Found: 33
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The contribution of GIGYF2 to Parkinson's disease: a meta-analysis.
- Published in:
- 2015
- By:
- Publication type:
- journal article
Clinical features and [11C]-CFT PET analysis of PARK2, PARK6, PARK7-linked autosomal recessive early onset Parkinsonism.
- Published in:
- 2011
- By:
- Publication type:
- journal article
Clinical features and [C]-CFT PET analysis of PARK2, PARK6, PARK7-linked autosomal recessive early onset Parkinsonism.
- Published in:
- Neurological Sciences, 2011, v. 32, n. 1, p. 35, doi. 10.1007/s10072-010-0360-z
- By:
- Publication type:
- Article
The Association Between Lysosomal Storage Disorder Genes and Parkinson's Disease: A Large Cohort Study in Chinese Mainland Population.
- Published in:
- Frontiers in Aging Neuroscience, 2021, v. 13, p. 1, doi. 10.3389/fnagi.2021.749109
- By:
- Publication type:
- Article
Reply: Assessing the NOTCH2NLC GGC expansion in essential tremor patients from eastern China.
- Published in:
- 2021
- By:
- Publication type:
- Letter
Reply: Assessing the NOTCH2NLC GGC expansion in European patients with essential tremor.
- Published in:
- 2020
- By:
- Publication type:
- Letter
Two cases of CLIPPERS with increased number of perivascular CD20-positive B lymphocytes.
- Published in:
- 2018
- By:
- Publication type:
- Letter
Lack of bidirectional association between age‐related macular degeneration and Alzheimer's disease: A Mendelian randomization study.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2022, v. 18, n. 12, p. 2725, doi. 10.1002/alz.12775
- By:
- Publication type:
- Article
The Progress of Induced Pluripotent Stem Cells as Models of Parkinson’s Disease.
- Published in:
- Thrombosis, 2016, p. 1, doi. 10.1155/2016/4126214
- By:
- Publication type:
- Article
BAG5 Interacts with DJ-1 and Inhibits the Neuroprotective Effects of DJ-1 to Combat Mitochondrial Oxidative Damage.
- Published in:
- Oxidative Medicine & Cellular Longevity, 2017, p. 1, doi. 10.1155/2017/5094934
- By:
- Publication type:
- Article
RAB39B gene mutations are not linked to familial Parkinson's disease in China.
- Published in:
- Scientific Reports, 2016, p. 34502, doi. 10.1038/srep34502
- By:
- Publication type:
- Article
Constructing Prediction Models for Freezing of Gait by Nomogram and Machine Learning: A Longitudinal Study.
- Published in:
- Frontiers in Neurology, 2021, v. 12, p. 1, doi. 10.3389/fneur.2021.684044
- By:
- Publication type:
- Article
Genetic Identification Is Critical for the Diagnosis of Parkinsonism: A Chinese Pedigree with Early Onset of Parkinsonism.
- Published in:
- PLoS ONE, 2015, v. 10, n. 8, p. 1, doi. 10.1371/journal.pone.0136245
- By:
- Publication type:
- Article
Genetic Diagnosis of Two Dopa-Responsive Dystonia Families by Exome Sequencing.
- Published in:
- PLoS ONE, 2014, v. 9, n. 9, p. 1, doi. 10.1371/journal.pone.0106388
- By:
- Publication type:
- Article
Analysis of EIF4G1 in ethnic Chinese.
- Published in:
- 2013
- By:
- Publication type:
- journal article
Association study between SNP rs150689919 in the DNA demethylation gene, TET1, and Parkinson's disease in Chinese Han population.
- Published in:
- 2013
- By:
- Publication type:
- journal article
Research advances on neurite outgrowth inhibitor B receptor.
- Published in:
- Journal of Cellular & Molecular Medicine, 2020, v. 24, n. 14, p. 7697, doi. 10.1111/jcmm.15391
- By:
- Publication type:
- Article
Identification of PRRT2 as the causative gene of paroxysmal kinesigenic dyskinesias.
