2471 - 2480 of 8587 Results
Title
Year
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RESTRICTEDTitle: Implications of DNA Methylation in Lewy Body PathologyJournal Name: Movement DisordersPublisher: WileyVol: 38Issue #: 1Start Page: 25End Page: 25Publication Date:Open Access(OA) Status: RESTRICTEDLicense:DOI - Digital Object Identifier: 10.1002/mds.29290Citation Count: 0
- De Novo and Dominantly Inherited SPTAN1 Mutations Cause Spastic Paraplegia and Cerebellar Ataxia2022OPENTitle: De Novo and Dominantly Inherited SPTAN1 Mutations Cause Spastic Paraplegia and Cerebellar AtaxiaJournal Name: Movement DisordersPublisher: WileyVol: 37Issue #: 6Start Page: 1175End Page: 1186Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1002/mds.28959Best OA location URL: https://www.ncbi.nlm.nih.gov/pmc/articles/9232883Citation Count: 21
- mTOR Inhibition with Sirolimus in Multiple System Atrophy: A Randomized, Double‐Blind, Placebo‐Controlled Futility Trial and 1‐Year Biomarker Longitudinal Analysis2022OPENTitle: mTOR Inhibition with Sirolimus in Multiple System Atrophy: A Randomized, Double‐Blind, Placebo‐Controlled Futility Trial and 1‐Year Biomarker Longitudinal AnalysisJournal Name: Movement DisordersPublisher: WileyVol: 37Issue #: 4Start Page: 778End Page: 789Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1002/mds.28923Best OA location URL: https://www.ncbi.nlm.nih.gov/pmc/articles/9018525Citation Count: 23
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RESTRICTEDTitle: Increased Free Water in the Substantia Nigra in Asymptomatic LRRK2 G2019S Mutation CarriersJournal Name: Movement DisordersPublisher: WileyVol: 38Issue #: 1Start Page: 138End Page: 142Publication Date:Open Access(OA) Status: RESTRICTEDLicense:DOI - Digital Object Identifier: 10.1002/mds.29253Citation Count: 4
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RESTRICTEDTitle: Unmet Needs of Women Living with Parkinson's Disease: Gaps and ControversiesJournal Name: Movement DisordersPublisher: WileyVol: 37Issue #: 3Start Page: 444End Page: 455Publication Date:Open Access(OA) Status: RESTRICTEDLicense:DOI - Digital Object Identifier: 10.1002/mds.28921Citation Count: 79
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RESTRICTEDTitle: 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: RESTRICTEDLicense:DOI - Digital Object Identifier: 10.1002/mds.29237Best OA location URL: https://www.ncbi.nlm.nih.gov/pmc/articles/9851940Citation Count: 5
- Digging into the Unknowns of the Human Genome Sequence: The T2T‐CHM13 Reference Assembly Release2022RESTRICTEDTitle: Digging into the Unknowns of the Human Genome Sequence: The T2T‐CHM13 Reference Assembly ReleaseJournal Name: Movement DisordersPublisher: WileyVol: 37Issue #: 11Start Page: 2192End Page: 2192Publication Date:Open Access(OA) Status: RESTRICTEDLicense:DOI - Digital Object Identifier: 10.1002/mds.29235Citation Count: 0
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RESTRICTEDTitle: The Dawn of Precision Medicine for Deep Brain Stimulation in Parkinson's Disease?Journal Name: Movement DisordersPublisher: WileyVol: 37Issue #: 11Start Page: 2191End Page: 2191Publication Date:Open Access(OA) Status: RESTRICTEDLicense:DOI - Digital Object Identifier: 10.1002/mds.29224Citation Count: 0
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RESTRICTEDTitle: Gaps, Controversies, and Proposed Roadmap for Research in Poststroke Movement DisordersJournal Name: Movement DisordersPublisher: WileyVol: 37Issue #: 10Start Page: 1996End Page: 2007Publication Date:Open Access(OA) Status: RESTRICTEDLicense:DOI - Digital Object Identifier: 10.1002/mds.29218Citation Count: 8
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