4831 - 4840 of 7877 Results
Title
Year
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RESTRICTEDTitle: Knowledge and attitudes of Parkinson’s disease risk in the Gaucher populationJournal Name: Journal of Genetic CounselingPublisher: WileyVol: 29Issue #: 1Start Page: 105End Page: 111Publication Date:Open Access(OA) Status: RESTRICTEDLicense:DOI - Digital Object Identifier: 10.1002/jgc4.1185Citation Count: 7
- Parkinson's Disease: Glucocerebrosidase 1 Mutation Severity Is Associated with CSF Alpha‐Synuclein Profiles2019RESTRICTEDTitle: Parkinson's Disease: Glucocerebrosidase 1 Mutation Severity Is Associated with CSF Alpha‐Synuclein ProfilesJournal Name: Movement DisordersPublisher: WileyVol: 35Issue #: 3Start Page: 495End Page: 499Publication Date:Open Access(OA) Status: RESTRICTEDLicense:DOI - Digital Object Identifier: 10.1002/mds.27884Citation Count: 36
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OPENTitle: PPM1H phosphatase counteracts LRRK2 signaling by selectively dephosphorylating Rab proteinsJournal Name: eLifePublisher: eLife Sciences Publications, LtdVol: 8Issue #:Start Page:End Page:Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.7554/elife.50416Best OA location URL: https://doi.org/10.7554/elife.50416Citation Count: 111
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RESTRICTEDTitle: Pathological Influences on Clinical Heterogeneity in Lewy Body DiseasesJournal Name: Movement DisordersPublisher: WileyVol: 35Issue #: 1Start Page: 5End Page: 19Publication Date:Open Access(OA) Status: RESTRICTEDLicense:DOI - Digital Object Identifier: 10.1002/mds.27867Best OA location URL: https://europepmc.org/articles/pmc7233798?pdf=renderCitation Count: 61
- The Genetic Architecture of Parkinson Disease in Spain: Characterizing Population‐Specific Risk, Differential Haplotype Structures, and Providing Etiologic Insight2019OPENTitle: The Genetic Architecture of Parkinson Disease in Spain: Characterizing Population‐Specific Risk, Differential Haplotype Structures, and Providing Etiologic InsightJournal Name: Movement DisordersPublisher: WileyVol: 34Issue #: 12Start Page: 1851End Page: 1863Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1002/mds.27864Best OA location URL: https://europepmc.org/articles/pmc8393828?pdf=renderCitation Count: 53
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OPENTitle: Distinct tau PET patterns in atrophy‐defined subtypes of Alzheimer's diseaseJournal Name: Alzheimer's & DementiaPublisher: WileyVol: 16Issue #: 2Start Page: 335End Page: 344Publication Date:Open Access(OA) Status: OPENLicense: cc-by-nc-ndDOI - Digital Object Identifier: 10.1016/j.jalz.2019.08.201Best OA location URL: https://doi.org/10.1016/j.jalz.2019.08.201Citation Count: 86
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RESTRICTEDTitle: Genetic, Structural, and Functional Evidence Link TMEM175 to SynucleinopathiesJournal Name: Annals of NeurologyPublisher: WileyVol: 87Issue #: 1Start Page: 139End Page: 153Publication Date:Open Access(OA) Status: RESTRICTEDLicense:DOI - Digital Object Identifier: 10.1002/ana.25629Citation Count: 81
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OPENTitle: Gender Differences in Functional Movement DisordersJournal Name: Movement Disorders Clinical PracticePublisher: WileyVol: 7Issue #: 2Start Page: 182End Page: 187Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1002/mdc3.12864Best OA location URL: https://movementdisorders.onlinelibrary.wiley.com/doi/pdfdirect/10.1002/mdc3.12864Citation Count: 45
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RESTRICTEDTitle: Autophagic- and Lysosomal-Related Biomarkers for Parkinson’s Disease: Lights and ShadowsJournal Name: CellsPublisher: MDPI AGVol: 8Issue #: 11Start Page: 1317End Page: 1317Publication Date:Open Access(OA) Status: RESTRICTEDLicense: cc-byDOI - Digital Object Identifier: 10.3390/cells8111317Best OA location URL: https://www.mdpi.com/2073-4409/8/11/1317/pdf?version=1571996609Citation Count: 23
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RESTRICTEDTitle: Driving genotype treatment options down the right path(way)Journal Name: Movement DisordersPublisher: WileyVol: 34Issue #: 12Start Page: 1811End Page: 1813Publication Date:Open Access(OA) Status: RESTRICTEDLicense:DOI - Digital Object Identifier: 10.1002/mds.27893Citation Count: 1