3251 - 3260 of 9156 Results
Title
Year
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OPENTitle: Proteomic Exploration of L1CAM+-Extracellular Vesicles from Plasma of Manifest and Prodromal Parkinson’s DiseaseJournal Name: International Journal of Molecular SciencesPublisher: MDPI AGVol: 26Issue #: 23Start Page: 11564End Page: 11564Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.3390/ijms262311564Best OA location URL: https://www.mdpi.com/1422-0067/26/23/11564/pdf?version=1764581678Citation Count: 1
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OPENTitle: Cerebral white matter rarefaction has both neurodegenerative and vascular causes and may primarily be a distal axonopathyJournal Name: Journal of Neuropathology & Experimental NeurologyPublisher: Oxford University Press (OUP)Vol: 82Issue #: 6Start Page: 457End Page: 466Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1093/jnen/nlad026Best OA location URL: https://pmc.ncbi.nlm.nih.gov/articles/PMC10209646/pdf/nlad026.pdfCitation Count: 24
- Neural correlates of executive functions in healthy G2019S LRRK2 mutation carriers2013RESTRICTEDTitle: Neural correlates of executive functions in healthy G2019S LRRK2 mutation carriersJournal Name: CortexPublisher: Elsevier BVVol: 49Issue #: 9Start Page: 2501End Page: 2511Publication Date:Open Access(OA) Status: RESTRICTEDLicense:DOI - Digital Object Identifier: 10.1016/j.cortex.2012.12.017Citation Count: 45
- Teaching program for the Unified Dyskinesia Rating Scale2009RESTRICTEDTitle: Teaching program for the Unified Dyskinesia Rating ScaleJournal Name: Movement DisordersPublisher: WileyVol: 24Issue #: 9Start Page: 1296End Page: 1298Publication Date:Open Access(OA) Status: RESTRICTEDLicense:DOI - Digital Object Identifier: 10.1002/mds.22563Citation Count: 12
- Parkinson's disease and LRRK2: Frequency of a common mutation in U.S. movement disorder clinics2005RESTRICTEDTitle: Parkinson's disease and LRRK2: Frequency of a common mutation in U.S. movement disorder clinicsJournal Name: Movement DisordersPublisher: WileyVol: 21Issue #: 4Start Page: 519End Page: 23Publication Date:Open Access(OA) Status: RESTRICTEDLicense:DOI - Digital Object Identifier: 10.1002/mds.20751Citation Count: 0
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OPENTitle: A simulative deep learning model of SNP interactions on chromosome 19 for predicting Alzheimer's disease risk and rates of disease progressionJournal Name: Alzheimer's & DementiaPublisher: WileyVol: 19Issue #: 12Start Page: 5690End Page: 5699Publication Date:Open Access(OA) Status: OPENLicense: cc-by-nc-ndDOI - Digital Object Identifier: 10.1002/alz.13319Best OA location URL: https://onlinelibrary.wiley.com/doi/pdfdirect/10.1002/alz.13319Citation Count: 13
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OPENTitle: Genetic screening of a large series of North American sporadic and familial frontotemporal dementia casesJournal Name: Alzheimer's & DementiaPublisher: WileyVol: 16Issue #: 1Start Page: 118End Page: 130Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1002/alz.12011Best OA location URL: https://www.ncbi.nlm.nih.gov/pmc/articles/7199807Citation Count: 78
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OPENTitle: Identifying gait differences between Alzheimer's disease and dementia with Lewy bodies and their associations with regional amyloid depositionJournal Name: Alzheimer's & DementiaPublisher: WileyVol: 21Issue #: 2Start Page: e14351End Page: e14351Publication Date:Open Access(OA) Status: OPENLicense: cc-by-nc-ndDOI - Digital Object Identifier: 10.1002/alz.14351Best OA location URL: https://onlinelibrary.wiley.com/doi/pdfdirect/10.1002/alz.14351Citation Count: 5
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OPENTitle: Longitudinal characterization of clinical, developmental, and behavioral phenotypes in 101 children and adults with FOXG1 syndromeJournal Name: Journal of Neurodevelopmental DisordersPublisher: Springer Science and Business Media LLCVol: 17Issue #: 1Start Page: 64End Page: 64Publication Date:Open Access(OA) Status: OPENLicense: cc-by-nc-ndDOI - Digital Object Identifier: 10.1186/s11689-025-09653-1Best OA location URL: https://jneurodevdisorders.biomedcentral.com/counter/pdf/10.1186/s11689-025-09653-1Citation Count: 3
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OPENTitle: Internal tremor in people with Parkinson’s Disease: Demographic characteristics and comorbid symptomsJournal Name: Clinical Parkinsonism & Related DisordersPublisher: Elsevier BVVol: 9Issue #:Start Page: 100229End Page: 100229Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.1016/j.prdoa.2023.100229Best OA location URL: https://doi.org/10.1016/j.prdoa.2023.100229Citation Count: 0