51 - 60 of 6082 Results
Title
Year
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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: 1
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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: Alzheimer's Disease Sequencing Project release 4 whole genome sequencing datasetJournal Name: Alzheimer's & DementiaPublisher: WileyVol: 21Issue #: 5Start Page:End Page:Publication Date:Open Access(OA) Status: OPENLicense: cc-by-ncDOI - Digital Object Identifier: 10.1002/alz.70237Best OA location URL: https://onlinelibrary.wiley.com/doi/pdfdirect/10.1002/alz.70237Citation Count: 0
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OPENTitle: Alzheimer's disease traits in Parkinson's disease without α‐synuclein seedingJournal Name: Alzheimer's & DementiaPublisher: WileyVol: 21Issue #: 5Start Page:End Page:Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.1002/alz.70284Best OA location URL: https://onlinelibrary.wiley.com/doi/pdfdirect/10.1002/alz.70284Citation Count: 0
- An unusual presentation of Huntington’s disease-like syndrome in a patient with Xeroderma pigmentosum type F: Case report and review of the literature2025OPENTitle: An unusual presentation of Huntington’s disease-like syndrome in a patient with Xeroderma pigmentosum type F: Case report and review of the literatureJournal Name: Clinical Parkinsonism & Related DisordersPublisher: Elsevier BVVol: 12Issue #:Start Page: 100340End Page: 100340Publication Date:Open Access(OA) Status: OPENLicense: cc-by-nc-ndDOI - Digital Object Identifier: 10.1016/j.prdoa.2025.100340Best OA location URL: https://doi.org/10.1016/j.prdoa.2025.100340Citation Count: 0
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OPENTitle: Comparative mapping of single‐cell transcriptomic landscapes in neurodegenerative diseasesJournal Name: Alzheimer's & DementiaPublisher: WileyVol: 21Issue #: 5Start Page:End Page:Publication Date:Open Access(OA) Status: OPENLicense: cc-by-nc-ndDOI - Digital Object Identifier: 10.1002/alz.70012Best OA location URL: https://doi.org/10.1002/alz.70012Citation Count: 0
- Distinct brain atrophy progression subtypes underlie phenoconversion in isolated REM sleep behaviour disorder2025OPENTitle: 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:DOI - 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: Examining the Relationship Between Physical Function and Anxiety/Depression in Parkinson'sJournal Name: Brain and BehaviorPublisher: WileyVol: 15Issue #: 5Start Page:End Page:Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.1002/brb3.70563Best OA location URL: https://onlinelibrary.wiley.com/doi/pdfdirect/10.1002/brb3.70563Citation Count: 0
- Increased burden of rare risk variants across gene expression networks predisposes to sporadic Parkinson’s disease2025OPENTitle: 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
- Motor asymmetry in Parkinson’s disease: Diagnostic thresholds based on clinical scores and DaTSCAN imaging2025OPENTitle: Motor asymmetry in Parkinson’s disease: Diagnostic thresholds based on clinical scores and DaTSCAN imagingJournal Name: Clinical Parkinsonism & Related DisordersPublisher: Elsevier BVVol: 12Issue #:Start Page: 100350End Page: 100350Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.1016/j.prdoa.2025.100350Best OA location URL: https://doi.org/10.1016/j.prdoa.2025.100350Citation Count: 0