1371 - 1380 of 9156 Results
Title
Year
- Genome‐wide variant by serum urate interaction in Parkinson's disease2015RESTRICTEDTitle: Genome‐wide variant by serum urate interaction in Parkinson's diseaseJournal Name: Annals of NeurologyPublisher: WileyVol: 78Issue #: 5Start Page: 731End Page: 741Publication Date:Open Access(OA) Status: RESTRICTEDLicense:DOI - Digital Object Identifier: 10.1002/ana.24504Citation Count: 12
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OPENTitle: Connectivity Predicts deep brain stimulation outcome in Parkinson diseaseJournal Name: Annals of NeurologyPublisher: WileyVol: 82Issue #: 1Start Page: 67End Page: 78Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1002/ana.24974Best OA location URL: https://www.ncbi.nlm.nih.gov/pmc/articles/5880678Citation Count: 734
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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
- Magnetic resonance T1w/T2w ratio: A parsimonious marker for Parkinson disease2018RESTRICTEDTitle: Magnetic resonance T1w/T2w ratio: A parsimonious marker for Parkinson diseaseJournal Name: Annals of NeurologyPublisher: WileyVol: 85Issue #: 1Start Page: 96End Page: 104Publication Date:Open Access(OA) Status: RESTRICTEDLicense:DOI - Digital Object Identifier: 10.1002/ana.25376Citation Count: 42
- Higher urate in LRRK2 mutation carriers resistant to Parkinson disease2019RESTRICTEDTitle: Higher urate in LRRK2 mutation carriers resistant to Parkinson diseaseJournal Name: Annals of NeurologyPublisher: WileyVol: 85Issue #: 4Start Page: 593End Page: 599Publication Date:Open Access(OA) Status: RESTRICTEDLicense:DOI - Digital Object Identifier: 10.1002/ana.25436Citation Count: 56
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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: Parkinson Disease and Subthalamic Nucleus Deep Brain Stimulation: Cognitive Effects in GBA Mutation CarriersJournal Name: Annals of NeurologyPublisher: WileyVol: 91Issue #: 3Start Page: 424End Page: 435Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1002/ana.26302Best OA location URL: https://www.ncbi.nlm.nih.gov/pmc/articles/8857042Citation Count: 99
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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
- Sex effects on brain structure in de novo Parkinson’s disease: a multimodal neuroimaging study2020RESTRICTEDTitle: Sex effects on brain structure in de novo Parkinson’s disease: a multimodal neuroimaging studyJournal Name: BrainPublisher: Oxford University Press (OUP)Vol: 143Issue #: 10Start Page: 3052End Page: 3066Publication Date:Open Access(OA) Status: RESTRICTEDLicense:DOI - Digital Object Identifier: 10.1093/brain/awaa234Citation Count: 97
- PTPA variants are rare in early-onset and familial Parkinson’s disease2023RESTRICTEDTitle: PTPA variants are rare in early-onset and familial Parkinson’s diseaseJournal Name: BrainPublisher: Oxford University Press (OUP)Vol: 146Issue #: 12Start Page: e125End Page: e127Publication Date:Open Access(OA) Status: RESTRICTEDLicense:DOI - Digital Object Identifier: 10.1093/brain/awad244Citation Count: 2