4481 - 4490 of 8826 Results
Title
Year
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OPENTitle: DOPA pheomelanin is increased in nigral neuromelanin of Parkinson’s diseaseJournal Name: Progress in NeurobiologyPublisher: Elsevier BVVol: 223Issue #:Start Page: 102414End Page: 102414Publication Date:Open Access(OA) Status: OPENLicense: cc-by, cc-byDOI - Digital Object Identifier: 10.1016/j.pneurobio.2023.102414Best OA location URL: https://doi.org/10.1016/j.pneurobio.2023.102414Citation Count: 18
- 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: e14448End Page: e14448Publication Date:Open Access(OA) Status: OPENLicense: cc-by-nc-ndDOI - Digital Object Identifier: 10.1002/alz.14448Best OA location URL: https://onlinelibrary.wiley.com/doi/pdfdirect/10.1002/alz.14448Citation Count: 1
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OPENTitle: α-Synuclein Seed Amplification Assay Amplification Parameters and the Risk of Progression in Prodromal Parkinson DiseaseJournal Name: NeurologyPublisher: Ovid Technologies (Wolters Kluwer Health)Vol: 104Issue #: 5Start Page: e210279End Page: e210279Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1212/wnl.0000000000210279Best OA location URL: https://doi.org/10.1212/wnl.0000000000210279Citation Count: 24
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OPENTitle: Sex‐specific mechanisms of cerebral microvascular BK Ca dysfunction in a mouse model of Alzheimer's diseaseJournal Name: Alzheimer's & DementiaPublisher: WileyVol: 21Issue #: 2Start Page: e14438End Page: e14438Publication Date:Open Access(OA) Status: OPENLicense: cc-by-nc-ndDOI - Digital Object Identifier: 10.1002/alz.14438Best OA location URL: https://onlinelibrary.wiley.com/doi/pdfdirect/10.1002/alz.14438Citation Count: 3
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OPENTitle: A simulative deep learning model of SNP interactions on chromosome 19 for predicting Alzheimer's disease risk and rates of disease progressionJournal Name: Alzheimer's & DementiaPublisher: WileyVol: 19Issue #: 12Start Page: 5690End Page: 5699Publication Date:Open Access(OA) Status: OPENLicense: cc-by-nc-ndDOI - Digital Object Identifier: 10.1002/alz.13319Best OA location URL: https://onlinelibrary.wiley.com/doi/pdfdirect/10.1002/alz.13319Citation Count: 13
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OPENTitle: Co‐Existent Probable RBD and PD: Disease Progression, Medication Response, and Clinical Trial ImplicationsJournal Name: Movement Disorders Clinical PracticePublisher: WileyVol: 11Issue #: 3Start Page: 312End Page: 314Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1002/mdc3.13890Best OA location URL: https://pmc.ncbi.nlm.nih.gov/articles/PMC10928330/pdf/MDC3-11-312.pdfCitation Count: 1
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OPENTitle: Outcome Selection for Research Studies in Movement DisordersJournal Name: Movement Disorders Clinical PracticePublisher: WileyVol: 11Issue #: S3Start Page: S26End Page: S30Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.1002/mdc3.14087Best OA location URL: https://onlinelibrary.wiley.com/doi/pdfdirect/10.1002/mdc3.14087Citation Count: 0
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OPENTitle: The Parkinson’s disease risk gene cathepsin B promotes fibrillar alpha-synuclein clearance, lysosomal function and glucocerebrosidase activity in dopaminergic neuronsJournal Name: Molecular NeurodegenerationPublisher: Springer Science and Business Media LLCVol: 19Issue #: 1Start Page: 88End Page: 88Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.1186/s13024-024-00779-9Best OA location URL: https://link.springer.com/content/pdf/10.1186/s13024-024-00779-9.pdfCitation Count: 28
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OPENTitle: Large-scale assessment of polyglutamine repeat expansions in Parkinson diseaseJournal Name: NeurologyPublisher: Ovid Technologies (Wolters Kluwer Health)Vol: 85Issue #: 15Start Page: 1283End Page: 1292Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1212/wnl.0000000000002016Best OA location URL: https://n.neurology.org/content/neurology/85/15/1283.full.pdfCitation Count: 31
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OPENTitle: Loss‐of‐Function Variants in HOPS Complex Genes VPS16 and VPS41 Cause Early Onset Dystonia Associated with Lysosomal AbnormalitiesJournal Name: Annals of NeurologyPublisher: WileyVol: 88Issue #: 5Start Page: 867End Page: 877Publication Date:Open Access(OA) Status: OPENLicense: cc-by, cc-byDOI - Digital Object Identifier: 10.1002/ana.25879Best OA location URL: https://onlinelibrary.wiley.com/doi/pdfdirect/10.1002/ana.25879Citation Count: 108