2861 - 2870 of 8808 Results
Title
Year
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OPENTitle: Predicting Parkinson’s disease trajectory using clinical and functional MRI features: A reproduction and replication studyJournal Name: PLOS ONEPublisher: Public Library of Science (PLoS)Vol: 20Issue #: 2Start Page: e0317566End Page: e0317566Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.1371/journal.pone.0317566Best OA location URL: https://doi.org/10.1371/journal.pone.0317566Citation Count: 1
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RESTRICTEDTitle: Progressive loss of raphe nuclei serotonin transporter in early Parkinson's disease: A longitudinal 123I-FP-CIT SPECT studyJournal Name: Parkinsonism & Related DisordersPublisher: Elsevier BVVol: 77Issue #:Start Page: 170End Page: 175Publication Date:Open Access(OA) Status: RESTRICTEDLicense:DOI - Digital Object Identifier: 10.1016/j.parkreldis.2019.03.025Citation Count: 38
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OPENTitle: Ethnicity and Parkinson’s Disease: Motor and Nonmotor Features and Disease Progression in Latino Patients Living in Rural CaliforniaJournal Name: The Journals of Gerontology: Series APublisher: Oxford University Press (OUP)Vol: 78Issue #: 7Start Page: 1258End Page: 1268Publication Date:Open Access(OA) Status: OPENLicense: cc-by-nc-ndDOI - Digital Object Identifier: 10.1093/gerona/glad016Best OA location URL: https://academic.oup.com/biomedgerontology/advance-article-pdf/doi/10.1093/gerona/glad016/48724731/glad016.pdfCitation Count: 12
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RESTRICTEDTitle: Disease-modifying therapies for Parkinson's diseaseJournal Name: The Biomedical & Life Sciences CollectionPublisher: Henry Stewart TalksVol: 2013Issue #: 3Start Page:End Page:Publication Date:Open Access(OA) Status: RESTRICTEDLicense:DOI - Digital Object Identifier: 10.69645/krxj9755Citation Count: 0
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OPENTitle: Protocol for the DeFOG trial: A randomized controlled trial on the effects of smartphone-based, on-demand cueing for freezing of gait in Parkinson's diseaseJournal Name: Contemporary Clinical Trials CommunicationsPublisher: Elsevier BVVol: 24Issue #:Start Page: 100817End Page: 100817Publication Date:Open Access(OA) Status: OPENLicense: cc-by-nc-ndDOI - Digital Object Identifier: 10.1016/j.conctc.2021.100817Best OA location URL: https://doi.org/10.1016/j.conctc.2021.100817Citation Count: 20
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OPENTitle: Nucleolar PARP-1 Expression Is Decreased in Alzheimer’s Disease: Consequences for Epigenetic Regulation of rDNA and CognitionJournal Name: Neural PlasticityPublisher: WileyVol: 2016Issue #:Start Page: 1End Page: 9Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.1155/2016/8987928Best OA location URL: http://downloads.hindawi.com/journals/np/2016/8987928.pdfCitation Count: 49
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OPENTitle: Automated Quality Control for Sensor Based Symptom Measurement Performed Outside the LabJournal Name: SensorsPublisher: MDPI AGVol: 18Issue #: 4Start Page: 1215End Page: 1215Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.3390/s18041215Best OA location URL: https://www.mdpi.com/1424-8220/18/4/1215/pdf?version=1525348690Citation Count: 22
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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: 32
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OPENTitle: Profiling migraine patients according to clinical and psychophysical characteristics: clinical validity of distinct migraine clustersJournal Name: Neurological SciencesPublisher: Springer Science and Business Media LLCVol: 45Issue #: 3Start Page: 1185End Page: 1200Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.1007/s10072-023-07118-8Best OA location URL: https://link.springer.com/content/pdf/10.1007/s10072-023-07118-8.pdfCitation Count: 5
- Bi-allelic truncating variants in CASP2 underlie a neurodevelopmental disorder with lissencephaly2023OPENTitle: Bi-allelic truncating variants in CASP2 underlie a neurodevelopmental disorder with lissencephalyJournal Name: European Journal of Human GeneticsPublisher: Springer Science and Business Media LLCVol: 32Issue #: 1Start Page: 52End Page: 60Publication Date:Open Access(OA) Status: OPENLicense: cc-by, cc-byDOI - Digital Object Identifier: 10.1038/s41431-023-01461-2Best OA location URL: https://www.nature.com/articles/s41431-023-01461-2.pdfCitation Count: 9