5721 - 5730 of 8606 Results
Title
Year
- 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
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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
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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: 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: 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: 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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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
- Joint Modeling Study Identifies Blood‐Based Transcripts Link to Cognitive Decline in Parkinson's Disease2022RESTRICTEDTitle: Joint Modeling Study Identifies Blood‐Based Transcripts Link to Cognitive Decline in Parkinson's DiseaseJournal Name: Movement DisordersPublisher: WileyVol: 37Issue #: 12Start Page: 2386End Page: 2395Publication Date:Open Access(OA) Status: RESTRICTEDLicense:DOI - Digital Object Identifier: 10.1002/mds.29213Citation Count: 0
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