1581 - 1590 of 9145 Results
Title
Year
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OPENTitle: Variable number tandem repeats – Their emerging role in sickness and healthJournal Name: Experimental Biology and MedicinePublisher: Frontiers Media SAVol: 246Issue #: 12Start Page: 1368End Page: 1376Publication Date:Open Access(OA) Status: OPENLicense: cc-by, cc-byDOI - Digital Object Identifier: 10.1177/15353702211003511Best OA location URL: https://doi.org/10.1177/15353702211003511Citation Count: 28
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OPENTitle: Loss‐of‐Function Variants in HOPS Complex Genes VPS16 and VPS41 Cause Early Onset Dystonia Associated with Lysosomal AbnormalitiesJournal Name: Annals of NeurologyPublisher: WileyVol: 88Issue #: 5Start Page: 867End Page: 877Publication Date:Open Access(OA) Status: OPENLicense: cc-by, cc-byDOI - Digital Object Identifier: 10.1002/ana.25879Best OA location URL: https://onlinelibrary.wiley.com/doi/pdfdirect/10.1002/ana.25879Citation Count: 110
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OPENTitle: Tossing and Turning in Bed: Nocturnal Movements in Parkinson's DiseaseJournal Name: Movement DisordersPublisher: WileyVol: 35Issue #: 6Start Page: 959End Page: 968Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1002/mds.28006Best OA location URL: https://onlinelibrary.wiley.com/doi/pdfdirect/10.1002/mds.28006Citation Count: 63
- Genetic determinants of survival in progressive supranuclear palsy: a genome-wide association study2020OPENTitle: Genetic determinants of survival in progressive supranuclear palsy: a genome-wide association studyJournal Name: The Lancet NeurologyPublisher: Elsevier BVVol: 20Issue #: 2Start Page: 107End Page: 116Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1016/s1474-4422(20)30394-xBest OA location URL: http://hdl.handle.net/10044/1/85602Citation Count: 120
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OPENTitle: Fibrillation and molecular characteristics are coherent with clinical and pathological features of 4-repeat tauopathy caused by MAPT variant G273RJournal Name: Neurobiology of DiseasePublisher: Elsevier BVVol: 146Issue #:Start Page: 105079End Page: 105079Publication Date:Open Access(OA) Status: OPENLicense: cc-by, cc-byDOI - Digital Object Identifier: 10.1016/j.nbd.2020.105079Best OA location URL: https://doi.org/10.1016/j.nbd.2020.105079Citation Count: 8
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OPENTitle: North American survey on impact of the COVID-19 pandemic shutdown on DBS careJournal Name: Parkinsonism & Related DisordersPublisher: Elsevier BVVol: 92Issue #:Start Page: 41End Page: 45Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1016/j.parkreldis.2021.10.011Best OA location URL: http://www.prd-journal.com/article/S1353802021003667/pdfCitation Count: 9
- Apolipoprotein E ε4 genotype and risk of freezing of gait in Parkinson's disease2020RESTRICTEDTitle: Apolipoprotein E ε4 genotype and risk of freezing of gait in Parkinson's diseaseJournal Name: Parkinsonism & Related DisordersPublisher: Elsevier BVVol: 81Issue #:Start Page: 173End Page: 178Publication Date:Open Access(OA) Status: RESTRICTEDLicense:DOI - Digital Object Identifier: 10.1016/j.parkreldis.2020.10.033Citation Count: 21
- REM sleep behavior disorder in early Parkinson’s disease predicts the rapid dopaminergic denervation2020OPENTitle: REM sleep behavior disorder in early Parkinson’s disease predicts the rapid dopaminergic denervationJournal Name: Parkinsonism & Related DisordersPublisher: Elsevier BVVol: 80Issue #:Start Page: 120End Page: 126Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1016/j.parkreldis.2020.09.032Best OA location URL: https://www.sciencedirect.com/science/article/pii/S1353802020307628Citation Count: 20
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OPENTitle: A novel approach to study markers of dopamine signaling in peripheral immune cellsJournal Name: Journal of Immunological MethodsPublisher: Elsevier BVVol: 476Issue #:Start Page: 112686End Page: 112686Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1016/j.jim.2019.112686Best OA location URL: https://www.ncbi.nlm.nih.gov/pmc/articles/6939127Citation Count: 23
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OPENTitle: Assessing the relationship between monoallelic PRKN mutations and Parkinson’s riskJournal Name: Human Molecular GeneticsPublisher: Oxford University Press (OUP)Vol: 30Issue #: 1Start Page: 78End Page: 86Publication Date:Open Access(OA) Status: OPENLicense: cc-by, cc-byDOI - Digital Object Identifier: 10.1093/hmg/ddaa273Best OA location URL: https://academic.oup.com/hmg/article-pdf/30/1/78/36989224/ddaa273.pdfCitation Count: 62