4761 - 4770 of 9145 Results
Title
Year
- Soluble CD163 Changes Indicate Monocyte Association With Cognitive Deficits in Parkinson's Disease2020OPENTitle: Soluble CD163 Changes Indicate Monocyte Association With Cognitive Deficits in Parkinson's DiseaseJournal Name: Movement DisordersPublisher: WileyVol: 36Issue #: 4Start Page: 963End Page: 976Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.1002/mds.28424Best OA location URL: https://pub.dzne.de/record/157801Citation Count: 60
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OPENTitle: The role of phosphodiesterase 4 in excessive daytime sleepiness in Parkinson's diseaseJournal Name: Parkinsonism & Related DisordersPublisher: Elsevier BVVol: 77Issue #:Start Page: 163End Page: 169Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1016/j.parkreldis.2019.02.027Best OA location URL: https://kclpure.kcl.ac.uk/ws/files/111216027/The_role_of_phosphodiesterase_WILSON_Accepted18February2019_GREEN_AAM.pdfCitation Count: 18
- Robust identification of Parkinson's disease subtypes using radiomics and hybrid machine learning2020RESTRICTEDTitle: Robust identification of Parkinson's disease subtypes using radiomics and hybrid machine learningJournal Name: Computers in Biology and MedicinePublisher: Elsevier BVVol: 129Issue #:Start Page: 104142End Page: 104142Publication Date:Open Access(OA) Status: RESTRICTEDLicense:DOI - Digital Object Identifier: 10.1016/j.compbiomed.2020.104142Citation Count: 58
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OPENTitle: Early Dysfunction of Substantia Nigra Dopamine Neurons in the ParkinQ311X MouseJournal Name: BiomedicinesPublisher: MDPI AGVol: 9Issue #: 5Start Page: 514End Page: 514Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.3390/biomedicines9050514Best OA location URL: https://www.mdpi.com/2227-9059/9/5/514/pdf?version=1620466923Citation Count: 6
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OPENTitle: α‐synuclein genetic variability: A biomarker for dementia in Parkinson diseaseJournal Name: Annals of NeurologyPublisher: WileyVol: 79Issue #: 6Start Page: 991End Page: 999Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1002/ana.24664Best OA location URL: http://hdl.handle.net/2027.42/137619Citation Count: 98
- Outcomes of genetic test disclosure and genetic counseling in a large Parkinson's disease research study2020RESTRICTEDTitle: Outcomes of genetic test disclosure and genetic counseling in a large Parkinson's disease research studyJournal Name: Journal of Genetic CounselingPublisher: WileyVol: 30Issue #: 3Start Page: 755End Page: 765Publication Date:Open Access(OA) Status: RESTRICTEDLicense:DOI - Digital Object Identifier: 10.1002/jgc4.1366Citation Count: 23
- Blood-Based Nanoparticle-Enhanced Quaking-Induced Conversion (Nano-QuIC): Inhibitor-Resistant Detection of Seeding Activity in Patients Diagnosed with Parkinson’s Disease2024RESTRICTEDTitle: Blood-Based Nanoparticle-Enhanced Quaking-Induced Conversion (Nano-QuIC): Inhibitor-Resistant Detection of Seeding Activity in Patients Diagnosed with Parkinson’s DiseaseJournal Name: Nano LettersPublisher: American Chemical Society (ACS)Vol: 24Issue #: 47Start Page: 15016End Page: 15024Publication Date:Open Access(OA) Status: RESTRICTEDLicense:DOI - Digital Object Identifier: 10.1021/acs.nanolett.4c03768Citation Count: 16
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OPENTitle: Subtype definition of vascular parkinsonismJournal Name: Parkinsonism & Related DisordersPublisher: Elsevier BVVol: 52Issue #:Start Page: 107End Page: 108Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1016/j.parkreldis.2018.03.005Best OA location URL: https://www.ncbi.nlm.nih.gov/pmc/articles/6019183Citation Count: 2
- Parkinson's disease motor subtypes and bilateral GPi deep brain stimulation: One-year outcomes2020RESTRICTEDTitle: Parkinson's disease motor subtypes and bilateral GPi deep brain stimulation: One-year outcomesJournal Name: Parkinsonism & Related DisordersPublisher: Elsevier BVVol: 75Issue #:Start Page: 7End Page: 13Publication Date:Open Access(OA) Status: RESTRICTEDLicense:DOI - Digital Object Identifier: 10.1016/j.parkreldis.2020.05.004Citation Count: 24
- RAB7L1-Mediated Relocalization of LRRK2 to the Golgi Complex Causes Centrosomal Deficits via RAB8A2018OPENTitle: RAB7L1-Mediated Relocalization of LRRK2 to the Golgi Complex Causes Centrosomal Deficits via RAB8AJournal Name: Frontiers in Molecular NeurosciencePublisher: Frontiers Media SAVol: 11Issue #:Start Page: 417End Page: 417Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.3389/fnmol.2018.00417Best OA location URL: https://www.frontiersin.org/articles/10.3389/fnmol.2018.00417/pdfCitation Count: 46