3871 - 3880 of 8823 Results
Title
Year
-
RESTRICTEDTitle: Advances in the genetics and pathology of Lewy body dementiaJournal Name: The Lancet NeurologyPublisher: Elsevier BVVol: 24Issue #: 12Start Page: 1026End Page: 1037Publication Date:Open Access(OA) Status: RESTRICTEDLicense:DOI - Digital Object Identifier: 10.1016/s1474-4422(25)00363-1Citation Count: 3
-
OPENTitle: Modelling cholinergic and dopaminergic function over time in Parkinson’s disease with and without GBA1 variantsJournal Name: npj Parkinson's DiseasePublisher: Springer Science and Business Media LLCVol: 11Issue #: 1Start Page: 316End Page: 316Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1038/s41531-025-01160-3Best OA location URL: https://www.nature.com/articles/s41531-025-01160-3.pdfCitation Count: 0
-
OPENTitle: The interplay between stress, inflammation and Parkinson’s disease: insights from the COVID-19 pandemicJournal Name: npj Parkinson's DiseasePublisher: Springer Science and Business Media LLCVol: 11Issue #: 1Start Page: 333End Page: 333Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1038/s41531-025-01178-7Best OA location URL: https://www.nature.com/articles/s41531-025-01178-7.pdfCitation Count: 0
-
OPENTitle: LRRK2 p.G2385R and p.R1628P variants in a multi-ethnic Asian Parkinson’s Cohort: epidemiology and clinical insightsJournal Name: npj Parkinson's DiseasePublisher: Springer Science and Business Media LLCVol: 11Issue #: 1Start Page: 320End Page: 320Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1038/s41531-025-01166-xBest OA location URL: https://www.nature.com/articles/s41531-025-01166-x.pdfCitation Count: 1
-
OPENTitle: Interferon gamma stimulates coordinated changes in LRRK2, GCase, and cathepsin activities in idiopathic and genetic Parkinson’s disease monocytesJournal Name: npj Parkinson's DiseasePublisher: Springer Science and Business Media LLCVol: 11Issue #: 1Start Page: 337End Page: 337Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1038/s41531-025-01185-8Best OA location URL: https://www.nature.com/articles/s41531-025-01185-8.pdfCitation Count: 2
-
OPENTitle: Inhibition or genetic reduction of ASAH1 /acid ceramidase restore α-synuclein clearance in mutant GBA1 dopamine neurons from Parkinson’s patientsJournal Name: Human Molecular GeneticsPublisher: Oxford University Press (OUP)Vol:Issue #:Start Page: 2075End Page: 2087Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1093/hmg/ddaf166Best OA location URL: https://academic.oup.com/hmg/advance-article-pdf/doi/10.1093/hmg/ddaf166/65278149/ddaf166.pdfCitation Count: 0
-
OPENTitle: Autophagy and mitophagy at the synapse and beyond: implications for learning, memory and neurological disordersJournal Name: AutophagyPublisher: Informa UK LimitedVol:Issue #:Start Page: 10End Page: 52Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1080/15548627.2025.2581217Best OA location URL: https://doi.org/10.1080/15548627.2025.2581217Citation Count: 0
-
OPENTitle: PBMCpedia: a harmonized PBMC scRNA-seq database with unified mapping and enhanced celltype annotationJournal Name: Nucleic Acids ResearchPublisher: Oxford University Press (OUP)Vol:Issue #:Start Page: D1216End Page: D1221Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1093/nar/gkaf1245Best OA location URL: https://academic.oup.com/nar/advance-article-pdf/doi/10.1093/nar/gkaf1245/65488636/gkaf1245.pdfCitation Count: 0
-
OPENTitle: CHCHD2 mutant mice link mitochondrial deficits to PD pathophysiologyJournal Name: Science AdvancesPublisher: American Association for the Advancement of Science (AAAS)Vol: 11Issue #: 46Start Page: eadu0726End Page: eadu0726Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1126/sciadv.adu0726Best OA location URL: https://doi.org/10.1126/sciadv.adu0726Citation Count: 2
-
OPENTitle: The Genetic Landscape of Hereditary Spastic Paraplegia in GreeceJournal Name: Clinical GeneticsPublisher: WileyVol:Issue #:Start Page:End Page:Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1111/cge.70113Best OA location URL: https://onlinelibrary.wiley.com/doi/pdfdirect/10.1111/cge.70113Citation Count: 0