1 - 10 of 8167 Results
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OPENTitle: Abundant non-inclusion α-synuclein pathology in Lewy body-negative LRRK2-mutant casesJournal Name: Acta NeuropathologicaPublisher: Springer Science and Business Media LLCVol: 149Issue #: 1Start Page:End Page:Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.1007/s00401-025-02871-wBest OA location URL: https://doi.org/10.1007/s00401-025-02871-wCitation Count: 0
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OPENTitle: Characterizing the expression profile of 3R tau pathology in Pick’s diseaseJournal Name: Science AdvancesPublisher: American Association for the Advancement of Science (AAAS)Vol: 11Issue #: 18Start Page:End Page:Publication Date:Open Access(OA) Status: OPENLicense: cc-by-ncDOI - Digital Object Identifier: 10.1126/sciadv.adt6105Best OA location URL: https://doi.org/10.1126/sciadv.adt6105Citation Count: 0
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OPENTitle: Increased burden of rare risk variants across gene expression networks predisposes to sporadic Parkinson’s diseaseJournal Name: Cell ReportsPublisher: Elsevier BVVol: 44Issue #: 5Start Page: 115636End Page: 115636Publication Date:Open Access(OA) Status: OPENLicense: cc-by-nc-ndDOI - Digital Object Identifier: 10.1016/j.celrep.2025.115636Best OA location URL: https://doi.org/10.1016/j.celrep.2025.115636Citation Count: 0
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OPENTitle: The role of alpha-synuclein in synucleinopathy: Impact on lipid regulation at mitochondria–ER membranesJournal Name: npj Parkinson's DiseasePublisher: Springer Science and Business Media LLCVol: 11Issue #: 1Start Page:End Page:Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1038/s41531-025-00960-xCitation Count: 0
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OPENTitle: Genome-Wide Association Study of Glucocerebrosidase Activity ModifiersJournal Name: Molecular NeurobiologyPublisher: Springer Science and Business Media LLCVol:Issue #:Start Page:End Page:Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.1007/s12035-025-04996-1Best OA location URL: https://doi.org/10.1007/s12035-025-04996-1Citation Count: 0
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OPENTitle: 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://doi.org/10.1038/s41531-025-00934-zCitation Count: 0
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OPENTitle: Mitochondrial complex I deficiency occurs in skeletal muscle of a subgroup of individuals with Parkinson’s diseaseJournal Name: Communications MedicinePublisher: Springer Science and Business Media LLCVol: 5Issue #: 1Start Page:End Page:Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.1038/s43856-025-00817-7Best OA location URL: https://doi.org/10.1038/s43856-025-00817-7Citation Count: 0
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OPENTitle: Parkinson’s disease is characterized by vitamin B6-dependent inflammatory kynurenine pathway dysfunctionJournal 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/s41531-025-00964-7Best OA location URL: https://doi.org/10.1038/s41531-025-00964-7Citation Count: 0
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OPENTitle: Four questions to predict cognitive decline in de novo 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/s41531-025-00958-5Best OA location URL: https://doi.org/10.1038/s41531-025-00958-5Citation Count: 0