4831 - 4840 of 8825 Results
Title
Year
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OPENTitle: Intronic Haplotypes in GBA Modify Age at Diagnosis of Parkinson's: Replication in a SubgroupJournal Name: Movement DisordersPublisher: WileyVol: 36Issue #: 6Start Page: 1468End Page: 1470Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1002/mds.28620Best OA location URL: https://onlinelibrary.wiley.com/doi/pdfdirect/10.1002/mds.28620Citation Count: 2
- Expectations of Benefit in a Trial of a Candidate Disease‐Modifying Treatment for Parkinson Disease2021RESTRICTEDTitle: Expectations of Benefit in a Trial of a Candidate Disease‐Modifying Treatment for Parkinson DiseaseJournal Name: Movement DisordersPublisher: WileyVol: 36Issue #: 8Start Page: 1964End Page: 1967Publication Date:Open Access(OA) Status: RESTRICTEDLicense:DOI - Digital Object Identifier: 10.1002/mds.28630Citation Count: 6
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OPENTitle: Heritability and genetic variance of dementia with Lewy bodiesJournal Name: Neurobiology of DiseasePublisher: Elsevier BVVol: 127Issue #:Start Page: 492End Page: 501Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1016/j.nbd.2019.04.004Best OA location URL: https://nottingham-repository.worktribe.com/output/1215394Citation Count: 44
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OPENTitle: Differences in the Presentation and Progression of Parkinson's Disease by SexJournal Name: Movement DisordersPublisher: WileyVol: 36Issue #: 1Start Page: 106End Page: 117Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1002/mds.28312Best OA location URL: https://onlinelibrary.wiley.com/doi/pdfdirect/10.1002/mds.28312Citation Count: 100
- Is the MC1R variant p.R160W associated with Parkinson's?2015RESTRICTEDTitle: Is the MC1R variant p.R160W associated with Parkinson's?Journal Name: Annals of NeurologyPublisher: WileyVol: 79Issue #: 1Start Page: 159End Page: 161Publication Date:Open Access(OA) Status: RESTRICTEDLicense:DOI - Digital Object Identifier: 10.1002/ana.24527Citation Count: 19
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OPENTitle: Specifically neuropathic Gaucher's mutations accelerate cognitive decline in Parkinson'sJournal Name: Annals of NeurologyPublisher: WileyVol: 80Issue #: 5Start Page: 674End Page: 685Publication Date:Open Access(OA) Status: OPENLicense: cc-by, cc-byDOI - Digital Object Identifier: 10.1002/ana.24781Best OA location URL: https://onlinelibrary.wiley.com/doi/pdfdirect/10.1002/ana.24781Citation Count: 276
- The Isolation and Deep Sequencing of Mitochondrial DNA2021RESTRICTEDTitle: The Isolation and Deep Sequencing of Mitochondrial DNAJournal Name: Methods in Molecular BiologyPublisher: Springer USVol:Issue #:Start Page: 433End Page: 447Publication Date:Open Access(OA) Status: RESTRICTEDLicense:DOI - Digital Object Identifier: 10.1007/978-1-0716-1270-5_27Citation Count: 8
- Astrocytic Changes in Mitochondrial Oxidative Phosphorylation Protein Levels in Parkinson's Disease2021OPENTitle: Astrocytic Changes in Mitochondrial Oxidative Phosphorylation Protein Levels in Parkinson's DiseaseJournal Name: Movement DisordersPublisher: WileyVol: 37Issue #: 2Start Page: 302End Page: 314Publication Date:Open Access(OA) Status: OPENLicense: cc-by, cc-byDOI - Digital Object Identifier: 10.1002/mds.28849Best OA location URL: https://eprints.ncl.ac.uk/278327Citation Count: 31
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OPENTitle: Suitability of Automated Writing Measures for Clinical Trial Outcome in Writer's CrampJournal Name: Movement DisordersPublisher: WileyVol: 38Issue #: 1Start Page: 123End Page: 132Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1002/mds.29237Best OA location URL: https://www.ncbi.nlm.nih.gov/pmc/articles/9851940Citation Count: 8
- Parkinson's Disease, NOTCH3 Genetic Variants, and White Matter Hyperintensities2020RESTRICTEDTitle: Parkinson's Disease, NOTCH3 Genetic Variants, and White Matter HyperintensitiesJournal Name: Movement DisordersPublisher: WileyVol: 35Issue #: 11Start Page: 2090End Page: 2095Publication Date:Open Access(OA) Status: RESTRICTEDLicense:DOI - Digital Object Identifier: 10.1002/mds.28171Citation Count: 28