1811 - 1820 of 8620 Results
Title
Year
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OPENTitle: KMT2B-related disorders: expansion of the phenotypic spectrum and long-term efficacy of deep brain stimulationJournal Name: BrainPublisher: Oxford University Press (OUP)Vol: 143Issue #: 11Start Page: 3242End Page: 3261Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1093/brain/awaa304Best OA location URL: https://academic.oup.com/brain/article-pdf/143/11/3242/36134972/awaa304.pdfCitation Count: 86
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OPENTitle: Microglial exosomes facilitate α-synuclein transmission in Parkinson’s diseaseJournal Name: BrainPublisher: Oxford University Press (OUP)Vol: 143Issue #: 5Start Page: 1476End Page: 1497Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1093/brain/awaa090Best OA location URL: https://academic.oup.com/brain/article-pdf/143/5/1476/33281811/awaa090.pdfCitation Count: 389
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OPENTitle: RFC1 expansions can mimic hereditary sensory neuropathy with cough and Sjögren syndromeJournal Name: BrainPublisher: Oxford University Press (OUP)Vol: 143Issue #: 10Start Page: e82End Page: e82Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1093/brain/awaa244Best OA location URL: https://academic.oup.com/brain/article-pdf/143/10/e82/34032248/awaa244.pdfCitation Count: 30
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RESTRICTEDTitle: Clinical spectrum of the pentanucleotide repeat expansion in the RFC1 gene in ataxia syndromesJournal Name: NeurologyPublisher: Ovid Technologies (Wolters Kluwer Health)Vol: 95Issue #: 21Start Page:End Page:Publication Date:Open Access(OA) Status: RESTRICTEDLicense:DOI - Digital Object Identifier: 10.1212/wnl.0000000000010744Citation Count: 40
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OPENTitle: Association of transient orthostatic hypotension with falls and syncope in patients with Parkinson diseaseJournal Name: NeurologyPublisher: Ovid Technologies (Wolters Kluwer Health)Vol: 95Issue #: 21Start Page:End Page:Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1212/wnl.0000000000010749Best OA location URL: https://www.ncbi.nlm.nih.gov/pmc/articles/7734734Citation Count: 40
- Disease progression and prognostic factors in multiple system atrophy: A prospective cohort study2020OPENTitle: Disease progression and prognostic factors in multiple system atrophy: A prospective cohort studyJournal Name: Neurobiology of DiseasePublisher: Elsevier BVVol: 139Issue #:Start Page: 104813End Page: 104813Publication Date:Open Access(OA) Status: OPENLicense: cc-by-nc-ndDOI - Digital Object Identifier: 10.1016/j.nbd.2020.104813Best OA location URL: https://www.sciencedirect.com/science/article/am/pii/S0969996120300887?via%3DihubCitation Count: 66
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OPENTitle: Neural connectivity predicts spreading of alpha-synuclein pathology in fibril-injected mouse models: Involvement of retrograde and anterograde axonal propagationJournal Name: Neurobiology of DiseasePublisher: Elsevier BVVol: 134Issue #:Start Page: 104623End Page: 104623Publication Date:Open Access(OA) Status: OPENLicense: cc-by-nc-ndDOI - Digital Object Identifier: 10.1016/j.nbd.2019.104623Best OA location URL: https://www.sciencedirect.com/science/article/pii/S0969996119302980?via%3DihubCitation Count: 74
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OPENTitle: Cerebrospinal fluid ceruloplasmin levels predict cognitive decline and brain atrophy in people with underlying β-amyloid pathologyJournal Name: Neurobiology of DiseasePublisher: Elsevier BVVol: 139Issue #:Start Page: 104810End Page: 104810Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.1016/j.nbd.2020.104810Best OA location URL: https://doi.org/10.1016/j.nbd.2020.104810Citation Count: 35
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OPENTitle: Artificial intelligence within the interplay between natural and artificial computation: Advances in data science, trends and applicationsJournal Name: NeurocomputingPublisher: Elsevier BVVol: 410Issue #:Start Page: 237End Page: 270Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1016/j.neucom.2020.05.078Best OA location URL: https://www.sciencedirect.com/science/article/am/pii/S0925231220309292Citation Count: 240
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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: 5