3111 - 3120 of 6230 Results
Title
Year
- Cognitive Performance in Early Neuronal Synuclein Disease with Hyposmia but without Motor Disability: Association with Dopamine Deficiency and Isolated Rapid Eye Movement Sleep Behavior Disorder2025OPENTitle: Cognitive Performance in Early Neuronal Synuclein Disease with Hyposmia but without Motor Disability: Association with Dopamine Deficiency and Isolated Rapid Eye Movement Sleep Behavior DisorderJournal Name: Annals of NeurologyPublisher: WileyVol: 98Issue #: 3Start Page:End Page:Publication Date:Open Access(OA) Status: OPENLicense: cc-by-ncDOI - Digital Object Identifier: 10.1002/ana.27263Citation Count: 0
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OPENTitle: Effects of parkinsonism on health status in welding exposed workersJournal Name: Parkinsonism & Related DisordersPublisher: Elsevier BVVol: 17Issue #: 9Start Page: 672End Page: 676Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1016/j.parkreldis.2011.05.021Best OA location URL: https://www.ncbi.nlm.nih.gov/pmc/articles/3200492Citation Count: 21
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OPENTitle: LRRK2 activation in idiopathic Parkinson’s diseaseJournal Name: Science Translational MedicinePublisher: American Association for the Advancement of Science (AAAS)Vol: 10Issue #: 451Start Page:End Page:Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1126/scitranslmed.aar5429Best OA location URL: https://www.ncbi.nlm.nih.gov/pmc/articles/6344941Citation Count: 547
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OPENTitle: PPM1H phosphatase counteracts LRRK2 signaling by selectively dephosphorylating Rab proteinsJournal Name: eLifePublisher: eLife Sciences Publications, LtdVol: 8Issue #:Start Page:End Page:Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.7554/elife.50416Best OA location URL: https://cdn.elifesciences.org/articles/50416/elife-50416-v2.pdfCitation Count: 118
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OPENTitle: Motor phenotype classification in moderate to advanced PD in BioFIND studyJournal Name: Parkinsonism & Related DisordersPublisher: Elsevier BVVol: 65Issue #:Start Page: 178End Page: 183Publication Date:Open Access(OA) Status: OPENLicense: other-oaDOI - Digital Object Identifier: 10.1016/j.parkreldis.2019.06.017Best OA location URL: https://www.ncbi.nlm.nih.gov/pmc/articles/6774826Citation Count: 23
- Diagnostic classification of Parkinson’s disease based on non-motor manifestations and machine learning strategies2022OPENTitle: Diagnostic classification of Parkinson’s disease based on non-motor manifestations and machine learning strategiesJournal Name: Neural Computing and ApplicationsPublisher: Springer Science and Business Media LLCVol: 35Issue #: 8Start Page: 5603End Page: 5617Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.1007/s00521-022-07256-8Best OA location URL: https://link.springer.com/content/pdf/10.1007/s00521-022-07256-8.pdfCitation Count: 22
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OPENTitle: A genetic and proteomic comparison of key AD biomarkers across tissuesJournal Name: Alzheimer's & DementiaPublisher: WileyVol: 20Issue #: 9Start Page: 6423End Page: 6440Publication Date:Open Access(OA) Status: OPENLicense: cc-by-ncDOI - Digital Object Identifier: 10.1002/alz.14139Best OA location URL: https://alz-journals.onlinelibrary.wiley.com/doi/pdf/10.1002/alz.14139Citation Count: 2
- Parkinson Sac Domain Mutation in Synaptojanin 1 Impairs Clathrin Uncoating at Synapses and Triggers Dystrophic Changes in Dopaminergic Axons2017OPENTitle: Parkinson Sac Domain Mutation in Synaptojanin 1 Impairs Clathrin Uncoating at Synapses and Triggers Dystrophic Changes in Dopaminergic AxonsJournal Name: NeuronPublisher: Elsevier BVVol: 93Issue #: 4Start Page: 882End Page: 896.e5Publication Date:Open Access(OA) Status: OPENLicense: publisher-specific-oa, publisher-specific-oaDOI - Digital Object Identifier: 10.1016/j.neuron.2017.01.019Best OA location URL: http://www.cell.com/article/S0896627317300430/pdfCitation Count: 174
- A proteomic network approach across the ALS ‐ FTD disease spectrum resolves clinical phenotypes and genetic vulnerability in human brain2017OPENTitle: A proteomic network approach across the ALS ‐ FTD disease spectrum resolves clinical phenotypes and genetic vulnerability in human brainJournal Name: EMBO Molecular MedicinePublisher: Springer Science and Business Media LLCVol: 10Issue #: 1Start Page: 48End Page: 62Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.15252/emmm.201708202Best OA location URL: https://onlinelibrary.wiley.com/doi/pdfdirect/10.15252/emmm.201708202Citation Count: 153
- Pathological α-syn aggregation is mediated by glycosphingolipid chain length and the physiological state of α-syn in vivo2021OPENTitle: Pathological α-syn aggregation is mediated by glycosphingolipid chain length and the physiological state of α-syn in vivoJournal Name: Proceedings of the National Academy of SciencesPublisher: Proceedings of the National Academy of SciencesVol: 118Issue #: 50Start Page:End Page:Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1073/pnas.2108489118Best OA location URL: https://www.ncbi.nlm.nih.gov/pmc/articles/8685670Citation Count: 28