7391 - 7400 of 9140 Results
Title
Year
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OPENTitle: Randomized controlled trial of intermittent hypoxia in Parkinson’s disease: study rationale and protocolJournal Name: BMC NeurologyPublisher: Springer Science and Business Media LLCVol: 24Issue #: 1Start Page: 212End Page: 212Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.1186/s12883-024-03702-3Best OA location URL: https://doi.org/10.1186/s12883-024-03702-3Citation Count: 7
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OPENTitle: Plasma extracellular vesicle tau and TDP-43 as diagnostic biomarkers in FTD and ALSJournal Name: Nature MedicinePublisher: Springer Science and Business Media LLCVol: 30Issue #: 6Start Page: 1771End Page: 1783Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.1038/s41591-024-02937-4Best OA location URL: https://doi.org/10.1038/s41591-024-02937-4Citation Count: 185
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OPENTitle: The hexosamine biosynthetic pathway rescues lysosomal dysfunction in Parkinson’s disease patient iPSC derived midbrain neuronsJournal Name: Nature CommunicationsPublisher: Springer Science and Business Media LLCVol: 15Issue #: 1Start Page: 5206End Page: 5206Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.1038/s41467-024-49256-3Best OA location URL: https://doi.org/10.1038/s41467-024-49256-3Citation Count: 14
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OPENTitle: Mitochondrial DNA Instability Supersedes Parkin Mutations in Driving Mitochondrial Proteomic Alterations and Functional Deficits in Polg Mutator MiceJournal Name: International Journal of Molecular SciencesPublisher: MDPI AGVol: 25Issue #: 12Start Page: 6441End Page: 6441Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.3390/ijms25126441Best OA location URL: https://doi.org/10.3390/ijms25126441Citation Count: 5
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OPENTitle: Prediction of motor and non-motor Parkinson’s disease symptoms using serum lipidomics and machine learning: a 2-year studyJournal Name: npj Parkinson's DiseasePublisher: Springer Science and Business Media LLCVol: 10Issue #: 1Start Page: 123End Page: 123Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.1038/s41531-024-00741-yBest OA location URL: https://doi.org/10.1038/s41531-024-00741-yCitation Count: 13
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OPENTitle: Neuroprotective Strategies and Cell-Based Biomarkers for Manganese-Induced Toxicity in Human Neuroblastoma (SH-SY5Y) CellsJournal Name: BiomoleculesPublisher: MDPI AGVol: 14Issue #: 6Start Page: 647End Page: 647Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.3390/biom14060647Best OA location URL: https://www.mdpi.com/2218-273X/14/6/647/pdf?version=1717136963Citation Count: 8
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OPENTitle: Increased mean diffusivity of the caudal motor SNc identifies patients with REM sleep behaviour disorder and Parkinson’s diseaseJournal Name: npj Parkinson's DiseasePublisher: Springer Science and Business Media LLCVol: 10Issue #: 1Start Page: 128End Page: 128Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.1038/s41531-024-00731-0Best OA location URL: http://dx.doi.org/10.1038/s41531-024-00731-0Citation Count: 1
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OPENTitle: Detection of mosaic and population-level structural variants with Sniffles2Journal Name: Nature BiotechnologyPublisher: Springer Science and Business Media LLCVol: 42Issue #: 10Start Page: 1571End Page: 1580Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.1038/s41587-023-02024-yBest OA location URL: https://www.nature.com/articles/s41587-023-02024-y.pdfCitation Count: 439
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OPENTitle: Genome sequence analyses identify novel risk loci for multiple system atrophyJournal Name: NeuronPublisher: Elsevier BVVol: 112Issue #: 13Start Page: 2142End Page: 2156.e5Publication Date:Open Access(OA) Status: OPENLicense: cc-by-nc-nd, cc-by-nc-ndDOI - Digital Object Identifier: 10.1016/j.neuron.2024.04.002Best OA location URL: http://www.cell.com/article/S089662732400240X/pdfCitation Count: 43
- RTN2 deficiency results in an autosomal recessive distal motor neuropathy with lower limb spasticity2024OPENTitle: RTN2 deficiency results in an autosomal recessive distal motor neuropathy with lower limb spasticityJournal Name: BrainPublisher: Oxford University Press (OUP)Vol: 147Issue #: 7Start Page: 2334End Page: 2343Publication Date:Open Access(OA) Status: OPENLicense: cc-by, cc-byDOI - Digital Object Identifier: 10.1093/brain/awae091Best OA location URL: https://academic.oup.com/brain/advance-article-pdf/doi/10.1093/brain/awae091/57089091/awae091.pdfCitation Count: 8