6431 - 6440 of 8620 Results
Title
Year
- 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
- 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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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: Profiling the NOTCH2NLC GGC Repeat Expansion in Parkinson's Disease in the European PopulationJournal Name: Movement DisordersPublisher: WileyVol: 37Issue #: 10Start Page: 2161End Page: 2162Publication Date:Open Access(OA) Status: RESTRICTEDLicense:DOI - Digital Object Identifier: 10.1002/mds.29155Best OA location URL: https://www.ncbi.nlm.nih.gov/pmc/articles/12159426Citation Count: 5
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OPENTitle: Disease Progression in Multiple System Atrophy—Novel Modeling Framework and Predictive FactorsJournal Name: Movement DisordersPublisher: WileyVol: 37Issue #: 8Start Page: 1719End Page: 1727Publication Date:Open Access(OA) Status: OPENLicense: cc-by-nc-ndDOI - Digital Object Identifier: 10.1002/mds.29077Best OA location URL: https://doi.org/10.1002/mds.29077Citation Count: 10
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RESTRICTEDTitle: Could Blood Hexosylsphingosine Be a Marker for Parkinson's Disease Linked with GBA1 Mutations?Journal Name: Movement DisordersPublisher: WileyVol: 37Issue #: 8Start Page: 1779End Page: 1781Publication Date:Open Access(OA) Status: RESTRICTEDLicense:DOI - Digital Object Identifier: 10.1002/mds.29132Citation Count: 11
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RESTRICTEDTitle: Mutation Screening of TFG in α‐Synucleinopathy and Amyotrophic Lateral SclerosisJournal Name: Movement DisordersPublisher: WileyVol: 37Issue #: 8Start Page: 1756End Page: 1761Publication Date:Open Access(OA) Status: RESTRICTEDLicense:DOI - Digital Object Identifier: 10.1002/mds.29079Citation Count: 5
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RESTRICTEDTitle: Corticobasal Syndrome with TAR Binding Protein 43–Positive Oligodendrocyte InclusionsJournal Name: Movement DisordersPublisher: WileyVol: 37Issue #: 7Start Page: 1564End Page: 1565Publication Date:Open Access(OA) Status: RESTRICTEDLicense:DOI - Digital Object Identifier: 10.1002/mds.29070Citation Count: 0
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RESTRICTEDTitle: Reply to: “Diabetes and Neuroaxonal Damage in Parkinson's Disease”Journal Name: Movement DisordersPublisher: WileyVol: 37Issue #: 7Start Page: 1569End Page: 1570Publication Date:Open Access(OA) Status: RESTRICTEDLicense:DOI - Digital Object Identifier: 10.1002/mds.29064Citation Count: 0