3371 - 3380 of 8404 Results
Title
Year
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OPENTitle: A Genetic Study of Cerebral Atherosclerosis Reveals Novel Associations with NTNG1 and CNOT3Journal Name: GenesPublisher: MDPI AGVol: 12Issue #: 6Start Page: 815End Page: 815Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.3390/genes12060815Best OA location URL: https://www.mdpi.com/2073-4425/12/6/815/pdf?version=1622161911Citation Count: 6
- Randomized Sham-Controlled Pilot Study of Neurocardiac Function in Patients With Acute Ischaemic Stroke Undergoing Heart Rate Variability Biofeedback2021OPENTitle: Randomized Sham-Controlled Pilot Study of Neurocardiac Function in Patients With Acute Ischaemic Stroke Undergoing Heart Rate Variability BiofeedbackJournal Name: Frontiers in NeurologyPublisher: Frontiers Media SAVol: 12Issue #:Start Page:End Page:Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.3389/fneur.2021.669843Best OA location URL: https://www.frontiersin.org/articles/10.3389/fneur.2021.669843/pdfCitation Count: 12
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OPENTitle: Swarm Learning for decentralized and confidential clinical machine learningJournal Name: NaturePublisher: Springer Science and Business Media LLCVol: 594Issue #: 7862Start Page: 265End Page: 270Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.1038/s41586-021-03583-3Best OA location URL: https://www.nature.com/articles/s41586-021-03583-3.pdfCitation Count: 610
- An update on the neurological short tandem repeat expansion disorders and the emergence of long-read sequencing diagnostics2021RESTRICTEDTitle: An update on the neurological short tandem repeat expansion disorders and the emergence of long-read sequencing diagnosticsJournal Name: Acta Neuropathologica CommunicationsPublisher: Springer Science and Business Media LLCVol: 9Issue #: 1Start Page:End Page:Publication Date:Open Access(OA) Status: RESTRICTEDLicense: cc-byDOI - Digital Object Identifier: 10.1186/s40478-021-01201-xBest OA location URL: https://actaneurocomms.biomedcentral.com/track/pdf/10.1186/s40478-021-01201-xCitation Count: 87
- Associations Between Amyloid and Tau Pathology, and Connectome Alterations, in Alzheimer’s Disease and Mild Cognitive Impairment2021RESTRICTEDTitle: Associations Between Amyloid and Tau Pathology, and Connectome Alterations, in Alzheimer’s Disease and Mild Cognitive ImpairmentJournal Name: Journal of Alzheimer's DiseasePublisher: SAGE PublicationsVol: 82Issue #: 2Start Page: 541End Page: 560Publication Date:Open Access(OA) Status: RESTRICTEDLicense:DOI - Digital Object Identifier: 10.3233/jad-201457Citation Count: 23
- Reference SVA insertion polymorphisms are associated with Parkinson’s Disease progression and differential gene expression2021OPENTitle: Reference SVA insertion polymorphisms are associated with Parkinson’s Disease progression and differential gene expressionJournal Name: npj Parkinson's DiseasePublisher: Springer Science and Business Media LLCVol: 7Issue #: 1Start Page:End Page:Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.1038/s41531-021-00189-4Best OA location URL: https://www.nature.com/articles/s41531-021-00189-4.pdfCitation Count: 34
- Predicting optimal deep brain stimulation parameters for Parkinson’s disease using functional MRI and machine learning2021OPENTitle: Predicting optimal deep brain stimulation parameters for Parkinson’s disease using functional MRI and machine learningJournal Name: Nature CommunicationsPublisher: Springer Science and Business Media LLCVol: 12Issue #: 1Start Page:End Page:Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.1038/s41467-021-23311-9Best OA location URL: https://www.nature.com/articles/s41467-021-23311-9.pdfCitation Count: 210
- A clinical, molecular genetics and pathological study of a FTDP-17 family with a heterozygous splicing variant c.823-10G>T at the intron 9/exon 10 of the MAPT gene2021OPENTitle: A clinical, molecular genetics and pathological study of a FTDP-17 family with a heterozygous splicing variant c.823-10G>T at the intron 9/exon 10 of the MAPT geneJournal Name: Neurobiology of AgingPublisher: Elsevier BVVol: 106Issue #:Start Page: 343.e1End Page: 343.e8Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.1016/j.neurobiolaging.2021.05.010Best OA location URL: https://doi.org/10.1016/j.neurobiolaging.2021.05.010Citation Count: 6
- Disruptions of neurological services, its causes and mitigation strategies during COVID-19: a global review2021RESTRICTEDTitle: Disruptions of neurological services, its causes and mitigation strategies during COVID-19: a global reviewJournal Name: Journal of NeurologyPublisher: Springer Science and Business Media LLCVol: 268Issue #: 11Start Page: 3947End Page: 3960Publication Date:Open Access(OA) Status: RESTRICTEDLicense: cc-byDOI - Digital Object Identifier: 10.1007/s00415-021-10588-5Best OA location URL: https://link.springer.com/content/pdf/10.1007/s00415-021-10588-5.pdfCitation Count: 28
- Effects of Gocovri (Amantadine) Extended-Release Capsules on Motor Aspects of Experiences of Daily Living in People with Parkinson’s Disease and Dyskinesia2021OPENTitle: Effects of Gocovri (Amantadine) Extended-Release Capsules on Motor Aspects of Experiences of Daily Living in People with Parkinson’s Disease and DyskinesiaJournal Name: Neurology and TherapyPublisher: Springer Science and Business Media LLCVol: 10Issue #: 2Start Page: 739End Page: 751Publication Date:Open Access(OA) Status: OPENLicense: cc-by-ncDOI - Digital Object Identifier: 10.1007/s40120-021-00256-1Best OA location URL: https://link.springer.com/content/pdf/10.1007/s40120-021-00256-1.pdfCitation Count: 11