631 - 640 of 8404 Results
Title
Year
-
RESTRICTEDTitle: If You Don’t Ask, You Won’t Know: Inclusive Recruitment Strategies for the Parkinson Progression Markers Initiative (PPMI)Journal Name: Parkinsonism & Related DisordersPublisher: Elsevier BVVol: 122Issue #:Start Page: 106689End Page: 106689Publication Date:Open Access(OA) Status: RESTRICTEDLicense:DOI - Digital Object Identifier: 10.1016/j.parkreldis.2024.106689Citation Count: 0
-
OPENTitle: Mutation of the ALS-/FTD-Associated RNA-Binding Protein FUS Affects Axonal DevelopmentJournal Name: The Journal of NeurosciencePublisher: Society for NeuroscienceVol: 44Issue #: 27Start Page: e2148232024End Page: e2148232024Publication Date:Open Access(OA) Status: OPENLicense: cc-by-nc-sa, cc-by-nc-sa, cc-by-nc-saDOI - Digital Object Identifier: 10.1523/jneurosci.2148-23.2024Citation Count: 1
-
RESTRICTEDTitle: Perceptual consequences of online group speech treatment for individuals with Parkinson’s disease: A pilot study case seriesJournal Name: International Journal of Speech-Language PathologyPublisher: Informa UK LimitedVol: 27Issue #: 2Start Page: 1End Page: 16Publication Date:Open Access(OA) Status: RESTRICTEDLicense:DOI - Digital Object Identifier: 10.1080/17549507.2024.2330538Citation Count: 2
-
OPENTitle: Positron Emission Tomography with [18F]ROStrace Reveals Progressive Elevations in Oxidative Stress in a Mouse Model of Alpha-SynucleinopathyJournal Name: International Journal of Molecular SciencesPublisher: MDPI AGVol: 25Issue #: 9Start Page: 4943End Page: 4943Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.3390/ijms25094943Best OA location URL: https://www.mdpi.com/1422-0067/25/9/4943/pdf?version=1714538058Citation Count: 5
-
OPENTitle: In vivo validation of late‐onset Alzheimer's disease genetic risk factorsJournal Name: Alzheimer's & DementiaPublisher: WileyVol: 20Issue #: 7Start Page: 4970End Page: 4984Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.1002/alz.13840Best OA location URL: https://onlinelibrary.wiley.com/doi/pdfdirect/10.1002/alz.13840Citation Count: 4
-
OPENTitle: Longitudinal study investigating the influence of COMT gene polymorphism on cortical thickness changes in Parkinson's disease over four yearsJournal Name: Scientific ReportsPublisher: Springer Science and Business Media LLCVol: 14Issue #: 1Start Page:End Page:Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.1038/s41598-024-60828-7Best OA location URL: https://www.nature.com/articles/s41598-024-60828-7.pdfCitation Count: 1
-
OPENTitle: Novel Variants Linked to the Prodromal Stage of Parkinson’s Disease (PD) PatientsJournal Name: DiagnosticsPublisher: MDPI AGVol: 14Issue #: 9Start Page: 929End Page: 929Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.3390/diagnostics14090929Best OA location URL: https://www.mdpi.com/2075-4418/14/9/929/pdf?version=1714465957Citation Count: 0
-
OPENTitle: Activation and Purification of ß‐Glucocerebrosidase by Exploiting its Transporter LIMP‐2 – Implications for Novel Treatment Strategies in Gaucher's and Parkinson's DiseaseJournal Name: Advanced SciencePublisher: WileyVol: 11Issue #: 25Start Page:End Page:Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.1002/advs.202401641Best OA location URL: https://doi.org/10.1002/advs.202401641Citation Count: 3
-
OPENTitle: Association of Misfolded α-Synuclein Derived from Neuronal Exosomes in Blood with Parkinson’s Disease Diagnosis and DurationJournal Name: Journal of Parkinson’s DiseasePublisher: SAGE PublicationsVol: 14Issue #: 4Start Page: 667End Page: 679Publication Date:Open Access(OA) Status: OPENLicense: cc-by-ncDOI - Digital Object Identifier: 10.3233/jpd-230390Best OA location URL: https://content.iospress.com:443/download/journal-of-parkinsons-disease/jpd230390?id=journal-of-parkinsons-disease%2Fjpd230390Citation Count: 13
-
OPENTitle: Autosomal Dominant Parkinson's Disease Caused by SNCA p.E46K Mutation in a Family with Russian AncestryJournal Name: Movement DisordersPublisher: WileyVol: 39Issue #: 8Start Page: 1424End Page: 1425Publication Date:Open Access(OA) Status: OPENLicense: cc-by-nc-ndDOI - Digital Object Identifier: 10.1002/mds.29821Best OA location URL: https://onlinelibrary.wiley.com/doi/pdfdirect/10.1002/mds.29821Citation Count: 0