4751 - 4760 of 8620 Results
Title
Year
- P4‐308: CSF α‐synuclein, BETA‐AMYLOID 1–42 and tau proteins: Relationship to clinical parameters in early Parkinson's disease2012RESTRICTEDTitle: P4‐308: CSF α‐synuclein, BETA‐AMYLOID 1–42 and tau proteins: Relationship to clinical parameters in early Parkinson's diseaseJournal Name: Alzheimer's & DementiaPublisher: WileyVol: 8Issue #: 4S_Part_21Start Page:End Page:Publication Date:Open Access(OA) Status: RESTRICTEDLicense:DOI - Digital Object Identifier: 10.1016/j.jalz.2013.08.089Citation Count: 0
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OPENTitle: A comprehensive screening of copy number variability in dementia with Lewy bodiesJournal Name: Neurobiology of AgingPublisher: Elsevier BVVol: 75Issue #:Start Page: 223.e1End Page: 223.e10Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1016/j.neurobiolaging.2018.10.019Best OA location URL: https://www.sciencedirect.com/science/article/pii/S019745801830383XCitation Count: 16
- It's a double knock‐out! The quaking mouse is a spontaneous deletion of parkin and parkin co‐regulated gene (PACRG)2004RESTRICTEDTitle: It's a double knock‐out! The quaking mouse is a spontaneous deletion of parkin and parkin co‐regulated gene (PACRG)Journal Name: Movement DisordersPublisher: WileyVol: 19Issue #: 1Start Page: 101End Page: 104Publication Date:Open Access(OA) Status: RESTRICTEDLicense:DOI - Digital Object Identifier: 10.1002/mds.20000Citation Count: 57
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OPENTitle: Therapeutic directions for Parkinson's diseaseJournal Name: Movement DisordersPublisher: WileyVol: 25Issue #: S1Start Page:End Page:Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1002/mds.22790Best OA location URL: https://europepmc.org/articles/pmc3110693?pdf=renderCitation Count: 7
- Prevalence of heterozygous mutations in Niemann-Pick type C genes in a cohort of progressive supranuclear palsy2020RESTRICTEDTitle: Prevalence of heterozygous mutations in Niemann-Pick type C genes in a cohort of progressive supranuclear palsyJournal Name: Parkinsonism & Related DisordersPublisher: Elsevier BVVol: 79Issue #:Start Page: 9End Page: 10Publication Date:Open Access(OA) Status: RESTRICTEDLicense:DOI - Digital Object Identifier: 10.1016/j.parkreldis.2020.08.013Citation Count: 4
- Evaluating the Utility of REVEL and CADD for Interpreting Variants in Amyotrophic Lateral Sclerosis Genes2023OPENTitle: Evaluating the Utility of REVEL and CADD for Interpreting Variants in Amyotrophic Lateral Sclerosis GenesJournal Name: Human MutationPublisher: WileyVol: 2023Issue #:Start Page: 1End Page: 16Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.1155/2023/8620557Best OA location URL: https://downloads.hindawi.com/journals/humu/2023/8620557.pdfCitation Count: 0
- Freesurfer cortical normative data for adults using Desikan-Killiany-Tourville and ex vivo protocols2017OPENTitle: Freesurfer cortical normative data for adults using Desikan-Killiany-Tourville and ex vivo protocolsJournal Name: NeuroImagePublisher: Elsevier BVVol: 156Issue #:Start Page: 43End Page: 64Publication Date:Open Access(OA) Status: OPENLicense: other-oaDOI - Digital Object Identifier: 10.1016/j.neuroimage.2017.04.035Best OA location URL: https://www.sciencedirect.com/science/article/am/pii/S1053811917303269?via%3DihubCitation Count: 45
- Chronic administration of cholesterol oximes in mice increases transcription of cytoprotective genes and improves transcriptome alterations induced by alpha-synuclein overexpression in nigrostriatal dopaminergic neurons2014OPENTitle: Chronic administration of cholesterol oximes in mice increases transcription of cytoprotective genes and improves transcriptome alterations induced by alpha-synuclein overexpression in nigrostriatal dopaminergic neuronsJournal Name: Neurobiology of DiseasePublisher: Elsevier BVVol: 69Issue #:Start Page: 263End Page: 275Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1016/j.nbd.2014.05.012Best OA location URL: https://www.ncbi.nlm.nih.gov/pmc/articles/4135465Citation Count: 31
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OPENTitle: A Novel PINK1 p.F385S Loss‐of‐Function Mutation in an Indian Family with Parkinson's DiseaseJournal Name: Movement DisordersPublisher: WileyVol: 39Issue #: 7Start Page: 1217End Page: 1225Publication Date:Open Access(OA) Status: OPENLicense: cc-by-nc-ndDOI - Digital Object Identifier: 10.1002/mds.29792Best OA location URL: https://onlinelibrary.wiley.com/doi/pdfdirect/10.1002/mds.29792Citation Count: 1
- Somatosensory-motor cortex interactions measured using dual-site transcranial magnetic stimulation2019RESTRICTEDTitle: Somatosensory-motor cortex interactions measured using dual-site transcranial magnetic stimulationJournal Name: Brain StimulationPublisher: Elsevier BVVol: 12Issue #: 5Start Page: 1229End Page: 1243Publication Date:Open Access(OA) Status: RESTRICTEDLicense:DOI - Digital Object Identifier: 10.1016/j.brs.2019.04.009Citation Count: 17