4781 - 4790 of 9145 Results
Title
Year
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OPENTitle: Motor and nonmotor symptoms in patients treated with 24-hour daily levodopa-carbidopa intestinal gel infusion: Analysis of the COmedication Study assessing Mono- and cOmbination therapy with levodopa-carbidopa inteStinal gel (COSMOS)Journal Name: Parkinsonism & Related DisordersPublisher: Elsevier BVVol: 105Issue #:Start Page: 139End Page: 144Publication Date:Open Access(OA) Status: OPENLicense: cc-by-nc-ndDOI - Digital Object Identifier: 10.1016/j.parkreldis.2022.08.002Best OA location URL: http://www.prd-journal.com/article/S1353802022002553/pdfCitation Count: 15
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OPENTitle: The LRRK2 Variant E193K Prevents Mitochondrial Fission Upon MPP+ Treatment by Altering LRRK2 Binding to DRP1Journal Name: Frontiers in Molecular NeurosciencePublisher: Frontiers Media SAVol: 11Issue #:Start Page: 64End Page: 64Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.3389/fnmol.2018.00064Best OA location URL: https://doi.org/10.3389/fnmol.2018.00064Citation Count: 38
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OPENTitle: Fine-Tuning ER Stress Signal Transducers to Treat Amyotrophic Lateral SclerosisJournal Name: Frontiers in Molecular NeurosciencePublisher: Frontiers Media SAVol: 10Issue #:Start Page: 216End Page: 216Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.3389/fnmol.2017.00216Best OA location URL: https://www.frontiersin.org/articles/10.3389/fnmol.2017.00216/pdfCitation Count: 29
- Transcriptome-wide Association Study in Frontotemporal Dementia Identifies New Disease Loci by In Silico Analysis2021RESTRICTEDTitle: Transcriptome-wide Association Study in Frontotemporal Dementia Identifies New Disease Loci by In Silico AnalysisJournal Name: Biological PsychiatryPublisher: Elsevier BVVol: 89Issue #: 8Start Page: e37End Page: e39Publication Date:Open Access(OA) Status: RESTRICTEDLicense:DOI - Digital Object Identifier: 10.1016/j.biopsych.2021.02.010Citation Count: 0
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OPENTitle: Identification of rare protein disulfide isomerase gene variants in amyotrophic lateral sclerosis patientsJournal Name: GenePublisher: Elsevier BVVol: 566Issue #: 2Start Page: 158End Page: 165Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1016/j.gene.2015.04.035Best OA location URL: http://doi.org/10.1016/j.gene.2015.04.035Citation Count: 78
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OPENTitle: Autoantibodies against α-synuclein inhibit its aggregation and cytotoxicityJournal Name: Journal of AutoimmunityPublisher: Elsevier BVVol: 152Issue #:Start Page: 103390End Page: 103390Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.1016/j.jaut.2025.103390Best OA location URL: https://doi.org/10.1016/j.jaut.2025.103390Citation Count: 7
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OPENTitle: Anodal tDCS modulates cortical activity and synchronization in Parkinson's disease depending on motor processingJournal Name: NeuroImage: ClinicalPublisher: Elsevier BVVol: 22Issue #:Start Page: 101689End Page: 101689Publication Date:Open Access(OA) Status: OPENLicense: cc-by-nc-ndDOI - Digital Object Identifier: 10.1016/j.nicl.2019.101689Best OA location URL: https://doi.org/10.1016/j.nicl.2019.101689Citation Count: 30
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OPENTitle: The Discovery of Central Nervous System Lymphatic Vessels: The Missing Link That Closes the Circle of Brain ImmunosurveillanceJournal Name: Movement Disorders Clinical PracticePublisher: WileyVol: 3Issue #: 1Start Page: 29End Page: 30Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1002/mdc3.12282Best OA location URL: https://onlinelibrary.wiley.com/doi/pdfdirect/10.1002/mdc3.12282Citation Count: 1
- End of life planning in parkinsonian diseases2019RESTRICTEDTitle: End of life planning in parkinsonian diseasesJournal Name: Parkinsonism & Related DisordersPublisher: Elsevier BVVol: 62Issue #:Start Page: 73End Page: 78Publication Date:Open Access(OA) Status: RESTRICTEDLicense:DOI - Digital Object Identifier: 10.1016/j.parkreldis.2019.01.026Citation Count: 10
- Clinical phenotype in carriers of intermediate alleles in the huntingtin gene2019RESTRICTEDTitle: Clinical phenotype in carriers of intermediate alleles in the huntingtin geneJournal Name: Journal of the Neurological SciencesPublisher: Elsevier BVVol: 402Issue #:Start Page: 57End Page: 61Publication Date:Open Access(OA) Status: RESTRICTEDLicense:DOI - Digital Object Identifier: 10.1016/j.jns.2019.05.010Citation Count: 33