1921 - 1930 of 6564 Results
Title
Year
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OPENTitle: Multiomic analyses direct hypotheses for Creutzfeldt-Jakob disease risk genesJournal Name: BrainPublisher: Oxford University Press (OUP)Vol: 148Issue #: 9Start Page: 3350End Page: 3363Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.1093/brain/awaf032Best OA location URL: https://doi.org/10.1093/brain/awaf032Citation Count: 9
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OPENTitle: Anti-Tetanus Vaccination Is Associated with Reduced Occurrence and Slower Progression of Parkinson’s Disease—A Retrospective StudyJournal Name: BiomedicinesPublisher: MDPI AGVol: 12Issue #: 12Start Page: 2687End Page: 2687Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.3390/biomedicines12122687Best OA location URL: https://www.mdpi.com/2227-9059/12/12/2687/pdf?version=1732544853Citation Count: 0
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OPENTitle: Differential Associations of Apolipoprotein E ε4 Genotype With Attentional Abilities Across the Life Span of Individuals With Down SyndromeJournal Name: JAMA Network OpenPublisher: American Medical Association (AMA)Vol: 3Issue #: 9Start Page: e2018221End Page: e2018221Publication Date:Open Access(OA) Status: OPENLicense: cc-by, cc-byDOI - Digital Object Identifier: 10.1001/jamanetworkopen.2020.18221Best OA location URL: https://jamanetwork.com/journals/jamanetworkopen/articlepdf/2770878/dsouza_2020_oi_200657_1605807465.21177.pdfCitation Count: 11
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OPENTitle: Altered network stability in progressive supranuclear palsyJournal Name: Neurobiology of AgingPublisher: Elsevier BVVol: 107Issue #:Start Page: 109End Page: 117Publication Date:Open Access(OA) Status: OPENLicense: cc-by, cc-byDOI - Digital Object Identifier: 10.1016/j.neurobiolaging.2021.07.007Best OA location URL: https://doi.org/10.1016/j.neurobiolaging.2021.07.007Citation Count: 15
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OPENTitle: Video-tutorial for the Movement Disorder Society criteria for progressive supranuclear palsyJournal Name: Parkinsonism & Related DisordersPublisher: Elsevier BVVol: 78Issue #:Start Page: 200End Page: 203Publication Date:Open Access(OA) Status: OPENLicense: cc-by-nc-nd, cc-by-nc-ndDOI - Digital Object Identifier: 10.1016/j.parkreldis.2020.06.030Best OA location URL: https://doi.org/10.1016/j.parkreldis.2020.06.030Citation Count: 13
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OPENTitle: Editorial: Non-neuronal cell heterogeneity in the nervous system during health and diseaseJournal Name: Frontiers in Cellular NeurosciencePublisher: Frontiers Media SAVol: 16Issue #:Start Page: 1047296End Page: 1047296Publication Date:Open Access(OA) Status: OPENLicense: cc-by, cc-byDOI - Digital Object Identifier: 10.3389/fncel.2022.1047296Best OA location URL: https://www.frontiersin.org/articles/10.3389/fncel.2022.1047296/pdfCitation Count: 1
- Combining Multimodal Biomarkers to Guide Deep Brain Stimulation Programming in Parkinson Disease2022OPENTitle: Combining Multimodal Biomarkers to Guide Deep Brain Stimulation Programming in Parkinson DiseaseJournal Name: Neuromodulation: Technology at the Neural InterfacePublisher: Elsevier BVVol: 26Issue #: 2Start Page: 320End Page: 332Publication Date:Open Access(OA) Status: OPENLicense: cc-by, cc-byDOI - Digital Object Identifier: 10.1016/j.neurom.2022.01.017Best OA location URL: http://www.neuromodulationjournal.org/article/S1094715922000381/pdfCitation Count: 57
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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: 110
- Genetic determinants of survival in progressive supranuclear palsy: a genome-wide association study2020OPENTitle: Genetic determinants of survival in progressive supranuclear palsy: a genome-wide association studyJournal Name: The Lancet NeurologyPublisher: Elsevier BVVol: 20Issue #: 2Start Page: 107End Page: 116Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1016/s1474-4422(20)30394-xBest OA location URL: http://hdl.handle.net/10044/1/85602Citation Count: 120
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OPENTitle: Fibrillation and molecular characteristics are coherent with clinical and pathological features of 4-repeat tauopathy caused by MAPT variant G273RJournal Name: Neurobiology of DiseasePublisher: Elsevier BVVol: 146Issue #:Start Page: 105079End Page: 105079Publication Date:Open Access(OA) Status: OPENLicense: cc-by, cc-byDOI - Digital Object Identifier: 10.1016/j.nbd.2020.105079Best OA location URL: https://doi.org/10.1016/j.nbd.2020.105079Citation Count: 8