4721 - 4730 of 8620 Results
Title
Year
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OPENTitle: Mapping dopaminergic projections in the human brain with resting-state fMRIJournal Name: eLifePublisher: eLife Sciences Publications, LtdVol: 11Issue #:Start Page:End Page:Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.7554/elife.71846Best OA location URL: https://doi.org/10.7554/elife.71846Citation Count: 33
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OPENTitle: Prevalence and Relationship of Rest Tremor and Action Tremor in Parkinson’s DiseaseJournal Name: Tremor and Other Hyperkinetic MovementsPublisher: Ubiquity Press, Ltd.Vol: 10Issue #: 0Start Page: 58End Page: 58Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.5334/tohm.552Best OA location URL: http://tremorjournal.org/articles/10.5334/tohm.552/galley/1480/download/Citation Count: 27
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OPENTitle: QRATER: a collaborative and centralized imaging quality control web-based applicationJournal Name: Aperture NeuroPublisher: Organization for Human Brain MappingVol: 4Issue #:Start Page:End Page:Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.52294/001c.118616Best OA location URL: https://doi.org/10.52294/001c.118616Citation Count: 0
- Shared and disease-specific pathways in frontotemporal dementia and Alzheimer’s and Parkinson’s diseases2025RESTRICTEDTitle: Shared and disease-specific pathways in frontotemporal dementia and Alzheimer’s and Parkinson’s diseasesJournal Name: Nature MedicinePublisher: Springer Science and Business Media LLCVol: 31Issue #: 8Start Page:End Page:Publication Date:Open Access(OA) Status: RESTRICTEDLicense: cc-by, cc-byDOI - Digital Object Identifier: 10.1038/s41591-025-03833-1Best OA location URL: https://www.nature.com/articles/s41591-025-03833-1.pdfCitation Count: 3
- Identifying and characterising sources of variability in digital outcome measures in Parkinson’s disease2022OPENTitle: Identifying and characterising sources of variability in digital outcome measures in Parkinson’s diseaseJournal Name: npj Digital MedicinePublisher: Springer Science and Business Media LLCVol: 5Issue #: 1Start Page:End Page:Publication Date:Open Access(OA) Status: OPENLicense: cc-by, cc-byDOI - Digital Object Identifier: 10.1038/s41746-022-00643-4Best OA location URL: https://www.nature.com/articles/s41746-022-00643-4.pdfCitation Count: 20
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OPENTitle: Triglycerides are an important fuel reserve for synapse function in the brainJournal Name: Nature MetabolismPublisher: Springer Science and Business Media LLCVol: 7Issue #: 7Start Page:End Page:Publication Date:Open Access(OA) Status: OPENLicense: cc-by, cc-byDOI - Digital Object Identifier: 10.1038/s42255-025-01321-xBest OA location URL: https://www.nature.com/articles/s42255-025-01321-x.pdfCitation Count: 1
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OPENTitle: Genome‐wide association analysis identifies APOE as a mitophagy modifier in Lewy body diseaseJournal Name: Alzheimer's & DementiaPublisher: WileyVol: 21Issue #: 4Start Page:End Page:Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.1002/alz.70198Best OA location URL: https://onlinelibrary.wiley.com/doi/pdfdirect/10.1002/alz.70198Citation Count: 2
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OPENTitle: Dopamine Transporter Imaging as Objective Monitoring Biomarker in Parkinson's DiseaseJournal Name: Annals of NeurologyPublisher: WileyVol: 98Issue #: 1Start Page:End Page:Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.1002/ana.27223Best OA location URL: https://doi.org/10.1002/ana.27223Citation Count: 2
- MAPT H2 haplotype and risk of Pick's disease in the Pick's disease International Consortium: a genetic association study2024OPENTitle: MAPT H2 haplotype and risk of Pick's disease in the Pick's disease International Consortium: a genetic association studyJournal Name: The Lancet NeurologyPublisher: Elsevier BVVol: 23Issue #: 5Start Page: 487End Page: 499Publication Date:Open Access(OA) Status: OPENLicense: cc-by, cc-by, cc-byDOI - Digital Object Identifier: 10.1016/s1474-4422(24)00083-8Best OA location URL: https://pub.dzne.de/record/269189Citation Count: 9
- LRRK2 rare-variant per-domain genetic burden in Parkinson’s Disease: association confined to the kinase domain2025OPENTitle: LRRK2 rare-variant per-domain genetic burden in Parkinson’s Disease: association confined to the kinase domainJournal Name: npj Parkinson's DiseasePublisher: Springer Science and Business Media LLCVol: 11Issue #: 1Start Page:End Page:Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.1038/s41531-025-00934-zBest OA location URL: https://www.nature.com/articles/s41531-025-00934-z.pdfCitation Count: 0