4521 - 4530 of 8808 Results
Title
Year
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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: 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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OPENTitle: 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
- It Is as It Was: MDS‐UPDRS Part III Scores Cannot Be Combined with Other Parts to Give a Valid Sum2022OPENTitle: It Is as It Was: MDS‐UPDRS Part III Scores Cannot Be Combined with Other Parts to Give a Valid SumJournal Name: Movement DisordersPublisher: WileyVol: 38Issue #: 2Start Page: 342End Page: 347Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1002/mds.29279Best OA location URL: https://www.ncbi.nlm.nih.gov/pmc/articles/9974855Citation Count: 14
- 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: 24
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OPENTitle: A Modified Progressive Supranuclear Palsy Rating Scale for Virtual AssessmentsJournal Name: Movement DisordersPublisher: WileyVol: 37Issue #: 6Start Page: 1265End Page: 1271Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1002/mds.28991Best OA location URL: https://www.ncbi.nlm.nih.gov/pmc/articles/9232989Citation Count: 12
- c‐Abl Inhibitors as Disease‐Modifying Therapies for Parkinson's Disease: Gaps and Opportunities2022RESTRICTEDTitle: c‐Abl Inhibitors as Disease‐Modifying Therapies for Parkinson's Disease: Gaps and OpportunitiesJournal Name: Movement DisordersPublisher: WileyVol: 37Issue #: 1Start Page: 3End Page: 5Publication Date:Open Access(OA) Status: RESTRICTEDLicense:DOI - Digital Object Identifier: 10.1002/mds.28907Citation Count: 3
- Lateralized Subthalamic Stimulation for Axial Dysfunction in Parkinson's Disease: A Randomized Trial2022RESTRICTEDTitle: Lateralized Subthalamic Stimulation for Axial Dysfunction in Parkinson's Disease: A Randomized TrialJournal Name: Movement DisordersPublisher: WileyVol: 37Issue #: 5Start Page: 1079End Page: 1087Publication Date:Open Access(OA) Status: RESTRICTEDLicense:DOI - Digital Object Identifier: 10.1002/mds.28953Citation Count: 13
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RESTRICTEDTitle: Validation of the Arabic Version of the Movement Disorder Society‐Unified Parkinson's Disease Rating ScaleJournal Name: Movement DisordersPublisher: WileyVol: 37Issue #: 4Start Page: 826End Page: 841Publication Date:Open Access(OA) Status: RESTRICTEDLicense:DOI - Digital Object Identifier: 10.1002/mds.28905Citation Count: 6
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OPENTitle: GRN Mutations Are Associated with Lewy Body DementiaJournal Name: Movement DisordersPublisher: WileyVol: 37Issue #: 9Start Page: 1943End Page: 1948Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1002/mds.29144Best OA location URL: http://orbilu.uni.lu/handle/10993/51636Citation Count: 14