5011 - 5020 of 8808 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: 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
- Low Frequency of p.S510G in PIAS1 Challenges its Relevance for Modifying Repeat Expansion Disorders2022OPENTitle: Low Frequency of p.S510G in PIAS1 Challenges its Relevance for Modifying Repeat Expansion DisordersJournal Name: Movement DisordersPublisher: WileyVol: 37Issue #: 10Start Page: 2168End Page: 2169Publication Date:Open Access(OA) Status: OPENLicense: cc-by-nc-ndDOI - Digital Object Identifier: 10.1002/mds.29191Best OA location URL: https://onlinelibrary.wiley.com/doi/pdfdirect/10.1002/mds.29191Citation Count: 1
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RESTRICTEDTitle: Epigenetic Clock Acceleration Is Linked to Age at Onset of Parkinson's DiseaseJournal Name: Movement DisordersPublisher: WileyVol: 37Issue #: 9Start Page: 1831End Page: 1840Publication Date:Open Access(OA) Status: RESTRICTEDLicense:DOI - Digital Object Identifier: 10.1002/mds.29157Citation Count: 30
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RESTRICTEDTitle: TDP‐43 Proteinopathy Presenting with Typical Symptoms of Parkinson's DiseaseJournal Name: Movement DisordersPublisher: WileyVol: 37Issue #: 7Start Page: 1561End Page: 1563Publication Date:Open Access(OA) Status: RESTRICTEDLicense:DOI - Digital Object Identifier: 10.1002/mds.29048Citation Count: 23
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RESTRICTEDTitle: Assessment of GGC Repeat Expansion in GIPC1 in Patients with Parkinson's DiseaseJournal Name: Movement DisordersPublisher: WileyVol: 37Issue #: 7Start Page: 1557End Page: 1559Publication Date:Open Access(OA) Status: RESTRICTEDLicense:DOI - Digital Object Identifier: 10.1002/mds.29041Citation Count: 10