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Can brain impermeable BACE1 inhibitors serve as anti-CAA medicine?
- Published in:
- 2017
- By:
- Publication type:
- journal article
Study of the Relationship between Gene Polymorphisms of Paraoxonase 2 and Stroke in a Chinese Population.
- Published in:
- Cerebrovascular Diseases, 2008, v. 25, n. 1/2, p. 87, doi. 10.1159/000111996
- By:
- Publication type:
- Article
The contribution of GIGYF2 to Parkinson's disease: a meta-analysis.
- Published in:
- 2015
- By:
- Publication type:
- journal article
A rare Von Hippel-Lindau disease that mimics acute myelitis: case report and review of the literature.
- Published in:
- Neurological Sciences, 2011, v. 32, n. 2, p. 305, doi. 10.1007/s10072-010-0413-3
- By:
- Publication type:
- 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
UQCRC1 variants in Parkinson's disease: a large cohort study in Chinese mainland population.
- Published in:
- 2021
- By:
- Publication type:
- journal 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
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
Identification of the Largest SCA36 Pedigree in Asia: with Multimodel Neuroimaging Evaluation for the First Time.
- Published in:
- Cerebellum, 2022, v. 21, n. 3, p. 358, doi. 10.1007/s12311-021-01304-0
- By:
- Publication type:
- Article
Lithium Chloride Alleviates Neurodegeneration Partly by Inhibiting Activity of GSK3β in a SCA3 Drosophila Model.
- Published in:
- Cerebellum, 2013, v. 12, n. 6, p. 892, doi. 10.1007/s12311-013-0498-3
- By:
- Publication type:
- Article
Influence of simvastatin on dopaminergic neurons of lipopolysaccharide–induced rat model of Parkinson's disease.
- Published in:
- Asian Pacific Journal of Tropical Medicine, 2015, v. 8, n. 1, p. 64, doi. 10.1016/S1995-7645(14)60189-9
- 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
Simvastatin Induces Neuroprotection in 6- OHDA-Lesioned PC12 via the PI3K/ AKT/Caspase 3 Pathway and Anti-Inflammatory Responses.
- Published in:
- CNS Neuroscience & Therapeutics, 2013, v. 19, n. 3, p. 170, doi. 10.1111/cns.12053
- By:
- Publication type:
- Article
Altered Functional Brain Connectomes between Sporadic and Familial Parkinson's Patients.
- Published in:
- Frontiers in Neuroanatomy, 2017, p. 1, doi. 10.3389/fnana.2017.00099
- By:
- Publication type:
- Article
Sortilin Fragments Deposit at Senile Plaques in Human Cerebrum.
- Published in:
- Frontiers in Neuroanatomy, 2017, p. 1, doi. 10.3389/fnana.2017.00045
- By:
- Publication type:
- Article
Two novel functional single nucleotide polymorphisms of ADRB3 are associated with type 2 diabetes in the Chinese population.
- Published in:
- 2013
- By:
- Publication type:
- Journal 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
Microglial Activation in the Pathogenesis of Huntington’s Disease.
- Published in:
- Frontiers in Aging Neuroscience, 2017, p. 1, doi. 10.3389/fnagi.2017.00193
- 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
SUMO-1 Modification on K166 of PolyQ-Expanded aTaxin-3 Strengthens Its Stability and Increases Its Cytotoxicity.
- Published in:
- PLoS ONE, 2013, v. 8, n. 1, p. 1, doi. 10.1371/journal.pone.0054214
- By:
- Publication type:
- Article
Analysis of EIF4G1 in ethnic Chinese.
- Published in:
- BMC Neurology, 2013, v. 13, n. 1, p. 1, doi. 10.1186/1471-2377-13-38
- By:
- Publication type:
- Article
Association study between SNP rs150689919 in the DNA demethylation gene, TET1, and Parkinson's disease in Chinese Han population.
- Published in:
- BMC Neurology, 2013, v. 13, n. 1, p. 1, doi. 10.1186/1471-2377-13-196
- 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
Mutation analysis of Parkin, PINK1 and DJ- 1 genes in Chinese patients with sporadic early onset parkinsonism.
