8491 - 8500 of 8808 Results
Title
Year
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OPENTitle: Expression of human E46K-mutated α-synuclein in BAC-transgenic rats replicates early-stage Parkinson's disease features and enhances vulnerability to mitochondrial impairmentJournal Name: Experimental NeurologyPublisher: Elsevier BVVol: 240Issue #:Start Page: 44End Page: 56Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1016/j.expneurol.2012.11.007Best OA location URL: https://www.ncbi.nlm.nih.gov/pmc/articles/3552027Citation Count: 67
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OPENTitle: Alternative splicing expands the clinical spectrum of NDUFS6-related mitochondrial disordersJournal Name: Genetics in MedicinePublisher: Elsevier BVVol: 26Issue #: 6Start Page: 101117End Page: 101117Publication Date:Open Access(OA) Status: OPENLicense: cc-by, cc-by, cc-byDOI - Digital Object Identifier: 10.1016/j.gim.2024.101117Best OA location URL: https://doi.org/10.1016/j.gim.2024.101117Citation Count: 2
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OPENTitle: Heart-brain synchronization breakdown in Parkinson’s diseaseJournal Name: npj Parkinson's DiseasePublisher: Springer Science and Business Media LLCVol: 8Issue #: 1Start Page:End Page:Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.1038/s41531-022-00323-wBest OA location URL: https://www.nature.com/articles/s41531-022-00323-w.pdfCitation Count: 15
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OPENTitle: In vitro evaluation of [3H]PI-2620 and structural derivatives in non-Alzheimer's tauopathiesJournal Name: Nuclear Medicine and BiologyPublisher: Elsevier BVVol: 130-131Issue #:Start Page: 108891End Page: 108891Publication Date:Open Access(OA) Status: OPENLicense: cc-by-nc-ndDOI - Digital Object Identifier: 10.1016/j.nucmedbio.2024.108891Citation Count: 9
- Gender disparities in deep brain stimulation surgery for Parkinson disease and essential tremor2023OPENTitle: Gender disparities in deep brain stimulation surgery for Parkinson disease and essential tremorJournal Name: Deep Brain StimulationPublisher: Elsevier BVVol: 1Issue #:Start Page: 26End Page: 33Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1016/j.jdbs.2023.04.001Best OA location URL: https://doi.org/10.1016/j.jdbs.2023.04.001Citation Count: 11
- Association of MAPT subhaplotypes with clinical and demographic features in Parkinson’s disease2020OPENTitle: Association of MAPT subhaplotypes with clinical and demographic features in Parkinson’s diseaseJournal Name: Annals of Clinical and Translational NeurologyPublisher: WileyVol: 7Issue #: 9Start Page: 1557End Page: 1563Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.1002/acn3.51139Best OA location URL: https://onlinelibrary.wiley.com/doi/pdfdirect/10.1002/acn3.51139Citation Count: 10
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OPENTitle: Large-scale genetic characterization of Parkinson’s disease in the African and African admixed populationsJournal Name: BrainPublisher: Oxford University Press (OUP)Vol:Issue #:Start Page:End Page:Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.1093/brain/awaf379Best OA location URL: https://academic.oup.com/brain/advance-article-pdf/doi/10.1093/brain/awaf379/64544330/awaf379.pdfCitation Count: 0
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OPENTitle: Subspace corrected relevance learning with application in neuroimagingJournal Name: Artificial Intelligence in MedicinePublisher: Elsevier BVVol: 149Issue #:Start Page: 102786End Page: 102786Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.1016/j.artmed.2024.102786Best OA location URL: https://doi.org/10.1016/j.artmed.2024.102786Citation Count: 6
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OPENTitle: Brain volumetric deficits in MAPT mutation carriers: a multisite studyJournal Name: Annals of Clinical and Translational NeurologyPublisher: WileyVol: 8Issue #: 1Start Page: 95End Page: 110Publication Date:Open Access(OA) Status: OPENLicense: cc-by-nc-ndDOI - Digital Object Identifier: 10.1002/acn3.51249Best OA location URL: https://onlinelibrary.wiley.com/doi/pdfdirect/10.1002/acn3.51249Citation Count: 25
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OPENTitle: Substantia nigra hyperechogenicity with LRRK2 G2019S mutationsJournal Name: Movement DisordersPublisher: WileyVol: 26Issue #: 5Start Page: 885End Page: 888Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1002/mds.23644Best OA location URL: https://www.ncbi.nlm.nih.gov/pmc/articles/3082617Citation Count: 36