5281 - 5290 of 8620 Results
Title
Year
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OPENTitle: Functional Impairment in Miro Degradation and Mitophagy Is a Shared Feature in Familial and Sporadic Parkinson’s DiseaseJournal Name: Cell Stem CellPublisher: Elsevier BVVol: 19Issue #: 6Start Page: 709End Page: 724Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1016/j.stem.2016.08.002Best OA location URL: http://doi.org/10.1016/j.stem.2016.08.002Citation Count: 429
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OPENTitle: Sex differences in brain atrophy and cognitive impairment in Parkinson’s disease patients with and without probable rapid eye movement sleep behavior disorderJournal Name: Journal of NeurologyPublisher: Springer Science and Business Media LLCVol: 269Issue #: 3Start Page: 1591End Page: 1599Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.1007/s00415-021-10728-xBest OA location URL: https://link.springer.com/content/pdf/10.1007/s00415-021-10728-x.pdfCitation Count: 32
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OPENTitle: Impact of excessive daytime sleepiness on the progression of freezing of gait in de novo Parkinson’s disease: a cohort studyJournal Name: Neurological SciencesPublisher: Springer Science and Business Media LLCVol: 46Issue #: 2Start Page:End Page:Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.1007/s10072-024-07738-8Best OA location URL: https://doi.org/10.1007/s10072-024-07738-8Citation Count: 0
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OPENTitle: An interpretable deep learning framework identifies proteomic drivers of Alzheimer’s diseaseJournal Name: Frontiers in Cell and Developmental BiologyPublisher: Frontiers Media SAVol: 12Issue #:Start Page:End Page:Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.3389/fcell.2024.1379984Best OA location URL: https://doi.org/10.3389/fcell.2024.1379984Citation Count: 5
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OPENTitle: Modelling human neuronal catecholaminergic pigmentation in rodents recapitulates age-related neurodegenerative deficitsJournal Name: Nature CommunicationsPublisher: Springer Science and Business Media LLCVol: 15Issue #: 1Start Page:End Page:Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.1038/s41467-024-53168-7Best OA location URL: https://www.nature.com/articles/s41467-024-53168-7.pdfCitation Count: 10
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OPENTitle: Single-cell somatic copy number variants in brain using different amplification methods and reference genomesJournal Name: Communications BiologyPublisher: Springer Science and Business Media LLCVol: 7Issue #: 1Start Page:End Page:Publication Date:Open Access(OA) Status: OPENLicense: cc-by-nc-ndDOI - Digital Object Identifier: 10.1038/s42003-024-06940-wBest OA location URL: https://doi.org/10.1038/s42003-024-06940-wCitation Count: 1
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OPENTitle: SNPs in cytochromes P450 catalyzing cholesterol degradation in brain are associated with Parkinson’s diseaseJournal Name: Frontiers in PharmacologyPublisher: Frontiers Media SAVol: 15Issue #:Start Page:End Page:Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.3389/fphar.2024.1477009Best OA location URL: http://doi.org/10.3389/fphar.2024.1477009Citation Count: 1
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OPENTitle: APOE contributes to longitudinal impulse control disorders progression in Parkinson’s diseaseJournal Name: BMC PsychiatryPublisher: Springer Science and Business Media LLCVol: 24Issue #: 1Start Page:End Page:Publication Date:Open Access(OA) Status: OPENLicense: cc-by-nc-ndDOI - Digital Object Identifier: 10.1186/s12888-024-06084-5Best OA location URL: http://doi.org/10.1186/s12888-024-06084-5Citation Count: 0
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OPENTitle: SVA Regulation of Transposable Element Clustered Transcription within the Major Histocompatibility Complex Genomic Class II Region of the Parkinson’s Progression Markers InitiativeJournal Name: GenesPublisher: MDPI AGVol: 15Issue #: 9Start Page: 1185End Page: 1185Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.3390/genes15091185Best OA location URL: https://doi.org/10.3390/genes15091185Citation Count: 2
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OPENTitle: A Novel MAG Variant Causes Hereditary Spastic Paraplegia in a Consanguineous Pakistani FamilyJournal Name: GenesPublisher: MDPI AGVol: 15Issue #: 9Start Page: 1203End Page: 1203Publication Date:Open Access(OA) Status: OPENLicense: cc-by, cc-by, cc-byDOI - Digital Object Identifier: 10.3390/genes15091203Best OA location URL: http://doi.org/10.3390/genes15091203Citation Count: 1