5051 - 5060 of 8571 Results
Title
Year
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OPENTitle: Intronic Haplotypes in the GBA Gene Do Not Predict Age at Diagnosis of Parkinson's DiseaseJournal Name: Movement DisordersPublisher: WileyVol: 36Issue #: 6Start Page: 1456End Page: 1460Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.1002/mds.28616Best OA location URL: https://onlinelibrary.wiley.com/doi/pdfdirect/10.1002/mds.28616Citation Count: 5
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OPENTitle: The Myelin‐Weighted Connectome in Parkinson's DiseaseJournal Name: Movement DisordersPublisher: WileyVol: 37Issue #: 4Start Page: 724End Page: 733Publication Date:Open Access(OA) Status: OPENLicense: cc-by, cc-byDOI - Digital Object Identifier: 10.1002/mds.28891Best OA location URL: https://onlinelibrary.wiley.com/doi/pdfdirect/10.1002/mds.28891Citation Count: 28
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OPENTitle: Genetic Stratification of Age‐Dependent Parkinson's Disease Risk by Polygenic Hazard ScoreJournal Name: Movement DisordersPublisher: WileyVol: 37Issue #: 1Start Page: 62End Page: 69Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.1002/mds.28808Best OA location URL: https://onlinelibrary.wiley.com/doi/pdfdirect/10.1002/mds.28808Citation Count: 15
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OPENTitle: Parkin Deficiency Appears Not to Be Associated with Cardiac Damage in Parkinson's DiseaseJournal Name: Movement DisordersPublisher: WileyVol: 36Issue #: 1Start Page: 271End Page: 273Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.1002/mds.28422Best OA location URL: https://onlinelibrary.wiley.com/doi/pdfdirect/10.1002/mds.28422Citation Count: 4
- Rapid Eye Movement Sleep Behavior Disorder: Abnormal Cardiac Image and Progressive Abnormal Metabolic Brain Pattern2021OPENTitle: Rapid Eye Movement Sleep Behavior Disorder: Abnormal Cardiac Image and Progressive Abnormal Metabolic Brain PatternJournal Name: Movement DisordersPublisher: WileyVol: 37Issue #: 3Start Page: 624End Page: 629Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.1002/mds.28859Best OA location URL: https://onlinelibrary.wiley.com/doi/pdfdirect/10.1002/mds.28859Citation Count: 9
- Solriamfetol for Excessive Daytime Sleepiness in Parkinson's Disease: Phase 2 Proof‐of‐Concept Trial2021OPENTitle: Solriamfetol for Excessive Daytime Sleepiness in Parkinson's Disease: Phase 2 Proof‐of‐Concept TrialJournal Name: Movement DisordersPublisher: WileyVol: 36Issue #: 10Start Page: 2408End Page: 2412Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.1002/mds.28702Best OA location URL: https://onlinelibrary.wiley.com/doi/pdf/10.1002/mds.28702Citation Count: 14
- Spontaneous Graft‐Induced Dyskinesias Are Independent of 5‐HT Neurons and Levodopa Priming in a Model of Parkinson's Disease2021OPENTitle: Spontaneous Graft‐Induced Dyskinesias Are Independent of 5‐HT Neurons and Levodopa Priming in a Model of Parkinson's DiseaseJournal Name: Movement DisordersPublisher: WileyVol: 37Issue #: 3Start Page: 613End Page: 619Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.1002/mds.28856Best OA location URL: https://onlinelibrary.wiley.com/doi/pdfdirect/10.1002/mds.28856Citation Count: 8
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OPENTitle: A Novel Variant of ATP5MC3 Associated with Both Dystonia and Spastic ParaplegiaJournal Name: Movement DisordersPublisher: WileyVol: 37Issue #: 2Start Page: 375End Page: 383Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1002/mds.28821Best OA location URL: https://www.ncbi.nlm.nih.gov/pmc/articles/8840961Citation Count: 13
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OPENTitle: Preexisting Bipolar Disorder Influences the Subsequent Phenotype of Parkinson's DiseaseJournal Name: Movement DisordersPublisher: WileyVol: 36Issue #: 12Start Page: 2840End Page: 2852Publication Date:Open Access(OA) Status: OPENLicense: cc-by-nc-ndDOI - Digital Object Identifier: 10.1002/mds.28745Best OA location URL: https://onlinelibrary.wiley.com/doi/pdfdirect/10.1002/mds.28745Citation Count: 18
- Neuropathological Findings in a Case of Parkinsonism and Developmental Delay Associated with a Monoallelic Variant in PLXNA12021RESTRICTEDTitle: Neuropathological Findings in a Case of Parkinsonism and Developmental Delay Associated with a Monoallelic Variant in PLXNA1Journal Name: Movement DisordersPublisher: WileyVol: 36Issue #: 11Start Page: 2681End Page: 2687Publication Date:Open Access(OA) Status: RESTRICTEDLicense:DOI - Digital Object Identifier: 10.1002/mds.28756Citation Count: 8