Found: 17
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Factors influencing cognitive function in patients with Huntington's disease from China: A cross‐sectional clinical study.
- Published in:
- Brain & Behavior, 2023, v. 13, n. 11, p. 1, doi. 10.1002/brb3.3258
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- Publication type:
- Article
The Role of Contrast Adaptation in Saccadic Suppression in Humans.
- Published in:
- PLoS ONE, 2014, v. 9, n. 1, p. 1, doi. 10.1371/journal.pone.0086542
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- Publication type:
- Article
Effect of adjunctive ranitidine for antipsychotic-induced weight gain: A systematic review of randomized placebo-controlled trials.
- Published in:
- Journal of International Medical Research, 2018, v. 46, n. 2, p. 22, doi. 10.1177/0300060517716783
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- Publication type:
- Article
Genetic factors for survival in amyotrophic lateral sclerosis: an integrated approach combining a systematic review, pairwise and network meta-analysis.
- Published in:
- 2022
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- Publication type:
- journal article
LncRNA GAS5 Suppresses Colorectal Cancer Progress by Target miR-21/LIFR Axis.
- Published in:
- Evidence-based Complementary & Alternative Medicine (eCAM), 2022, p. 1, doi. 10.1155/2022/3298939
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- Publication type:
- Article
Enrichment of rare variants of BIN1 but not APOE genes in Chinese patients with Parkinson's disease.
- Published in:
- Journal of Internal Medicine, 2022, v. 291, n. 5, p. 698, doi. 10.1111/joim.13444
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- Publication type:
- Article
Expanding causal genes for Parkinson's disease via multi-omics analysis.
- Published in:
- NPJ Parkinson's Disease, 2023, v. 9, n. 1, p. 1, doi. 10.1038/s41531-023-00591-0
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- Publication type:
- Article
Identifying novel genes for amyotrophic lateral sclerosis by integrating human brain proteomes with genome-wide association data.
- Published in:
- Journal of Neurology, 2023, v. 270, n. 8, p. 4013, doi. 10.1007/s00415-023-11757-4
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- Publication type:
- Article
The mutation spectrum of Parkinson‐disease‐related genes in early‐onset Parkinson's disease in ethnic Chinese.
- Published in:
- European Journal of Neurology, 2022, v. 29, n. 11, p. 3218, doi. 10.1111/ene.15509
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- Publication type:
- Article
Association Analysis of WNT3 , HLA-DRB5 and IL1R2 Polymorphisms in Chinese Patients With Parkinson's Disease and Multiple System Atrophy.
- Published in:
- Frontiers in Genetics, 2021, v. 12, p. 1, doi. 10.3389/fgene.2021.765833
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- Publication type:
- Article
Multivariable clinical-genetic model for predicting dyskinesia in early-onset Parkinson's disease.
- Published in:
- 2021
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- Publication type:
- Letter
Systematic druggable genome‐wide Mendelian randomization identifies therapeutic targets for sarcopenia.
- Published in:
- Journal of Cachexia, Sarcopenia & Muscle, 2024, v. 15, n. 4, p. 1324, doi. 10.1002/jcsm.13479
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- Publication type:
- Article
Loss of CHCHD2 Stability Coordinates with C1QBP/CHCHD2/CHCHD10 Complex Impairment to Mediate PD-Linked Mitochondrial Dysfunction.
- Published in:
- Molecular Neurobiology, 2024, v. 61, n. 10, p. 7968, doi. 10.1007/s12035-024-04090-y
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- Publication type:
- Article
Discovery and Exploration of Lipid-Modifying Drug Targets for ALS by Mendelian Randomization.
- Published in:
- Molecular Neurobiology, 2024, v. 61, n. 9, p. 6572, doi. 10.1007/s12035-024-04007-9
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- Publication type:
- Article
Genetic Analysis of ZNF Protein Family Members for Early-Onset Parkinson's Disease in Chinese Population.
- Published in:
- Molecular Neurobiology, 2021, v. 58, n. 7, p. 3435, doi. 10.1007/s12035-021-02354-5
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- Publication type:
- Article
Genetic Analysis of Prosaposin, the Lysosomal Storage Disorder Gene in Parkinson's Disease.
- Published in:
- Molecular Neurobiology, 2021, v. 58, n. 4, p. 1583, doi. 10.1007/s12035-020-02218-4
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- Publication type:
- Article
TBK1, a prioritized drug repurposing target for amyotrophic lateral sclerosis: evidence from druggable genome Mendelian randomization and pharmacological verification in vitro.
- Published in:
- BMC Medicine, 2024, v. 22, n. 1, p. 1, doi. 10.1186/s12916-024-03314-1
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- Publication type:
- Article