3741 - 3750 of 6456 Results
Title
Year
-
OPENTitle: Dopamine genetic risk score predicts impulse control behaviors in Parkinson’s diseaseJournal Name: Clinical Parkinsonism & Related DisordersPublisher: Elsevier BVVol: 5Issue #:Start Page: 100113End Page: 100113Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.1016/j.prdoa.2021.100113Best OA location URL: https://doi.org/10.1016/j.prdoa.2021.100113Citation Count: 12
-
OPENTitle: Evaluating the Role of α‐Synuclein Seed Amplification as a Disease Progression Marker: Evidence and UncertaintiesJournal Name: Movement Disorders Clinical PracticePublisher: WileyVol: 13Issue #: 5Start Page: 1228End Page: 1235Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1002/mdc3.70434Best OA location URL: https://onlinelibrary.wiley.com/doi/pdfdirect/10.1002/mdc3.70434Citation Count: 0
-
OPENTitle: Association study of DNAJC13, UCHL1, HTRA2, GIGYF2, and EIF4G1 with Parkinson's diseaseJournal Name: Neurobiology of AgingPublisher: Elsevier BVVol: 100Issue #:Start Page: 119.e7End Page: 119.e13Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1016/j.neurobiolaging.2020.10.019Best OA location URL: https://www.ncbi.nlm.nih.gov/pmc/articles/7940813Citation Count: 44
-
OPENTitle: Different Circulating Trace Amine Profiles in De Novo and Treated Parkinson’s Disease PatientsJournal Name: Scientific ReportsPublisher: Springer Science and Business Media LLCVol: 9Issue #: 1Start Page: 6151End Page: 6151Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.1038/s41598-019-42535-wBest OA location URL: https://www.nature.com/articles/s41598-019-42535-w.pdfCitation Count: 48
-
OPENTitle: A functionalized hydroxydopamine quinone links thiol modification to neuronal cell deathJournal Name: Redox BiologyPublisher: Elsevier BVVol: 28Issue #:Start Page: 101377End Page: 101377Publication Date:Open Access(OA) Status: OPENLicense: cc-by-nc-ndDOI - Digital Object Identifier: 10.1016/j.redox.2019.101377Best OA location URL: https://doi.org/10.1016/j.redox.2019.101377Citation Count: 30
-
OPENTitle: Tetrabenazine‐induced acute dystonic reaction during the treatment of comorbid tics in a young woman with autism spectrum disorderJournal Name: Psychiatry and Clinical NeurosciencesPublisher: WileyVol: 78Issue #: 9Start Page: 558End Page: 559Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1111/pcn.13705Best OA location URL: https://onlinelibrary.wiley.com/doi/pdfdirect/10.1111/pcn.13705Citation Count: 1
- Factors in the disease severity of ATP1A3 mutations: Impairment, misfolding, and allele competition2019OPENTitle: Factors in the disease severity of ATP1A3 mutations: Impairment, misfolding, and allele competitionJournal Name: Neurobiology of DiseasePublisher: Elsevier BVVol: 132Issue #:Start Page: 104577End Page: 104577Publication Date:Open Access(OA) Status: OPENLicense: cc-by-nc-ndDOI - Digital Object Identifier: 10.1016/j.nbd.2019.104577Best OA location URL: https://doi.org/10.1016/j.nbd.2019.104577Citation Count: 45
-
OPENTitle: N-type Ca2+ channels mediate the stimuli-dependent α-synuclein secretion in mouse striatumJournal Name: npj Parkinson's DiseasePublisher: Springer Science and Business Media LLCVol: 11Issue #: 1Start Page: 276End Page: 276Publication Date:Open Access(OA) Status: OPENLicense: cc-by-nc-ndDOI - Digital Object Identifier: 10.1038/s41531-025-01110-zBest OA location URL: https://www.nature.com/articles/s41531-025-01110-z.pdfCitation Count: 0
-
OPENTitle: PathoFact: a pipeline for the prediction of virulence factors and antimicrobial resistance genes in metagenomic dataJournal Name: MicrobiomePublisher: Springer Science and Business Media LLCVol: 9Issue #: 1Start Page: 49End Page: 49Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.1186/s40168-020-00993-9Best OA location URL: https://microbiomejournal.biomedcentral.com/track/pdf/10.1186/s40168-020-00993-9Citation Count: 196
-
OPENTitle: Potential genetic modifiers of disease risk and age at onset in patients with frontotemporal lobar degeneration and GRN mutations: a genome-wide association studyJournal Name: The Lancet NeurologyPublisher: Elsevier BVVol: 17Issue #: 6Start Page: 548End Page: 558Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1016/s1474-4422(18)30126-1Best OA location URL: https://research.vumc.nl/en/publications/57d02919-2cda-42ec-b013-51bcf8175201Citation Count: 128