Chinese population with sporadic Parkinson's disease.
- Published in:
- Molecular Genetics & Genomic Medicine, 2020, v. 8, n. 10, p. 1, doi. 10.1002/mgg3.1449
- By:
- Publication type:
- Article
Association Between Dystonia-Related Genetic Loci and Parkinson's Disease in Eastern China.
- Published in:
- Frontiers in Neurology, 2022, v. 13, p. 1, doi. 10.3389/fneur.2021.711050
- By:
- Publication type:
- Article