- Published in:
- Journal of Neurology, 2010, v. 257, n. 7, p. 1170, doi. 10.1007/s00415-010-5485-8
- By:
- Publication type:
- Article
Small heat-shock protein 22 mutated in autosomal dominant Charcot-Marie-Tooth disease type 2L.
- Published in:
- Human Genetics, 2005, v. 116, n. 3, p. 222, doi. 10.1007/s00439-004-1218-3
- By:
- Publication type:
- Article
A new locus for autosomal dominant Charcot-Marie-Tooth disease type 2 (CMT2L) maps to chromosome 12q24.
- Published in:
- Human Genetics, 2004, v. 114, n. 6, p. 527, doi. 10.1007/s00439-004-1102-1
- By:
- Publication type:
- Article
Associations of multiple visual rating scales based on structural magnetic resonance imaging with disease severity and cerebrospinal fluid biomarkers in patients with Alzheimer’s disease.
- Published in:
- Frontiers in Aging Neuroscience, 2022, v. 14, p. 1, doi. 10.3389/fnagi.2022.906519
- By:
- Publication type:
- Article
Lack of variation of ATTCT pentanucleotide repeats at ATXN10 gene between clinically diagnosed ataxia patients and normal individuals originated from Chinese Han.
- Published in:
- Journal of Genetics, 2008, v. 87, n. 3, p. 283, doi. 10.1007/s12041-008-0045-z
- By:
- Publication type:
- Article
HCFC1 variants in the proteolysis domain are associated with X‐linked idiopathic partial epilepsy: Exploring the underlying mechanism.
- Published in:
- Clinical & Translational Medicine, 2023, v. 13, n. 6, p. 1, doi. 10.1002/ctm2.1289
- By:
- Publication type:
- Article
Identification of clinically actionable secondary genetic variants from whole‐genome sequencing in a large‐scale Chinese population.
- Published in:
- Clinical & Translational Medicine, 2022, v. 12, n. 5, p. 1, doi. 10.1002/ctm2.866
- By:
- Publication type:
- Article
C9orf72 mutation is rare in Alzheimer's disease, Parkinson's disease, and essential tremor in China.
- Published in:
- Frontiers in Cellular Neuroscience, 2013, v. 7, p. 1, doi. 10.3389/fncel.2013.00164
- By:
- Publication type:
- 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
High-depth whole-genome sequencing identifies structure variants, copy number variants and short tandem repeats associated with Parkinson's disease.
- Published in:
- NPJ Parkinson's Disease, 2024, v. 10, n. 1, p. 1, doi. 10.1038/s41531-024-00722-1
- 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
Identification of a Locus for Disseminated Superficial Actinic Porokeratosis at Chromosome 12q23.2–24.1.
- Published in:
- Journal of Investigative Dermatology, 2000, v. 114, n. 6, p. 1071, doi. 10.1046/j.1523-1747.2000.00978.x
- By:
- Publication type:
- Article
SPG46 and SPG56 are rare causes of hereditary spastic paraplegia in China.
- Published in:
- 2016
- By:
- Publication type:
- Letter
Association of the DRD2 and DRD3 polymorphisms with response to pramipexole in Parkinson’s disease patients.
- Published in:
- European Journal of Clinical Pharmacology, 2009, v. 65, n. 7, p. 679, doi. 10.1007/s00228-009-0658-z
- 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
- By:
- Publication type:
- Article
VPS35-deficiency results in an impaired AMPA receptor trafficking and decreased dendritic spine maturation.
- Published in:
- Molecular Brain, 2015, v. 8, p. 1, doi. 10.1186/s13041-015-0156-4
- By:
- 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
Gluten ataxia of sporadic and hereditary cerebellar ataxia in patients from mainland China.
- Published in:
- 2013
- By:
- Publication type:
- journal article
Gluten ataxia of sporadic and hereditary cerebellar ataxia in patients from mainland China.
- Published in:
- Neurology India, 2013, v. 61, n. 3, p. 226, doi. 10.4103/0028-3886.115056
- 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