6671 - 6680 of 8808 Results
Title
Year
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OPENTitle: Unified Staging System for Lewy Body Disorders: Clinicopathologic Correlations and Comparison to Braak StagingJournal Name: Journal of Neuropathology & Experimental NeurologyPublisher: Oxford University Press (OUP)Vol: 78Issue #: 10Start Page: 891End Page: 899Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1093/jnen/nlz080Best OA location URL: https://academic.oup.com/jnen/article-pdf/78/10/891/30026987/nlz080.pdfCitation Count: 69
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OPENTitle: Cadherin‐8 expression, synaptic localization, and molecular control of neuronal form in prefrontal corticostriatal circuitsJournal Name: Journal of Comparative NeurologyPublisher: WileyVol: 523Issue #: 1Start Page: 75End Page: 92Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1002/cne.23666Best OA location URL: https://www.ncbi.nlm.nih.gov/pmc/articles/4232472Citation Count: 40
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OPENTitle: Human Dopaminergic Neurons Lacking PINK1 Exhibit Disrupted Dopamine Metabolism Related to Vitamin B6 Co-FactorsJournal Name: iSciencePublisher: Elsevier BVVol: 23Issue #: 12Start Page: 101797End Page: 101797Publication Date:Open Access(OA) Status: OPENLicense: cc-by-nc-ndDOI - Digital Object Identifier: 10.1016/j.isci.2020.101797Best OA location URL: http://www.cell.com/article/S2589004220309949/pdfCitation Count: 30
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RESTRICTEDTitle: Clinical phenotype in carriers of intermediate alleles in the huntingtin geneJournal Name: Journal of the Neurological SciencesPublisher: Elsevier BVVol: 402Issue #:Start Page: 57End Page: 61Publication Date:Open Access(OA) Status: RESTRICTEDLicense:DOI - Digital Object Identifier: 10.1016/j.jns.2019.05.010Citation Count: 31
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OPENTitle: Subthalamic deep brain stimulation alleviates the gait sequence effect and freezing of gait in Parkinson's diseaseJournal Name: Parkinsonism & Related DisordersPublisher: Elsevier BVVol:Issue #:Start Page: 108062End Page: 108062Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1016/j.parkreldis.2025.108062Best OA location URL: https://www.prd-journal.com/article/S1353-8020(25)00803-X/pdfCitation Count: 0
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OPENTitle: Interaction of Mitochondrial Polygenic Score and Lifestyle Factors in LRRK2 p.Gly2019Ser ParkinsonismJournal Name: Movement DisordersPublisher: WileyVol: 38Issue #: 10Start Page: 1837End Page: 1849Publication Date:Open Access(OA) Status: OPENLicense: cc-by-nc-ndDOI - Digital Object Identifier: 10.1002/mds.29563Best OA location URL: https://onlinelibrary.wiley.com/doi/pdfdirect/10.1002/mds.29563Citation Count: 15
- Cortical atrophy patterns in early Parkinson's disease patients using hierarchical cluster analysis2018OPENTitle: Cortical atrophy patterns in early Parkinson's disease patients using hierarchical cluster analysisJournal Name: Parkinsonism & Related DisordersPublisher: Elsevier BVVol: 50Issue #:Start Page: 3End Page: 9Publication Date:Open Access(OA) Status: OPENLicense: cc-by-nc-ndDOI - Digital Object Identifier: 10.1016/j.parkreldis.2018.02.006Best OA location URL: http://www.prd-journal.com/article/S1353802018300427/pdfCitation Count: 71
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OPENTitle: Higher Urine bis(Monoacylglycerol)Phosphate Levels in LRRK2 G2019S Mutation Carriers: Implications for Therapeutic DevelopmentJournal Name: Movement DisordersPublisher: WileyVol: 35Issue #: 1Start Page: 134End Page: 141Publication Date:Open Access(OA) Status: OPENLicense: cc-by-nc-ndDOI - Digital Object Identifier: 10.1002/mds.27818Best OA location URL: https://doi.org/10.1002/mds.27818Citation Count: 69
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OPENTitle: Proteomic and functional data sets on synaptic mitochondria from rats with genetic ablation of ParkinJournal Name: Data in BriefPublisher: Elsevier BVVol: 20Issue #:Start Page: 568End Page: 572Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.1016/j.dib.2018.08.053Best OA location URL: https://doi.org/10.1016/j.dib.2018.08.053Citation Count: 2
- Parkinson disease-associated mutations in LRRK2 cause centrosomal defects via Rab8a phosphorylation2018OPENTitle: Parkinson disease-associated mutations in LRRK2 cause centrosomal defects via Rab8a phosphorylationJournal Name: Molecular NeurodegenerationPublisher: Springer Science and Business Media LLCVol: 13Issue #: 1Start Page:End Page:Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.1186/s13024-018-0235-yBest OA location URL: https://molecularneurodegeneration.biomedcentral.com/track/pdf/10.1186/s13024-018-0235-yCitation Count: 106