5871 - 5880 of 6568 Results
Title
Year
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OPENTitle: Passive Monitoring of Parkinson Tremor in Daily Life: A Prototypical Network ApproachJournal Name: SensorsPublisher: MDPI AGVol: 25Issue #: 2Start Page: 366End Page: 366Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.3390/s25020366Best OA location URL: https://www.mdpi.com/1424-8220/25/2/366/pdf?version=1736439033Citation Count: 6
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OPENTitle: Functionally active modulators targeting the LRRK2 WD40 repeat domain identified by FRASE-bot in CACHE Challenge #1Journal Name: Chemical SciencePublisher: Royal Society of Chemistry (RSC)Vol: 16Issue #: 8Start Page: 3430End Page: 3439Publication Date:Open Access(OA) Status: OPENLicense: cc-by-ncDOI - Digital Object Identifier: 10.1039/d4sc07532cBest OA location URL: https://pubs.rsc.org/en/content/articlepdf/2025/sc/d4sc07532cCitation Count: 4
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OPENTitle: Association between serum sodium and sporadic Parkinson’s diseaseJournal Name: Frontiers in NeurosciencePublisher: Frontiers Media SAVol: 19Issue #:Start Page: 1555831End Page: 1555831Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.3389/fnins.2025.1555831Best OA location URL: https://www.frontiersin.org/journals/neuroscience/articles/10.3389/fnins.2025.1555831/pdfCitation Count: 2
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OPENTitle: Tet2 loss and enhanced ciliogenesis suppress α-synuclein pathologyJournal Name: Acta Neuropathologica CommunicationsPublisher: Springer Science and Business Media LLCVol: 13Issue #: 1Start Page: 71End Page: 71Publication Date:Open Access(OA) Status: OPENLicense: cc-by-nc-ndDOI - Digital Object Identifier: 10.1186/s40478-025-01988-zBest OA location URL: https://actaneurocomms.biomedcentral.com/counter/pdf/10.1186/s40478-025-01988-zCitation Count: 5
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OPENTitle: Application of new biologic disease criteria for synucleinopathies to the systemic synuclein sampling study cohortJournal Name: npj Parkinson's DiseasePublisher: Springer Science and Business Media LLCVol: 11Issue #: 1Start Page: 69End Page: 69Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.1038/s41531-025-00919-yBest OA location URL: https://www.nature.com/articles/s41531-025-00919-y.pdfCitation Count: 1
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OPENTitle: Structural pathway for PI3-kinase regulation by VPS15 in autophagyJournal Name: SciencePublisher: American Association for the Advancement of Science (AAAS)Vol:Issue #:Start Page: eadl3787End Page: eadl3787Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.1126/science.adl3787Best OA location URL: https://doi.org/10.1126/science.adl3787Citation Count: 29
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OPENTitle: GRAMD1B is a regulator of lipid homeostasis, autophagic flux and phosphorylated tauJournal Name: Nature CommunicationsPublisher: Springer Science and Business Media LLCVol: 16Issue #: 1Start Page: 3312End Page: 3312Publication Date:Open Access(OA) Status: OPENLicense: cc-by-nc-ndDOI - Digital Object Identifier: 10.1038/s41467-025-58585-wBest OA location URL: https://www.nature.com/articles/s41467-025-58585-w.pdfCitation Count: 7
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OPENTitle: Somatic instability of the FGF14 -SCA27B GAA•TTC repeat reveals a marked expansion bias in the cerebellumJournal Name: BrainPublisher: Oxford University Press (OUP)Vol: 148Issue #: 4Start Page: 1258End Page: 1270Publication Date:Open Access(OA) Status: OPENLicense: cc-by, cc-byDOI - Digital Object Identifier: 10.1093/brain/awae312Best OA location URL: https://academic.oup.com/brain/advance-article-pdf/doi/10.1093/brain/awae312/59644388/awae312.pdfCitation Count: 16
- Elevated cholesterol is a common phenotype for dominant and recessive ATAD3- associated disorders2024OPENTitle: Elevated cholesterol is a common phenotype for dominant and recessive ATAD3- associated disordersJournal Name: BrainPublisher: Oxford University Press (OUP)Vol: 148Issue #: 4Start Page: e24End Page: e28Publication Date:Open Access(OA) Status: OPENLicense: cc-by-ncDOI - Digital Object Identifier: 10.1093/brain/awae402Best OA location URL: https://academic.oup.com/brain/advance-article-pdf/doi/10.1093/brain/awae402/61091141/awae402.pdfCitation Count: 2
- Clinical and genetic characterization of a progressive RBL2-associated neurodevelopmental disorder2024OPENTitle: Clinical and genetic characterization of a progressive RBL2-associated neurodevelopmental disorderJournal Name: BrainPublisher: Oxford University Press (OUP)Vol: 148Issue #: 4Start Page: 1194End Page: 1211Publication Date:Open Access(OA) Status: OPENLicense: cc-by, cc-byDOI - Digital Object Identifier: 10.1093/brain/awae363Best OA location URL: https://academic.oup.com/brain/advance-article-pdf/doi/10.1093/brain/awae363/61226784/awae363.pdfCitation Count: 1