- Published in:
- Brain: A Journal of Neurology, 2011, v. 134, n. 12, p. 3490
- By:
- Publication type:
- Article
Parkinson’s Disease and Cognitive Impairment.
- Published in:
- Parkinson's Disease (20420080), 2016, p. 1, doi. 10.1155/2016/6734678
- By:
- Publication type:
- Article
Neuroimaging uncovers distinct relationships of glymphatic dysfunction and motor symptoms in Parkinson's disease.
- Published in:
- Journal of Neurology, 2023, v. 270, n. 5, p. 2649, doi. 10.1007/s00415-023-11594-5
- By:
- Publication type:
- Article
Distribution of Transglutaminase 6 in the Central Nervous System of Adult Mice.
- Published in:
- Anatomical Record: Advances in Integrative Anatomy & Evolutionary Biology, 2013, v. 296, n. 10, p. 1576, doi. 10.1002/ar.22741
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- Publication type:
- Article
Associations between gut microbiota and Parkinson disease: A bidirectional Mendelian randomization analysis.
- Published in:
- European Journal of Neurology, 2023, v. 30, n. 11, p. 3471, doi. 10.1111/ene.15848
- By:
- Publication type:
- Article
Preliminary Study of hsa-mir-626 Change in the Cerebrospinal Fluid in Parkinson's Disease.
- Published in:
- 2021
- By:
- Publication type:
- journal article
Reply to: Has Parkinson Disease Gone to the Dogs?
- Published in:
- Movement Disorders, 2023, v. 38, n. 2, p. 359, doi. 10.1002/mds.29305
- By:
- Publication type:
- Article
Telomere Length and COVID-19 Outcomes: A Two-Sample Bidirectional Mendelian Randomization Study.
- Published in:
- Frontiers in Genetics, 2022, p. 1, doi. 10.3389/fgene.2022.805903
- By:
- Publication type:
- Article
The Progress of Induced Pluripotent Stem Cells as Models of Parkinson’s Disease.
- Published in:
- Stem Cells International, 2016, p. 1, doi. 10.1155/2016/4126214
- By:
- Publication type:
- Article
Effect of GBA Mutations on Phenotype of Parkinson’s Disease: A Study on Chinese Population and a Meta-Analysis.
- Published in:
- Parkinson's Disease (20420080), 2015, v. 2015, p. 1, doi. 10.1155/2015/916971
- By:
- Publication type:
- Article
Performance on adsorption of toluene by ionic liquid-modified AC in high-humidity exhaust gas.
- Published in:
- Environmental Science & Pollution Research, 2024, v. 31, n. 24, p. 35553, doi. 10.1007/s11356-024-33578-2
- By:
- Publication type:
- Article
The Phenotypes and Mechanisms of NOTCH2NLC-Related GGC Repeat Expansion Disorders: a Comprehensive Review.
- Published in:
- Molecular Neurobiology, 2022, v. 59, n. 1, p. 523, doi. 10.1007/s12035-021-02616-2
- By:
- Publication type:
- Article
Glucocerebrosidase Gene L444P mutation is a risk factor for Parkinson's disease in Chinese population.
- Published in:
- Movement Disorders, 2010, v. 25, n. 8, p. 1005, doi. 10.1002/mds.23009
- By:
- Publication type:
- Article
Analysis of SCA2 and SCA3/MJD repeats in Parkinson's disease in mainland China: Genetic, clinical, and positron emission tomography findings.
- Published in:
- Movement Disorders, 2009, v. 24, n. 13, p. 2007, doi. 10.1002/mds.22727
- By:
- Publication type:
- Article
Mutation analysis of Parkin, PINK1, DJ-1 and ATP13A2 genes in Chinese patients with autosomal recessive early-onset Parkinsonism.
- Published in:
- Movement Disorders, 2008, v. 23, n. 14, p. 2074, doi. 10.1002/mds.22156
- By:
- Publication type:
- Article
Novel compound heterozygous mutations in the PANK2 gene in a Chinese patient with atypical pantothenate kinase-associated neurodegeneration.
- Published in:
- 2005
- By:
- Publication type:
- journal article