7181 - 7190 of 8808 Results
Title
Year
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RESTRICTEDTitle: Validation of Fox Insight Cohort via Virtual Research Visits (4749)Journal Name: NeurologyPublisher: Ovid Technologies (Wolters Kluwer Health)Vol: 94Issue #: 15_supplementStart Page:End Page:Publication Date:Open Access(OA) Status: RESTRICTEDLicense:DOI - Digital Object Identifier: 10.1212/wnl.94.15_supplement.4749Citation Count: 1
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OPENTitle: Whole proteome copy number dataset in primary mouse cortical neuronsJournal Name: Data in BriefPublisher: Elsevier BVVol: 49Issue #:Start Page: 109336End Page: 109336Publication Date:Open Access(OA) Status: OPENLicense: cc-by, cc-by, cc-byDOI - Digital Object Identifier: 10.1016/j.dib.2023.109336Best OA location URL: https://doi.org/10.1016/j.dib.2023.109336Citation Count: 4
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OPENTitle: Genetic variability and potential effects on clinical trial outcomes: perspectives in Parkinson’s diseaseJournal Name: Journal of Medical GeneticsPublisher: BMJVol: 57Issue #: 5Start Page: 331End Page: 338Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1136/jmedgenet-2019-106283Best OA location URL: https://www.ncbi.nlm.nih.gov/pmc/articles/8474559Citation Count: 64
- Progression of two Progressive Supranuclear Palsy phenotypes with comparable initial disability2019RESTRICTEDTitle: Progression of two Progressive Supranuclear Palsy phenotypes with comparable initial disabilityJournal Name: Parkinsonism & Related DisordersPublisher: Elsevier BVVol: 66Issue #:Start Page: 87End Page: 93Publication Date:Open Access(OA) Status: RESTRICTEDLicense:DOI - Digital Object Identifier: 10.1016/j.parkreldis.2019.07.010Citation Count: 28
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OPENTitle: Pathogenic LRRK2 regulates ciliation probability upstream of tau tubulin kinase 2 via Rab10 and RILPL1 proteinsJournal Name: Proceedings of the National Academy of SciencesPublisher: Proceedings of the National Academy of SciencesVol: 118Issue #: 10Start Page:End Page:Publication Date:Open Access(OA) Status: OPENLicense: cc-by-nc-ndDOI - Digital Object Identifier: 10.1073/pnas.2005894118Best OA location URL: https://www.ncbi.nlm.nih.gov/pmc/articles/7958464Citation Count: 81
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OPENTitle: Efficacy of Nilotinib in Patients With Moderately Advanced Parkinson DiseaseJournal Name: JAMA NeurologyPublisher: American Medical Association (AMA)Vol: 78Issue #: 3Start Page: 312End Page: 312Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.1001/jamaneurol.2020.4725Best OA location URL: https://jamanetwork.com/journals/jamaneurology/articlepdf/2773698/jamaneurology_simuni_2020_oi_200091_1614894403.37383.pdfCitation Count: 111
- A novel alpha-synuclein G14R missense variant is associated with atypical neuropathological features2025OPENTitle: A novel alpha-synuclein G14R missense variant is associated with atypical neuropathological featuresJournal Name: Molecular NeurodegenerationPublisher: Springer Science and Business Media LLCVol: 20Issue #: 1Start Page:End Page:Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.1186/s13024-025-00889-yBest OA location URL: https://molecularneurodegeneration.biomedcentral.com/counter/pdf/10.1186/s13024-025-00889-yCitation Count: 0
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OPENTitle: Assessment of heterogeneity among participants in the Parkinson's Progression Markers Initiative cohort using α-synuclein seed amplification: a cross-sectional studyJournal Name: The Lancet NeurologyPublisher: Elsevier BVVol: 22Issue #: 5Start Page: 407End Page: 417Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1016/s1474-4422(23)00109-6Best OA location URL: https://pmc.ncbi.nlm.nih.gov/articles/PMC10627170/pdf/nihms-1937442.pdfCitation Count: 465
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RESTRICTEDTitle: Microstructural patterns in substantia nigra subregions are associated with depression and olfactory impairments in Parkinson’s diseaseJournal Name: Clinical Neurology and NeurosurgeryPublisher: Elsevier BVVol: 251Issue #:Start Page: 108817End Page: 108817Publication Date:Open Access(OA) Status: RESTRICTEDLicense:DOI - Digital Object Identifier: 10.1016/j.clineuro.2025.108817Citation Count: 1
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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: 3