6401 - 6410 of 9131 Results
Title
Year
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OPENTitle: Deep gray matter volume loss drives disability worsening in multiple sclerosisJournal Name: Annals of NeurologyPublisher: WileyVol: 83Issue #: 2Start Page: 210End Page: 222Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.1002/ana.25145Best OA location URL: https://onlinelibrary.wiley.com/doi/pdfdirect/10.1002/ana.25145Citation Count: 441
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OPENTitle: Fine‐Mapping of SNCA in Rapid Eye Movement Sleep Behavior Disorder and Overt SynucleinopathiesJournal Name: Annals of NeurologyPublisher: WileyVol: 87Issue #: 4Start Page: 584End Page: 598Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1002/ana.25687Best OA location URL: http://hdl.handle.net/11380/1205937Citation Count: 65
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OPENTitle: Plasma MIA , CRP , and Albumin Predict Cognitive Decline in Parkinson's DiseaseJournal Name: Annals of NeurologyPublisher: WileyVol: 92Issue #: 2Start Page: 255End Page: 269Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1002/ana.26410Best OA location URL: https://www.ncbi.nlm.nih.gov/pmc/articles/9329215Citation Count: 33
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OPENTitle: Interaction of an α-synuclein epitope with HLA-DRB1∗15:01 triggers enteric features in mice reminiscent of prodromal Parkinson’s diseaseJournal Name: NeuronPublisher: Elsevier BVVol: 111Issue #: 21Start Page: 3397End Page: 3413.e5Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.1016/j.neuron.2023.07.015Best OA location URL: http://www.cell.com/article/S0896627323005482/pdfCitation Count: 55
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OPENTitle: Large-scale pathway specific polygenic risk and transcriptomic community network analysis identifies novel functional pathways in Parkinson diseaseJournal Name: Acta NeuropathologicaPublisher: Springer Science and Business Media LLCVol: 140Issue #: 3Start Page: 341End Page: 358Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.1007/s00401-020-02181-3Best OA location URL: https://link.springer.com/content/pdf/10.1007/s00401-020-02181-3.pdfCitation Count: 119
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OPENTitle: ggtranscript : an R package for the visualization and interpretation of transcript isoforms using ggplot2Journal Name: BioinformaticsPublisher: Oxford University Press (OUP)Vol: 38Issue #: 15Start Page: 3844End Page: 3846Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.1093/bioinformatics/btac409Best OA location URL: https://academic.oup.com/bioinformatics/article-pdf/38/15/3844/49884398/btac409.pdfCitation Count: 726
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OPENTitle: Trait Anxiety as a Risk Factor for Impulse Control Disorders in de novo Parkinson’s DiseaseJournal Name: Journal of Parkinson's DiseasePublisher: SAGE PublicationsVol: 12Issue #: 2Start Page: 689End Page: 697Publication Date:Open Access(OA) Status: OPENLicense: cc-by-ncDOI - Digital Object Identifier: 10.3233/jpd-212959Best OA location URL: https://content.iospress.com:443/download/journal-of-parkinsons-disease/jpd212959?id=journal-of-parkinsons-disease%2Fjpd212959Citation Count: 13
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OPENTitle: Pathway-specific dysregulation of striatal excitatory synapses by LRRK2 mutationsJournal Name: eLifePublisher: eLife Sciences Publications, LtdVol: 9Issue #:Start Page:End Page:Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.7554/elife.58997Best OA location URL: https://doi.org/10.7554/elife.58997Citation Count: 59
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OPENTitle: Cerebrospinal fluid and blood profiles of transfer RNA fragments show age, sex, and Parkinson's disease‐related changesJournal Name: Journal of NeurochemistryPublisher: WileyVol: 164Issue #: 5Start Page: 671End Page: 683Publication Date:Open Access(OA) Status: OPENLicense: cc-by-nc-ndDOI - Digital Object Identifier: 10.1111/jnc.15723Best OA location URL: https://onlinelibrary.wiley.com/doi/pdfdirect/10.1111/jnc.15723Citation Count: 31
- Compound heterozygous variants in Wiskott-Aldrich syndrome like (WASL) gene segregating in a family with early onset Parkinson's disease2021RESTRICTEDTitle: Compound heterozygous variants in Wiskott-Aldrich syndrome like (WASL) gene segregating in a family with early onset Parkinson's diseaseJournal Name: Parkinsonism & Related DisordersPublisher: Elsevier BVVol: 84Issue #:Start Page: 61End Page: 67Publication Date:Open Access(OA) Status: RESTRICTEDLicense:DOI - Digital Object Identifier: 10.1016/j.parkreldis.2021.02.001Citation Count: 19