6071 - 6080 of 6466 Results
Title
Year
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OPENTitle: Characterizing resting‐state networks in Parkinson’s disease: A multi‐aspect functional connectivity studyJournal Name: Brain and BehaviorPublisher: WileyVol: 11Issue #: 5Start Page: e02101End Page: e02101Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.1002/brb3.2101Best OA location URL: https://doi.org/10.1002/brb3.2101Citation Count: 15
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OPENTitle: DNA Methylation and Expression Profiles of Whole Blood in Parkinson’s DiseaseJournal Name: Frontiers in GeneticsPublisher: Frontiers Media SAVol: 12Issue #:Start Page: 640266End Page: 640266Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.3389/fgene.2021.640266Best OA location URL: https://www.frontiersin.org/articles/10.3389/fgene.2021.640266/pdfCitation Count: 81
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OPENTitle: Computational medication regimen for Parkinson’s disease using reinforcement learningJournal Name: Scientific ReportsPublisher: Springer Science and Business Media LLCVol: 11Issue #: 1Start Page: 9313End Page: 9313Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.1038/s41598-021-88619-4Best OA location URL: https://www.nature.com/articles/s41598-021-88619-4.pdfCitation Count: 28
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OPENTitle: Integrating human brain proteomes with genome-wide association data implicates new proteins in Alzheimer’s disease pathogenesisJournal Name: Nature GeneticsPublisher: Springer Science and Business Media LLCVol: 53Issue #: 2Start Page: 143End Page: 146Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1038/s41588-020-00773-zBest OA location URL: https://www.ncbi.nlm.nih.gov/pmc/articles/8130821Citation Count: 401
- Exploring new uses for existing drugs: innovative mechanisms to fund independent clinical research2021OPENTitle: Exploring new uses for existing drugs: innovative mechanisms to fund independent clinical researchJournal Name: TrialsPublisher: Springer Science and Business Media LLCVol: 22Issue #: 1Start Page: 322End Page: 322Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.1186/s13063-021-05273-xBest OA location URL: https://trialsjournal.biomedcentral.com/counter/pdf/10.1186/s13063-021-05273-xCitation Count: 45
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OPENTitle: Incidence and Progression of Rapid Eye Movement Behavior Disorder in Early Parkinson's DiseaseJournal Name: Movement Disorders Clinical PracticePublisher: WileyVol: 8Issue #: 4Start Page: 534End Page: 540Publication Date:Open Access(OA) Status: OPENLicense: cc-by-nc-ndDOI - Digital Object Identifier: 10.1002/mdc3.13168Best OA location URL: https://resolver.sub.uni-goettingen.de/purl?gro-2/134137Citation Count: 30
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OPENTitle: High-throughput generation of midbrain dopaminergic neuron organoids from reporter human pluripotent stem cellsJournal Name: STAR ProtocolsPublisher: Elsevier BVVol: 2Issue #: 2Start Page: 100463End Page: 100463Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.1016/j.xpro.2021.100463Best OA location URL: https://doi.org/10.1016/j.xpro.2021.100463Citation Count: 24
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OPENTitle: Rare CASP6N73T variant associated with hippocampal volume exhibits decreased proteolytic activity, synaptic transmission defect, and neurodegenerationJournal Name: Scientific ReportsPublisher: Springer Science and Business Media LLCVol: 11Issue #: 1Start Page: 12695End Page: 12695Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.1038/s41598-021-91367-0Best OA location URL: https://www.nature.com/articles/s41598-021-91367-0.pdfCitation Count: 13
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OPENTitle: Autosomal recessive VWA1-related disorder: comprehensive analysis of phenotypic variability and genetic mutationsJournal Name: Brain CommunicationsPublisher: Oxford University Press (OUP)Vol: 6Issue #: 6Start Page: fcae377End Page: fcae377Publication Date:Open Access(OA) Status: OPENLicense: cc-by, cc-byDOI - Digital Object Identifier: 10.1093/braincomms/fcae377Best OA location URL: https://doi.org/10.1093/braincomms/fcae377Citation Count: 6
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OPENTitle: Biallelic NDUFA13 variants lead to a neurodevelopmental phenotype with gradual neurological impairmentJournal Name: Brain CommunicationsPublisher: Oxford University Press (OUP)Vol: 7Issue #: 1Start Page: fcae453End Page: fcae453Publication Date:Open Access(OA) Status: OPENLicense: cc-by, cc-byDOI - Digital Object Identifier: 10.1093/braincomms/fcae453Best OA location URL: https://academic.oup.com/braincomms/advance-article-pdf/doi/10.1093/braincomms/fcae453/61218229/fcae453.pdfCitation Count: 3