4631 - 4640 of 9016 Results
Title
Year
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OPENTitle: S-Nitrosylation of PINK1 Attenuates PINK1/Parkin-Dependent Mitophagy in hiPSC-Based Parkinson’s Disease ModelsJournal Name: Cell ReportsPublisher: Elsevier BVVol: 21Issue #: 8Start Page: 2171End Page: 2182Publication Date:Open Access(OA) Status: OPENLicense: cc-by-nc-ndDOI - Digital Object Identifier: 10.1016/j.celrep.2017.10.068Best OA location URL: http://www.cell.com/article/S2211124717315310/pdfCitation Count: 127
- NILO-PD: A Phase 2A Study of Nilotinib in Patients with Advanced and Early Parkinson’s Disease: Study Design and Status Update (P3.8-035)2019RESTRICTEDTitle: NILO-PD: A Phase 2A Study of Nilotinib in Patients with Advanced and Early Parkinson’s Disease: Study Design and Status Update (P3.8-035)Journal Name: NeurologyPublisher: Ovid Technologies (Wolters Kluwer Health)Vol: 92Issue #: 15_supplementStart Page:End Page:Publication Date:Open Access(OA) Status: RESTRICTEDLicense:DOI - Digital Object Identifier: 10.1212/wnl.92.15_supplement.p3.8-035Citation Count: 2
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OPENTitle: Brain volumetric deficits in MAPT mutation carriers: a multisite studyJournal Name: Annals of Clinical and Translational NeurologyPublisher: WileyVol: 8Issue #: 1Start Page: 95End Page: 110Publication Date:Open Access(OA) Status: OPENLicense: cc-by-nc-ndDOI - Digital Object Identifier: 10.1002/acn3.51249Best OA location URL: https://onlinelibrary.wiley.com/doi/pdfdirect/10.1002/acn3.51249Citation Count: 35
- Heartbeat signature for predicting motor and non-motor involvement among nonparkinsonian LRRK2 G2019S mutation carriers2025RESTRICTEDTitle: Heartbeat signature for predicting motor and non-motor involvement among nonparkinsonian LRRK2 G2019S mutation carriersJournal Name: Clinical Autonomic ResearchPublisher: Springer Science and Business Media LLCVol: 35Issue #: 3Start Page: 407End Page: 419Publication Date:Open Access(OA) Status: RESTRICTEDLicense:DOI - Digital Object Identifier: 10.1007/s10286-024-01104-6Citation Count: 0
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OPENTitle: Genome‐Wide Analysis of Structural Variants in Parkinson DiseaseJournal Name: Annals of NeurologyPublisher: WileyVol: 93Issue #: 5Start Page: 1012End Page: 1022Publication Date:Open Access(OA) Status: OPENLicense: cc-by-ncDOI - Digital Object Identifier: 10.1002/ana.26608Best OA location URL: https://onlinelibrary.wiley.com/doi/pdfdirect/10.1002/ana.26608Citation Count: 37
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OPENTitle: Breakthrough News in Adenoviral Vector‐Mediated AADC Gene Therapy: Lessons from the Success in AADC Deficiency and Possible Future ApplicationsJournal Name: Movement Disorders Clinical PracticePublisher: WileyVol: 9Issue #: 6Start Page: 737End Page: 738Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1002/mdc3.13503Best OA location URL: https://www.ncbi.nlm.nih.gov/pmc/articles/9346230Citation Count: 1
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OPENTitle: Autonomic dysfunction is associated with neuropsychological impairment in Lewy body diseaseJournal Name: Journal of NeurologyPublisher: Springer Science and Business Media LLCVol: 267Issue #: 7Start Page: 1941End Page: 1951Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1007/s00415-020-09783-7Best OA location URL: http://hdl.handle.net/10810/65454Citation Count: 29
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OPENTitle: Cryogel microcarriers loaded with glial cell line-derived neurotrophic factor enhance the engraftment of primary dopaminergic neurons in a rat model of Parkinson’s diseaseJournal Name: Journal of Neural EngineeringPublisher: IOP PublishingVol: 21Issue #: 5Start Page: 056011End Page: 056011Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.1088/1741-2552/ad7761Best OA location URL: https://doi.org/10.1088/1741-2552/ad7761Citation Count: 2
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OPENTitle: External delay and dispersion correction of automatically sampled arterial blood with dual flow ratesJournal Name: Biomedical Physics & Engineering ExpressPublisher: IOP PublishingVol: 11Issue #: 2Start Page: 025021End Page: 025021Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.1088/2057-1976/adae13Best OA location URL: https://doi.org/10.1088/2057-1976/adae13Citation Count: 2
- Increased substantia nigra echogenicity in LRRK2 family members without mutations2018RESTRICTEDTitle: Increased substantia nigra echogenicity in LRRK2 family members without mutationsJournal Name: Movement DisordersPublisher: WileyVol: 33Issue #: 9Start Page: 1504End Page: 1505Publication Date:Open Access(OA) Status: RESTRICTEDLicense:DOI - Digital Object Identifier: 10.1002/mds.27443Citation Count: 2