4071 - 4080 of 8587 Results
Title
Year
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OPENTitle: APOE genetic variability in an Egyptian cohort of PDJournal Name: Frontiers in NeurosciencePublisher: Frontiers Media SAVol: 19Issue #:Start Page:End Page:Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.3389/fnins.2025.1579968Best OA location URL: https://www.frontiersin.org/journals/neuroscience/articles/10.3389/fnins.2025.1579968/pdfCitation Count: 0
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OPENTitle: Distinct brain atrophy progression subtypes underlie phenoconversion in isolated REM sleep behaviour disorderJournal Name: eBioMedicinePublisher: Elsevier BVVol: 117Issue #:Start Page: 105753End Page: 105753Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.1016/j.ebiom.2025.105753Best OA location URL: https://www.thelancet.com/action/showPdf?pii=S2352396425001975Citation Count: 0
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OPENTitle: Identifying gait differences between Alzheimer's disease and dementia with Lewy bodies and their associations with regional amyloid depositionJournal Name: Alzheimer's & DementiaPublisher: WileyVol: 21Issue #: 2Start Page:End Page:Publication Date:Open Access(OA) Status: OPENLicense: cc-by-nc-ndDOI - Digital Object Identifier: 10.1002/alz.14351Best OA location URL: https://www.ncbi.nlm.nih.gov/pmc/articles/11815204Citation Count: 1
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OPENTitle: Alzheimer's disease‐associated CD83(+) microglia are linked with increased immunoglobulin G4 and human cytomegalovirus in the gut, vagal nerve, and brainJournal Name: Alzheimer's & DementiaPublisher: WileyVol: 21Issue #: 1Start Page:End Page:Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.1002/alz.14401Best OA location URL: https://doi.org/10.1002/alz.14401Citation Count: 2
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OPENTitle: Genome Aggregation Database Version 4—Allele Frequency Changes and Impact on Variant Interpretation in DystoniaJournal Name: Movement DisordersPublisher: WileyVol: 40Issue #: 2Start Page:End Page:Publication Date:Open Access(OA) Status: OPENLicense: cc-by-nc-ndDOI - Digital Object Identifier: 10.1002/mds.30066Best OA location URL: https://www.ncbi.nlm.nih.gov/pmc/articles/11832811Citation Count: 3
- Updated MDSGene review on the clinical and genetic spectrum of LRRK2 variants in Parkinson´s disease2025OPENTitle: Updated MDSGene review on the clinical and genetic spectrum of LRRK2 variants in Parkinson´s diseaseJournal 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/s41531-025-00881-9Best OA location URL: https://www.nature.com/articles/s41531-025-00881-9.pdfCitation Count: 8
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OPENTitle: Exome sequencing in Asian populations identifies low-frequency and rare coding variation influencing Parkinson’s disease riskJournal Name: Nature AgingPublisher: Springer Science and Business Media LLCVol: 5Issue #: 2Start Page:End Page:Publication Date:Open Access(OA) Status: OPENLicense: cc-by-nc-ndDOI - Digital Object Identifier: 10.1038/s43587-024-00760-7Best OA location URL: https://www.ncbi.nlm.nih.gov/pmc/articles/11839463Citation Count: 5
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OPENTitle: Endogenous LRRK2 and PINK1 function in a convergent neuroprotective ciliogenesis pathway in the brainJournal Name: Proceedings of the National Academy of SciencesPublisher: Proceedings of the National Academy of SciencesVol: 122Issue #: 5Start Page:End Page:Publication Date:Open Access(OA) Status: OPENLicense: cc-by, cc-by, cc-byDOI - Digital Object Identifier: 10.1073/pnas.2412029122Best OA location URL: https://pnas.org/doi/pdf/10.1073/pnas.2412029122Citation Count: 3
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OPENTitle: Sex‐specific mechanisms of cerebral microvascular BKCa dysfunction in a mouse model of Alzheimer's diseaseJournal Name: Alzheimer's & DementiaPublisher: WileyVol: 21Issue #: 2Start Page:End Page:Publication Date:Open Access(OA) Status: OPENLicense: cc-by-nc-ndDOI - Digital Object Identifier: 10.1002/alz.14438Best OA location URL: https://alz-journals.onlinelibrary.wiley.com/doi/pdf/10.1002/alz.14438Citation Count: 1
- Psychotropic medication usage in sporadic versus genetic behavioral‐variant frontotemporal dementia2024OPENTitle: Psychotropic medication usage in sporadic versus genetic behavioral‐variant frontotemporal dementiaJournal Name: Alzheimer's & DementiaPublisher: WileyVol: 21Issue #: 2Start Page:End Page:Publication Date:Open Access(OA) Status: OPENLicense: cc-by-nc-ndDOI - Digital Object Identifier: 10.1002/alz.14448Best OA location URL: https://escholarship.org/content/qt0tm1495f/qt0tm1495f.pdfCitation Count: 0