Found: 26
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Disease-Specific Changes in Reelin Protein and mRNA in Neurodegenerative Diseases.
- Published in:
- Cells (2073-4409), 2020, v. 9, n. 5, p. 1252, doi. 10.3390/cells9051252
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- Publication type:
- Article
Pleiotropic Effects of Variants in Dementia Genes in Parkinson Disease.
- Published in:
- Frontiers in Neuroscience, 2018, p. 1, doi. 10.3389/fnins.2018.00230
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- Publication type:
- Article
Assessing the NOTCH2NLC GGC expansion in European patients with essential tremor.
- Published in:
- 2020
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- Publication type:
- letter
ARSA variants in α-synucleinopathies.
- Published in:
- 2019
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- Publication type:
- letter
Mendelian Randomisation Confirms the Role of Y-Chromosome Loss in Alzheimer's Disease Aetiopathogenesis in Men.
- Published in:
- International Journal of Molecular Sciences, 2023, v. 24, n. 2, p. 898, doi. 10.3390/ijms24020898
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- Publication type:
- Article
The Genetic Landscape of Parkinsonism-Related Dystonias and Atypical Parkinsonism-Related Syndromes.
- Published in:
- International Journal of Molecular Sciences, 2021, v. 22, n. 15, p. 8100, doi. 10.3390/ijms22158100
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- Publication type:
- Article
Genetic Risk Profiling in Parkinson's Disease and Utilizing Genetics to Gain Insight into Disease-Related Biological Pathways.
- Published in:
- International Journal of Molecular Sciences, 2020, v. 21, n. 19, p. 7332, doi. 10.3390/ijms21197332
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- Publication type:
- Article
Vitamin D Receptor and Binding Protein Gene Variants in Patients with Essential Tremor.
- Published in:
- Molecular Neurobiology, 2022, v. 59, n. 6, p. 3458, doi. 10.1007/s12035-022-02804-8
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- Publication type:
- Article
Correction to: A nonsynonymous mutation in PLCG2 reduces the risk of Alzheimer's disease, dementia with Lewy bodies and frontotemporal dementia, and increases the likelihood of longevity.
- Published in:
- 2020
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- Publication type:
- Correction Notice
A nonsynonymous mutation in PLCG2 reduces the risk of Alzheimer's disease, dementia with Lewy bodies and frontotemporal dementia, and increases the likelihood of longevity.
- Published in:
- Acta Neuropathologica, 2019, v. 138, n. 2, p. 237, doi. 10.1007/s00401-019-02026-8
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- Publication type:
- Article
Association Between Insulin‐Like Growth Factor‐1 and Social Cognition in Huntington's Disease.
- Published in:
- Movement Disorders Clinical Practice, 2023, v. 10, n. 2, p. 279, doi. 10.1002/mdc3.13613
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- Publication type:
- Article
Functional genomic analyses uncover APOE-mediated regulation of brain and cerebrospinal fluid beta-amyloid levels in Parkinson disease.
- Published in:
- Acta Neuropathologica Communications, 2020, v. 8, n. 1, p. 1, doi. 10.1186/s40478-020-01072-8
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- Publication type:
- Article
P1‐260: ALZHEIMER'S DISEASE CSF BIOMARKERS VALIDATION WITH FLORBETAPIR PET USING NOVEL EUROIMMUN'S Aβ 1–42 ADJUSTED VALUES.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2019, v. 15, p. P339, doi. 10.1016/j.jalz.2019.06.815
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- Publication type:
- Article
Correction to: Serum vitamin D, vitamin D receptor and binding protein genes polymorphisms in restless legs syndrome.
- Published in:
- 2021
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- Publication type:
- Correction Notice
Serum vitamin D, vitamin D receptor and binding protein genes polymorphisms in restless legs syndrome.
- Published in:
- Journal of Neurology, 2021, v. 268, n. 4, p. 1461, doi. 10.1007/s00415-020-10312-9
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- Publication type:
- Article
Association between the missense alcohol dehydrogenase rs1229984T variant with the risk for Parkinson's disease in women.
- Published in:
- Journal of Neurology, 2019, v. 266, n. 2, p. 346, doi. 10.1007/s00415-018-9136-9
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- Publication type:
- Article
Polymorphisms in the oxytocin receptor and their association with apathy and impaired social cognition in Huntington's disease.
- Published in:
- 2022
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- Publication type:
- journal article
Common Endothelial Nitric Oxide Synthase Single Nucleotide Polymorphisms are not Related With the Risk for Restless Legs Syndrome.
- Published in:
- Frontiers in Pharmacology, 2021, v. 11, p. N.PAG, doi. 10.3389/fphar.2021.618989
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- Publication type:
- Article
Association of Essential Tremor With Novel Risk Loci: A Genome-Wide Association Study and Meta-analysis.
- Published in:
- JAMA Neurology, 2022, v. 79, n. 2, p. 185, doi. 10.1001/jamaneurol.2021.4781
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- Publication type:
- Article
The Parkinson's Disease Genome‐Wide Association Study Locus Browser.
- Published in:
- Movement Disorders, 2020, v. 35, n. 11, p. 2056, doi. 10.1002/mds.28197
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- Publication type:
- Article
The Genetic Architecture of Parkinson Disease in Spain: Characterizing Population-Specific Risk, Differential Haplotype Structures, and Providing Etiologic Insight.
- Published in:
- 2019
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- Publication type:
- journal article
A rare heterozygous TREM2 coding variant identified in familial clustering of dementia affects an intrinsically disordered protein region and function of TREM2.
- Published in:
- Human Mutation, 2020, v. 41, n. 1, p. 169, doi. 10.1002/humu.23904
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- Publication type:
- Article
Genomic Characterization of Host Factors Related to SARS-CoV-2 Infection in People with Dementia and Control Populations: The GR@ACE/DEGESCO Study.
- Published in:
- Journal of Personalized Medicine, 2021, v. 11, n. 12, p. 1318, doi. 10.3390/jpm11121318
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- Publication type:
- Article
Serum Trace Elements Concentrations in Patients with Restless Legs Syndrome.
- Published in:
- Antioxidants, 2022, v. 11, n. 2, p. 272, doi. 10.3390/antiox11020272
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- Publication type:
- Article
Added value of cerebrospinal fluid multimarker analysis in diagnosis and progression of dementia.
- Published in:
- European Journal of Neurology, 2021, v. 28, n. 4, p. 1142, doi. 10.1111/ene.14658
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- Publication type:
- Article
A polygenic risk score for mosaic loss of chromosome Y susceptibility is associated with higher risk of MCI to AD conversion.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2021, v. 17, n. 3, p. 1, doi. 10.1002/alz.053745
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- Publication type:
- Article