1811 - 1820 of 8654 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
- 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
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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
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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
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OPENTitle: Elevated Urinary Rab10 Phosphorylation in Idiopathic Parkinson DiseaseJournal Name: Movement DisordersPublisher: WileyVol: 37Issue #: 7Start Page: 1454End Page: 1464Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.1002/mds.29043Best OA location URL: https://doi.org/10.1002/mds.29043Citation Count: 26
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OPENTitle: Accumulation of Brain Hypointense Foci on Susceptibility-Weighted Imaging in Childhood Ataxia TelangiectasiaJournal Name: American Journal of NeuroradiologyPublisher: American Society of Neuroradiology (ASNR)Vol: 42Issue #: 6Start Page: 1144End Page: 1150Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.3174/ajnr.a7107Best OA location URL: http://www.ajnr.org/content/ajnr/42/6/1144.full.pdfCitation Count: 7
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OPENTitle: Deficiency of the frontotemporal dementia gene GRN results in gangliosidosisJournal Name: Nature CommunicationsPublisher: Springer Science and Business Media LLCVol: 13Issue #: 1Start Page:End Page:Publication Date:Open Access(OA) Status: OPENLicense: cc-by, cc-by, cc-byDOI - Digital Object Identifier: 10.1038/s41467-022-33500-9Best OA location URL: https://escholarship.org/uc/item/7p7865xxCitation Count: 73
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OPENTitle: DNA Sequence Analysis for Brain Disorder Using Deep Learning and Secure StorageJournal Name: Computers, Materials & ContinuaPublisher: Tech Science PressVol: 71Issue #: 3Start Page: 5949End Page: 5962Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.32604/cmc.2022.022028Best OA location URL: https://www.techscience.com/cmc/v71n3/46465/pdfCitation Count: 5
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OPENTitle: The genetic regulation of protein expression in cerebrospinal fluidJournal Name: EMBO Molecular MedicinePublisher: Springer Science and Business Media LLCVol: 15Issue #: 1Start Page:End Page:Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.15252/emmm.202216359Best OA location URL: https://onlinelibrary.wiley.com/doi/pdfdirect/10.15252/emmm.202216359Citation Count: 35